{"title":"Musculoskeletal System","description":"","products":[{"product_id":"nurofen-24-cpr-riv-200-mg","title":"NUROFEN 200 MG COATED TABLETS 24 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNUROFEN 200 mg coated tablets\u003cbr\u003e NUROFEN 400 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eNurofen contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) which work by reducing pain and swelling caused by inflammation and fever.\u003cbr\u003e\u003cbr\u003e Nurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003e Nurofen is also indicated as an adjuvant for the symptomatic treatment of fever and influenza.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema) and chest pain. Stop Nurofen immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e \u003cbr\u003e• are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • have previously experienced allergic reactions such as difficulty breathing (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or hives after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e • suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e • suffer from severe heart disease (severe heart failure);\u003cbr\u003e • have suffered from stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e • suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e • is in the last trimester of pregnancy;\u003cbr\u003e • has or must have had heart surgery.\u003cbr\u003e   \u003cbr\u003eDo not give Nurofen to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Nurofen if:\u003cbr\u003e • you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen\"); \u003cbr\u003e• are elderly and\/or have had stomach and intestinal problems (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of stomach-protective medicines (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen\"). Bleeding, ulceration and perforation of the stomach or intestine, which may be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop taking Nurofen and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • are taking medicines which may increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines which may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen\");\u003cbr\u003e • suffer from high blood pressure and\/or severe heart disease (heart failure) as fluid retention, high blood pressure and swelling have been reported in association with NSAID therapy; \u003cbr\u003e• suffer from reduced liver and\/or kidney function, as the habitual use of painkillers such as Nurofen can lead to serious permanent kidney problems (with possible onset of kidney failure). Your doctor will advise you to carry out periodic tests during treatment;\u003cbr\u003e • suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e • suffers from clotting problems; \u003cbr\u003e• suffer from a chronic autoimmune disease that causes problems in various parts of the body, especially the skin (systemic lupus erythematosus) or mixed connective tissue disease, as the risk of aseptic meningitis increases; manifests the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or is suspected, you should stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptoms;\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs containing ibuprofen may cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e • have an infection – see section “Infections” below.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Nurofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eDo not\u003c\/b\u003e give this medicine to children under 12 years of age.\u003cbr\u003e Caution is advised in dehydrated adolescents (12-18 years) as there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • Widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • stomach disturbances, such as heartburn, stomach pain and nausea\u003cbr\u003e • heachache\u003cbr\u003e • dizziness\u003cbr\u003e • skin rashes\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, flatulence, constipation\u003cbr\u003e • increased transaminases, increased alkaline phosphatase, decreased haematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e • brain attack or stroke\u003cbr\u003e • liver damage (hepatotoxicity)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, perforation and bleeding of the stomach and intestines, black stools and vomiting blood\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis)\u003cbr\u003e • severe heart disease (heart failure), swelling and high blood pressure (hypertension) \u003cbr\u003e• severe kidney disease (renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (haematuria), inflammation of the kidney (nephritis), a set of signs and symptoms such as loss of protein in the urine, decreased levels of protein in the blood, accumulation of fluid in the body resulting in swelling, increased levels of lipids or fats in the blood, hypercoagulability of the blood, related to kidney disease (nephrotic syndrome)\u003cbr\u003e • liver damage especially following long-term treatments, hepatitis, jaundice \u003cbr\u003e• reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nose and skin bleeding, bruising on the skin (hematomas)\u003cbr\u003e • aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more common if you have systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e • decrease in hemoglobin levels in the blood\u003cbr\u003e • visual disturbances\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e • respiratory tract disorders including asthma, worsening of asthma, shortness of breath (bronchospasm) and difficulty breathing (dyspnoea) \u003cbr\u003e• worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • inflammation of the pancreas (pancreatitis)\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e • the skin becomes sensitive to light\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day) may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218917658958,"sku":"025634041","price":10.48,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000702.jpg?v=1768737847"},{"product_id":"moment-12-cpr-riv-200-mg","title":"MOMENT 200 MG COATED TABLETS 12 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENT 200 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Moment contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e   \u003cbr\u003eMoment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for: - treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain);\u003cbr\u003e - reduction of feverish and flu symptoms.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Moment\");\u003cbr\u003e - if the patient is a child under 12 years of age; \u003cbr\u003e- if you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines;\u003cbr\u003e - if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - in the presence of serious heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop Moment immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Moment: \u003cbr\u003e- if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Moment\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and if necessary contact your doctor to obtain a prescription for a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"); \u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or anti-blood coagulation agents (e.g. acetylsalicylic acid). See also the section \"Other medicines and Moment\". If gastrointestinal bleeding or ulceration occurs in patients taking Moment, the treatment should be discontinued; \u003cbr\u003e- if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have lost a significant amount of fluid, or if you develop swelling, heart problems or high blood pressure; \u003cbr\u003e- if you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure, as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e- if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Moment can: \u003cbr\u003e- be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys;\u003cbr\u003e - cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Moment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment may hide the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e \u003cbr\u003eIf the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer, or bleeding from the stomach and\/or intestines, or lesions of the skin and\/or mucous membranes, you should stop taking Moment and contact your doctor. These side effects are usually more common in older people.\u003cbr\u003e\u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e   \u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e •pain in the chest, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis); \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the above allergic reactions, go to a hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e   \u003cbr\u003eThe risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function); \u003cbr\u003e• inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations; \u003cbr\u003e• inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase); \u003cbr\u003e• abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly on the skin sores, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218917691726,"sku":"025669019","price":6.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000345.jpg?v=1768737849"},{"product_id":"moment-24-cpr-riv-200-mg","title":"MOMENT 200 MG COATED TABLETS 24 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENT 200 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Moment contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e\u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for: - treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain); \u003cbr\u003e- reduction of feverish and flu symptoms.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Moment\");\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines; \u003cbr\u003e- if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - in the presence of serious heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop Moment immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs; \u003cbr\u003e- if you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Moment\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and if necessary contact your doctor to obtain a prescription for a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"); \u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or anti-blood coagulation agents (e.g. acetylsalicylic acid). See also the section \"Other medicines and Moment\". If gastrointestinal bleeding or ulceration occurs in patients taking Moment, the treatment should be discontinued; \u003cbr\u003e- if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have lost a significant amount of fluid, or if you develop swelling, heart problems or high blood pressure; \u003cbr\u003e- if you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure, as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e- if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Moment can: \u003cbr\u003e- be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys;\u003cbr\u003e - cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Moment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment may hide the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e \u003cbr\u003eIf the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer, or bleeding from the stomach and\/or intestines, or lesions of the skin and\/or mucous membranes, you should stop taking Moment and contact your doctor. These side effects are usually more common in older people.\u003cbr\u003e\u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e   \u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e •pain in the chest, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis); \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the above allergic reactions, go to a hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e   \u003cbr\u003eThe risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function); \u003cbr\u003e• inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations; \u003cbr\u003e• inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase); \u003cbr\u003e• abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly on the skin sores, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218917724494,"sku":"025669072","price":11.36,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005707_9a8e4d39-3bdf-47fe-b093-2641ca6c0001.png?v=1768737852"},{"product_id":"moment-36-cpr-riv-200-mg","title":"MOMENT \"200 MG COATED TABLETS\"36 TABLETS\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENT 200 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Moment contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e\u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for: - treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain); \u003cbr\u003e- reduction of feverish and flu symptoms.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Moment\");\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines; \u003cbr\u003e- if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - in the presence of serious heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop Moment immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs; \u003cbr\u003e- if you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Moment\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and if necessary contact your doctor to obtain a prescription for a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"); \u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or anti-blood coagulation agents (e.g. acetylsalicylic acid). See also the section \"Other medicines and Moment\". If gastrointestinal bleeding or ulceration occurs in patients taking Moment, the treatment should be discontinued; \u003cbr\u003e- if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have lost a significant amount of fluid, or if you develop swelling, heart problems or high blood pressure; \u003cbr\u003e- if you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure, as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e- if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Moment can: \u003cbr\u003e- be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys;\u003cbr\u003e - cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Moment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment may hide the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e \u003cbr\u003eIf the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer, or bleeding from the stomach and\/or intestines, or lesions of the skin and\/or mucous membranes, you should stop taking Moment and contact your doctor. These side effects are usually more common in older people.\u003cbr\u003e\u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e   \u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e •pain in the chest, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis); \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the above allergic reactions, go to a hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e   \u003cbr\u003eThe risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function); \u003cbr\u003e• inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations; \u003cbr\u003e• inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase); \u003cbr\u003e• abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly on the skin sores, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218917790030,"sku":"025669185","price":12.72,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000347.png?v=1768737852"},{"product_id":"moment-12-bust-grat-200-mg","title":"MOMENT 200 MG GRANULES FOR ORAL SOLUTION IN SACHET 12 SACHETS IN PAPER\/PE\/ALU\/SURLYN","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENT 200 mg granules for oral solution\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Moment contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e   \u003cbr\u003eMoment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for the treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain).\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDon't take Moment\u003c\/b\u003e\u003cbr\u003e - If you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6).\u003cbr\u003e - If you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Moment\").\u003cbr\u003e - If the patient is a child under 12 years of age.\u003cbr\u003e - If you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\"). \u003cbr\u003e- If you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer).\u003cbr\u003e - If you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines.\u003cbr\u003e - If you have had two or more distinct episodes of stomach ulcers or bleeding in the past.\u003cbr\u003e - In the presence of serious heart disease (severe heart failure).\u003cbr\u003e - If you have severe liver or kidney disease.\u003cbr\u003e - If you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e - If you suffer from a disease of the metabolism of amino acids, which make up proteins, called phenylketonuria.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop taking Moment immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment.\u003cbr\u003e Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Moment: \u003cbr\u003e- If you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs.\u003cbr\u003e - If you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs).\u003cbr\u003e - If you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Moment\"). \u003cbr\u003e- If you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Moment\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and if necessary contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Moment\").\u003cbr\u003e - If you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"). \u003cbr\u003e- If you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment.\u003cbr\u003e - If you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or anti-blood aggregants (e.g. acetylsalicylic acid). See also the section \"Other medicines and Moment\". If gastrointestinal bleeding or ulceration occurs in patients taking Moment, the treatment should be discontinued. \u003cbr\u003e- If you have high blood pressure and your medicines do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these conditions (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke).\u003cbr\u003e - If you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Moment\").\u003cbr\u003e - If you have lost a significant amount of fluid, or if you develop swelling, heart problems or high blood pressure. \u003cbr\u003e- If you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure, as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk.\u003cbr\u003e - If you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Moment\").\u003cbr\u003e - If you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a disease of the connective tissue, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. \u003cbr\u003eAlthough this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without underlying chronic diseases.\u003cbr\u003e - If you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Moment\").\u003cbr\u003e - If you intend to become pregnant (see section \"Pregnancy, breast-feeding and fertility\").\u003cbr\u003e - If you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\").\u003cbr\u003e - If you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e   \u003cbr\u003eYou should discuss your treatment with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Moment can:\u003cbr\u003e - be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys; \u003cbr\u003e- cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Moment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment may hide the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e\u003cbr\u003e If the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Moment can cause side effects, although not everybody gets them. \u003cbr\u003eThe side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer, or bleeding from the stomach and\/or intestines, or lesions of the skin and\/or mucous membranes, you should stop taking Moment and contact your doctor. These side effects are usually more common in older people.\u003cbr\u003e\u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e\u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e •chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e • skin rashes or lesions, \u003cbr\u003e• mucosal lesions,\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock),\u003cbr\u003e • flaking skin,\u003cbr\u003e • reddish, non-raised, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis),\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome),\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis),\u003cbr\u003e • vision problems,\u003cbr\u003e • liver disease (liver dysfunction), \u003cbr\u003e• bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the allergic reactions listed above, go to the hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e\u003cbr\u003e The risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e   \u003cbr\u003e\u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body (paraesthesia), drowsiness\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea)\u003cbr\u003e • temporary interruption of breathing (apnea)\u003cbr\u003e • vision disorders\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (altered liver function)\u003cbr\u003e • inflammation of the liver (hepatitis)\u003cbr\u003e • yellowing of the skin and eyes (jaundice)\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure) \u003cbr\u003e• hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia)\u003cbr\u003e • reduced clotting ability\u003cbr\u003e • depression, confusion, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis) \u003cbr\u003e• inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome)\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e • high levels of nitrogen in the blood\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase)\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid)\u003cbr\u003e   \u003cbr\u003e\u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling your heart beating (palpitations)\u003cbr\u003e • heart disease (heart failure)\u003cbr\u003e • heart attack (myocardial infarction)\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema)\u003cbr\u003e • liver disease (liver failure)\u003cbr\u003e • hypertension\u003cbr\u003e • serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection\u003cbr\u003e   \u003cbr\u003e\u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach\u003cbr\u003e • nausea\u003cbr\u003e • vomit\u003cbr\u003e • diarrhea\u003cbr\u003e • flatulence\u003cbr\u003e • constipation\u003cbr\u003e • difficulty digesting\u003cbr\u003e • abdominal pain\u003cbr\u003e • heartburn\u003cbr\u003e • blood in the stool\u003cbr\u003e • blood in vomit\u003cbr\u003e • lesions inside the mouth\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease)\u003cbr\u003e • increased risk of sudden reduction in blood circulation in the brain (stroke)\u003cbr\u003e • allergic reactions, anaphylaxis\u003cbr\u003e • Drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell) \u003cbr\u003e• a widespread, red, scaly rash with pustules under the skin and blisters mainly on the skin sores, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218917822798,"sku":"025669211","price":7.12,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000349.png?v=1768737855"},{"product_id":"momendol-24-cpr-riv-220-mg","title":"MOMENDOL \"220 MG FILM-COATED TABLETS\"24 TABLETS\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENDOL 220 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Naproxen sodium\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Momendol belongs to the class of nonsteroidal analgesic-anti-inflammatory-antirheumatic drugs, that is, medicines that fight pain, inflammation, fever and are useful in the symptomatic treatment of rheumatic diseases. \u003cbr\u003eMomendol is used for the short-term symptomatic treatment of mild to moderate pain, such as muscle and joint pain (e.g. back pain, stiff neck), headache, toothache and menstrual pain.\u003cbr\u003e Momendol can also be used to treat fever.\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 7 days of treatment for pain, and after 3 days of treatment for fever.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take MOMENDOL:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to naproxen sodium or any of the other ingredients of this medicine (listed in section 6), or to other chemically related substances;\u003cbr\u003e • if you suffer from allergic reactions, such as asthma, urticaria, rhinitis, nasal polyps, angioedema and allergic reactions induced by acetylsalicylic acid, analgesics, anti-inflammatory and\/or antirheumatic drugs; \u003cbr\u003e• if you have had a history of gastrointestinal bleeding or perforation, active or previous recurrent peptic ulcer, chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease), severe liver failure, severe heart failure, severe renal failure (creatinine clearance \u0026lt;30 ml\/min), angioedema, during intensive therapy with diuretics, in subjects with active haemorrhage and at risk of haemorrhage during therapy with anticoagulants (See \"Other medicines and MOMENDOL\" and \"Warnings and precautions\");\u003cbr\u003e • during pregnancy, starting from the third trimester and during breastfeeding (See \"Pregnancy, breastfeeding and fertility\");\u003cbr\u003e • the medicine cannot be administered to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Momendol: \u003cbr\u003e• since there is a close correlation between dosage and the appearance of severe gastrointestinal side effects. Therefore, the minimum effective dosage should always be used;\u003cbr\u003e • medicines such as MOMENDOL may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke. Any risk is more likely with high doses and prolonged treatment. Do not exceed the recommended dose or duration of treatment (7 days for pain and 3 days for the treatment of fever); \u003cbr\u003e• when MOMENDOL is used in hypertensive patients and\/or in patients with reduced cardiac and\/or renal function. During treatment with MOMENDOL, diuresis and renal function should be well monitored, particularly in the elderly, in patients with cardiac insufficiency or chronic renal insufficiency and in patients treated with diuretics, following major surgical interventions involving large blood loss;\u003cbr\u003e • if you have heart problems, or a history of stroke or think you may be at risk of these conditions (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke) you should discuss your treatment with your doctor or pharmacist;\u003cbr\u003e • when MOMENDOL is used in patients with severe heart failure, worsening of the conditions may occur; \u003cbr\u003e• when MOMENDOL is used in patients with a history of gastrointestinal diseases or liver failure and in patients with current or previous allergic reactions, as in these subjects the product may cause bronchospasm, asthma, or other allergic phenomena. In these cases, particular caution is recommended;\u003cbr\u003e • MOMENDOL must be discontinued at the first appearance of skin rash, mucosal lesions or any other sign of allergy and\/or hypersensitivity;\u003cbr\u003e • if visual disturbances occur, treatment with MOMENDOL must be discontinued;\u003cbr\u003e • since naproxen, like any other anti-inflammatory drug, can mask concomitant symptoms of infectious diseases;\u003cbr\u003e • since in isolated cases, in temporal connection with the use of anti-inflammatory drugs, an aggravation of inflammation on an infectious basis has been reported; \u003cbr\u003e• if used in elderly patients, who generally have some degree of impairment of renal, hepatic and cardiac functions, since this group of patients is more exposed to the risk of developing side effects related to the use of anti-inflammatory drugs. The prolonged use of anti-inflammatory drugs in the elderly is not recommended;\u003cbr\u003e • since naproxen inhibits platelet aggregation and may prolong bleeding time. Patients with coagulation disorders or taking medicinal products that interfere with coagulation should be carefully monitored while taking MOMENDOL;\u003cbr\u003e • when MOMENDOL is used by habitual consumers of high daily doses of alcohol there is a high risk of stomach bleeding; \u003cbr\u003e• the use of the product should be avoided in cases of pain of gastrointestinal origin. It is in fact known that bleeding in the stomach or intestine may occur in patients taking anti-inflammatory drugs;\u003cbr\u003e • in asthmatic patients, the product is generally contraindicated;\u003cbr\u003e • when MOMENDOL is used in combination with other drugs that require caution, see \"Other medicines and MOMENDOL\";\u003cbr\u003e • serious skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with Momendol. If you notice any symptoms of these serious skin reactions, described in section 4, stop taking Momendol and contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e If you are under 16 years of age, it is recommended to contact your doctor.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e \u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most commonly observed adverse effects are gastrointestinal in nature.\u003cbr\u003e The following adverse effects have been reported with NSAIDs and naproxen:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - Headache, drowsiness, dizziness;\u003cbr\u003e - Nausea, dyspepsia, vomiting, heartburn, gastralgia, flatulence.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e - Allergic reaction (including facial swelling and angioedema);\u003cbr\u003e - Sleep disturbances, excitement;\u003cbr\u003e - Vision disturbances;\u003cbr\u003e - Tinnitus, hearing disorders;\u003cbr\u003e - Contusion;\u003cbr\u003e - Diarrhea, constipation;\u003cbr\u003e - Skin rash\/itching;\u003cbr\u003e - Abnormal kidney function;\u003cbr\u003e - Chills, edema (including peripheral edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e \u003cbr\u003e- Peptic ulcer, perforation or gastrointestinal bleeding, sometimes fatal, may occur especially in the elderly, haematemesis, ulcerative stomatitis, aggravated colitis and aggravated Crohn's disease.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e - Hemolytic or aplastic anemia, thrombocytopenia, granulocytopenia;\u003cbr\u003e - Meningitis-like reaction;\u003cbr\u003e - Tachycardia, edema, hypertension and cardiac failure have been observed in association with treatment with NSAIDs;\u003cbr\u003e - Dyspnea, asthma;\u003cbr\u003e - Colitis, stomatitis. Less frequently, gastritis has been observed;\u003cbr\u003e - Jaundice, hepatitis, reduced liver function;\u003cbr\u003e - Photosensitivity, alopecia, bullous disorder including Stevens-Johnson syndrome and toxic epidermal necrolysis;\u003cbr\u003e - Increased blood pressure.\u003cbr\u003e\u003cbr\u003e Stop taking Momendol and contact your doctor immediately if you notice any of the following side effects:\u003cbr\u003e   \u003cbr\u003e\u003cem\u003eNot known:\u003c\/em\u003e frequency cannot be estimated from the available data\u003cbr\u003e - Extensive skin rash, high body temperature, increased liver enzymes, blood abnormalities (eosinophilia), swollen lymph nodes and involvement of other organs (Drug Reaction with Eosinophilia and Systemic Symptoms, also known as DRESS). See also section 2;\u003cbr\u003e - A distinctive allergic skin reaction known as a fixed drug eruption, which usually recurs at the same site or sites with new exposure to the medicine and may appear as round or oval patches with redness and swelling of the skin, a rash with blisters (hives), or an itchy sensation.\u003cbr\u003e\u003cbr\u003e As with other anti-inflammatory drugs, anaphylactic or anaphylactoid allergic reactions may occur in patients with or without previous exposure to drugs of the same class.\u003cbr\u003e   \u003cbr\u003eThe characteristic symptoms of an anaphylactic reaction are: sudden severe hypotension, acceleration or slowing of the heartbeat, unusual tiredness or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, hives with or without angioedema, redness of the skin, nausea, vomiting, crampy abdominal pain, diarrhea.\u003cbr\u003e Medicines like MOMENDOL may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218917888334,"sku":"025829185","price":11.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005490_dc230c28-4bce-451c-8044-c7d9d7a368d4.png?v=1768737857"},{"product_id":"buscofen-12-cps-molli-200-mg","title":"BUSCOFEN \"200 MG SOFT CAPSULES\"12 CAPSULES\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBUSCOFEN 200 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Buscofen contains ibuprofen, a medicine that belongs to the class of anti-inflammatory analgesics, i.e. medicines that fight pain and inflammation.\u003cbr\u003e Buscofen is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for:\u003cbr\u003e - treatment of pain of various origins and natures (menstrual pain, headache, toothache, neuralgia, osteoarticular and muscular pain); \u003cbr\u003e- reduction of feverish and flu symptoms.\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after three days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Buscofen\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Buscofen\");\u003cbr\u003e • if you have ever had bleeding or perforation of the stomach or intestine after taking other medicines;\u003cbr\u003e • if you suffer from stomach and intestinal diseases (for example, active or severe gastrointestinal ulcer);\u003cbr\u003e • if you have had two or more distinct episodes of stomach ulcer or bleeding in the past;\u003cbr\u003e • if you suffer from severe liver or kidney disease; \u003cbr\u003e• if you suffer from severe heart disease (severe heart failure);\u003cbr\u003e • if you suffer from alterations in blood composition (blood dyscrasias);\u003cbr\u003e • if you are in the third trimester (7th-9th month) of pregnancy or if you are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e • if the patient is a child under 12 years of age;\u003cbr\u003e • if you are severely dehydrated (due to vomiting, diarrhoea or insufficient fluid intake).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eTake special care with Buscofen:\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop Buscofen immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cem\u003e\u003cb\u003eSkin reactions\u003c\/b\u003e\u003c\/em\u003e \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Buscofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Buscofen:\u003cbr\u003e • if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs; \u003cbr\u003e• if you suffer from asthma, runny nose (chronic rhinitis), presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e • if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you are elderly or have suffered from ulcers, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Buscofen\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or drugs that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you have suffered from stomach or intestinal diseases related to the use of drugs, and in particular if you are elderly, you should report to your doctor any unusual symptoms of your stomach and intestines (especially bleeding), particularly in the initial stages of treatment;\u003cbr\u003e • if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or blood aggregation inhibitors (e.g. acetylsalicylic acid). See also the section \"Other medicines and Buscofen\". If gastrointestinal bleeding or ulceration occurs in patients taking Buscofen, the treatment should be discontinued; \u003cbr\u003e• if you have suffered or suffer from chronic intestinal diseases such as ulcerative colitis or Crohn's disease, as they may worsen (see section 4 \"Possible side effects\");\u003cbr\u003e • if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported in association with NSAID treatment. NSAIDs may reduce the action of medicines taken to lower blood pressure (see section \"Other medicines and Buscofen\"). Your doctor will prescribe Buscofen only after carefully assessing your condition;\u003cbr\u003e • if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke); \u003cbr\u003e• if you have lost a significant amount of fluid or develop swelling, heart problems or high blood pressure;\u003cbr\u003e • if you have impaired kidney function, heart or liver function problems, or if you are elderly or are taking medicines for high blood pressure as you may be more susceptible to kidney problems. Furthermore, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e • if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you suffer from an autoimmune disease that can affect several organs and tissues of the body (systemic lupus erythematosus), or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without any concomitant chronic diseases;\u003cbr\u003e • if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Buscofen\");\u003cbr\u003e • if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e • if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e• if you have an infection – see section “Infections” below;\u003cbr\u003e • if you develop a skin rash or skin symptoms, you should stop taking ibuprofen immediately, seek medical advice immediately and tell your doctor that you are taking this medicine;\u003cbr\u003e • if you develop symptoms or signs of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) which include rash, fever, swollen lymph nodes and an increase in a type of white blood cell (eosinophilia).\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving medicines such as ibuprofen may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke (loss of blood flow to the brain), especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Buscofen if you have: \u003cbr\u003e• heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Buscofen can:\u003cbr\u003e • be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the functionality of your kidneys;\u003cbr\u003e • cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Buscofen.\u003cbr\u003e\u003cbr\u003e \u003cem\u003e\u003cb\u003eInfections\u003c\/b\u003e\u003c\/em\u003e \u003cbr\u003eBuscofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Buscofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e\u003cbr\u003e Dehydrated adolescents are at risk of kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them. The side effects of the medicine can be minimised if you use the lowest recommended dose and if you use the medicine only for as long as necessary to control your symptoms. \u003cbr\u003eIf you develop an ulcer or bleeding in the stomach and\/or intestine or lesions of the skin and\/or mucous membranes, you must stop treatment with Buscofen and contact your doctor.\u003cbr\u003e These side effects are usually more common in older people.\u003cbr\u003e The use of Buscofen can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP using Buscofen immediately\u003c\/b\u003e and contact your doctor or the nearest hospital where you will be given appropriate and specific treatment:\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly. \u003cbr\u003eIf you experience any of the allergic reactions listed above, go to the hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e\u003cbr\u003e The risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Buscofen and which are listed below according to frequency:\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety; \u003cbr\u003e• numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity).\u003cbr\u003e   \u003cbr\u003e\u003cb\u003erare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome); \u003cbr\u003e• worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using Buscofen if you develop these symptoms and contact your doctor immediately. See also section 2;\u003cbr\u003e • fixed drug eruption (which manifests itself with redness in round or oval patches and swelling of the skin, possibly associated with itching); \u003cbr\u003e• chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"OPELLA HEALTHCARE ITALY SRL","offers":[{"title":"Default Title","offer_id":50218918314318,"sku":"029396037","price":6.8,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0008650_d264b688-bee0-4456-a354-2c249dafdbe7.png?v=1768737880"},{"product_id":"buscofen-24-cps-molli-200-mg","title":"BUSCOFEN 200 MG SOFT CAPSULES, 24 CAPSULES IN AL\/PVC\/PE\/PVDC BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBUSCOFEN 200 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Buscofen contains ibuprofen, a medicine that belongs to the class of anti-inflammatory analgesics, i.e. medicines that fight pain and inflammation. \u003cbr\u003eBuscofen is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for:\u003cbr\u003e - treatment of pain of various origins and natures (menstrual pain, headache, toothache, neuralgia, osteoarticular and muscular pain);\u003cbr\u003e - reduction of feverish and flu symptoms.\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after three days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Buscofen\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Buscofen\");\u003cbr\u003e • if you have ever had bleeding or perforation of the stomach or intestine after taking other medicines; \u003cbr\u003e• if you suffer from stomach and intestinal diseases (for example, active or severe gastrointestinal ulcer);\u003cbr\u003e • if you have had two or more distinct episodes of stomach ulcer or bleeding in the past;\u003cbr\u003e • if you suffer from severe liver or kidney disease;\u003cbr\u003e • if you suffer from severe heart disease (severe heart failure);\u003cbr\u003e • if you suffer from alterations in blood composition (blood dyscrasias);\u003cbr\u003e • if you are in the third trimester (7th-9th month) of pregnancy or if you are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e • if the patient is a child under 12 years of age;\u003cbr\u003e • if you are severely dehydrated (due to vomiting, diarrhoea or insufficient fluid intake).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eTake special care with Buscofen:\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop Buscofen immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cem\u003e\u003cb\u003eSkin reactions\u003c\/b\u003e\u003c\/em\u003e\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Buscofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Buscofen:\u003cbr\u003e • if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs; \u003cbr\u003e• if you suffer from asthma, runny nose (chronic rhinitis), presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e • if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you are elderly or have suffered from ulcers, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Buscofen\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or drugs that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you have suffered from stomach or intestinal diseases related to the use of drugs, and in particular if you are elderly, you should report to your doctor any unusual symptoms of your stomach and intestines (especially bleeding), particularly in the initial stages of treatment;\u003cbr\u003e • if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or blood aggregation inhibitors (e.g. acetylsalicylic acid). See also the section \"Other medicines and Buscofen\". If gastrointestinal bleeding or ulceration occurs in patients taking Buscofen, the treatment should be discontinued; \u003cbr\u003e• if you have suffered or suffer from chronic intestinal diseases such as ulcerative colitis or Crohn's disease, as they may worsen (see section 4 \"Possible side effects\");\u003cbr\u003e • if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported in association with NSAID treatment. NSAIDs may reduce the action of medicines taken to lower blood pressure (see section \"Other medicines and Buscofen\"). Your doctor will prescribe Buscofen only after carefully assessing your condition;\u003cbr\u003e • if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke); \u003cbr\u003e• if you have lost a significant amount of fluid or develop swelling, heart problems or high blood pressure;\u003cbr\u003e • if you have impaired kidney function, heart or liver function problems, or if you are elderly or are taking medicines for high blood pressure as you may be more susceptible to kidney problems. Furthermore, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e • if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Buscofen\"); \u003cbr\u003e• if you suffer from an autoimmune disease that can affect several organs and tissues of the body (systemic lupus erythematosus), or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without any concomitant chronic diseases;\u003cbr\u003e • if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Buscofen\");\u003cbr\u003e • if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e • if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e• if you have an infection – see section “Infections” below;\u003cbr\u003e • if you develop a skin rash or skin symptoms, you should stop taking ibuprofen immediately, seek medical advice immediately and tell your doctor that you are taking this medicine;\u003cbr\u003e • if you develop symptoms or signs of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) which include rash, fever, swollen lymph nodes and an increase in a type of white blood cell (eosinophilia).\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving medicines such as ibuprofen may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke (loss of blood flow to the brain), especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Buscofen if you have: \u003cbr\u003e• heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Buscofen can:\u003cbr\u003e • be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the functionality of your kidneys;\u003cbr\u003e • cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Buscofen.\u003cbr\u003e\u003cbr\u003e \u003cem\u003e\u003cb\u003eInfections\u003c\/b\u003e\u003c\/em\u003e \u003cbr\u003eBuscofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Buscofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e\u003cbr\u003e Dehydrated adolescents are at risk of kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them. The side effects of the medicine can be minimised if you use the lowest recommended dose and if you use the medicine only for as long as necessary to control your symptoms. \u003cbr\u003eIf you develop an ulcer or bleeding in the stomach and\/or intestine or lesions of the skin and\/or mucous membranes, you must stop treatment with Buscofen and contact your doctor.\u003cbr\u003e These side effects are usually more common in older people.\u003cbr\u003e The use of Buscofen can cause side effects that are generally mild or moderate or more serious reactions, even of an allergic type, although rarely.\u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP using Buscofen immediately\u003c\/b\u003e and contact your doctor or the nearest hospital where you will be given appropriate and specific treatment:\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly. \u003cbr\u003eIf you experience any of the allergic reactions listed above, go to the hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e\u003cbr\u003e The risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Buscofen and which are listed below according to frequency:\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety; \u003cbr\u003e• numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity).\u003cbr\u003e   \u003cbr\u003e\u003cb\u003erare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome); \u003cbr\u003e• worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using Buscofen if you develop these symptoms and contact your doctor immediately. See also section 2;\u003cbr\u003e • fixed drug eruption (which manifests itself with redness in round or oval patches and swelling of the skin, possibly associated with itching); \u003cbr\u003e• chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"OPELLA HEALTHCARE ITALY SRL","offers":[{"title":"Default Title","offer_id":50218918347086,"sku":"029396052","price":11.6,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0008649.png?v=1768737880"},{"product_id":"nurofen-febbre-e-dolore-bb-orale-sosp-150-ml-100-mg-5-ml-arancia-senza-zucchero-con-siringa","title":"NUROFEN FEVER D CHILDREN 100 MG\/5 ML ORAL SUSPENSION ORANGE FLAVOUR SUGAR FREE 150 ML BOTTLE WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNurofen Fever and Pain Children 100mg\/5ml oral suspension orange flavour sugar free\u003cbr\u003e Nurofen Fever and Pain Children 100mg\/5ml oral suspension strawberry flavour sugar free\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eNurofen Fever and Pain contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation.\u003cbr\u003e Nurofen Fever and Pain is indicated in \u003cb\u003echildren aged 3 months to 12 years\u003c\/b\u003e for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earache).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking Nurofen Fever and Pain immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not use Nurofen Fever and Pain if the child\u003c\/b\u003e \u003cbr\u003e- are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - you experience or have experienced in the past allergic reactions such as shortness of breath, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, particularly if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - suffer from a serious heart disease (heart failure);\u003cbr\u003e - suffer or have suffered from bleeding in the stomach and\/or intestine (gastrointestinal haemorrhage) or perforation following previous treatments with NSAIDs;\u003cbr\u003e - suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding); \u003cbr\u003e- if you are taking other non-steroidal anti-inflammatory drugs (NSAIDs, including selective COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\");\u003cbr\u003e - if you have any disease that increases the risk of bleeding;\u003cbr\u003e - in case of unclear blood disorders;\u003cbr\u003e - if you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or if you drink very little;\u003cbr\u003e - is less than 3 months old or weighs less than 5.6 kg;\u003cbr\u003e - is in the last trimester of pregnancy (see section \"Pregnancy and breast-feeding\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Nurofen Fever and Pain if your child: \u003cbr\u003e• you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), seasonal allergies (hay fever), polyps in the nose, if you have severe breathing or chest problems, e.g. chronic obstructive pulmonary disease, swelling of the face, lips and throat (angioedema);\u003cbr\u003e • you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen Fever and Pain\"). Bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with Nurofen Fever and Pain and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section \"Possible side effects\");\u003cbr\u003e • if you are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have heart disease (uncontrolled hypertension, congestive heart failure, known ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think your child may be at risk of these conditions (for example, if you have high blood pressure, high levels of sugar (diabetes) or fats in your blood, or if you smoke). Medicines like Nurofen Fever and Pain may be associated with a slightly increased risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses and during prolonged treatment. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e • have an infection (see section \"Infections\" below); \u003cbr\u003e• have chickenpox, in which case it is advisable to avoid the use of Nurofen Fever and Pain.\u003cbr\u003e\u003cbr\u003e The use of Nurofen Fever and Pain requires adequate precautions, especially if the child:\u003cbr\u003e • suffer or have suffered from asthma as it could make breathing difficulties worse;\u003cbr\u003e • suffers from clotting problems or high blood pressure;\u003cbr\u003e • suffers from kidney, heart or liver disease, if he\/she takes drugs that increase urine production (diuretics), or if he\/she has undergone major surgery resulting in loss of fluids, since in these cases your doctor will advise you to perform periodic blood and urine tests on your child;\u003cbr\u003e • has undergone major surgery; \u003cbr\u003e• suffers from certain congenital diseases affecting blood formation (for example acute intermittent porphyria); is dehydrated (for example due to fever, vomiting or diarrhoea), in this case rehydrate him before starting and during treatment to avoid the risk of altering kidney function.\u003cbr\u003e\u003cbr\u003e During prolonged treatment with Nurofen Fever and Pain, you must pay particular attention and inform your doctor immediately if the following occur:\u003cbr\u003e • signs or symptoms of ulceration or bleeding in the stomach and intestines (e.g. black, foul-smelling stools, vomiting blood);\u003cbr\u003e • signs or symptoms of liver damage (e.g. hepatitis and jaundice);\u003cbr\u003e • signs or symptoms of kidney damage (e.g. increased urine production, blood in the urine);\u003cbr\u003e • visual disturbances (blurred or reduced vision, areas of complete or partial blindness, alteration of color perception); \u003cbr\u003e• symptoms such as frequent or daily headaches despite regular use of headache medicines, as they may be caused by excessive use of these medicines;\u003cbr\u003e • symptoms such as headache, disorientation, nausea, vomiting, stiff neck and fever as these could be symptoms due to aseptic meningitis (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen Fever and Pain and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eNurofen Fever and Pain may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen Fever and Pain may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If your child experiences any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e taking Nurofen Fever and Pain and contact your doctor: \u003cbr\u003e• allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), abnormal heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, severe shock and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases);\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis]; \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia);\u003cbr\u003e • skin rashes;\u003cbr\u003e • vision disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing problems;\u003cbr\u003e • cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting; \u003cbr\u003e• hair loss (alopecia);\u003cbr\u003e • the skin becomes sensitive to light;\u003cbr\u003e • severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis); \u003cbr\u003e• simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice);\u003cbr\u003e • severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood;\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotising fasciitis) associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the esophagus (esophagitis); \u003cbr\u003e• a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen Fever and Pain if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218920771918,"sku":"034102020","price":11.44,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0001770.jpg?v=1768737907"},{"product_id":"nurofen-febbre-e-dolore-bb-orale-sosp-150-ml-100-mg-5-ml-fragola-senza-zucchero-con-siringa","title":"NUROFEN FEVER D CHILDREN 100 MG\/5 ML ORAL SUSPENSION STRAWBERRY FLAVOUR SUGAR FREE 150 ML BOTTLE WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eNurofen Fever and Pain Children 100mg\/5ml oral suspension orange flavour sugar free\u003cbr\u003e Nurofen Fever and Pain Children 100mg\/5ml oral suspension strawberry flavour sugar free\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen Fever and Pain contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation.\u003cbr\u003e Nurofen Fever and Pain is indicated in \u003cb\u003echildren aged 3 months to 12 years\u003c\/b\u003e for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earache).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop taking Nurofen Fever and Pain immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not use Nurofen Fever and Pain if the child\u003c\/b\u003e\u003cbr\u003e - are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - you experience or have experienced in the past allergic reactions such as shortness of breath, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, particularly if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - suffer from a serious heart disease (heart failure);\u003cbr\u003e - suffer or have suffered from bleeding in the stomach and\/or intestine (gastrointestinal haemorrhage) or perforation following previous treatments with NSAIDs; \u003cbr\u003e- suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you are taking other non-steroidal anti-inflammatory drugs (NSAIDs, including selective COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\");\u003cbr\u003e - if you have any disease that increases the risk of bleeding;\u003cbr\u003e - in case of unclear blood disorders;\u003cbr\u003e - if you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or if you drink very little;\u003cbr\u003e - is less than 3 months old or weighs less than 5.6 kg;\u003cbr\u003e - is in the last trimester of pregnancy (see section \"Pregnancy and breast-feeding\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Nurofen Fever and Pain if your child: \u003cbr\u003e• you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), seasonal allergies (hay fever), polyps in the nose, if you have severe breathing or chest problems, e.g. chronic obstructive pulmonary disease, swelling of the face, lips and throat (angioedema);\u003cbr\u003e • you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen Fever and Pain\"). Bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with Nurofen Fever and Pain and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section \"Possible side effects\");\u003cbr\u003e • if you are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have heart disease (uncontrolled hypertension, congestive heart failure, known ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think your child may be at risk of these conditions (for example, if you have high blood pressure, high levels of sugar (diabetes) or fats in your blood, or if you smoke). Medicines like Nurofen Fever and Pain may be associated with a slightly increased risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses and during prolonged treatment. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e • have an infection (see section \"Infections\" below); \u003cbr\u003e• have chickenpox, in which case it is advisable to avoid the use of Nurofen Fever and Pain.\u003cbr\u003e\u003cbr\u003e The use of Nurofen Fever and Pain requires adequate precautions, especially if the child:\u003cbr\u003e • suffer or have suffered from asthma as it could make breathing difficulties worse;\u003cbr\u003e • suffers from clotting problems or high blood pressure;\u003cbr\u003e • suffers from kidney, heart or liver disease, if he\/she takes drugs that increase urine production (diuretics), or if he\/she has undergone major surgery resulting in loss of fluids, since in these cases your doctor will advise you to perform periodic blood and urine tests on your child;\u003cbr\u003e • has undergone major surgery; \u003cbr\u003e• suffers from certain congenital diseases affecting blood formation (for example acute intermittent porphyria); is dehydrated (for example due to fever, vomiting or diarrhoea), in this case rehydrate him before starting and during treatment to avoid the risk of altering kidney function.\u003cbr\u003e\u003cbr\u003e During prolonged treatment with Nurofen Fever and Pain, you must pay particular attention and inform your doctor immediately if the following occur:\u003cbr\u003e • signs or symptoms of ulceration or bleeding in the stomach and intestines (e.g. black, foul-smelling stools, vomiting blood);\u003cbr\u003e • signs or symptoms of liver damage (e.g. hepatitis and jaundice);\u003cbr\u003e • signs or symptoms of kidney damage (e.g. increased urine production, blood in the urine);\u003cbr\u003e • visual disturbances (blurred or reduced vision, areas of complete or partial blindness, alteration of color perception); \u003cbr\u003e• symptoms such as frequent or daily headaches despite regular use of headache medicines, as they may be caused by excessive use of these medicines;\u003cbr\u003e • symptoms such as headache, disorientation, nausea, vomiting, stiff neck and fever as these could be symptoms due to aseptic meningitis (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen Fever and Pain and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eNurofen Fever and Pain may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen Fever and Pain may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If your child experiences any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e taking Nurofen Fever and Pain and contact your doctor: \u003cbr\u003e• allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), abnormal heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, severe shock and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases);\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis]; \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia);\u003cbr\u003e • skin rashes;\u003cbr\u003e • vision disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing problems;\u003cbr\u003e • cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting; \u003cbr\u003e• hair loss (alopecia);\u003cbr\u003e • the skin becomes sensitive to light;\u003cbr\u003e • severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis); \u003cbr\u003e• simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice);\u003cbr\u003e • severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood;\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotising fasciitis) associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the esophagus (esophagitis); \u003cbr\u003e• a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen Fever and Pain if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218920804686,"sku":"034102261","price":11.44,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0001769_aceeecf3-e45d-4aa0-96bb-f78a1127acb9.jpg?v=1768737908"},{"product_id":"nurofen-febbre-e-dolore-orale-sosp-100-ml-200-mg-5-ml-arancia-senza-zucchero-con-siringa","title":"NUROFEN FEVER D 200 MG\/5 ML ORAL SUSPENSION ORANGE FLAVOUR SUGAR FREE 100 ML BOTTLE WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eNurofen Fever and Pain 200mg\/5ml oral suspension orange flavour sugar free\u003cbr\u003e Nurofen Fever and Pain 200mg\/5ml oral suspension strawberry flavour sugar free\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen Fever and Pain contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation.\u003cbr\u003e Nurofen Fever and Pain is indicated in \u003cb\u003echildren aged 2 to 12 years, adolescents and adults\u003c\/b\u003e for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earache).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop taking Nurofen Fever and Pain immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not use Nurofen Fever and Pain if:\u003c\/b\u003e\u003cbr\u003e - are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - you experience or have experienced in the past allergic reactions such as shortness of breath, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, particularly if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - suffer from a serious heart disease (heart failure);\u003cbr\u003e - suffer or have suffered from bleeding in the stomach and\/or intestine (gastrointestinal haemorrhage) or perforation following previous treatments with NSAIDs; \u003cbr\u003e- suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you are taking other non-steroidal anti-inflammatory drugs (NSAIDs, including selective COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\");\u003cbr\u003e - the child is under 2 years old;\u003cbr\u003e - is in the last trimester of pregnancy (see section \"Pregnancy, breast-feeding and fertility\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Nurofen Fever and Pain if:\u003cbr\u003e • you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), polyps in the nose, swelling of the face, lips and throat (angioedema); \u003cbr\u003e• you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen Fever and Pain\"). Bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with Nurofen Fever and Pain and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section \"Possible side effects\");\u003cbr\u003e • if you are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen Fever and Pain\"); \u003cbr\u003e• have heart disease (uncontrolled hypertension, congestive heart failure, established ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think you or your child may be at risk of these conditions (for example if you have high blood pressure, high levels of sugar (diabetes) or fats in your blood or if you smoke). Medicines like Nurofen Fever and Pain may be associated with a slightly increased risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses and during prolonged treatment. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e • have an infection (see section \"Infections\" below); \u003cbr\u003e• have chickenpox, in which case it is advisable to avoid the use of Nurofen Fever and Pain.\u003cbr\u003e\u003cbr\u003e The use of Nurofen Fever and Pain requires adequate precautions, particularly if:\u003cbr\u003e • suffer or have suffered from asthma as it could make breathing difficulties worse;\u003cbr\u003e • suffers from clotting problems;\u003cbr\u003e • suffers from kidney, heart, liver disease and hypertension;\u003cbr\u003e • the child or adolescent is dehydrated (for example due to fever, vomiting or diarrhoea), in this case rehydrate them before starting and during treatment to avoid the risk of altering kidney function.\u003cbr\u003e\u003cbr\u003e During prolonged treatment with Nurofen Fever and Pain, you must pay particular attention and inform your doctor immediately if the following occur:\u003cbr\u003e • signs or symptoms of ulceration or bleeding in the stomach and intestines (e.g. black, foul-smelling stools, vomiting blood);\u003cbr\u003e • signs or symptoms of liver damage (e.g. hepatitis and jaundice); \u003cbr\u003e• signs or symptoms of kidney damage (e.g. increased urine production, blood in the urine);\u003cbr\u003e • visual disturbances (blurred or reduced vision, areas of complete or partial blindness, alteration of color perception);\u003cbr\u003e • symptoms such as headache, disorientation, nausea, vomiting, stiff neck and fever as these could be symptoms due to aseptic meningitis (more common if you suffer from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen Fever and Pain and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eNurofen Fever and Pain may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen Fever and Pain may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e taking Nurofen Fever and Pain and contact your doctor: \u003cbr\u003e• allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more frequent if you suffer from systemic lupus erythematosus or other collagen diseases);\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis]; \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia);\u003cbr\u003e • skin rashes.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing and vision problems;\u003cbr\u003e • cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting;\u003cbr\u003e • hair loss (alopecia); \u003cbr\u003e• the skin becomes sensitive to light;\u003cbr\u003e • severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis);\u003cbr\u003e • simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice); \u003cbr\u003e• severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood;\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotising fasciitis) associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite; \u003cbr\u003e• abnormal perception of noises such as buzzing, ringing or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the esophagus (esophagitis);\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell); \u003cbr\u003e• a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen Fever and Pain if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218920837454,"sku":"034102424","price":14.56,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0001768.jpg?v=1768737909"},{"product_id":"nurofen-influenza-e-raffreddore-12-cpr-riv-200-mg-30-mg","title":"NUROFEN FLU COOL 200 MG + 30 MG COATED TABLETS 12 COATED TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNUROFEN FLU AND COLD 200 mg + 30 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen + Pseudoephedrine hydrochloride\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen Cold and Flu contains two active ingredients:\u003cbr\u003e • ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce the pain and swelling caused by inflammation and to lower fever;\u003cbr\u003e • pseudoephedrine hydrochloride, belongs to a group of medicines called vasoconstrictors which act on the blood vessels inside the nose to relieve nasal congestion.\u003cbr\u003e   \u003cbr\u003eNurofen Cold and Flu is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of cold and flu symptoms such as blocked nose (nasal and sinus congestion), aches, headache, fever and sore throat.\u003cbr\u003e Contact your doctor if you do not feel better or feel worse after 3 days in adolescents over 12 years and after 5 days in adults.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofen Cold and Flu:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen, pseudoephedrine or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if in the past after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs), other medicines to treat fever or pain, you have experienced allergic reactions such as polyps in the nose, wheezing and\/or difficulty breathing (asthma), rhinitis, swelling of the face, lips and throat (angioedema) or hives; \u003cbr\u003e• if you suffer or have suffered from recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of ulcers or bleeding diagnosed);\u003cbr\u003e • if you suffer from severe liver disease (liver failure);\u003cbr\u003e • if you suffer from severe acute (sudden) or chronic (long-term) kidney disease or kidney failure;\u003cbr\u003e • if you suffer from severe heart disease (severe heart failure);\u003cbr\u003e • if you suffer from serious heart or circulation problems such as increased heart rate (tachycardia), very high blood pressure (severe hypertension) or high blood pressure not controlled by medicines, chest pain that occurs when the heart does not receive enough oxygen (angina pectoris);\u003cbr\u003e • if you suffer from overactive thyroid (hyperthyroidism);\u003cbr\u003e • if you suffer from a disease characterised by a high concentration of glucose in the blood (diabetes);\u003cbr\u003e • if you suffer from a tumor affecting the kidney (pheochromocytoma); \u003cbr\u003e• if you suffer from increased intraocular pressure (glaucoma);\u003cbr\u003e • if you suffer from difficulty urinating related to prostate problems;\u003cbr\u003e • if you are under 12 years of age;\u003cbr\u003e • if you are a pregnant or breastfeeding woman;\u003cbr\u003e • if you are taking medicines for depression, such as non-selective monoamine oxidase inhibitors (known as MAOIs) or if you have taken them in the last 14 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Nurofen Cold \u0026amp; Flu if:\u003cbr\u003e • you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors). The concomitant use of these medicines may increase the risk of side effects and should be avoided (see section \"Other medicines and Nurofen Cold and Flu\"); \u003cbr\u003e• suffer from clotting problems or are taking medicines to thin the blood (oral anticoagulants). Your doctor will carefully assess whether you can take this medicine as it may lead to a reduction in clotting (see section \"Other medicines and Nurofen Cold and Flu\");\u003cbr\u003e • you are elderly and\/or have had stomach and intestinal problems (history of ulcer), especially with bleeding or perforation, or if you are taking medicines that may increase the risk of gastrointestinal events. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors);\u003cbr\u003e • suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease); \u003cbr\u003e• are taking medicines that could increase the risk of ulceration or bleeding, medicines used to treat inflammation (oral corticosteroids), medicines used to thin the blood (such as warfarin), antiplatelet drugs (aspirin) and medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen Cold and Flu\");\u003cbr\u003e • have heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or are a smoker;\u003cbr\u003e • suffer from reduced kidney function; \u003cbr\u003e• suffer or have suffered from allergic reactions or episodes of asthma (difficulty breathing) as you may experience shortness of breath;\u003cbr\u003e • suffers from liver disorders;\u003cbr\u003e • in dehydrated adolescents (i.e. those who have lost a lot of fluids through fever, vomiting or diarrhoea) due to the risk of altered kidney function;\u003cbr\u003e • suffers from a chronic autoimmune disease that causes disorders in various parts of the body, particularly the skin (systemic lupus erythematosus) or mixed connective tissue disease, as it increases the risk of aseptic meningitis;\u003cbr\u003e • if you suffer from hyperexcitement;\u003cbr\u003e • if you take medicines that mimic the effects of sympathetic nervous system stimulation on various tissues such as nasal decongestants, appetite suppressants and amphetamine stimulants (see \"Other medicines and Nurofen Cold and Flu\") your doctor will carefully evaluate co-administration; \u003cbr\u003e• if you develop a generalised feverish rash associated with pustules, stop taking Nurofen Cold and Flu and contact your doctor or seek medical advice immediately.\u003cbr\u003e See paragraph 4;\u003cbr\u003e • sudden abdominal pain or rectal bleeding may occur with Nurofen Cold \u0026amp; Flu, due to inflammation of the colon (ischaemic colitis). If you develop these gastrointestinal symptoms, stop taking Nurofen Cold \u0026amp; Flu and contact your doctor or seek medical help immediately. See section 4;\u003cbr\u003e • have an infection. See section \"Infections\" below.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking Nurofen Cold \u0026amp; Flu immediately and contact your doctor or emergency department immediately if you notice any of these signs.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e Bleeding, ulceration or perforation of the stomach or intestine, which can be fatal, has been reported with all NSAIDs at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. If bleeding or ulceration occurs, stop taking Nurofen Cold and Flu and contact your doctor (see section \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e If you have suffered from gastrointestinal problems (gastrointestinal toxicity) in the past, especially if you are elderly, inform your doctor of any uncommon symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment.\u003cbr\u003e   \u003cbr\u003eWith Nurofen Cold and Flu, there may be a reduction in blood flow to the optic nerve. If you experience sudden loss of vision, stop taking Nurofen Cold and Flu and contact your doctor or healthcare provider immediately. See section 4.\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions have been reported in association with treatment with Nurofen Cold and Flu. Stop taking Nurofen Cold and Flu and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eNurofen Cold \u0026amp; Flu may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen Cold \u0026amp; Flu may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e Cases of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS) have been reported following the use of medicinal products containing pseudoephedrine.\u003cbr\u003e PRES and RCVS are rare conditions that can result in reduced blood supply to the brain. \u003cbr\u003eStop using NUROFEN COLD \u0026amp; FLU immediately and seek immediate medical attention if you develop symptoms that could be signs of PRES or RCVS (see section 4 \"Possible side effects\" for symptoms).\u003cbr\u003e\u003cbr\u003e \u003cu\u003e\u003cem\u003eFor those who do sports activities\u003c\/em\u003e\u003c\/u\u003e\u003cbr\u003e The use of the drug without therapeutic need constitutes doping and may still result in positive anti-doping tests.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Do not give this medicine to children under 12 years of age.\u003cbr\u003e In dehydrated adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e   \u003cbr\u003eStop taking NUROFEN COLD \u0026amp; FLU immediately and see a doctor urgently if you develop symptoms that could be signs of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS). These include: sudden onset of severe headache, nausea, vomiting, confusion, convulsions, changes in vision.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • ulcerations or bleeding of the stomach and intestines, not necessarily preceded by warning symptoms or a previous history of serious stomach and intestinal diseases; \u003cbr\u003e• changes in the skin and mucous membranes (rashes, redness, itching, blisters), as they could be signs of serious allergic reactions (exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis). The onset of reactions occurs in most cases in the early stages of treatment;\u003cbr\u003e • difficulty breathing (bronchospasm);\u003cbr\u003e • hallucinations, restlessness or sleep disturbances (see section \"Warnings and precautions\").\u003cbr\u003e\u003cbr\u003e The sudden onset of fever, redness of the skin or numerous small pustules (possible symptoms of Acute Generalised Exanthematous Pustulosis) may occur within the first 2 days of treatment with Nurofen Cold and Flu. See section 2.\u003cbr\u003e Stop using Nurofen Cold \u0026amp; Flu if you develop these symptoms and contact your doctor or seek medical help immediately.\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e \u003cbr\u003e• digestive disorders (dyspepsia), abdominal pain and nausea;\u003cbr\u003e • headache, tremors;\u003cbr\u003e • allergic reactions manifested by hives and itching*;\u003cbr\u003e • skin rashes*;\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, passing gas from the intestines (flatulence) and difficulty in going to the toilet (constipation).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, perforation and bleeding of the stomach and intestines, black stools and vomiting of blood sometimes fatal particularly in the elderly (see section \"Warnings and precautions\");\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis);\u003cbr\u003e • severe kidney disease (severe renal failure including papillary necrosis). Especially during long-term treatment, associated with increased levels of urea in the blood and swelling (oedema);\u003cbr\u003e • liver damage; \u003cbr\u003e• reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis), the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, unexplained bleeding, bruising on the skin (hematomas);\u003cbr\u003e • severe allergic reactions (anaphylaxis, angioedema or severe shock). Symptoms may include swelling of the face, tongue and larynx, difficulty breathing (dyspnoea), rapid heartbeat (tachycardia), low blood pressure (hypotension);\u003cbr\u003e • central nervous system disease of viral origin (aseptic meningitis), with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more frequent if you suffer from systemic lupus erythematosus or mixed connective tissue disease);\u003cbr\u003e • decreased levels of hemoglobin (the substance that carries oxygen) in the blood; \u003cbr\u003e• Blistering skin reactions including Stevens-Johnson syndrome, erythema multiforme and toxic epidermal necrolysis may occur.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • serious conditions affecting the blood vessels in the brain known as posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS);\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • respiratory tract disorders, due to allergic reactions, including shortness of breath and\/or difficulty breathing (asthma), wheezing (bronchospasm) and difficulty breathing (dyspnoea)*;\u003cbr\u003e • high blood pressure (hypertension) (see section \"Warnings and precautions\");\u003cbr\u003e • palpitations, alterations in heart rhythm (tachycardia, arrhythmia);\u003cbr\u003e • swelling (edema);\u003cbr\u003e • chest pain; \u003cbr\u003e• heart failure (see section \"Warnings and precautions\");\u003cbr\u003e • insomnia;\u003cbr\u003e • anxiety;\u003cbr\u003e • agitation;\u003cbr\u003e • restlessness;\u003cbr\u003e • hallucinations;\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease) (see section \"Warnings and precautions\");\u003cbr\u003e • dry mouth;\u003cbr\u003e • excessive sweating;\u003cbr\u003e • muscle weakness;\u003cbr\u003e • reduction in the normal amount of urine during the day;\u003cbr\u003e • irritability;\u003cbr\u003e • thirst;\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen Cold \u0026amp; Flu if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2;\u003cbr\u003e • inflammation of the colon due to insufficient blood supply (ischemic colitis); \u003cbr\u003e• reduction of blood flow to the optic nerve (ischemic optic neuropathy);\u003cbr\u003e • the skin becomes sensitive to light.\u003cbr\u003e\u003cbr\u003e A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell).\u003cbr\u003e   \u003cbr\u003e*Allergic reactions include a) non-specific allergic reactions and anaphylaxis, b) respiratory tract reactivity including asthma, worsening of asthma, bronchospasm or dyspnoea or c) various skin conditions such as various rashes, itching, hives, redness of the skin with bleeding (purpura), marks on the skin and swelling in the area of ​​the eyes and lips (angioedema) and very rarely bullous and exfoliative dermatitis including toxic epidermal necrolysis, Stevens-Johnson syndrome and erythema multiforme) allergic reactions due to pseudoephedrine or similar compounds (cross-reactivity reactions with pseudoephedrine).\u003cbr\u003e\u003cbr\u003e The following side effects have also been reported: gastrointestinal intolerance, bleeding, sweating, dizziness, chest pain (precordial pain), difficulty urinating, and insomnia.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218920870222,"sku":"034246013","price":8.39,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000699.png?v=1768737910"},{"product_id":"nurofen-influenza-e-raffreddore-24-cpr-riv-200-mg-30-mg","title":"NUROFEN INFLUENZA COOL 200 MG + 30 MG COATED TABLETS 24 COATED TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNUROFEN FLU AND COLD 200 mg + 30 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen + Pseudoephedrine hydrochloride\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen Cold and Flu contains two active ingredients:\u003cbr\u003e • ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce the pain and swelling caused by inflammation and to lower fever; \u003cbr\u003e• pseudoephedrine hydrochloride, belongs to a group of medicines called vasoconstrictors which act on the blood vessels inside the nose to relieve nasal congestion.\u003cbr\u003e\u003cbr\u003e Nurofen Cold and Flu is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of cold and flu symptoms such as blocked nose (nasal and sinus congestion), aches, headache, fever and sore throat.\u003cbr\u003e Contact your doctor if you do not feel better or feel worse after 3 days in adolescents over 12 years and after 5 days in adults.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofen Cold and Flu:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen, pseudoephedrine or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e• if in the past after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs), other medicines to treat fever or pain, you have experienced allergic reactions such as polyps in the nose, wheezing and\/or difficulty breathing (asthma), rhinitis, swelling of the face, lips and throat (angioedema) or hives;\u003cbr\u003e • if you suffer or have suffered from recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of ulcers or bleeding diagnosed);\u003cbr\u003e • if you suffer from severe liver disease (liver failure);\u003cbr\u003e • if you suffer from severe acute (sudden) or chronic (long-term) kidney disease or kidney failure;\u003cbr\u003e • if you suffer from severe heart disease (severe heart failure); \u003cbr\u003e• if you suffer from serious heart or circulation problems such as increased heart rate (tachycardia), very high blood pressure (severe hypertension) or high blood pressure not controlled by medicines, chest pain that occurs when the heart does not receive enough oxygen (angina pectoris);\u003cbr\u003e • if you suffer from overactive thyroid (hyperthyroidism);\u003cbr\u003e • if you suffer from a disease characterised by a high concentration of glucose in the blood (diabetes);\u003cbr\u003e • if you suffer from a tumor affecting the kidney (pheochromocytoma);\u003cbr\u003e • if you suffer from increased intraocular pressure (glaucoma);\u003cbr\u003e • if you suffer from difficulty urinating related to prostate problems;\u003cbr\u003e • if you are under 12 years of age;\u003cbr\u003e • if you are a pregnant or breastfeeding woman;\u003cbr\u003e • if you are taking medicines for depression, such as non-selective monoamine oxidase inhibitors (known as MAOIs) or if you have taken them in the last 14 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eTalk to your doctor or pharmacist before taking Nurofen Cold \u0026amp; Flu if:\u003cbr\u003e • you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors). The concomitant use of these medicines may increase the risk of side effects and should be avoided (see section \"Other medicines and Nurofen Cold and Flu\");\u003cbr\u003e • suffer from clotting problems or are taking medicines to thin the blood (oral anticoagulants). Your doctor will carefully assess whether you can take this medicine as it may lead to a reduction in clotting (see section \"Other medicines and Nurofen Cold and Flu\"); \u003cbr\u003e• you are elderly and\/or have suffered from stomach and intestinal disorders (history of ulcer), especially with bleeding or perforation or if you are taking medicines that may increase the risk of gastrointestinal events. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors);\u003cbr\u003e • suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • are taking medicines that could increase the risk of ulceration or bleeding, medicines used to treat inflammation (oral corticosteroids), medicines used to thin the blood (such as warfarin), antiplatelet drugs (aspirin) and medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen Cold and Flu\"); \u003cbr\u003e• have heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or are a smoker;\u003cbr\u003e • suffer from reduced kidney function;\u003cbr\u003e • suffer or have suffered from allergic reactions or episodes of asthma (difficulty breathing) as you may experience shortness of breath;\u003cbr\u003e • suffers from liver disorders;\u003cbr\u003e • in dehydrated adolescents (i.e. those who have lost a lot of fluids through fever, vomiting or diarrhoea) due to the risk of altered kidney function; \u003cbr\u003e• suffers from a chronic autoimmune disease that causes disorders in various parts of the body, particularly the skin (systemic lupus erythematosus) or mixed connective tissue disease, as it increases the risk of aseptic meningitis;\u003cbr\u003e • if you suffer from hyperexcitement;\u003cbr\u003e • if you take medicines that mimic the effects of sympathetic nervous system stimulation on various tissues such as nasal decongestants, appetite suppressants and amphetamine stimulants (see \"Other medicines and Nurofen Cold and Flu\") your doctor will carefully evaluate co-administration;\u003cbr\u003e • if you develop a generalised feverish rash associated with pustules, stop taking Nurofen Cold and Flu and contact your doctor or seek medical advice immediately.\u003cbr\u003e See paragraph 4; \u003cbr\u003e• sudden abdominal pain or rectal bleeding may occur with Nurofen Cold \u0026amp; Flu, due to inflammation of the colon (ischaemic colitis). If you develop these gastrointestinal symptoms, stop taking Nurofen Cold \u0026amp; Flu and contact your doctor or seek medical help immediately. See section 4;\u003cbr\u003e • have an infection. See section \"Infections\" below.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking Nurofen Cold \u0026amp; Flu immediately and contact your doctor or emergency department immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e   \u003cbr\u003eBleeding, ulceration or perforation of the stomach or intestine, which can be fatal, has been reported with all NSAIDs at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. If bleeding or ulceration occurs, stop taking Nurofen Cold and Flu and contact your doctor (see section \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e If you have suffered from gastrointestinal problems (gastrointestinal toxicity) in the past, especially if you are elderly, inform your doctor of any uncommon symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment.\u003cbr\u003e   \u003cbr\u003eWith Nurofen Cold and Flu, there may be a reduction in blood flow to the optic nerve. If you experience sudden loss of vision, stop taking Nurofen Cold and Flu and contact your doctor or healthcare provider immediately. See section 4.\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions have been reported in association with treatment with Nurofen Cold and Flu. Stop taking Nurofen Cold and Flu and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eNurofen Cold \u0026amp; Flu may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen Cold \u0026amp; Flu may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e Cases of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS) have been reported following the use of medicinal products containing pseudoephedrine.\u003cbr\u003e PRES and RCVS are rare conditions that can result in reduced blood supply to the brain. \u003cbr\u003eStop using NUROFEN COLD \u0026amp; FLU immediately and seek immediate medical attention if you develop symptoms that could be signs of PRES or RCVS (see section 4 \"Possible side effects\" for symptoms).\u003cbr\u003e\u003cbr\u003e \u003cu\u003e\u003cem\u003eFor those who do sports activities\u003c\/em\u003e\u003c\/u\u003e\u003cbr\u003e The use of the drug without therapeutic need constitutes doping and may still result in positive anti-doping tests.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Do not give this medicine to children under 12 years of age.\u003cbr\u003e In dehydrated adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e   \u003cbr\u003eStop taking NUROFEN COLD \u0026amp; FLU immediately and see a doctor urgently if you develop symptoms that could be signs of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS). These include: sudden onset of severe headache, nausea, vomiting, confusion, convulsions, changes in vision.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • ulcerations or bleeding of the stomach and intestines, not necessarily preceded by warning symptoms or a previous history of serious stomach and intestinal diseases; \u003cbr\u003e• changes in the skin and mucous membranes (rashes, redness, itching, blisters), as they could be signs of serious allergic reactions (exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis). The onset of reactions occurs in most cases in the early stages of treatment;\u003cbr\u003e • difficulty breathing (bronchospasm);\u003cbr\u003e • hallucinations, restlessness or sleep disturbances (see section \"Warnings and precautions\").\u003cbr\u003e\u003cbr\u003e The sudden onset of fever, redness of the skin or numerous small pustules (possible symptoms of Acute Generalised Exanthematous Pustulosis) may occur within the first 2 days of treatment with Nurofen Cold and Flu. See section 2.\u003cbr\u003e Stop using Nurofen Cold \u0026amp; Flu if you develop these symptoms and contact your doctor or seek medical help immediately.\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e \u003cbr\u003e• digestive disorders (dyspepsia), abdominal pain and nausea;\u003cbr\u003e • headache, tremors;\u003cbr\u003e • allergic reactions manifested by hives and itching*;\u003cbr\u003e • skin rashes*;\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, passing gas from the intestines (flatulence) and difficulty in going to the toilet (constipation).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, perforation and bleeding of the stomach and intestines, black stools and vomiting of blood sometimes fatal particularly in the elderly (see section \"Warnings and precautions\");\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis);\u003cbr\u003e • severe kidney disease (severe renal failure including papillary necrosis). Especially during long-term treatment, associated with increased levels of urea in the blood and swelling (oedema);\u003cbr\u003e • liver damage; \u003cbr\u003e• reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis), the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, unexplained bleeding, bruising on the skin (hematomas);\u003cbr\u003e • severe allergic reactions (anaphylaxis, angioedema or severe shock). Symptoms may include swelling of the face, tongue and larynx, difficulty breathing (dyspnoea), rapid heartbeat (tachycardia), low blood pressure (hypotension);\u003cbr\u003e • central nervous system disease of viral origin (aseptic meningitis), with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more frequent if you suffer from systemic lupus erythematosus or mixed connective tissue disease);\u003cbr\u003e • decreased levels of hemoglobin (the substance that carries oxygen) in the blood; \u003cbr\u003e• Blistering skin reactions including Stevens-Johnson syndrome, erythema multiforme and toxic epidermal necrolysis may occur.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • serious conditions affecting the blood vessels in the brain known as posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS);\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • respiratory tract disorders, due to allergic reactions, including shortness of breath and\/or difficulty breathing (asthma), wheezing (bronchospasm) and difficulty breathing (dyspnoea)*;\u003cbr\u003e • high blood pressure (hypertension) (see section \"Warnings and precautions\");\u003cbr\u003e • palpitations, alterations in heart rhythm (tachycardia, arrhythmia);\u003cbr\u003e • swelling (edema);\u003cbr\u003e • chest pain; \u003cbr\u003e• heart failure (see section \"Warnings and precautions\");\u003cbr\u003e • insomnia;\u003cbr\u003e • anxiety;\u003cbr\u003e • agitation;\u003cbr\u003e • restlessness;\u003cbr\u003e • hallucinations;\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease) (see section \"Warnings and precautions\");\u003cbr\u003e • dry mouth;\u003cbr\u003e • excessive sweating;\u003cbr\u003e • muscle weakness;\u003cbr\u003e • reduction in the normal amount of urine during the day;\u003cbr\u003e • irritability;\u003cbr\u003e • thirst;\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen Cold \u0026amp; Flu if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2;\u003cbr\u003e • inflammation of the colon due to insufficient blood supply (ischemic colitis); \u003cbr\u003e• reduction of blood flow to the optic nerve (ischemic optic neuropathy);\u003cbr\u003e • the skin becomes sensitive to light.\u003cbr\u003e\u003cbr\u003e A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell).\u003cbr\u003e   \u003cbr\u003e*Allergic reactions include a) non-specific allergic reactions and anaphylaxis, b) respiratory tract reactivity including asthma, worsening of asthma, bronchospasm or dyspnoea or c) various skin conditions such as various rashes, itching, hives, redness of the skin with bleeding (purpura), marks on the skin and swelling in the area of ​​the eyes and lips (angioedema) and very rarely bullous and exfoliative dermatitis including toxic epidermal necrolysis, Stevens-Johnson syndrome and erythema multiforme) allergic reactions due to pseudoephedrine or similar compounds (cross-reactivity reactions with pseudoephedrine).\u003cbr\u003e\u003cbr\u003e The following side effects have also been reported: gastrointestinal intolerance, bleeding, sweating, dizziness, chest pain (precordial pain), difficulty urinating, and insomnia.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218920935758,"sku":"034246025","price":16.56,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0003537.jpg?v=1768737911"},{"product_id":"voltaren-emulgel-gel-derm-120-g-1","title":"VOLTAREN EMULGEL 1% GEL 120 G TUBE IN LDPE\/AL\/LLDPE-HDPE MIXTURE-ANTI-BLOCKING ADDITIVE WITH APPLICATOR CAP","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eVoltaren Emulgel 1% gel\u003c\/b\u003e\u003cbr\u003e diclofenac diethylammonium\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Voltaren Emulgel contains the active substance diclofenac diethylammonium. Diclofenac belongs to the class of nonsteroidal anti-inflammatory drugs (NSAIDs) and is used to reduce pain and inflammation.\u003cbr\u003e\u003cbr\u003e Voltaren Emulgel is indicated for the local treatment of painful and inflammatory conditions of rheumatic or traumatic nature affecting:\u003cbr\u003e • joints, e.g. osteoarthritis and arthritis\u003cbr\u003e • muscles, e.g. contractures or injuries\u003cbr\u003e • tendons and ligaments, e.g. tendonitis\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 7 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use Voltaren Emulgel\u003c\/b\u003e \u003cbr\u003e• if you are allergic to diclofenac diethylammonium or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if in the past after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs) you have had an allergic reaction manifested by asthma (difficulty breathing caused by inflammation and narrowing of the bronchi), angioedema (swelling of the face, lips, tongue and\/or throat with difficulty swallowing and\/or breathing), urticaria (itchy skin rash), or acute rhinitis (runny nose due to acute forms of inflammation of the nasal mucosa);\u003cbr\u003e • if you are in the last 3 months of pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e • if the patient is a child or adolescent under 14 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Voltaren Emulgel.\u003cbr\u003e\u003cbr\u003e Pay special attention: \u003cbr\u003e• do not ingest Voltaren Emulgel; after use, in case of contact with the gel, clean your hands with absorbent paper and then wash them (see paragraph 3);\u003cbr\u003e • do not apply Voltaren Emulgel on broken, diseased or open wounds;\u003cbr\u003e • avoid contact of Voltaren Emulgel with your eyes or mucous membranes, such as those of the mouth or vagina. If this occurs, wash the area immediately with running water and contact your doctor;\u003cbr\u003e • do not use Voltaren Emulgel with an occlusive dressing, i.e. covering the affected area with a plastic film that does not allow air to pass through. Instead, you can use Voltaren Emulgel with a gauze that allows air to pass through;\u003cbr\u003e • if you experience skin rashes, stop taking Voltaren Emulgel;\u003cbr\u003e • if you use diclofenac on large areas of skin and for long periods of time, you may experience side effects that involve the whole body; do not exceed the recommended dose.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003eVoltaren Emulgel should not be used in children and adolescents under 14 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • various types of skin reactions characterised by rash, skin irritation, redness, itching and swelling (dermatitis, eczema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the skin with the appearance of blisters (bullous dermatitis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • allergic reactions including hives;\u003cbr\u003e • angioedema (swelling of the face, lips, tongue and\/or throat with difficulty swallowing and\/or breathing)\u003cbr\u003e • skin rash with the appearance of pustules; \u003cbr\u003e• asthma (difficulty breathing caused by inflammation and narrowing of the bronchi);\u003cbr\u003e • appearance of spots or redness on the skin following exposure to sunlight or sunlamps.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSide effects with unknown frequency\u003c\/b\u003e\u003cbr\u003e • burning sensation at the application site;\u003cbr\u003e • dry skin.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"NOVARTIS FARMA SPA","offers":[{"title":"Default Title","offer_id":50218924507470,"sku":"034548204","price":13.52,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/034548204.jpg?v=1768737925"},{"product_id":"voltadvance-20-cpr-riv-25-mg","title":"VOLTADVANCE 25 MG FILM-COATED TABLETS 20 TABLETS IN OPA\/AL\/PVC\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eVoltadvance 25 mg film-coated tablets\u003cbr\u003e Voltadvance 25 mg powder for oral solution\u003c\/b\u003e\u003cbr\u003e Diclofenac sodium\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Voltadvance contains the active substance diclofenac sodium, which belongs to the class of medicines known as nonsteroidal anti-inflammatory drugs (NSAIDs). Voltadvance works by reducing pain and inflammation.\u003cbr\u003e\u003cbr\u003e Voltadvance is indicated for the treatment of pain of various origins and natures, such as:\u003cbr\u003e • joint pain\u003cbr\u003e • back pain (lumbago)\u003cbr\u003e • muscle pain, including stiff neck\u003cbr\u003e • heachache\u003cbr\u003e • toothache\u003cbr\u003e • menstrual cramps\u003cbr\u003e   \u003cbr\u003eTalk to your doctor if you do not feel better or if you feel worse after 2-3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Voltadvance\u003c\/b\u003e\u003cbr\u003e • if you are allergic to diclofenac sodium, acetylsalicylic acid or any other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in section 6)\u003cbr\u003e • if you have an ongoing ulcer, bleeding or perforation of the stomach or intestine\u003cbr\u003e • if you have had bleeding (haemorrhage) from the stomach or intestine or perforation after previous treatments with NSAIDs\u003cbr\u003e • if you have had bleeding or ulcers that occur repeatedly (two or more distinct episodes of proven ulceration or bleeding)\u003cbr\u003e • if you have a severe form of liver or kidney failure \u003cbr\u003e• if you suffer from established heart disease and\/or cerebrovascular disease, e.g. you have had a heart attack, stroke, mini-stroke (TIA) or blockage of the blood vessels to the heart or brain or an operation to remove or avoid such blockages\u003cbr\u003e • if you suffer or have suffered from blood circulation problems (peripheral arterial disease)\u003cbr\u003e • if you think you may be allergic to diclofenac sodium, acetylsalicylic acid, ibuprofen or any other NSAID or any other ingredients of this medicine. Signs of a hypersensitivity reaction include swelling of the face, lips, tongue and\/or throat with difficulty swallowing (angioedema), breathing problems (difficulty breathing, asthma), chest pain, acute rhinitis (runny nose), skin rashes (hives) or any other type of allergic reaction\u003cbr\u003e • if you have an alteration in the production of blood cells \u003cbr\u003e• if you are taking high doses of medicines that increase urine production (diuretics) (see \"Other medicines and Voltadvance\")\u003cbr\u003e • if your stool is dark or contains blood\u003cbr\u003e • if you are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\")\u003cbr\u003e • if you are in the last three months of pregnancy (see section \"Pregnancy, breast-feeding and fertility\")\u003cbr\u003e • if you are under 14 years old\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Voltadvance.\u003cbr\u003e\u003cbr\u003e \u003cu\u003e\u003cb\u003eBefore taking Voltadvance make sure your doctor knows\u003c\/b\u003e\u003c\/u\u003e :\u003cbr\u003e • if you have asthma\u003cbr\u003e • if you have seasonal colds on an allergic basis (allergic rhinitis), swelling of the nasal mucosa (e.g. nasal polyps)\u003cbr\u003e • if you have chronic obstructive pulmonary disease or chronic respiratory tract infections \u003cbr\u003e• if you have liver or kidney problems, unless you have severe liver or kidney failure because in these cases you should not take Voltadvance (see section 2 \"Do not take Voltadvance\"). If you are not sure, ask your doctor.\u003cbr\u003e • if you have hepatic porphyria\u003cbr\u003e • if you have ulcerative colitis or Crohn's disease as these conditions may get worse\u003cbr\u003e • if you are using medicines that increase urine production (diuretics) or other medicines that may affect the way your kidneys work\u003cbr\u003e • if you have low body fluid volume (for example before or after major surgery)\u003cbr\u003e • if you are undergoing or have undergone major surgery\u003cbr\u003e • if you have blood clotting defects (haemostasis defects)\u003cbr\u003e • if you have or have had heart problems\u003cbr\u003e • if he smokes\u003cbr\u003e • if you suffer from diabetes\u003cbr\u003e • if you suffer from angina, blood clots, high blood pressure, increased cholesterol or increased triglycerides \u003cbr\u003e• if you experience signs or symptoms of heart or blood vessel problems such as chest pain, shortness of breath, weakness or difficulty speaking, contact your doctor immediately\u003cbr\u003e • if you have stomach or intestinal problems, unless you have one or more conditions why you should not take Voltadvance (see section \"Do not take Voltadvance\")\u003cbr\u003e • if you are taking medicines that may increase the risk of bleeding, ulceration and perforation such as acetylsalicylic acid (e.g. aspirin) and other NSAIDs, corticosteroids given by mouth, injection or rectally (e.g. cortisone), medicines to thin the blood (anticoagulants and antiplatelet agents), selective serotonin reuptake inhibitors (antidepressants) (see section \"Other medicines and Voltadvance\") \u003cbr\u003e• Tell your doctor if you have recently had or are about to have surgery on your stomach or intestinal tract before receiving\/taking\/using Voltadvance, as Voltadvance can sometimes worsen the healing of the wound in your intestine following surgery.\u003cbr\u003e\u003cbr\u003e In these cases, your doctor will monitor you closely and periodically reassess the need for treatment with Voltadvance. In addition, your doctor may perform periodic tests (such as monitoring of kidney or liver function) to assess your condition during treatment with Voltadvance.\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eStop treatment and tell your doctor if during treatment with Voltadvance you develop\u003c\/u\u003e :\u003c\/b\u003e • gastrointestinal bleeding or ulceration\u003cbr\u003e • skin reactions, because serious skin reactions which may even be fatal have been reported very rarely (see section 4.8) \u003cbr\u003e• mucosal lesions or any other signs of allergic reaction\u003cbr\u003e • fluid retention and swelling from fluid accumulation (edema)\u003cbr\u003e • signs and symptoms of liver problems or if liver function parameters are not normal (visible in blood tests)\u003cbr\u003e • unusual stomach and intestinal symptoms\u003cbr\u003e • worsening of headaches because prolonged use of medicines to reduce headaches can in some cases make them worse\u003cbr\u003e • symptoms of an infection (e.g. headache, fever) or if you notice a worsening of an infection as Voltadvance may hide the signs and symptoms of infection.\u003cbr\u003e\u003cbr\u003e In these cases, your doctor will evaluate whether to continue or stop treatment with Voltadvance.\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eOther important information\u003c\/u\u003e :\u003c\/b\u003e \u003cbr\u003e• Gastrointestinal bleeding, ulceration or perforation, which may be fatal, may occur during treatment with NSAIDs, including diclofenac. The risk of gastrointestinal bleeding is higher with high doses of NSAIDs and in patients who have had ulcers, particularly if complicated by bleeding or perforation. You should take the lowest effective dose of diclofenac to reduce the risk of gastrointestinal toxicity and your doctor may also prescribe medicines (e.g. misoprostol or proton pump inhibitors) to protect the gastrointestinal mucosa.\u003cbr\u003e • Medicines such as Voltadvance may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. Any risk is more likely with high doses or prolonged treatment. \u003cbr\u003e• Undesirable effects can be minimised by using the lowest effective dose for the shortest duration necessary (see section 3 \"How to take Voltadvance\")\u003cbr\u003e • Avoid using diclofenac during treatment with other NSAIDs administered by mouth, injection and rectal administration, including selective cyclooxygenase-2 inhibitors, because it increases the possibility of you experiencing side effects.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Voltadvance is contraindicated in children and adolescents under 14 years of age.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eElderly patients\u003c\/b\u003e\u003cbr\u003e Elderly patients are more likely to experience adverse reactions, especially stomach or intestinal bleeding and perforation, which are usually more severe and can be fatal.\u003cbr\u003e If you are elderly you should take the lowest dose of Voltadvance. \u003cbr\u003eAs a precaution, your doctor may check your kidney function and prescribe medications that work by protecting the gastrointestinal mucosa, such as misoprostol or proton pump inhibitors.\u003cbr\u003e Tell your doctor about any unusual stomach and intestinal symptoms.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If any of these effects occur during treatment with Voltadvance, \u003cb\u003eit is advisable to stop taking the medicine and consult your doctor.\u003c\/b\u003e\u003cbr\u003e Undesirable effects can be minimised by using the lowest effective dose for the shortest duration necessary.\u003cbr\u003e\u003cbr\u003e Some side effects can be serious.\u003cbr\u003e\u003cbr\u003e Stop taking Voltadvance and tell your doctor immediately if you notice: \u003cbr\u003e• Mild abdominal cramps and tenderness that occur shortly after starting treatment with Voltadvance, followed by rectal bleeding or bloody diarrhoea usually within 24 hours of the onset of abdominal pain (frequency not known, cannot be estimated from the available data).\u003cbr\u003e • Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, vertigo\u003cbr\u003e • nausea, vomiting\u003cbr\u003e • diarrhea, gas emission (flatulence)\u003cbr\u003e • problems with digestion (dyspepsia), abdominal pain\u003cbr\u003e • lack or reduction of appetite (anorexia)\u003cbr\u003e • alterations in tests to evaluate liver function (increased transaminases)\u003cbr\u003e • skin rash\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects (may affect up to 1 in 100 people)\u003c\/b\u003e \u003cbr\u003eThese effects occurred after treatment for a long period and with a high dose (150 mg per day).\u003cbr\u003e • heart attack\u003cbr\u003e • heart problems (heart failure)\u003cbr\u003e • awareness of one's heartbeat (palpitations)\u003cbr\u003e • chest pain\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e • allergic reactions, severe allergic reactions even after first use of the medicine (anaphylactic and anaphylactoid reactions) including hypotension and collapse (shock)\u003cbr\u003e • drowsiness\u003cbr\u003e • asthma, difficulty breathing (dyspnea)\u003cbr\u003e • inflammation of the stomach (gastritis), bleeding from the stomach or intestine, vomiting blood (haematemesis), ulcer of the stomach or intestine with or without bleeding and perforation (with possible inflammation of the peritoneum called peritonitis), narrowing of the gastrointestinal tract (stenosis)\u003cbr\u003e • diarrhea accompanied by bleeding, dark stools with blood (melena)\u003cbr\u003e • dry mouth and mucous membranes \u003cbr\u003e• inflammation of the liver (hepatitis), yellowing of the skin, mucous membranes and eyes (jaundice), liver disorders\u003cbr\u003e • urticaria\u003cbr\u003e • swelling from fluid accumulation (edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • abnormal values ​​in blood tests\u003cbr\u003e - reduction in the number of platelets (thrombocytopenia)\u003cbr\u003e - reduction in the number of white blood cells (leukopenia, agranulocytosis)\u003cbr\u003e - anemia (including haemolytic and aplastic anemia)\u003cbr\u003e • abnormal values ​​in urine tests\u003cbr\u003e - presence of blood in the urine (hematuria)\u003cbr\u003e - presence of proteins in the urine (proteinuria)\u003cbr\u003e • swelling of the skin and mucous membranes (angioedema) including facial edema\u003cbr\u003e • disorientation, depression, insomnia, nightmares, irritability, severe mental changes (psychotic reactions)\u003cbr\u003e • worsening of memory, convulsions, anxiety, tremors\u003cbr\u003e • alteration of sensation in the limbs or other parts of the body (paraesthesia)\u003cbr\u003e • taste alterations \u003cbr\u003e• inflammation of the membranes covering the brain and spinal cord (aseptic meningitis), damage to the blood vessels in the brain (cerebrovascular accidents)\u003cbr\u003e • vision disturbances, blurred vision, double vision (diplopia)\u003cbr\u003e • ringing or buzzing in the ears (tinnitus), worsening hearing\u003cbr\u003e • high blood pressure (hypertension)\u003cbr\u003e • inflammation of the blood vessels (vasculitis)\u003cbr\u003e • pneumonia\u003cbr\u003e • inflammation of the colon (colitis) including colitis with bleeding and worsening of ulcerative colitis or Crohn's disease\u003cbr\u003e • constipation (constipation)\u003cbr\u003e • inflammation of the mucosa of the mouth (stomatitis) including stomatitis with ulcers\u003cbr\u003e • inflammation of the tongue (glossitis)\u003cbr\u003e • problems with the esophagus, narrowing of the intestine (intestinal diaphragm disease)\u003cbr\u003e • inflammation of the pancreas (pancreatitis) \u003cbr\u003e• very severe and sudden form of hepatitis (fulminant hepatitis), liver necrosis, impairment of liver function (liver failure)\u003cbr\u003e • skin reactions ranging from mild to life-threatening (bullous eruptions, eczema, erythema, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell's syndrome), exfoliative dermatitis)\u003cbr\u003e • appearance of red-brown spots on the skin (purpura), Henoch-Schonlein purpura, itching\u003cbr\u003e • hair loss\u003cbr\u003e • appearance of spots or redness on the skin following exposure to sunlight or sunlamps\u003cbr\u003e • impairment of kidney function (acute renal failure), nephrotic syndrome, interstitial nephritis, renal papillary necrosis.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSide effects with unknown frequency (frequency cannot be estimated from the available data):\u003c\/b\u003e \u003cbr\u003e• sudden, severe chest pain which may be a symptom of a serious allergic reaction (Kounis syndrome) Medicines like Voltadvance may be associated with a small increased risk of heart attack (infarction) or stroke (see \"Warnings and precautions\" above).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"HALEON ITALY SRL","offers":[{"title":"Default Title","offer_id":50218924671310,"sku":"035500026","price":10.8,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000636_b5b7e2c2-1076-4262-be7e-ae0beda5a2f0.jpg?v=1768753974"},{"product_id":"momentact-12-cpr-riv-400-mg","title":"MOMENTACT 400 MG FILM-COATED TABLETS 12 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENTACT 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eMomentact contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e\u003cbr\u003e Momentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and above\u003c\/b\u003e to treat:\u003cbr\u003e - pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain) and to help reduce the symptoms of fever and flu.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Momentact\"), or allergic to any of the other ingredients of this medicine;\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines;\u003cbr\u003e - if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - in the presence of serious heart disease;\u003cbr\u003e - in the presence of severe liver or kidney disease; \u003cbr\u003e- if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e What you need to know before taking Momentact\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop Momentact immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Serious skin reactions have been reported in association with ibuprofen treatment including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP). \u003cbr\u003eStop taking Momentact and see your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Momentact:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs); \u003cbr\u003e- if you are taking other anti-inflammatory medicines, including selective inhibitors of COX-2 (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Momentact\"); \u003cbr\u003e- if you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Momentact\"), since the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Momentact\");\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"); \u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (serotonin inhibitors), or anti-platelet drugs (e.g. acetylsalicylic acid). See also the section \"Other medicines and Momentact\". If gastrointestinal bleeding or ulceration occurs in patients taking Momentact, the treatment should be discontinued; \u003cbr\u003e- if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or around the edges or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Momentact\");\u003cbr\u003e - if you have lost a significant amount of fluid, or if you develop swelling, heart problems or high blood pressure; \u003cbr\u003e- if you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure, as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from heart disease;\u003cbr\u003e - if you suffer from liver disease (liver dysfunction);\u003cbr\u003e - if you are elderly, as the risk of bleeding, ulcers and perforations is increased compared to other patients;\u003cbr\u003e - if you suffer from a bleeding disorder or are taking medicines to thin your blood (anticoagulants) (see section \"Other medicines and Momentact\"); \u003cbr\u003e- if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a disease of the connective tissue, which is present in many parts of the body, such as bones and cartilage, since on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen.\u003cbr\u003e Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without underlying chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Momentact\");\u003cbr\u003e - if you intend to start a pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e- If you have an infection – see section “Infections” below;\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Momentact can: \u003cbr\u003e- be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys;\u003cbr\u003e - cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, discontinue treatment with Momentact.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Momentact may hide the symptoms of infections such as fever and pain. It is therefore possible that Momentact may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e \u003cbr\u003eIf the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Momentact can cause side effects, although not everybody gets them. The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer, or bleeding from the stomach and\/or intestines, or lesions of the skin and\/or mucous membranes, you should stop taking Momentact and contact your doctor. These side effects are usually more common in older people.\u003cbr\u003e\u003cbr\u003e The use of Momentact can cause side effects that are generally mild or moderate or more serious, allergic-type reactions, although rarely.\u003cbr\u003e   \u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using Momentact immediately\u003c\/b\u003e and contact your doctor or the nearest hospital where you will be given appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome);\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome); \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the allergic reactions listed above, go to the hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e\u003cbr\u003e The risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e   \u003cbr\u003eIn addition, you may experience additional side effects that have also been reported with other medicines similar to Momentact and which are listed below by frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body, drowsiness\u003cbr\u003e • nasal congestion (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea)\u003cbr\u003e • temporary interruption of breathing (apnea)\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (altered liver function)\u003cbr\u003e • inflammation of the liver (hepatitis)\u003cbr\u003e • yellowing of the skin and eyes (jaundice)\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure) \u003cbr\u003e• hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, difficulty breathing (bronchospasm or dyspnoea), asthma attacks with low blood pressure\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia)\u003cbr\u003e • depression, confusion, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis)\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis), especially in patients with pre-existing autoimmune disorders (see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation \u003cbr\u003e• eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling your heart beating (palpitations)*\u003cbr\u003e • heart disease (heart failure)*\u003cbr\u003e • heart attack (myocardial infarction)*\u003cbr\u003e • increased fluid around the lungs (acute pulmonary edema)*\u003cbr\u003e • liver disease (liver failure)\u003cbr\u003e • hypertension* \u003cbr\u003e• serious allergic reactions, which may include symptoms such as swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection\u003cbr\u003e\u003cbr\u003e \u003cb\u003e*these side effects tend to regress with the interruption of treatment\u003cbr\u003e\u003cbr\u003e not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach\u003cbr\u003e • nausea\u003cbr\u003e • vomit\u003cbr\u003e • diarrhea\u003cbr\u003e • flatulence\u003cbr\u003e • constipation\u003cbr\u003e • difficulty digesting\u003cbr\u003e • stomach pain\u003cbr\u003e • heartburn\u003cbr\u003e • blood in the stool\u003cbr\u003e • blood in vomit\u003cbr\u003e • lesions inside the mouth \u003cbr\u003e• worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease)\u003cbr\u003e • increased risk of heart attack (myocardial infarction), or failure of blood supply to the brain (stroke)\u003cbr\u003e • high blood pressure\u003cbr\u003e • severe heart disease (heart failure)\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also section 2 \u003cbr\u003e• chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50218924704078,"sku":"035618026","price":9.36,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005556_96b19da3-946c-4c9a-9e66-df2d4f13d0ca.png?v=1768737934"},{"product_id":"buscofenact-12-cps-molli-400-mg","title":"BUSCOFENACT \"400 MG SOFT CAPSULES\"12 CAPSULES IN BLISTER PVC\/PE\/PVDC-AL\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBuscofenAct 400 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat is it and what is it used for?\u003c\/b\u003e \u003cbr\u003eBuscofenAct contains the active ingredient ibuprofen, which belongs to a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs relieve symptoms by altering the body's response to pain and fever.\u003cbr\u003e\u003cbr\u003e BuscofenAct is indicated for the short-term symptomatic treatment of:\u003cbr\u003e - mild to moderate pain such as headache, toothache, and menstrual cramps;\u003cbr\u003e - fever and pain associated with the common cold.\u003cbr\u003e\u003cbr\u003e BuscofenAct is indicated in adults and adolescents with a body weight greater than 40 kg (12 years and older).\u003cbr\u003e\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse:\u003cbr\u003e - after 3 days in adolescents;\u003cbr\u003e - after 3 days in case of fever, or after 4 days for the treatment of pain in adults.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take BuscofenAct\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you have ever suffered from shortness of breath, asthma, runny nose, swelling or hives after using acetylsalicylic acid or other NSAIDs;\u003cbr\u003e - if you have or have had a history of recurrent stomach\/duodenal ulcer (peptic ulcer) or bleeding (two or more distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you have had a history of gastrointestinal bleeding or perforation related to previous NSAID therapy;\u003cbr\u003e - if you suffer from severe heart failure;\u003cbr\u003e - if you suffer from severe liver failure or severe kidney failure;\u003cbr\u003e - if you suffer from cerebrovascular haemorrhages, or other haemorrhages;\u003cbr\u003e - if you suffer from haematological disorders of unknown origin;\u003cbr\u003e - if you are severely dehydrated (due to vomiting, diarrhea or poor fluid intake);\u003cbr\u003e - if you are in your last trimester of pregnancy.\u003cbr\u003e Do not use BuscofenAct in adolescents with body weight \u0026lt;40 kg and in children under 12 years of age due to the high content of the active ingredient.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eYou should discuss your treatment with your doctor or pharmacist before taking BuscofenAct:\u003cbr\u003e - if you suffer or have suffered from asthma or allergic diseases as shortness of breath may occur;\u003cbr\u003e - if you have liver problems;\u003cbr\u003e - if you have reduced kidney function;\u003cbr\u003e - if you have or have ever had intestinal diseases (ulcerative colitis or Crohn's disease);\u003cbr\u003e - if you have heart problems including heart attack, angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a \"mini stroke\" or \"TIA\" - transient ischaemic attack);\u003cbr\u003e - if you have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - if you suffer from certain skin diseases (Systemic Lupus Erythematosus (SLE) or a mixed connective tissue disease); \u003cbr\u003e- if you have any hereditary disease related to the production of blood cells (acute intermittent porphyria);\u003cbr\u003e - if you have had high blood pressure and\/or heart failure;\u003cbr\u003e - if you have undergone major surgery. In this case, medical supervision is particularly required;\u003cbr\u003e - if you suffer from hay fever, nasal polyps, or chronic obstructive pulmonary disease, as these conditions increase the risk of allergic reactions. Allergic reactions may manifest as asthma attacks (so-called \"pain-induced asthma\"), Quincke's edema, or urticaria;\u003cbr\u003e - if you have a chickenpox infection it is advisable to avoid using BuscofenAct;\u003cbr\u003e - if you suffer from blood clotting disorders;\u003cbr\u003e - in cases of prolonged administration of BuscofenAct, periodic monitoring of liver function, kidney function and blood count is necessary; \u003cbr\u003e- concomitant use of NSAIDs, including specific cyclooxygenase-2 inhibitors, increases the risk of adverse reactions (see paragraph \"Taking BuscofenAct with other medicines\") and should be avoided;\u003cbr\u003e - if you have an infection – see section “Infections” below;\u003cbr\u003e - if you develop a rash or skin symptoms, you should stop taking ibuprofen immediately, seek medical advice immediately, and tell your doctor that you are taking this medicine;\u003cbr\u003e - if you develop symptoms or signs of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) which include rash, fever, swollen lymph nodes and an increase in a type of white blood cell (eosinophilia).\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using BuscofenAct and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e BuscofenAct may mask the symptoms of infections, such as fever and pain. Therefore, BuscofenAct may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms persist or worsen, contact your doctor immediately. \u003cbr\u003eThese side effects can be minimized by using the lowest effective dose for the shortest duration of treatment. Elderly people are at higher risk of side effects.\u003cbr\u003e In general, the habitual use of painkillers can lead to serious, permanent kidney problems. This risk may be increased by physical exertion associated with salt loss and dehydration. Therefore, this should be avoided.\u003cbr\u003e Prolonged use of any type of painkiller for headaches can lead to worsening of the headache. If this occurs or is suspected, you should notify your doctor and discontinue treatment.\u003cbr\u003e The diagnosis of medication-overuse headache (MOH) should be suspected in patients with frequent or daily headaches despite (or because of) the regular use of headache medications.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/painkiller medications such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking BuscofenAct immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e If you think any of the above conditions apply to you, consult your doctor before using BuscofenAct.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated adolescents there is a risk of impaired kidney function.\u003cbr\u003e Do not use BuscofenAct in adolescents with body weight \u0026lt;40 kg and in children under 12 years of age due to the high content of the active ingredient.\u003cbr\u003e\u003cbr\u003e \u003cbr\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e If you experience any of the following known side effects of NSAIDs, or if you have any concerns, stop taking this medicine and consult your doctor as soon as possible. Elderly patients are at greater risk of developing problems associated with side effects.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop taking BuscofenAct immediately and inform your doctor if any of the following conditions occur, which may be a sign of serious adverse events:\u003c\/b\u003e\u003cbr\u003e - severe stomach problems, heartburn or abdominal pain;\u003cbr\u003e - vomit containing blood that looks like coffee grounds;\u003cbr\u003e - black stools or blood in the urine;\u003cbr\u003e - skin reactions, such as itchy rashes;\u003cbr\u003e - difficulty breathing and\/or swelling in the face or throat;\u003cbr\u003e - tiredness associated with loss of appetite;\u003cbr\u003e - sore throat, associated with mouth ulcers, tiredness and fever; \u003cbr\u003e- heavy nosebleeds and skin bleeding;\u003cbr\u003e - abnormal fatigue associated with reduced urine output;\u003cbr\u003e - swelling of the face, feet or legs;\u003cbr\u003e - chest pain;\u003cbr\u003e - vision problems;\u003cbr\u003e - flat, reddish, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e - widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e - widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eTell your doctor if you experience any of the following side effects, if they get worse, or if you notice any side effects not listed.\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cu\u003eCommon frequency (may affect up to 1 in 10 people)\u003c\/u\u003e\u003cbr\u003e - gastrointestinal disorders such as heartburn, abdominal pain, nausea and indigestion, vomiting, flatulence, diarrhea, constipation, and slight bleeding in the stomach and\/or intestines which may cause anemia in exceptional cases.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eUncommon frequency (may affect up to 1 in 100 people)\u003c\/u\u003e\u003cbr\u003e - gastrointestinal ulcers, sometimes with bleeding and perforation, inflammation of the mucosa of the mouth with ulcers (ulcerative stomatitis), inflammation of the stomach (gastritis), worsening of colitis and Crohn's disease;\u003cbr\u003e - central nervous system disorders such as headache, dizziness, insomnia, agitation, irritability or tiredness;\u003cbr\u003e - vision problems;\u003cbr\u003e - various skin rashes; \u003cbr\u003e- allergic reactions such as skin rashes, itching, and asthma attacks (with possible drop in blood pressure). Stop taking BuscofenAct and inform your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRare frequency (may affect up to 1 in 1000 people)\u003c\/u\u003e\u003cbr\u003e - tinnitus (ringing in the ears);\u003cbr\u003e - kidney damage (papillary necrosis) and high concentrations of uric acid in the blood.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eVery rare frequency (may affect up to 1 in 10,000 people)\u003c\/u\u003e\u003cbr\u003e - swelling (edema), high blood pressure (hypertension) and heart failure have been reported in association with NSAID treatment;\u003cbr\u003e - inflammation of the esophagus or pancreas, formation of narrowing in the small and large intestine (in the form of diaphragmatic and intestinal stenosis);\u003cbr\u003e - serious skin infections and soft tissue complications have occurred during chickenpox infection; \u003cbr\u003e- decreased urine output and swelling (especially in patients with high blood pressure or impaired kidney function), swelling (edema) and cloudy urine (nephrotic syndrome), inflammatory kidney disease (interstitial nephritis), which can lead to acute kidney failure. If any of the above symptoms occur or if you feel generally unwell, stop taking BuscofenAct and consult your doctor immediately, as these may be the first signs of kidney damage or kidney failure;\u003cbr\u003e - Disturbances in blood cell production. The first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds, and skin bleeding. In these cases, you should stop treatment immediately and consult your doctor. You should not self-medicate with painkillers or antipyretics;\u003cbr\u003e - psychotic reactions and depression; \u003cbr\u003e- worsening of inflammation associated with infections (e.g., necrotizing fasciitis) has been observed in association with the use of certain painkillers (NSAIDs). If signs of infection develop or worsen while using BuscofenAct, consult your doctor immediately. Antibiotic therapy should be considered;\u003cbr\u003e - hypertension (high blood pressure), vasculitis, palpitations, heart failure, heart attack;\u003cbr\u003e - liver dysfunction (an early sign may be yellowing of the skin), liver damage, especially during long-term treatment, liver failure, acute inflammation of the liver (acute hepatitis);\u003cbr\u003e - Symptoms of aseptic meningitis, including neck stiffness, headache, nausea, vomiting, fever, and blurred consciousness, have been observed with ibuprofen use. Patients with autoimmune diseases (SLE, mixed connective tissue disease) may be more susceptible. \u003cbr\u003eContact your doctor immediately if these symptoms occur;\u003cbr\u003e - severe forms of skin reactions, such as rash with redness and blistering (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis, Lyell's syndrome), hair loss (alopecia);\u003cbr\u003e - severe generalized hypersensitivity reactions.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eFrequency not known (cannot be estimated from the available data)\u003c\/u\u003e\u003cbr\u003e - a widespread, red, scaly rash with pustules under the skin and vesicles located mainly in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using BuscofenAct if you develop these symptoms and contact your doctor immediately. \u003cbr\u003eSee also section 2; - a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell);\u003cbr\u003e - the skin becomes sensitive to light;\u003cbr\u003e - fixed drug eruption (which manifests itself as redness in round or oval patches and swelling of the skin, possibly associated with itching);\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e Medicines such as BuscofenAct may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you experience any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"OPELLA HEALTHCARE ITALY SRL","offers":[{"title":"Default Title","offer_id":50218925850958,"sku":"041631021","price":7.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0008659.png?v=1768737948"},{"product_id":"buscofenact-20-cps-molli-400-mg","title":"BUSCOFENACT 400 MG SOFT CAPSULES, 20 CAPSULES IN PVC\/PE\/PVDC-AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBuscofenAct 400 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat is it and what is it used for?\u003c\/b\u003e\u003cbr\u003e BuscofenAct contains the active ingredient ibuprofen, which belongs to a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs relieve symptoms by altering the body's response to pain and fever.\u003cbr\u003e\u003cbr\u003e BuscofenAct is indicated for the short-term symptomatic treatment of:\u003cbr\u003e - mild to moderate pain such as headache, toothache, and menstrual cramps;\u003cbr\u003e - fever and pain associated with the common cold. \u003cbr\u003e\u003cbr\u003eBuscofenAct is indicated in adults and adolescents with a body weight greater than 40 kg (12 years and older).\u003cbr\u003e\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse:\u003cbr\u003e - after 3 days in adolescents;\u003cbr\u003e - after 3 days in case of fever, or after 4 days for the treatment of pain in adults.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take BuscofenAct\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you have ever suffered from shortness of breath, asthma, runny nose, swelling or hives after using acetylsalicylic acid or other NSAIDs;\u003cbr\u003e - if you have or have had a history of recurrent stomach\/duodenal ulcer (peptic ulcer) or bleeding (two or more distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you have had a history of gastrointestinal bleeding or perforation related to previous NSAID therapy;\u003cbr\u003e - if you suffer from severe heart failure; \u003cbr\u003e- if you suffer from severe liver failure or severe kidney failure;\u003cbr\u003e - if you suffer from cerebrovascular haemorrhages, or other haemorrhages;\u003cbr\u003e - if you suffer from haematological disorders of unknown origin;\u003cbr\u003e - if you are severely dehydrated (due to vomiting, diarrhea or poor fluid intake);\u003cbr\u003e - if you are in your last trimester of pregnancy.\u003cbr\u003e Do not use BuscofenAct in adolescents with body weight \u0026lt;40 kg and in children under 12 years of age due to the high content of the active ingredient.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking BuscofenAct:\u003cbr\u003e - if you suffer or have suffered from asthma or allergic diseases as shortness of breath may occur;\u003cbr\u003e - if you have liver problems;\u003cbr\u003e - if you have reduced kidney function;\u003cbr\u003e - if you have or have ever had intestinal diseases (ulcerative colitis or Crohn's disease); \u003cbr\u003e- if you have heart problems including heart attack, angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a \"mini stroke\" or \"TIA\" - transient ischaemic attack);\u003cbr\u003e - if you have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - if you suffer from certain skin diseases (Systemic Lupus Erythematosus (SLE) or a mixed connective tissue disease);\u003cbr\u003e - if you have any hereditary disease related to the production of blood cells (acute intermittent porphyria);\u003cbr\u003e - if you have had high blood pressure and\/or heart failure;\u003cbr\u003e - if you have undergone major surgery. In this case, medical supervision is particularly required; \u003cbr\u003e- if you suffer from hay fever, nasal polyps, or chronic obstructive pulmonary disease, as these conditions increase the risk of allergic reactions. Allergic reactions may manifest as asthma attacks (so-called \"pain-induced asthma\"), Quincke's edema, or urticaria;\u003cbr\u003e - if you have a chickenpox infection it is advisable to avoid using BuscofenAct;\u003cbr\u003e - if you suffer from blood clotting disorders;\u003cbr\u003e - in cases of prolonged administration of BuscofenAct, periodic monitoring of liver function, kidney function and blood count is necessary;\u003cbr\u003e - concomitant use of NSAIDs, including specific cyclooxygenase-2 inhibitors, increases the risk of adverse reactions (see paragraph \"Taking BuscofenAct with other medicines\") and should be avoided;\u003cbr\u003e - if you have an infection – see section “Infections” below; \u003cbr\u003e- if you develop a rash or skin symptoms, you should stop taking ibuprofen immediately, seek medical advice immediately, and tell your doctor that you are taking this medicine;\u003cbr\u003e - if you develop symptoms or signs of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) which include rash, fever, swollen lymph nodes and an increase in a type of white blood cell (eosinophilia).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using BuscofenAct and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eBuscofenAct may mask the symptoms of infections, such as fever and pain. Therefore, BuscofenAct may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms persist or worsen, contact your doctor immediately.\u003cbr\u003e These side effects can be minimized by using the lowest effective dose for the shortest duration of treatment. Elderly people are at higher risk of side effects.\u003cbr\u003e In general, the habitual use of painkillers can lead to serious, permanent kidney problems. This risk may be increased by physical exertion associated with salt loss and dehydration. Therefore, this should be avoided. \u003cbr\u003eProlonged use of any type of painkiller for headaches can lead to worsening of the headache. If this occurs or is suspected, you should notify your doctor and discontinue treatment.\u003cbr\u003e The diagnosis of medication-overuse headache (MOH) should be suspected in patients with frequent or daily headaches despite (or because of) the regular use of headache medications.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/painkiller medications such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop taking BuscofenAct immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e If you think any of the above conditions apply to you, consult your doctor before using BuscofenAct.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated adolescents there is a risk of impaired kidney function.\u003cbr\u003e Do not use BuscofenAct in adolescents with body weight \u0026lt;40 kg and in children under 12 years of age due to the high content of the active ingredient.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e If you experience any of the following known side effects of NSAIDs, or if you have any concerns, stop taking this medicine and consult your doctor as soon as possible. Elderly patients are at greater risk of developing problems associated with side effects.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eStop taking BuscofenAct immediately and inform your doctor if any of the following conditions occur, which may be a sign of serious adverse events:\u003c\/b\u003e\u003cbr\u003e - severe stomach problems, heartburn or abdominal pain;\u003cbr\u003e - vomit containing blood that looks like coffee grounds;\u003cbr\u003e - black stools or blood in the urine;\u003cbr\u003e - skin reactions, such as itchy rashes;\u003cbr\u003e - difficulty breathing and\/or swelling in the face or throat;\u003cbr\u003e - tiredness associated with loss of appetite;\u003cbr\u003e - sore throat, associated with mouth ulcers, tiredness and fever;\u003cbr\u003e - heavy nosebleeds and skin bleeding;\u003cbr\u003e - abnormal fatigue associated with reduced urine output;\u003cbr\u003e - swelling of the face, feet or legs;\u003cbr\u003e - chest pain;\u003cbr\u003e - vision problems; \u003cbr\u003e- flat, reddish, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e - widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e - widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTell your doctor if you experience any of the following side effects, if they get worse, or if you notice any side effects not listed.\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cu\u003eCommon frequency (may affect up to 1 in 10 people)\u003c\/u\u003e \u003cbr\u003e- gastrointestinal disorders such as heartburn, abdominal pain, nausea and indigestion, vomiting, flatulence, diarrhea, constipation, and slight bleeding in the stomach and\/or intestines which may cause anemia in exceptional cases.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eUncommon frequency (may affect up to 1 in 100 people)\u003c\/u\u003e\u003cbr\u003e - gastrointestinal ulcers, sometimes with bleeding and perforation, inflammation of the mucosa of the mouth with ulcers (ulcerative stomatitis), inflammation of the stomach (gastritis), worsening of colitis and Crohn's disease;\u003cbr\u003e - central nervous system disorders such as headache, dizziness, insomnia, agitation, irritability or tiredness;\u003cbr\u003e - vision problems;\u003cbr\u003e - various skin rashes;\u003cbr\u003e - allergic reactions such as skin rashes, itching, and asthma attacks (with possible drop in blood pressure). Stop taking BuscofenAct and inform your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRare frequency (may affect up to 1 in 1000 people)\u003c\/u\u003e \u003cbr\u003e- tinnitus (ringing in the ears);\u003cbr\u003e - kidney damage (papillary necrosis) and high concentrations of uric acid in the blood.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eVery rare frequency (may affect up to 1 in 10,000 people)\u003c\/u\u003e\u003cbr\u003e - swelling (edema), high blood pressure (hypertension) and heart failure have been reported in association with NSAID treatment;\u003cbr\u003e - inflammation of the esophagus or pancreas, formation of narrowing in the small and large intestine (in the form of diaphragmatic and intestinal stenosis);\u003cbr\u003e - serious skin infections and soft tissue complications have occurred during chickenpox infection; \u003cbr\u003e- decreased urine output and swelling (especially in patients with high blood pressure or impaired kidney function), swelling (edema) and cloudy urine (nephrotic syndrome), inflammatory kidney disease (interstitial nephritis), which can lead to acute kidney failure. If any of the above symptoms occur or if you feel generally unwell, stop taking BuscofenAct and consult your doctor immediately, as these may be the first signs of kidney damage or kidney failure;\u003cbr\u003e - Disturbances in blood cell production. The first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds, and skin bleeding. In these cases, you should stop treatment immediately and consult your doctor. You should not self-medicate with painkillers or antipyretics;\u003cbr\u003e - psychotic reactions and depression; \u003cbr\u003e- worsening of inflammation associated with infections (e.g., necrotizing fasciitis) has been observed in association with the use of certain painkillers (NSAIDs). If signs of infection develop or worsen while using BuscofenAct, consult your doctor immediately. Antibiotic therapy should be considered;\u003cbr\u003e - hypertension (high blood pressure), vasculitis, palpitations, heart failure, heart attack;\u003cbr\u003e - liver dysfunction (an early sign may be yellowing of the skin), liver damage, especially during long-term treatment, liver failure, acute inflammation of the liver (acute hepatitis);\u003cbr\u003e - Symptoms of aseptic meningitis, including neck stiffness, headache, nausea, vomiting, fever, and blurred consciousness, have been observed with ibuprofen use. Patients with autoimmune diseases (SLE, mixed connective tissue disease) may be more susceptible. \u003cbr\u003eContact your doctor immediately if these symptoms occur;\u003cbr\u003e - severe forms of skin reactions, such as rash with redness and blistering (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis, Lyell's syndrome), hair loss (alopecia);\u003cbr\u003e - severe generalized hypersensitivity reactions.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eFrequency not known (cannot be estimated from the available data)\u003c\/u\u003e\u003cbr\u003e - a widespread, red, scaly rash with pustules under the skin and vesicles located mainly in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using BuscofenAct if you develop these symptoms and contact your doctor immediately. \u003cbr\u003eSee also section 2; - a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell);\u003cbr\u003e - the skin becomes sensitive to light;\u003cbr\u003e - fixed drug eruption (which manifests itself as redness in round or oval patches and swelling of the skin, possibly associated with itching);\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e Medicines such as BuscofenAct may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you experience any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"OPELLA HEALTHCARE ITALY SRL","offers":[{"title":"Default Title","offer_id":50218925883726,"sku":"041631033","price":11.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0008658.png?v=1768737949"},{"product_id":"nurofencaps-10-cps-molli-400-mg","title":"NUROFENCAPS 400 MG SOFT CAPSULES 10 CAPSULES IN PVC\/PVDC\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNurofencaps 400 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat is it and what is it for?\u003c\/b\u003e\u003cbr\u003e Ibuprofen belongs to a group of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). These medications provide relief by altering the body's response to pain and fever.\u003cbr\u003e\u003cbr\u003e Nurofencaps is used in adults and adolescents weighing more than 40 kg (from 12 years of age) for the short-term symptomatic treatment of:\u003cbr\u003e • mild to moderate pain such as headache, menstrual cramps and toothache; \u003cbr\u003e• fever and pain associated with the common cold.\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after 3 days in adolescents or after 3 days for fever and 4 days for pain treatment in adults.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofencaps if:\u003c\/b\u003e\u003cbr\u003e • are allergic to the active substance, ponceau 4R (E124) or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • have ever suffered from breathing difficulties, asthma, runny nose, swelling or hives after taking acetylsalicylic acid or other similar pain relievers (NSAIDs);\u003cbr\u003e • have (or have had two or more distinct episodes of) gastric\/duodenal ulcer (peptic ulcer) or stomach bleeding;\u003cbr\u003e • have had gastrointestinal bleeding or perforation following previous treatment with NSAIDs (nonsteroidal anti-inflammatory drugs);\u003cbr\u003e • suffers from unexplained blood formation disorders; \u003cbr\u003e• suffer from severe liver, kidney or heart failure;\u003cbr\u003e • is in the last 3 months of pregnancy (see section \"Pregnancy and breastfeeding\");\u003cbr\u003e • suffers from severe dehydration (caused by vomiting, diarrhea or insufficient fluid intake);\u003cbr\u003e • have bleeding in the brain (cerebrovascular bleeding) or other active bleeding.\u003cbr\u003e\u003cbr\u003e Do not administer to adolescents weighing less than 40 kg or to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Nurofencaps if:\u003cbr\u003e • have an infection – see section “Infections” below;\u003cbr\u003e • have systemic lupus erythematosus (SLE) or mixed connective tissue disease (immune system conditions that cause joint pain, skin rashes, and fever);\u003cbr\u003e • suffer from a certain hereditary disorder of blood formation (e.g. acute intermittent porphyria) or have problems with blood clotting; \u003cbr\u003e• have or have had intestinal diseases (ulcerative colitis or Crohn's disease);\u003cbr\u003e • has reduced kidney function;\u003cbr\u003e • has liver problems;\u003cbr\u003e • has recently undergone major surgery;\u003cbr\u003e • suffer or have suffered from asthma or allergies, as you may experience shortness of breath;\u003cbr\u003e • suffer from hay fever, nasal polyps, or chronic obstructive pulmonary disease, as there is an increased risk of developing allergic reactions. Allergic reactions may manifest themselves in the form of asthma attacks (so-called analgesic asthma), acute swelling (Quincke's edema), or skin rash;\u003cbr\u003e • if you are taking other medicines that may increase the risk of ulceration or bleeding such as oral corticosteroids, medicines to thin the blood (such as warfarin), selective serotonin reuptake inhibitors (medicines for depression) or antiplatelet agents such as acetylsalicylic acid.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther warnings\u003c\/b\u003e \u003cbr\u003e• Prolonged use of painkillers for headaches can worsen symptoms. If this occurs or you suspect this, you should stop taking Nurofencaps and consult your doctor.\u003cbr\u003e • You should avoid taking Nurofencaps if you have chickenpox.\u003cbr\u003e • If you take Nurofencaps for long periods of time, you need to have regular blood tests and have your liver and kidneys checked regularly.\u003cbr\u003e • Taking Nurofencaps in combination with other NSAIDs, including cyclooxygenase-2 selective inhibitors, may increase the risk of side effects and should be avoided (see section \"Other medicines and Nurofencaps\").\u003cbr\u003e • Generally, the habitual use of (different types of) painkillers can lead to serious, long-lasting kidney problems and should be avoided. The risk is further increased by salt loss and dehydration.\u003cbr\u003e • In dehydrated adolescents there is a risk of altered renal function.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e \u003cbr\u003eNurofencaps may mask the symptoms of infections, such as fever and pain. Therefore, Nurofencaps may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Serious skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment.\u003cbr\u003e Stop using Nurofencaps and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/painkiller medications such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Nurofencaps if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain), or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a \"mini-stroke\" or \"TIA\" - transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker. \u003cbr\u003eSigns of an allergic reaction to ibuprofen have been reported, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop taking Nurofencaps immediately and contact your doctor or emergency services immediately if you notice any of these signs. \u003cb\u003eSide effects can be minimized by using the lowest effective dose for the shortest period of time. Elderly people are more at risk of experiencing side effects.\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e Talk to your doctor before taking Nurofencaps if any of the above conditions worry you.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Nurofencaps can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Undesirable effects can be minimized by using the lowest effective dose for the shortest duration possible for symptom relief. \u003cbr\u003eYou may experience one of the known side effects of NSAIDs (see below). If this happens, or if you are concerned, stop taking this medicine and tell your doctor as soon as possible. Elderly people taking this medicine are at greater risk of developing problems associated with side effects.\u003cbr\u003e\u003cbr\u003e STOP TAKING this medicine and consult your doctor immediately if you experience:\u003cbr\u003e • signs of intestinal bleeding such as: severe abdominal pain, dark stools, vomiting blood or dark particles resembling coffee grounds;\u003cbr\u003e • signs of very rare but serious allergic reactions such as worsening of asthma, unexplained wheezing or shortness of breath, swelling of the face, tongue, or throat, difficulty breathing, rapid heartbeat, or a drop in blood pressure leading to shock. These symptoms may occur even when you first use this medicine; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central vesicles, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes.\u003cbr\u003e These serious skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis] [very rare - may affect up to 1 in 10,000 people];\u003cbr\u003e • widespread skin rash, high body temperature, swollen lymph nodes and increased eosinophils (a type of white blood cell) (DRESS syndrome) [not known - frequency cannot be estimated from the available data]; \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters, mainly located in the skin folds, on the trunk and upper limbs, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis) [not known - frequency cannot be estimated from the available data].\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConsult your doctor if you experience any of the following adverse reactions, if they become serious, or if you notice any adverse reactions not listed in the package leaflet.\u003cbr\u003e\u003cbr\u003e Common (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • Gastrointestinal disorders such as heartburn, abdominal pain, nausea, and indigestion, vomiting, flatulence, diarrhea, constipation and slight bleeding in the stomach and\/or intestine which in exceptional cases may cause anemia.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e \u003cbr\u003e• Gastric or intestinal ulcers, sometimes with bleeding and perforation, inflammation of the oral mucosa with ulceration (ulcerative stomatitis), inflammation of the stomach (gastritis), worsening of colitis and Crohn's disease;\u003cbr\u003e • Central nervous system disorders such as headache, dizziness, insomnia, agitation, irritability or tiredness;\u003cbr\u003e • Vision disturbances;\u003cbr\u003e • Allergic reactions, such as skin rashes, itching, and asthma attacks. You should stop taking Nurofencaps and consult your doctor immediately;\u003cbr\u003e • Various skin rashes.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • Tinnitus (ringing in the ears);\u003cbr\u003e • Kidney damage (papillary necrosis) and high concentrations of uric acid in the blood;\u003cbr\u003e • Hearing impairment;\u003cbr\u003e • Increased concentration of urea in the blood;\u003cbr\u003e • Reduction in hemoglobin levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e \u003cbr\u003e• Swelling (edema), high blood pressure (hypertension), and heart failure have been reported in association with NSAID treatment;\u003cbr\u003e • Inflammation of the esophagus or pancreas, formation of membranous strictures in the small and large intestine (diaphragmatic-like intestinal strictures);\u003cbr\u003e • Serious skin infections and soft tissue complications have been reported during chickenpox infection;\u003cbr\u003e • Decreased urine output and swelling (especially in patients with high blood pressure or reduced kidney function); swelling (edema) and cloudy urine (nephrotic syndrome); inflammatory kidney disease (interstitial nephritis), which may lead to acute kidney failure. If you experience any of the above symptoms or if you feel generally unwell, stop taking Nurofencaps and consult your doctor immediately, as these may be the first signs of kidney damage or kidney failure. \u003cbr\u003e• Disturbances in blood cell production. The first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nosebleeds, and skin bleeding. In these cases, you should stop treatment immediately and consult your doctor. Do not treat these symptoms with painkillers or fever-reducing medications (antipyretics);\u003cbr\u003e • Psychotic reactions and depression;\u003cbr\u003e • Worsening of infection-related inflammation (e.g. necrotising fasciitis) has been described in association with the use of some analgesics (NSAIDs). If signs of an infection appear or worsen while using Nurofencaps, contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary;\u003cbr\u003e • High blood pressure, palpitations, heart failure, myocardial infarction; \u003cbr\u003e• Liver dysfunction, liver damage, especially with long periods of treatment, liver failure, acute inflammation of the liver (hepatitis);\u003cbr\u003e • Symptoms of aseptic meningitis, including stiff neck, headache, malaise, nausea, fever, or disorientation, have been observed during ibuprofen use. Patients with autoimmune disorders (SLE, mixed connective tissue disease) may be more susceptible. Contact your doctor immediately if these symptoms occur;\u003cbr\u003e • hair loss (alopecia);\u003cbr\u003e • Severe generalized hypersensitivity reactions;\u003cbr\u003e • Worsening of asthma and bronchospasm;\u003cbr\u003e • Inflammation of blood vessels (vasculitis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • the skin becomes sensitive to light.\u003cbr\u003e   \u003cbr\u003eNurofencaps contains Ponceau 4R (E124) which may cause allergic reactions.\u003cbr\u003e\u003cbr\u003e Medicines such as Nurofencaps may be associated with a small increased risk of heart attack ('myocardial infarction') or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you experience any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50218926145870,"sku":"041860053","price":9.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/041860053.jpg?v=1768737965"},{"product_id":"okitask-orale-grat-10-bust-40-mg","title":"OKITASK 40 MG GRANULES 10 SACHETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eOkitask 40 mg granules\u003c\/b\u003e\u003cbr\u003e Ketoprofen lysine salt\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eOkitask contains ketoprofen which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for treating pain of different origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscular pain and osteoarticular pain (of the bones and joints).\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after a few days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Okitask\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ketoprofen, to other non-steroidal anti-inflammatory drugs (NSAIDs) or to any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you have a history of hypersensitivity (allergy) reactions triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatory drugs) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), urticaria, skin rashes, nasal polyps, angioneurotic oedema (swelling of the skin and mucous membranes) or other allergic-type reactions;\u003cbr\u003e - if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - if you have severe heart failure (inability of the heart to pump an adequate amount of blood to meet the body's needs);\u003cbr\u003e - if you suffer from gastritis (an inflammation of the stomach lining); \u003cbr\u003e- if you currently have a peptic ulcer (a sore in the stomach or upper intestine) or bleeding, or if you have had recurrent peptic ulcer or bleeding in the past (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - if you have suffered in the past from gastrointestinal haemorrhage (bleeding from the stomach or intestine), ulceration, perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - if you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - if you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - if you have severe liver failure (reduced liver function due to liver cirrhosis, severe hepatitis) or renal failure (reduced kidney function);\u003cbr\u003e - if you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets); \u003cbr\u003e- if you suffer from haemorrhagic diathesis (predisposition to developing haemorrhages) and other coagulation disorders or if you have haemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - if you are taking high doses of diuretics;\u003cbr\u003e - if you are in the third trimester of pregnancy;\u003cbr\u003e - if the subject to be treated is under 15 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Okitask.\u003cbr\u003e \u003cem\u003e\u003cu\u003eWarnings\u003c\/u\u003e\u003c\/em\u003e\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose and for the shortest duration necessary to control symptoms (see \"How to take Okitask\" and the sections below on gastrointestinal and cardiovascular risks).\u003cbr\u003e\u003cbr\u003e Concomitant use of Okitask with other anti-inflammatory drugs should be avoided. \u003cbr\u003eGastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported with all NSAIDs, such as Okitask, at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. Patients who have suffered from these conditions in the past are at increased risk (see \"Do not take Okitask\"). \u003cbr\u003eReport any abdominal signs or symptoms (including gastrointestinal bleeding) also at the start of treatment. Tell your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting) such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelets from aggregating) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e Elderly patients are at increased risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which may be fatal.\u003cbr\u003e \u003cb\u003eDiscontinue treatment with Okitask immediately at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e \u003cbr\u003eSerious skin reactions, some of them fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the early stages of treatment. Stop using Okitask if you experience a skin rash, mucosal lesions, or any other sign of hypersensitivity (allergic reaction).\u003cbr\u003e \u003cem\u003e\u003cu\u003ePrecautions\u003c\/u\u003e\u003c\/em\u003e\u003cbr\u003e \u003cb\u003eAsk your doctor or pharmacist for advice before taking Okitask:\u003c\/b\u003e\u003cbr\u003e - if your kidneys are not working well because in this case Okitask must be taken with caution. If you use Okitask you must monitor your kidneys, especially if you are elderly or if you are taking diuretics (medicines that lower blood pressure);\u003cbr\u003e - if you have liver problems you should have periodic check-ups;\u003cbr\u003e - if you have an infection – see section “Infections” below; \u003cbr\u003e- if you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (accumulation of fluid in the lungs, abdominal organs and peripheral tissues due to inadequate pumping function of the heart), established ischaemic heart disease (heart disease that occurs following a reduction in blood flow due to a narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and vessels of the brain), as you should take Okitask only after careful consideration by your doctor;\u003cbr\u003e - if you have risk factors for these conditions, for example if you have high blood pressure, diabetes (a disease caused by high blood glucose levels), hyperlipidaemia (high levels of fats in the blood), or if you smoke;\u003cbr\u003e - if you have allergic reactions or have suffered from allergies in the past, as the medicine must be administered with caution; \u003cbr\u003e- if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or with allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), chronic sinusitis and\/or nasal polyposis;\u003cbr\u003e - if you suffer from haematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (immune system disease) or mixed connective tissue diseases, as Okitask must be used with caution;\u003cbr\u003e - if you have hepatic porphyria (a rare blood disease characterised by the alteration of the activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). There are currently insufficient data to exclude such a risk for OKITASK. \u003cbr\u003eAn increased risk of atrial fibrillation (disturbance in the rhythm of the heartbeat) has been reported with the use of NSAIDs.\u003cbr\u003e Hyperkalaemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, renal insufficiency and\/or are taking medicines that can cause hyperkalaemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Okitask may hide the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately. \u003cbr\u003eContact your doctor if you experience any visual disturbances, such as blurred vision, as treatment should be stopped.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people):\u003cbr\u003e - dyspepsia (difficulty digestion), nausea, abdominal pain and vomiting.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people):\u003cbr\u003e - headache, dizziness, drowsiness;\u003cbr\u003e - constipation, diarrhea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach mucosa);\u003cbr\u003e - skin rash, itching and fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1,000 people): \u003cbr\u003e- haemorrhagic anaemia (reduction of haemoglobin in the blood, the substance that carries oxygen in the blood caused by bleeding);\u003cbr\u003e - paresthesia (sensation of numbness, tingling);\u003cbr\u003e - blurred vision (see \"Warnings and precautions\");\u003cbr\u003e - tinnitus (persistent perception of noises in the ear);\u003cbr\u003e - asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine);\u003cbr\u003e - hepatitis (inflammation of the liver), increased transaminases (increase in some enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function);\u003cbr\u003e - increased weight.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare\u003c\/b\u003e (may affect up to 1 in 10,000 people):\u003cbr\u003e - edema (swelling) of the face and erythema (redness of the skin).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFrequency not known\u003c\/b\u003e (frequency cannot be estimated from the available data): \u003cbr\u003e- thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cell), bone marrow failure (reduction in the production of blood cells by the bone marrow), haemolytic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (reduction in the number of white blood cells), neutropenia (reduction in the number of a type of white blood cells), aplastic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets);\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy); \u003cbr\u003e- jaundice (yellowing of the skin and whites of the eyes);\u003cbr\u003e - depression, hallucination (perception of things that do not exist in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital oedema (swelling around the eye), peripheral oedema;\u003cbr\u003e - chills, asthenia (weakness);\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of the heart rhythm), palpitations (awareness of the heartbeat), tachycardia (increased number of heartbeats), hypertension (high blood pressure), hypotension (low blood pressure); \u003cbr\u003e- vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoplastic vasculitis (inflammation of small vessels);\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with known hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnoea (difficulty breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one case, with fatal outcome, has been reported in an asthmatic patient sensitive to acetylsalicylic acid); \u003cbr\u003e- exacerbation of colitis (worsening of inflammation of the intestine), exacerbation of Crohn's disease (worsening of inflammation of the intestine), gastrointestinal haemorrhage (bleeding from the stomach or intestine), gastrointestinal perforation (sometimes fatal, especially in the elderly, see \"Warnings\"), gastric ulcer (injury to the stomach), mouth ulceration, duodenal ulcer (injury to the upper part of the intestine), duodenal perforation, heartburn, mouth oedema (swelling), pancreatitis (inflammation of the pancreas), melaena (presence of digested blood in the stool), haematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue oedema (swelling of the tongue); \u003cbr\u003e- photosensitivity reactions (sensitivity reaction to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat which may cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (serious skin reactions), oedema (fluid retention), exanthema (skin rash), maculopapular exanthema (patchy skin rash), purpura (purple spots on the skin due to abnormal accumulation of blood), acute generalized exanthematous pustulosis (skin rash with the formation of purulent collections), dermatitis (skin irritation); \u003cbr\u003e- acute renal failure (decrease in kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (kidney impairment resulting in loss of protein in the urine), glomerulonephritis (inflammatory disease of the kidneys), water\/sodium retention with possible oedema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decrease in urine production), abnormal kidney function test, haematuria (blood in the urine);\u003cbr\u003e - aseptic meningitis (inflammation of the membranes covering the brain not caused by infection), lymphangitis (inflammation of the lymph vessels);\u003cbr\u003e - hyperkalemia (increased amount of potassium in the blood), hyponatremia (decreased amount of sodium in the blood).\u003cbr\u003e\u003cbr\u003e Following the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"DOMPE' FARMACEUTICI SPA","offers":[{"title":"Default Title","offer_id":50218926309710,"sku":"042028011","price":5.93,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005071.png?v=1768737970"},{"product_id":"okitask-20-cpr-riv-40-mg","title":"OKITASK 40 MG FILM-COATED TABLET 20 TABLETS IN AL\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eOkitask 40 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ketoprofen lysine salt\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Okitask contains ketoprofen which belongs to a group of medicines called “Non-Steroidal Anti-Inflammatory Drugs” (NSAIDs). Ketoprofen blocks chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for treating pain of different origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscular pain and osteoarticular pain (of the bones and joints).\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - If you are allergic to ketoprofen, to other non-steroidal anti-inflammatory drugs (NSAIDs) or to any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- If you have a history of hypersensitivity (allergy) reactions triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatory drugs) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), urticaria, skin rashes, nasal polyps, angioneurotic oedema (swelling of the skin and mucous membranes) or other allergic-type reactions;\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - If you have severe heart failure (inability of the heart to pump an adequate amount of blood to meet the body's needs);\u003cbr\u003e - If you suffer from gastritis (an inflammation of the stomach lining); \u003cbr\u003e- If you currently have a peptic ulcer (a sore in the stomach or upper intestine) or bleeding, or if you have had recurrent peptic ulcer or bleeding in the past (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - If you have suffered in the past from gastrointestinal haemorrhage (bleeding from the stomach or intestine), ulceration or perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - If you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - If you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - If you have severe liver failure (reduced liver function due to liver cirrhosis, severe hepatitis) or renal failure (reduced kidney function);\u003cbr\u003e - If you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets); \u003cbr\u003e- If you suffer from haemorrhagic diathesis (predisposition to developing haemorrhages) and other coagulation disorders or if you have haemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - If you are taking high doses of diuretics;\u003cbr\u003e - If you are in your third trimester of pregnancy;\u003cbr\u003e - If the subject to be treated is under 15 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Okitask.\u003cbr\u003e \u003cu\u003e\u003cem\u003eWarnings\u003c\/em\u003e\u003c\/u\u003e\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose and for the shortest duration necessary to control symptoms (see \"How to take Okitask\" and the sections below on gastrointestinal and cardiovascular risks). \u003cbr\u003eConcomitant use of Okitask with other anti-inflammatory drugs should be avoided. Gastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported with all NSAIDs, such as Okitask, at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. Patients who have suffered from these conditions in the past are at increased risk (see \"Do not take Okitask\"). \u003cbr\u003eReport any abdominal signs or symptoms (including gastrointestinal bleeding) also at the start of treatment. Tell your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting) such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelets from aggregating) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e The elderly are at increased risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which may be fatal. \u003cb\u003eDiscontinue treatment with Okitask immediately at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e \u003cbr\u003eSerious skin reactions, some of them fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the early stages of treatment. Stop using Okitask if you experience a skin rash, mucosal lesions, or any other sign of hypersensitivity (allergic reaction).\u003cbr\u003e\u003cbr\u003e \u003cem\u003ePrecautions\u003c\/em\u003e\u003cbr\u003e \u003cb\u003eAsk your doctor or pharmacist for advice before taking Okitask\u003c\/b\u003e\u003cbr\u003e - If your kidneys are not working well because in this case Okitask must be taken with caution. If you use Okitask you must monitor your kidneys, especially if you are elderly or if you are taking diuretics (medicines that lower blood pressure).\u003cbr\u003e - If you have liver problems you should have regular check-ups.\u003cbr\u003e - If you have an infection – see section “Infections” below. \u003cbr\u003e- If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (accumulation of fluid in the lungs, abdominal organs and peripheral tissues due to inadequate pumping function of the heart), established ischaemic heart disease (heart disease that occurs following reduced blood flow due to narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and blood vessels of the brain), as you should only take Okitask after careful consideration by your doctor.\u003cbr\u003e - If you have risk factors for these conditions, for example if you have high blood pressure, diabetes (a disease caused by high blood glucose levels), hyperlipidaemia (high levels of fats in the blood), if you smoke.\u003cbr\u003e - If you have allergic reactions or have suffered from allergies in the past, as the medicine should be administered with caution. \u003cbr\u003e- If you suffer from bronchial asthma (inflammation of the bronchi and narrowing of the airways) or allergic diathesis (predisposition to the onset of allergies), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e - If you suffer from haematopoietic disorders (which modify the formation and maturation of blood cells), systemic lupus erythematosus (a disease of the immune system) or mixed connective tissue diseases, as Okitask must be used with caution.\u003cbr\u003e - If you have hepatic porphyria (a rare blood disease characterised by the alteration of the activity of one of the liver enzymes), as the medicine could trigger an attack. \u003cbr\u003eSome NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). There are currently insufficient data to exclude such a risk for OKITASK. An increased risk of atrial fibrillation (alteration of the rhythm of the heartbeat) associated with the use of NSAIDs has been reported. Hyperkalaemia (increase in the amount of potassium in the blood) may occur, especially if you suffer from diabetes, kidney failure and\/or are taking medicines that can cause hyperkalaemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e\u003cbr\u003e Infections \u003cbr\u003eOkitask may hide the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e Contact your doctor if you experience any visual disturbances, such as blurred vision, as treatment should be stopped.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e \u003cbr\u003e- dyspepsia (difficulty digestion), nausea, abdominal pain and vomiting.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - headache, dizziness, drowsiness, constipation, diarrhea, flatulence (passing of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e - skin rash, itching and fatigue\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e - hemorrhagic anemia (reduction of hemoglobin in the blood, the substance that carries oxygen in the blood caused by bleeding)\u003cbr\u003e - paresthesia (sensation of numbness, tingling)\u003cbr\u003e - blurred vision (see \"Warnings and precautions\")\u003cbr\u003e - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e - asthma (bronchial inflammation and narrowing of the airways)\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine) \u003cbr\u003e- hepatitis (inflammation of the liver), increased transaminases (increase in some enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function)\u003cbr\u003e - increased weight.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e - edema (swelling) of the face and erythema (redness of the skin)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFrequency not known (frequency cannot be estimated from the available data)\u003c\/b\u003e \u003cbr\u003e- thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cell), bone marrow failure (reduction in the production of blood cells by the bone marrow), haemolytic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (reduction in the number of white blood cells), neutropenia (reduction in the number of a type of white blood cells), aplastic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets)\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy) \u003cbr\u003e- jaundice (yellowing of the skin and whites of the eyes)\u003cbr\u003e - depression, hallucination (perception of things that do not exist in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital oedema (swelling around the eye), peripheral oedema\u003cbr\u003e - chills, asthenia (weakness)\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of the heart rhythm), palpitations (awareness of the heartbeat), tachycardia (increased number of heartbeats), hypertension (high blood pressure), hypotension (low blood pressure) \u003cbr\u003e- vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoplastic vasculitis (inflammation of small vessels)\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with known hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnoea (difficulty breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one case, with fatal outcome, has been reported in an asthmatic patient sensitive to acetylsalicylic acid) \u003cbr\u003e- exacerbation of colitis (worsening of inflammation of the intestine), exacerbation of Crohn's disease (worsening of inflammation of the intestine), gastrointestinal haemorrhage (bleeding from the stomach or intestine), gastrointestinal perforation (sometimes fatal, especially in the elderly, see \"Warnings\"), gastric ulcer (injury to the stomach), mouth ulceration, duodenal ulcer (injury to the upper part of the intestine), duodenal perforation, heartburn, mouth oedema (swelling), pancreatitis (inflammation of the pancreas), melaena (presence of digested blood in the stool), haematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue oedema (swelling of the tongue) \u003cbr\u003e- photosensitivity reactions (sensitivity reaction to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat which may cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (serious skin reactions), oedema (fluid retention), exanthema (skin rash), maculopapular exanthema (patchy rash), purpura (purple spots on the skin due to abnormal accumulation of blood), acute generalized exanthematous pustulosis (skin rash with the formation of pus-filled collections), dermatitis (skin irritation) \u003cbr\u003e- acute renal failure (decrease in kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (kidney impairment resulting in loss of protein in the urine), glomerulonephritis (inflammatory disease of the kidneys), water\/sodium retention with possible oedema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decrease in urine production), abnormal kidney function test, haematuria (blood in the urine)\u003cbr\u003e - aseptic meningitis (inflammation of the membranes covering the brain not caused by infection), lymphangitis (inflammation of the lymph vessels)\u003cbr\u003e - hyperkalemia (increased amount of potassium in the blood) and hyponatremia (decreased amount of sodium in the blood).\u003cbr\u003e\u003cbr\u003e Following the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"DOMPE' FARMACEUTICI SPA","offers":[{"title":"Default Title","offer_id":50218926342478,"sku":"042028047","price":9.52,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0003827_ba031f9a-5a9e-4b20-8683-26ddf8443044.png?v=1768737969"},{"product_id":"okitask-orale-grat-30-bust-40-mg","title":"OKITASK 40 MG GRANULES 30 PET\/AL\/PE SACHETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eOkitask 40 mg granules\u003c\/b\u003e\u003cbr\u003e Ketoprofen lysine salt\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Okitask contains ketoprofen which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks chemicals that cause inflammation. \u003cbr\u003eOkitask is indicated for treating pain of different origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscular pain and osteoarticular pain (of the bones and joints).\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after a few days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Okitask\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ketoprofen, to other non-steroidal anti-inflammatory drugs (NSAIDs) or to any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you have a history of hypersensitivity (allergy) reactions triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatory drugs) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), urticaria, skin rashes, nasal polyps, angioneurotic oedema (swelling of the skin and mucous membranes) or other allergic-type reactions;\u003cbr\u003e - if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - if you have severe heart failure (inability of the heart to pump an adequate amount of blood to meet the body's needs);\u003cbr\u003e - if you suffer from gastritis (an inflammation of the stomach lining); \u003cbr\u003e- if you currently have a peptic ulcer (a sore in the stomach or upper intestine) or bleeding, or if you have had recurrent peptic ulcer or bleeding in the past (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - if you have suffered in the past from gastrointestinal haemorrhage (bleeding from the stomach or intestine), ulceration, perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - if you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - if you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - if you have severe liver failure (reduced liver function due to liver cirrhosis, severe hepatitis) or renal failure (reduced kidney function);\u003cbr\u003e - if you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets); \u003cbr\u003e- if you suffer from haemorrhagic diathesis (predisposition to developing haemorrhages) and other coagulation disorders or if you have haemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - if you are taking high doses of diuretics;\u003cbr\u003e - if you are in the third trimester of pregnancy;\u003cbr\u003e - if the subject to be treated is under 15 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Okitask.\u003cbr\u003e \u003cem\u003e\u003cu\u003eWarnings\u003c\/u\u003e\u003c\/em\u003e\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose and for the shortest duration necessary to control symptoms (see \"How to take Okitask\" and the sections below on gastrointestinal and cardiovascular risks).\u003cbr\u003e\u003cbr\u003e Concomitant use of Okitask with other anti-inflammatory drugs should be avoided. \u003cbr\u003eGastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported with all NSAIDs, such as Okitask, at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. Patients who have suffered from these conditions in the past are at increased risk (see \"Do not take Okitask\"). \u003cbr\u003eReport any abdominal signs or symptoms (including gastrointestinal bleeding) also at the start of treatment. Tell your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting) such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelets from aggregating) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e Elderly patients are at increased risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which may be fatal.\u003cbr\u003e \u003cb\u003eDiscontinue treatment with Okitask immediately at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e \u003cbr\u003eSerious skin reactions, some of them fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the early stages of treatment. Stop using Okitask if you experience a skin rash, mucosal lesions, or any other sign of hypersensitivity (allergic reaction).\u003cbr\u003e \u003cem\u003e\u003cu\u003ePrecautions\u003c\/u\u003e\u003c\/em\u003e\u003cbr\u003e \u003cb\u003eAsk your doctor or pharmacist for advice before taking Okitask:\u003c\/b\u003e\u003cbr\u003e - if your kidneys are not working well because in this case Okitask must be taken with caution. If you use Okitask you must monitor your kidneys, especially if you are elderly or if you are taking diuretics (medicines that lower blood pressure);\u003cbr\u003e - if you have liver problems you should have periodic check-ups;\u003cbr\u003e - if you have an infection – see section “Infections” below; \u003cbr\u003e- if you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (accumulation of fluid in the lungs, abdominal organs and peripheral tissues due to inadequate pumping function of the heart), established ischaemic heart disease (heart disease that occurs following a reduction in blood flow due to a narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and vessels of the brain), as you should take Okitask only after careful consideration by your doctor;\u003cbr\u003e - if you have risk factors for these conditions, for example if you have high blood pressure, diabetes (a disease caused by high blood glucose levels), hyperlipidaemia (high levels of fats in the blood), or if you smoke;\u003cbr\u003e - if you have allergic reactions or have suffered from allergies in the past, as the medicine must be administered with caution; \u003cbr\u003e- if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or with allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (inflammation of the nasal mucosa of an allergic nature), chronic sinusitis and\/or nasal polyposis;\u003cbr\u003e - if you suffer from haematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (immune system disease) or mixed connective tissue diseases, as Okitask must be used with caution;\u003cbr\u003e - if you have hepatic porphyria (a rare blood disease characterised by the alteration of the activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). There are currently insufficient data to exclude such a risk for OKITASK. \u003cbr\u003eAn increased risk of atrial fibrillation (disturbance in the rhythm of the heartbeat) has been reported with the use of NSAIDs.\u003cbr\u003e Hyperkalaemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, renal insufficiency and\/or are taking medicines that can cause hyperkalaemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Okitask may hide the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately. \u003cbr\u003eContact your doctor if you experience any visual disturbances, such as blurred vision, as treatment should be stopped.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people):\u003cbr\u003e - dyspepsia (difficulty digestion), nausea, abdominal pain and vomiting.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people):\u003cbr\u003e - headache, dizziness, drowsiness;\u003cbr\u003e - constipation, diarrhea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach mucosa);\u003cbr\u003e - skin rash, itching and fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1,000 people): \u003cbr\u003e- haemorrhagic anaemia (reduction of haemoglobin in the blood, the substance that carries oxygen in the blood caused by bleeding);\u003cbr\u003e - paresthesia (sensation of numbness, tingling);\u003cbr\u003e - blurred vision (see \"Warnings and precautions\");\u003cbr\u003e - tinnitus (persistent perception of noises in the ear);\u003cbr\u003e - asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine);\u003cbr\u003e - hepatitis (inflammation of the liver), increased transaminases (increase in some enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function);\u003cbr\u003e - increased weight.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare\u003c\/b\u003e (may affect up to 1 in 10,000 people):\u003cbr\u003e - edema (swelling) of the face and erythema (redness of the skin).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFrequency not known\u003c\/b\u003e (frequency cannot be estimated from the available data): \u003cbr\u003e- thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cell), bone marrow failure (reduction in the production of blood cells by the bone marrow), haemolytic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (reduction in the number of white blood cells), neutropenia (reduction in the number of a type of white blood cells), aplastic anaemia (reduction in the amount of haemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets);\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy); \u003cbr\u003e- jaundice (yellowing of the skin and whites of the eyes);\u003cbr\u003e - depression, hallucination (perception of things that do not exist in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital oedema (swelling around the eye), peripheral oedema;\u003cbr\u003e - chills, asthenia (weakness);\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of the heart rhythm), palpitations (awareness of the heartbeat), tachycardia (increased number of heartbeats), hypertension (high blood pressure), hypotension (low blood pressure); \u003cbr\u003e- vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoplastic vasculitis (inflammation of small vessels);\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with known hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnoea (difficulty breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one case, with fatal outcome, has been reported in an asthmatic patient sensitive to acetylsalicylic acid); \u003cbr\u003e- exacerbation of colitis (worsening of inflammation of the intestine), exacerbation of Crohn's disease (worsening of inflammation of the intestine), gastrointestinal haemorrhage (bleeding from the stomach or intestine), gastrointestinal perforation (sometimes fatal, especially in the elderly, see \"Warnings\"), gastric ulcer (injury to the stomach), mouth ulceration, duodenal ulcer (injury to the upper part of the intestine), duodenal perforation, heartburn, mouth oedema (swelling), pancreatitis (inflammation of the pancreas), melaena (presence of digested blood in the stool), haematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue oedema (swelling of the tongue); \u003cbr\u003e- photosensitivity reactions (sensitivity reaction to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat which may cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (serious skin reactions), oedema (fluid retention), exanthema (skin rash), maculopapular exanthema (patchy skin rash), purpura (purple spots on the skin due to abnormal accumulation of blood), acute generalized exanthematous pustulosis (skin rash with the formation of purulent collections), dermatitis (skin irritation); \u003cbr\u003e- acute renal failure (decrease in kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (kidney impairment resulting in loss of protein in the urine), glomerulonephritis (inflammatory disease of the kidneys), water\/sodium retention with possible oedema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decrease in urine production), abnormal kidney function test, haematuria (blood in the urine);\u003cbr\u003e - aseptic meningitis (inflammation of the membranes covering the brain not caused by infection), lymphangitis (inflammation of the lymph vessels);\u003cbr\u003e - hyperkalemia (increased amount of potassium in the blood), hyponatremia (decreased amount of sodium in the blood).\u003cbr\u003e\u003cbr\u003e Following the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"DOMPE' FARMACEUTICI SPA","offers":[{"title":"Default Title","offer_id":50218926375246,"sku":"042028050","price":10.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005045_60971964-71b6-4a25-b251-7b7d1e945736.png?v=1768737978"},{"product_id":"lasonil-antidolore-gel-120-g-10","title":"LASONIL PAIN RELIEF 10% GEL 1 TUBE OF 120 G","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eLasonil anti-pain 10% gel\u003c\/b\u003e\u003cbr\u003e Ibuprofen lysine salt\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e This medicine contains Ibuprofen lysine salt, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs), which work to relieve pain and reduce symptoms related to inflammation.\u003cbr\u003e   \u003cbr\u003eLasonil anti-pain is used for the local treatment of bruises, sprains, myalgia (muscle pain), muscle strains, stiff neck.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if your symptoms get worse.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use Lasonil pain reliever\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6).\u003cbr\u003e - if you are allergic to other analgesics (painkillers), antipyretics (feverkillers), non-steroidal anti-inflammatory drugs (NSAIDs) that have previously caused asthma, rhinitis, urticaria or other allergic reactions.\u003cbr\u003e - if you are in the last 3 months of pregnancy (see \" \u003cem\u003ePregnancy, breast-feeding and fertility\u003c\/em\u003e \").\u003cbr\u003e - if you are breast-feeding (see \" \u003cem\u003ePregnancy, breast-feeding and fertility\u003c\/em\u003e \").\u003cbr\u003e - if you are under 14 years old (see \" \u003cem\u003eChildren and adolescents\u003c\/em\u003e \").\u003cbr\u003e - if you use other NSAIDs (see \" \u003cem\u003eOther medicines and Lasonil anti-pain\u003c\/em\u003e \").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eTalk to your doctor or pharmacist before using Lasonil pain reliever:\u003cbr\u003e - if you suffer or have ever suffered from asthma, allergic rhinitis, urticaria or other allergic reactions after using acetylsalicylic acid or other similar anti-inflammatories.\u003cbr\u003e - if you are using anticoagulant medicines (drugs used to thin the blood) such as warfarin at the same time (see \"Other medicines and Lasonil anti-pain\")\u003cbr\u003e\u003cbr\u003e It is advisable to avoid applying Lasonil pain reliever on open wounds or skin lesions.\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e\u003cbr\u003e The use of Lasonil pain reliever, especially if prolonged, may give rise to local sensitization phenomena: at the first appearance of skin rash (eruption), mucosal lesions or any other sign of hypersensitivity, discontinue treatment and consult your doctor who will be able to adopt appropriate therapeutic measures.\u003cbr\u003e   \u003cbr\u003eTo avoid more serious hypersensitivity or photosensitivity phenomena (skin erythema after application of the product and subsequent exposure to light, solar or UV), do not expose yourself to direct sunlight, including solarium, during treatment and for two weeks thereafter (see section 4. Possible side effects).\u003cbr\u003e\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with treatment with Lasonil antidolore. Stop using Lasonil antidolore and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e The use of the medicine is reserved only for patients over 14 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e \u003cbr\u003eStop using Lasonil Antidolore and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e\u003cbr\u003e - reddish, non-elevated, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e - widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome).\u003cbr\u003e - widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e   \u003cbr\u003eUndesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms.\u003cbr\u003e\u003cbr\u003e Skin reactions with erythema, itching, irritation, sensation of heat or burning and contact dermatitis have been reported with some nonsteroidal anti-inflammatory drugs applied to the skin.\u003cbr\u003e\u003cbr\u003e The skin becomes sensitive to light. Photosensitivity reactions (skin erythema after application of the product and subsequent exposure to light, solar or UV) are possible, side effects reported with an unknown frequency (i.e. the frequency cannot be estimated from the available data). See also paragraph 2.\u003cbr\u003e\u003cbr\u003e Following the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"BAYER SPA","offers":[{"title":"Default Title","offer_id":50218926932302,"sku":"042154029","price":11.1,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005143.png?v=1768737974"},{"product_id":"algopirina-febbre-e-dolore-bborale-sosp-150-ml-100-mg-5-ml-gusto-fragola-senza-zucchero","title":"ALGOPIRINA FEVER DOL CHILDREN 100 MG\/5 ML ORAL SUSPENSION STRAWBERRY FLAVOUR SUGAR FREE 1 BOTTLE OF 150 ML WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eALGOPIRINA FEVER AND PAIN Children 100mg\/5ml oral suspension strawberry flavour sugar free\u003cbr\u003e ALGOPIRINA FEVER AND PAIN Children 100mg\/5ml sugar-free orange-flavoured oral suspension\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e Equivalent medicine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eAlgopirina Febbre e Dolore contains ibuprofen which belongs to a group of drugs called nonsteroidal anti-inflammatory\/antirheumatic drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e Algopirina Febbre e Dolore is indicated in children aged 3 months to 12 years for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earaches).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use Algopirina Fever and Pain if:\u003c\/b\u003e\u003cbr\u003e - are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- you experience or have experienced in the past allergic reactions such as shortness of breath, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, particularly if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - suffer from serious heart problems (severe heart failure);\u003cbr\u003e - suffer or have suffered from bleeding in the stomach and\/or intestine (gastrointestinal haemorrhage) or periferation following previous treatments with NSAIDs;\u003cbr\u003e - suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of ulceration or bleeding); \u003cbr\u003e- are using other medicines from the same family of non-steroidal anti-inflammatory drugs (NSAIDs) at the same time, including those that act by selectively inhibiting the action of an enzyme called COX-2 (see section \"Other medicines and Algopirina Fever and Pain\");\u003cbr\u003e - have any disease that increases the risk of bleeding;\u003cbr\u003e - in case of unclear blood disorders;\u003cbr\u003e - is severely dehydrated, for example has had severe vomiting, diarrhoea or drinks very little;\u003cbr\u003e - is less than 3 months old or weighs less than 5.6 kg;\u003cbr\u003e - is in the last trimester of pregnancy (see Pregnancy and breast-feeding).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Algopirina Febbre e Dolore and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Algopirina Fever and Pain if:\u003cbr\u003e - you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), seasonal allergies (hay fever), polyps in the nose, if you have severe breathing or chest problems, e.g. chronic obstructive pulmonary disease, swelling of the face, lips and throat (angioedema); \u003cbr\u003e- are taking other medicines used to treat pain, lower fever and\/or treat inflammation (non-steroidal anti-inflammatory drugs (NSAIDs), including those that act by selectively inhibiting the action of an enzyme called COX-2 (see \"Other medicines and Algopirina Fever and Pain\"); \u003cbr\u003e- have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that can increase the risk of stomach and intestinal diseases (see section \"Other medicines and Algopirina Fever and Pain\"). During treatment with all NSAIDs, at any time, with or without warning symptoms or a previous history of serious gastrointestinal events, bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur. Therefore, inform your doctor of any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with Algopirina Febbre e Dolore and contact your doctor; \u003cbr\u003e- you suffer or have suffered from gastrointestinal diseases such as Crohn's disease or ulcerative colitis, inform your doctor because the use of NSAIDs could intensify these diseases (see section 4 \"Possible side effects\");\u003cbr\u003e - are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Algopirina Fever and Pain\"); \u003cbr\u003e- have heart disease (uncontrolled hypertension, congestive heart failure, known ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think your child may be at risk of these conditions (for example, if you have high blood pressure, high levels of sugar (diabetes) or fat in your blood, or if you smoke). Medicines such as Algopirina Febbre e Dolore may be associated with a slightly increased risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses and during prolonged therapy. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e - suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e - have an infection – see section “Infections” below. \u003cbr\u003e- has chickenpox, in which case it is advisable to avoid the use of Algopirina Fever and Pain.\u003cbr\u003e\u003cbr\u003e The use of Algopirina Fever and Pain requires adequate precautions, especially if the child:\u003cbr\u003e - suffer or have suffered from asthma as it could worsen breathing difficulties;\u003cbr\u003e - suffers from coagulation problems or high blood pressure;\u003cbr\u003e - suffer from kidney, heart or liver disease;\u003cbr\u003e - takes medicines that increase urine production (diuretics), or if you have undergone major surgery resulting in fluid loss, as in these cases your doctor will recommend that you perform periodic blood and urine tests on your child;\u003cbr\u003e - has undergone major surgery;\u003cbr\u003e - suffers from certain congenital diseases affecting blood formation (for example acute intermittent porphyria); \u003cbr\u003e- you are dehydrated due to fever, vomiting or diarrhoea, your doctor will advise you to re-establish your hydration status both before and during treatment to avoid the risk of altering kidney function.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before using Algopirina Fever and Pain if your child has:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack); \u003cbr\u003e- high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking Algopirina Fever and Pain immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e During prolonged treatments with Algopirina Febbre e Dolore, you must pay particular attention and immediately inform your doctor if the following appear:\u003cbr\u003e - signs or symptoms of lesions (ulcerations) or bleeding in the stomach and intestines (e.g. black, foul-smelling stools, vomiting blood);\u003cbr\u003e - signs and symptoms of liver damage (e.g. hepatitis and jaundice);\u003cbr\u003e - signs and symptoms of kidney damage (e.g. increased urine production, blood in the urine); \u003cbr\u003e- visual disturbances blurred or reduced vision, partial or complete blindness (scotomas), alteration of colour perception: in this case, stop treatment immediately and consult your ophthalmologist;\u003cbr\u003e - symptoms such as frequent or daily headaches despite regular use of headache medicines, as they may be caused by excessive use of these medicines;\u003cbr\u003e - symptoms such as headache, disorientation, nausea, vomiting, stiff neck and fever as these could be symptoms due to aseptic meningitis (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e \u003cbr\u003eSerious skin reactions have been reported in association with ibuprofen treatment. Stop taking Algopirina Febbre e Dolore and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Algopirina Febbre e Dolore may hide the symptoms of infections such as fever and pain. It is therefore possible that Algopirina Febbre e Dolore may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eTo reduce the possible side effects mentioned above, the lowest effective dose should be used for the shortest duration necessary to control symptoms.\u003cbr\u003e Children and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If your child experiences any of the following side effects STOP treatment with Algopirina\u003cbr\u003e Fever and Pain and seek medical attention immediately:\u003cbr\u003e • severe skin and mucous membrane disorders characterized by rashes, redness, itching and blisters (bullous and exfoliative dermatitis including erythema multiforme, Stevens-Johnson syndrome and toxic epidermal necrolysis); \u003cbr\u003e• allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases);\u003cbr\u003e • reddish, non-raised, target-shaped or circular patches on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome); \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia);\u003cbr\u003e • skin rashes;\u003cbr\u003e • vision disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing problems;\u003cbr\u003e • cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting;\u003cbr\u003e • hair loss (alopecia), the skin becomes sensitive to light; \u003cbr\u003e• severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis);\u003cbr\u003e • simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice); \u003cbr\u003e• severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood;\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotizing fasciitis);\u003cbr\u003e • associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing or rustling (tinnitus); \u003cbr\u003e• severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the esophagus (esophagitis);\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell); \u003cbr\u003e• a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using Algopirina Febbre e Dolore if you develop these symptoms and contact your doctor immediately. See also section 2;\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.","brand":"SO.SE.PHARM SRL","offers":[{"title":"Default Title","offer_id":50218926965070,"sku":"042178018","price":8.72,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0011133.png?v=1768737976"},{"product_id":"brufen-analgesico-12-cpr-riv-400-mg","title":"BRUFEN ANALGESIC 400 MG FILM-COATED TABLETS 12 TABLETS IN PVC\/ACLAR\/AL\/VMCH BLISTER\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBRUFEN ANALGESIC 200 mg film-coated tablets\u003cbr\u003e BRUFEN ANALGESIC 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen (as lysine salt)\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat is it and what is it used for?\u003c\/b\u003e\u003cbr\u003e BRUFEN ANALGESIC contains the active substance ibuprofen. It belongs to a group of medicines known as nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs provide relief by modifying the body's response to pain and fever.\u003cbr\u003e\u003cbr\u003e BRUFEN ANALGESICO tablets are used for the symptomatic treatment of mild to moderate pain, such as headache, dental pain, menstrual pain, and pain and fever associated with colds.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take BRUFEN ANALGESIC:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e• if you have suffered from an allergic reaction, such as asthma, difficulty breathing, swelling of the face, tongue or throat, hives, runny or itchy nose, caused by acetylsalicylic acid (ASA) or other NSAIDs;\u003cbr\u003e • if you have (or have had two or more episodes of) stomach ulcer or bleeding;\u003cbr\u003e • if you have had gastrointestinal perforation or bleeding while using NSAIDs;\u003cbr\u003e • if you suffer from cerebrovascular bleeding or other active bleeding;\u003cbr\u003e • if you suffer from blood formation disorders of unknown nature;\u003cbr\u003e • if you have severe dehydration (caused by vomiting, diarrhoea or insufficient fluid intake);\u003cbr\u003e • if you suffer from severe liver, kidney or heart failure;\u003cbr\u003e • if you are in the last 3 months of pregnancy.\u003cbr\u003e\u003cbr\u003e \u003cem\u003e(Only 200 mg)\u003c\/em\u003e\u003cbr\u003e BRUFEN ANALGESIC is contraindicated in children under 6 years of age (less than 20 kg of body weight).\u003cbr\u003e   \u003cbr\u003e\u003cem\u003e(Only 400 mg)\u003c\/em\u003e BRUFEN ANALGESIC is contraindicated in adolescents under 40 kg of body weight or in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking BRUFEN ANALGESIC:\u003cbr\u003e • if you have recently undergone major surgery;\u003cbr\u003e • if you suffer or have suffered from asthma or an allergic disease, because breathing difficulties may occur;\u003cbr\u003e • if you suffer from hay fever, nasal polyps, or chronic obstructive pulmonary disease, as there is an increased risk of allergic reactions. Allergic reactions may present as asthma attacks (so-called analgesic asthma), Quincke's edema, or hives;\u003cbr\u003e • if you suffer from heart problems;\u003cbr\u003e • if you have a history of gastrointestinal diseases (such as ulcerative colitis, Crohn's disease);\u003cbr\u003e • if you suffer from systemic lupus erythematosus or mixed connective tissue disease (a disease affecting the skin, joints and kidneys); \u003cbr\u003e• if you suffer from certain hereditary blood formation disorders (e.g. acute intermittent porphyria);\u003cbr\u003e • if you suffer from blood clotting disorders;\u003cbr\u003e • if you are taking other NSAIDs. Concomitant use with other NSAIDs, including specific cyclooxygenase-2 inhibitors, increases the risk of adverse reactions (see section \"Other medicines and BRUFEN ANALGESIC\", below) and should be avoided;\u003cbr\u003e • if you have chickenpox it is advisable to avoid the use of BRUFEN ANALGESIC;\u003cbr\u003e • if he is elderly;\u003cbr\u003e • if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Patients with kidney or liver problems should consult a doctor before taking ibuprofen tablets.\u003cbr\u003e\u003cbr\u003e Anti-inflammatories such as ibuprofen may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke, particularly when used in high doses.\u003cbr\u003e Do not exceed the recommended dose or duration of treatment (see section 3).\u003cbr\u003e   \u003cbr\u003eYou should discuss your treatment with your doctor or pharmacist before taking BRUFEN ANALGESICO, if:\u003cbr\u003e • have heart problems, including heart failure, angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral arterial disease (circulation problems in the legs or feet due to narrowed or blocked arteries), or any type of stroke (including a \"mini-stroke\" or transient ischemic attack, \"TIA\");\u003cbr\u003e • have high blood pressure, diabetes, high cholesterol, have a family history of heart disease or stroke, or are a smoker.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to ibuprofen have been reported, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop taking BRUFEN ANALAGESICO immediately and contact your doctor or emergency medical services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e \u003cbr\u003eSerious skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment.\u003cbr\u003e Stop using BRUFEN ANALGESICO and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Brufen Analgesic may hide the symptoms of infections, such as fever and pain. Brufen Analgesic may therefore delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately. \u003cbr\u003eSide effects can be minimized by using the lowest effective dose for the shortest period of time. Elderly people are at increased risk of side effects.\u003cbr\u003e\u003cbr\u003e In general, the habitual use of painkillers (even of different types) can lead to serious and persistent kidney problems. This risk may increase during exercise, associated with salt loss and dehydration. Therefore, it should be avoided. There is a risk of impaired kidney function in dehydrated children and adolescents.\u003cbr\u003e\u003cbr\u003e Prolonged use of any type of painkiller for headaches can worsen them. If this condition is present or suspected, medical advice should be sought and treatment should be discontinued. The diagnosis of medication-overuse headache should be suspected in patients who experience headaches despite (or because of) the regular use of headache medications.\u003cbr\u003e   \u003cbr\u003eIf you take BRUFEN ANALGESIC for a long time, regular checks of your liver and kidney function, as well as your blood count, are required. Your doctor may require blood tests during treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Side effects can be minimized by taking the lowest dose for the shortest period of time necessary to relieve symptoms. Elderly people using this product are at greater risk of developing problems associated with side effects.\u003cbr\u003e\u003cbr\u003e Medicines such as BRUFEN ANALGESICO may be associated with a small increased risk of a heart attack (myocardial infarction) or stroke.\u003cbr\u003e   \u003cbr\u003eSome of the side effects listed below are less frequent when the maximum daily dose is 1200 mg compared to high-dose therapy in rheumatic patients.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eIf you think you have any of the following side effects or symptoms, stop taking this medicine and seek immediate medical help:\u003c\/b\u003e\u003cbr\u003e • stomach or intestinal ulcers, sometimes with bleeding and perforation, vomiting blood or black, tarry stools (common may affect up to 1 in 10 people);\u003cbr\u003e • kidney problems with blood in the urine which may be associated with kidney failure (uncommon: may affect up to 1 in 100 people);\u003cbr\u003e • serious allergic reactions (very rare: may affect up to 1 in 10,000 people) such as:\u003cbr\u003e - difficulty breathing or unexplained wheezing;\u003cbr\u003e - dizziness or rapid heartbeat;\u003cbr\u003e - drop in blood pressure causing shock;\u003cbr\u003e - swelling of the face, tongue and throat; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis] (very rare: may affect up to 1 in 10,000 people);\u003cbr\u003e • a serious skin condition that can affect the mouth and other parts of the body with symptoms including red, often itchy patches, similar to a measles rash, starting on the limbs and sometimes on the face and body. The patches may swell or progress to form raised, red spots with a pale center. Affected patients may have fever, sore throat, headache, and\/or diarrhoea (very rare: may affect up to 1 in 10,000 people); \u003cbr\u003e• severe flaking or peeling of the skin (very rare: may affect up to 1 in 10,000 people);\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome) (not known: frequency cannot be estimated from the available data);\u003cbr\u003e • inflammation of the pancreas with severe epigastric pain, often with nausea and vomiting (very rare: may affect up to 1 in 10,000 people);\u003cbr\u003e • nausea, vomiting, loss of appetite, feeling generally unwell, fever, itching, yellowing of the skin and eyes, light-coloured stools, dark-coloured urine, which may be signs of hepatitis or liver failure (very rare: may affect up to 1 in 10,000 people);\u003cbr\u003e • heart disorder with shortness of breath and swelling of the feet or legs due to fluid retention (heart failure) (not known: frequency cannot be estimated from the available data); \u003cbr\u003e• aseptic meningitis (infection around the brain or spinal cord, with symptoms including: fever, nausea, vomiting, headache, stiff neck and extreme sensitivity to bright light and clouding of the mental state such that you are completely out of touch with your environment (very rare: may affect up to 1 in 10,000 people);\u003cbr\u003e • heart attack ('myocardial infarction', very rare: may affect up to 1 in 10,000 people) or stroke (frequency not known: cannot be estimated from the available data);\u003cbr\u003e • severe kidney damage (papillary necrosis), particularly with long-term use (rare: may affect up to 1 in 1,000 people);\u003cbr\u003e • worsening of inflammation related to an infection (e.g. development of 'flesh-eating bacteria' syndrome) particularly with the use of other NSAIDs (very rare: may affect up to 1 in 10,000 people); \u003cbr\u003e• Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome (not known: frequency cannot be estimated from the available data).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop taking\u003c\/b\u003e the medicine and tell your doctor if you experience:\u003cbr\u003e Very common (may affect more than 1 in 10 people):\u003cbr\u003e • indigestion or heartburn;\u003cbr\u003e • abdominal pain (stomach pain) or other stomach abnormalities.\u003cbr\u003e\u003cbr\u003e Not known (frequency cannot be estimated from the available data):\u003cbr\u003e • visual disturbances;\u003cbr\u003e • a widespread, red, scaly rash, with pustules and vesicles forming on the skin, mainly in the skin folds, trunk, and upper limbs, accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using BRUFEN ANALGESICO if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e   \u003cbr\u003eTell your doctor if any of the following side effects occur:\u003cbr\u003e Very common (may affect more than 1 in 10 people):\u003cbr\u003e • nausea, flatulence, diarrhea, constipation, vomiting.\u003cbr\u003e\u003cbr\u003e Common (may affect up to 1 in 10 people):\u003cbr\u003e • headache, drowsiness, dizziness, spinning sensation, tiredness, agitation, inability to sleep, irritability;\u003cbr\u003e • gastric and duodenal ulcers, sometimes with bleeding and perforation, occult blood loss which can lead to anaemia, a condition in which there is a decrease in red blood cells (symptoms include tiredness, headache, shortness of breath during exercise, dizziness and paleness), black, tarry stools, vomiting blood, mouth ulcers and cold sores, inflammation of the colon (symptoms include diarrhoea, usually with blood and mucus, stomach pain and fever), worsening of inflammatory bowel disease, inflammation of the gut wall.\u003cbr\u003e   \u003cbr\u003eUncommon (may affect up to 1 in 100 people):\u003cbr\u003e • hives, itching, unusual bleeding or bruising under the skin, rash, asthma attack (sometimes with low blood pressure);\u003cbr\u003e • runny or stuffy nose, sneezing, facial pain or pressure, difficulty breathing;\u003cbr\u003e • inflammation of the stomach (symptoms include: pain, nausea, vomiting, vomiting blood, blood in the stool);\u003cbr\u003e • increased sensitivity of the skin to the sun;\u003cbr\u003e • swelling of the face, lips, mouth, tongue, or throat, which may cause difficulty swallowing or breathing, sometimes with high blood pressure;\u003cbr\u003e • fluid retention in body tissues, especially in patients with hypertension or kidney problems.\u003cbr\u003e\u003cbr\u003e Rare (may affect up to 1 in 1,000 people):\u003cbr\u003e • a disease affecting the skin, joints and kidneys (lupus erythematosus syndrome);\u003cbr\u003e • depression, confusion, hallucinations, mental illness with strange or disturbing thoughts or mood; \u003cbr\u003e• persistent ringing, buzzing, hissing, whistling, or other noises in the ears;\u003cbr\u003e • increased blood urea nitrogen, transaminases and alkaline phosphatase, decreased hemoglobin and hematocrit values, inhibition of platelet aggregation, prolongation of bleeding time, decreased serum calcium, increased serum uric acid, all observed with a blood test;\u003cbr\u003e • loss of vision.\u003cbr\u003e\u003cbr\u003e Very rare (may affect up to 1 in 10,000 people):\u003cbr\u003e • rapid or irregular heartbeat (palpitations);\u003cbr\u003e • increased fluid in body tissues;\u003cbr\u003e • inflammation of the esophagus, narrowing of the intestine;\u003cbr\u003e • liver disorders, liver damage (especially with long-term use), liver failure, yellowing of the skin and\/or eyes, also called jaundice;\u003cbr\u003e • serious skin infections, with soft tissue complications, may occur if you have chickenpox; \u003cbr\u003e• fluid buildup in the lungs, symptoms include shortness of breath, which can be very severe and usually worsens when lying down.\u003cbr\u003e\u003cbr\u003e Not known (frequency cannot be estimated from the available data):\u003cbr\u003e • worsening of an inflammatory disease that may affect any part of the gastrointestinal tract (symptoms include pain, fever, diarrhea, and weight loss), worsening of inflammation of the colon (symptoms: diarrhea, usually with blood and mucus, stomach pain, fever);\u003cbr\u003e • high blood pressure;\u003cbr\u003e • unusual hair loss or baldness;\u003cbr\u003e • menstrual disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you experience any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"MYLAN SPA","offers":[{"title":"Default Title","offer_id":50218927030606,"sku":"042386348","price":9.12,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0004064.jpg?v=1768737979"},{"product_id":"ibuprofene-doc-12-cpr-riv-400-mg","title":"IBUPROFENE DOC 400 MG FILM-COATED TABLETS 12 TABLETS IN PVC\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eIBUPROFENE DOC 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Equivalent medicine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eIBUPROFENE DOC contains ibuprofen, an active ingredient belonging to a group of medicines called NSAIDs (nonsteroidal anti-inflammatory drugs). NSAIDs are medicines against pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e IBUPROFENE DOC is used:\u003cbr\u003e • to treat pain of various kinds, due to toothache (for example after extraction or dental and oral surgery), menstrual pain, headache, muscle, joint (osteoarticular) and nerve pain (nervralgia);\u003cbr\u003e • together with other medicines, to treat symptoms due to flu or fever.\u003cbr\u003e\u003cbr\u003e IBUPROFENE DOC can be used by adults and children over 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take IBUPROFENE DOC:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e• if you have had allergic reactions after taking aspirin (acetylsalicylic acid), other medicines for pain, fever, or other non-steroidal anti-inflammatory drugs (NSAIDs), particularly if associated with nasal polyps, swelling of the face (angioedema) and\/or asthma;\u003cbr\u003e • if you have a lesion of the stomach or intestinal wall (severe or active peptic ulcer);\u003cbr\u003e • if you have had a history of perforation or bleeding in the stomach or intestine caused by taking medicines;\u003cbr\u003e • if you have had two or more distinct episodes of bleeding or injury to the wall of your stomach or intestine (recurrent peptic ulcer);\u003cbr\u003e • if you have severe liver or kidney problems;\u003cbr\u003e • if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e • if you have any disease that increases the risk of bleeding;\u003cbr\u003e • if you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or drink very little; \u003cbr\u003e• after the sixth month of pregnancy.\u003cbr\u003e\u003cbr\u003e Do not use IBUPROFENE DOC in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor before taking IBUPROFENE DOC if:\u003cbr\u003e • suffer from systemic lupus erythematosus (SLE) or mixed connective tissue disease, diseases that affect the connective tissue causing joint or muscle pain, skin changes and problems with other organs;\u003cbr\u003e • have had stomach or intestinal problems, for example ulcer, Crohn's disease, ulcerative colitis (see paragraph below \"WARNING\" on gastrointestinal risks and \"Do not take IBUPROFENE DOC\");\u003cbr\u003e • has reduced kidney function;\u003cbr\u003e • has liver problems;\u003cbr\u003e • has blood clotting problems;\u003cbr\u003e • have or have had allergies (e.g. hay fever);\u003cbr\u003e • has inflammation of the nose (chronic rhinitis) or nasal polyps;\u003cbr\u003e • suffers from asthma or respiratory diseases that have lasted for a long time (chronic); \u003cbr\u003e• have had swelling of the face, throat, lips or other parts of the body (angioedema) in the past;\u003cbr\u003e • are elderly, as they are more likely to develop adverse events from this medicine, particularly bleeding and perforations of the stomach and intestines which may be life-threatening (see section below BE CAREFUL about gastrointestinal risks);\u003cbr\u003e • have chickenpox, as pain and inflammation medicines (NSAIDs) may make the skin lesions caused by it worse. In such cases your doctor may advise you not to use this medicine;\u003cbr\u003e • if you are a dehydrated teenager or elderly as they are more likely to have kidney problems;\u003cbr\u003e • have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHeart attack and stroke\u003c\/b\u003e \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking IBUPROFENE DOC if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSkin reactions\u003c\/b\u003e\u003cbr\u003e Severe skin reactions have been reported in association with treatment with IBUPROFENE DOC. \u003cbr\u003eStop taking IBUPROFENE DOC and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e IBUPROFENE DOC may hide the symptoms of infections such as fever and pain. It is therefore possible that IBUPROFENE DOC may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePLEASE NOTE\u003c\/b\u003e , as during treatment with all nonsteroidal anti-inflammatory drugs for pain and inflammation (NSAIDs): \u003cbr\u003e• at any time, with or without warning symptoms, even in patients without previous serious stomach or intestinal (gastrointestinal) problems, bleeding, ulceration or perforation of the stomach or intestine, which may be life-threatening, has been reported (see section \"Do not take IBUPROFENE DOC\"). If you are elderly or have had these types of problems in the past, the risk of experiencing these events will be higher if you take higher doses of the medicine. In this case, your doctor will tell you to start treatment with the lowest available dose, and may also prescribe a medicine to protect your stomach (gastroprotectors such as misoprostol or proton pump inhibitors) to be taken together with IBUPROFENE DOC; \u003cbr\u003e• serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with treatment with IBUPROFENE DOC. Stop using IBUPROFENE DOC and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4;\u003cbr\u003e • serious allergic reactions (anaphylactoid reactions, up to anaphylactic shock) may occur;\u003cbr\u003e • eye changes may occur if IBUPROFENE DOC is used. During therapy it is necessary to carry out periodic eye checks, especially for prolonged treatments;\u003cbr\u003e • especially if used for prolonged periods and at high doses, headache may occur; in this case, do not increase the dose of IBUPROFENE DOC to relieve the pain.\u003cbr\u003e   \u003cbr\u003eIf you have reduced heart, liver or kidney function (particularly if you suffer from systemic lupus erythematosus), your doctor will prescribe specific periodic tests, particularly in the case of prolonged treatments, and will prescribe the lowest effective dose and for the shortest duration of treatment necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e The risk of side effects can be reduced by using the lowest effective dose and for the shortest duration of treatment necessary to control symptoms. Do not take more than the recommended dose of IBUPROFENE DOC and do not take it for long periods; always follow your doctor's instructions carefully.\u003cbr\u003e\u003cbr\u003e STOP treatment and contact your doctor if: \u003cbr\u003e• note any symptoms affecting your stomach and intestines (gastrointestinal), especially bleeding, particularly if this occurs early in treatment, if you are an elderly patient or if you have had gastrointestinal problems in the past;\u003cbr\u003e • a skin rash, mucosal lesions or any other sign of an allergic reaction appears (e.g. redness, itching, swelling of the face and throat, sudden drop in blood pressure);\u003cbr\u003e • exhibits vision problems;\u003cbr\u003e • has liver problems;\u003cbr\u003e • signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema) and chest pain, have been reported with ibuprofen. Stop IBUPROFENE DOC immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren\u003c\/b\u003e \u003cbr\u003eDo not use IBUPROFENE DOC in children under 12 years of age. If necessary, ask your doctor for advice, as specific (lower) dosages are available for these patients.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSerious side effects\u003cbr\u003e Stop taking IBUPROFENE DOC and contact your doctor immediately if you experience any of the following conditions:\u003c\/b\u003e\u003cbr\u003e • severe stomach problems, heartburn or abdominal pain due to lesions in the stomach or intestine (peptic ulcers), sudden severe pain in the pit of the stomach or belly (gastrointestinal perforation). These side effects are uncommon;\u003cbr\u003e • vomiting containing blood (haematemesis) or black stools (melena), bleeding from the stomach or intestines (gastrointestinal haemorrhages). These conditions are common side effects; \u003cbr\u003e• allergic reactions, even serious ones, which manifest themselves with the more or less sudden appearance of skin lesions, for example with widespread or blotchy redness (rash, purpura), hives, itching, swelling of the face, eyes, lips, swelling of the throat with possible difficulty in breathing and swallowing (angioedema). These conditions occur with uncommon frequency. Rarely, a serious allergic reaction may also occur, which can be life-threatening, characterised by an increase in heart rate and a sudden drop in blood pressure (anaphylactic reactions, anaphylaxis); \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • difficulty breathing (even severe asthma, bronchospasm or dyspnoea). These conditions are uncommon side effects;\u003cbr\u003e • systemic lupus erythematosus (SLE), a disease that affects connective tissue, causing joint or muscle pain, skin changes, and problems with other organs. This condition occurs rarely; \u003cbr\u003e• worsening of infections such as the onset of necrotizing fasciitis which manifests itself with fever, chills, weakness, sweating, diarrhoea, vomiting, redness, pain, swelling, bruising in an area of ​​the body due to tissue necrosis (death of tissue cells);\u003cbr\u003e • inflammation of the meninges (aseptic meningitis) which manifests itself with: very high fever, sudden headache, inability to bend the head, nausea, vomiting, confusion, drowsiness and sensitivity to light. This condition occurs rarely;\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome). Symptoms of DRESS also include increased eosinophils (a type of white blood cell); \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters located mainly in the skin folds, trunk and upper limbs, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects\u003c\/b\u003e\u003cbr\u003e Tell your doctor if you notice:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects\u003c\/b\u003e (may affect up to 1 in 10 people)\u003cbr\u003e • nausea, vomiting, diarrhoea, intestinal gas (flatulence), constipation, indigestion (dyspepsia), abdominal pain;\u003cbr\u003e • headache, dizziness;\u003cbr\u003e • fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects\u003c\/b\u003e (may affect up to 1 in 100 people)\u003cbr\u003e • inflammation of the nose (rhinitis);\u003cbr\u003e • stomach inflammation (gastritis), mouth ulcers;\u003cbr\u003e • dizziness, drowsiness, difficulty falling asleep (insomnia), anxiety, changes in sensation (paraesthesia);\u003cbr\u003e • impaired hearing, ringing in the ears (tinnitus), vision disturbances; \u003cbr\u003e• skin reactions following exposure to the sun (photosensitivity);\u003cbr\u003e • changes in liver function, yellowing of the eyes or skin (jaundice), dark urine, pale stools, itching or pain in the abdomen, inflammation of the liver (hepatitis);\u003cbr\u003e • kidney problems such as nephrotic syndrome, inflammation of the kidney (tubulointerstitial nephritis), changes in function (renal failure).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects\u003c\/b\u003e (may affect up to 1 in 1,000 people)\u003cbr\u003e • decrease in the number of white blood cells (leukopenia) or certain types of white blood cells (neutropenia, agranulocytosis), decrease in the number of platelets (thrombocytopenia), decrease in the number of red blood cells due to destruction (haemolytic anaemia) or problems with the bone marrow (aplastic anaemia);\u003cbr\u003e • depression, confusion;\u003cbr\u003e • alteration of vision due for example to inflammation of the optic nerve (optic neuritis) or to toxic optic neuropathy; \u003cbr\u003e• swelling (edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects\u003c\/b\u003e (may affect up to 1 in 10,000 people)\u003cbr\u003e • reduced liver function, inflammation of the pancreas (pancreatitis);\u003cbr\u003e • feeling of heart in the throat (palpitations), heart attack (myocardial infarction), reduced heart function (failure), high blood pressure (hypertension);\u003cbr\u003e • problems breathing due to swelling in the lungs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects\u003c\/b\u003e\u003cbr\u003e • pain or burning (heartburn) in the pit of the stomach, inflammation of the mucosa of the mouth with ulcers (ulcerative stomatitis);\u003cbr\u003e • worsening of inflammation of the colon (colitis) or Crohn's disease;\u003cbr\u003e • worsening of skin infections caused by chickenpox;\u003cbr\u003e • stroke;\u003cbr\u003e • hallucinations, malaise;\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"DOC GENERICI SRL","offers":[{"title":"Default Title","offer_id":50218927194446,"sku":"043109040","price":4.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/043109040.jpg?v=1768737983"},{"product_id":"buscofenpocket-orale-polv-10-bust-400-mg","title":"BUSCOFENPOCKET 400 MG ORAL POWDER IN SACHET 10 SINGLE-DOSE SACHETS IN PAP\/AL\/MEEA","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBUSCOFENPOCKET 400 mg oral powder in sachet\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Ibuprofen belongs to a group of medicines known as Nonsteroidal Anti-Inflammatory Drugs (NSAIDs). These medicines work by changing the body's response to pain, inflammation, and high body temperature.\u003cbr\u003e   \u003cbr\u003eBUSCOFENPOCKET is used for the short-term symptomatic treatment of mild-moderate pain such as headache, toothache, menstrual pain and\/or fever.\u003cbr\u003e\u003cbr\u003e BUSCOFENPOCKET 400 mg is recommended for adults and adolescents with a body weight of 40 kg or more (aged 12 years or over).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take BUSCOFENPOCKET\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you have experienced shortness of breath, asthma, runny nose, hives or angioedema (serious allergic reaction causing swelling of the face or throat) after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - if you have ever had bleeding or perforation of the stomach or intestine related to previous NSAID therapy; \u003cbr\u003e- if you have an active or recurrent ulcer (peptic ulcers) or bleeding in your stomach or duodenum or if you have had this problem repeatedly (two or more episodes of proven ulceration or bleeding) in the past;\u003cbr\u003e - if you suffer from severe liver, kidney or heart failure;\u003cbr\u003e - if you have bleeding in the brain (cerebrovascular haemorrhage) or other active bleeding;\u003cbr\u003e - if you suffer from a blood formation disorder of unknown origin, e.g. thrombocytopenia;\u003cbr\u003e - if you are severely dehydrated (due to vomiting, diarrhoea or insufficient fluid intake);\u003cbr\u003e - in the last three months of pregnancy (see \"Pregnancy and breast-feeding\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking BUSCOFENPOCKET if:\u003cbr\u003e - suffer from certain hereditary blood formation diseases (e.g. acute intermittent porphyria);\u003cbr\u003e - suffer from certain skin diseases (systemic lupus erythematosus (SLE) or mixed connective tissue disease); \u003cbr\u003e- suffer or have suffered from intestinal diseases (ulcerative colitis or Crohn's disease), as they may worsen (see section 4 \"Possible side effects\");\u003cbr\u003e - has reduced kidney function;\u003cbr\u003e - has liver problems;\u003cbr\u003e - are taking other medicines which may increase the risk of ulceration or bleeding, such as oral corticosteroids (e.g. prednisolone), medicines to thin the blood (e.g. warfarin), selective serotonin reuptake inhibitors (medicines used for depression) or antiplatelet agents (e.g. acetylsalicylic acid);\u003cbr\u003e - are taking other NSAIDs (including COX-2 inhibitors such as celecoxib or etoricoxib), as their concomitant use should be avoided; \u003cbr\u003e- have heart problems, including heart failure, angina (chest pain), or have had a heart attack, bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a \"mini-stroke\" or transient ischaemic attack, \"TIA\");\u003cbr\u003e - have high blood pressure, diabetes, high cholesterol, or a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - suffer from allergies (e.g. skin reactions to other substances, asthma, hay fever), nasal polyps, chronic swelling of the nasal mucosa or chronic obstructive respiratory diseases, as in that case you are at higher risk of allergic reactions;\u003cbr\u003e - has just undergone major surgery;\u003cbr\u003e - have problems with blood clotting (thickening);\u003cbr\u003e - if you have a chickenpox infection it is advisable to avoid using BUSCOFENPOCKET; \u003cbr\u003e- have an infection – see section “Infections” below;\u003cbr\u003e - have ever developed a fixed drug eruption (round or oval patches of redness and swelling of the skin, blisters, hives and itching) after taking ibuprofen (see section 4).\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop BUSCOFENPOCKET immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Undesirable effects can be limited by using the lowest effective dose for the shortest duration necessary to control symptoms.\u003cbr\u003e\u003cbr\u003e In general, the habitual intake of (different types of) painkillers can cause serious and permanent kidney problems. This risk can be increased under physical exertion associated with salt loss and dehydration. Therefore it should be avoided.\u003cbr\u003e   \u003cbr\u003eIn prolonged use of BUSCOFENPOCKET, regular monitoring of liver values, renal function, and blood count is necessary.\u003cbr\u003e\u003cbr\u003e Prolonged use of any type of painkiller for headaches may worsen these values. If this situation occurs, contact your doctor for advice and stop treatment with BUSCOFENPOCKET.\u003cbr\u003e\u003cbr\u003e If you suffer or have suffered from asthma or allergic diseases, shortness of breath may occur.\u003cbr\u003e\u003cbr\u003e Take special care with BUSCOFENPOCKET:\u003cbr\u003e\u003cbr\u003e Severe skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. \u003cbr\u003eStop using BUSCOFENPOCKET and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e BUSCOFENPOCKET may hide the symptoms of infections such as fever and pain. It is therefore possible that BUSCOFENPOCKET may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e The use of anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or maximum duration of treatment.\u003cbr\u003e   \u003cbr\u003eGastrointestinal bleeding (bleeding into the stomach or intestines), ulceration or perforation, which can be fatal, has been reported with all NSAIDs at any time during treatment, with or without warning symptoms or a previous history of serious GI events. If GI bleeding or ulceration occurs, stop taking this medicine immediately. The risk of GI bleeding, ulceration or perforation is higher with increasing NSAID doses, in patients with a history of ulcer, particularly if complicated with haemorrhage or perforation (see section 2 \"Do not take BUSCOFENPOCKET\"), and in the elderly. These patients should start treatment on the lowest available dose. Combination therapy with protective agents (e.g. misoprostol or proton pump inhibitors) should be considered for these patients, as well as for patients who require concomitant use of low dose acetylsalicylic acid or other drugs likely to increase gastrointestinal risk. If gastrointestinal bleeding or ulceration occurs during treatment with ibuprofen, treatment should be discontinued and a doctor should be consulted. \u003cbr\u003e\u003cbr\u003eThe use of NSAIDs in association with alcohol may aggravate the adverse reactions caused by the active ingredient, especially those affecting the gastrointestinal tract or the central nervous system.\u003cbr\u003e\u003cbr\u003e If any of the above conditions apply to you, consult your doctor before using BUSCOFENPOCKET.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eElderly people\u003c\/b\u003e\u003cbr\u003e Elderly people taking NSAIDs are at increased risk of side effects, especially those related to the stomach and intestines. For more information, see section 4 \"Possible side effects\".\u003cbr\u003e If you have a history of gastrointestinal toxicity, particularly if you are elderly, report any unusual abdominal symptoms (especially bleeding in the stomach or intestines), particularly in the early stages of treatment.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e There is a risk of renal impairment in dehydrated adolescents.\u003cbr\u003e BUSCOFENPOCKET 400 mg is not suitable for children under 12 years of age and adolescents with a body weight of less than 40 kg.\u003cbr\u003e\u003cbr\u003e \u003cbr\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Side effects can be limited by using the lowest dose for the shortest time necessary to relieve symptoms. You may experience one of the known side effects of NSAIDs. If this happens, or if you are in any doubt, stop taking this medicine and consult your doctor as soon as possible.\u003cbr\u003e\u003cbr\u003e Older people using this medicine are at greater risk of developing problems associated with side effects.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop taking this medicine and see a doctor immediately if you experience:\u003c\/b\u003e\u003cbr\u003e - signs of intestinal bleeding such as: severe abdominal pain, dark, tarry stools, vomiting blood or dark particles that look like coffee grounds; \u003cbr\u003e- signs of rare but serious allergic reactions, such as worsening of asthma, wheezing or shortness of breath of unknown origin, swelling of the face, tongue or throat, difficulty breathing, rapid heartbeat, drop in blood pressure resulting in shock. These may also happen when you first start taking this medicine. If you experience any of these symptoms, call your doctor straight away;\u003cbr\u003e - reddish, non-elevated, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e - widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome); \u003cbr\u003e- widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTalk to your doctor if you experience any of the following side effects, if they get worse, or if you notice any effects not listed.\u003cbr\u003e\u003cbr\u003e Common (may affect up to 1 in 10 people):\u003c\/b\u003e - feeling dizzy or tired, headache;\u003cbr\u003e - stomach ache, digestive disorders, diarrhea, heartburn, nausea, vomiting, flatulence, constipation;\u003cbr\u003e - various skin rashes.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e - sneezing, stuffy or runny nose or itchy nose (rhinitis); \u003cbr\u003e- hypersensitivity reactions with skin rashes and itching, as well as asthma attacks (possibly with a drop in blood pressure). In this case, the doctor must be informed immediately and the intake of ibuprofen must be stopped;\u003cbr\u003e - sensation of tingling or prickling, drowsiness, agitation, irritability;\u003cbr\u003e - difficulty sleeping, feeling anxious;\u003cbr\u003e - hives, itching, small bruises on the skin or inside the mouth, nose or ears, sensitivity of the skin to light;\u003cbr\u003e - visual disturbance. In this case, the doctor must be informed immediately and the intake of ibuprofen must be stopped;\u003cbr\u003e - hearing problems, feeling dizzy or spinning (vertigo), ringing in the ears (tinnitus);\u003cbr\u003e - difficulty breathing, wheezing or coughing, asthma or worsening of asthma; \u003cbr\u003e- inflammation of the stomach lining, gastrointestinal ulcers, in some cases with bleeding and perforation, ulcerative stomatitis, exacerbation of colitis and Crohn's disease;\u003cbr\u003e - hepatitis, yellowing of the skin or eyes, reduced liver function;\u003cbr\u003e - nephrotic syndrome (accumulation of fluid within the body (edema) and accumulation of protein in the urine); inflammation of the kidneys (interstitial nephritis), which may be accompanied by acute kidney dysfunction. Reduced urine output, accumulation of fluid within the body (edema) and generally feeling unwell may be signs of kidney disease and even kidney failure. If any of the above symptoms occur, stop taking BUSCOFENPOCKET and consult your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e - feeling depressed or confused; \u003cbr\u003e- Symptoms of aseptic meningitis with stiff neck, headache, nausea, vomiting, fever or blurred consciousness have been observed during treatment with ibuprofen. Patients with autoimmune disorders (SLE, mixed connective tissue disease) seem to be predisposed. If such symptoms occur, contact a doctor immediately;\u003cbr\u003e - damage to the optic nerve;\u003cbr\u003e - damage to kidney tissue (papillary necrosis), especially in long-term treatment, and increased uric acid and urea concentration in the blood;\u003cbr\u003e - water retention (edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e \u003cbr\u003e- worsening of infection-related inflammation (e.g. necrotizing fasciitis) associated with the use of some painkillers (NSAIDs) has been described. If signs of infection occur or worsen during the use of BUSCOFENPOCKET, consult a doctor immediately. It should be examined whether there is an indication for anti-infective\/antibiotic therapy;\u003cbr\u003e - changes in blood count - pancytopenia, anaemia, leucopenia, thrombocytopenia, neutropenia, agranulocytosis, aplastic anaemia, haemolytic anaemia (the first symptoms are fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nose and skin bleeding, unusual or unexplained bruising). In these cases, treatment should be stopped immediately and a doctor should be consulted. No treatment with painkillers or medicines that reduce fever (antipyretic drugs) should be undertaken;\u003cbr\u003e - psychotic reactions; \u003cbr\u003e- high blood pressure, heart failure, heart attack;\u003cbr\u003e - inflammation of blood vessels;\u003cbr\u003e - inflammation of the pancreas and esophagus;\u003cbr\u003e - diaphragm-like intestinal stenosis;\u003cbr\u003e - liver failure or damage, especially with long-term use, manifested by yellowing of the skin and eyes or pale stools and dark urine;\u003cbr\u003e - in exceptional cases, serious skin infections and soft tissue complications have occurred during chickenpox infection;\u003cbr\u003e - hair loss (alopecia);\u003cbr\u003e - reduced urine output and increased tissue fluid formation (edema), particularly in patients with high blood pressure or impaired renal function.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data)\u003c\/b\u003e \u003cbr\u003e- a widespread, red, scaly rash with pustules under the skin and vesicles located mainly in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using BUSCOFENPOCKET if you develop these symptoms and contact your doctor immediately. See also section 2;\u003cbr\u003e - a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e - fixed drug eruption (such as round or oval patches of redness, swelling of the skin, blisters, hives, and itching);\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e   \u003cbr\u003eMedicines like this may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"OPELLA HEALTHCARE ITALY SRL","offers":[{"title":"Default Title","offer_id":50218927685966,"sku":"045386075","price":8.72,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005847.png?v=1768737988"},{"product_id":"brufenkids-febbre-e-dolore-orale-sosp-150-ml-20-mg-ml","title":"BRUFENKIDS FEB DOL 20 MG\/ML ORAL SUSPENSION 150 ML BOTTLE WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBRUFENKIDS FEVER AND PAIN 20 mg\/ml oral suspension\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eBRUFENKIDS FEVER AND PAIN contains ibuprofen, an active ingredient belonging to a group of medicines called NSAIDs (nonsteroidal anti-inflammatory drugs). NSAIDs are medicines against pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e BRUFENKIDS FEVER AND PAIN is used to treat:\u003cbr\u003e • fever;\u003cbr\u003e • mild to moderate pain.\u003cbr\u003e\u003cbr\u003e BRUFENKIDS FEVER AND PAIN can be used in infants and children aged between 3 months and 12 years.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take BRUFENKIDS FEVER AND PAIN:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to the active substance or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you have had allergic symptoms (e.g. difficulty breathing, nasal congestion, skin rashes) after taking aspirin or other anti-inflammatory medicines, particularly if associated with nasal polyps, swelling of the face (angioedema) and\/or asthma;\u003cbr\u003e • if you have a stomach or duodenal ulcer; \u003cbr\u003e• if you have had even one episode of ulcer, perforation or bleeding in the stomach or intestines (including blood in vomiting or during bowel movements or black, tarry stools) caused by taking medicines;\u003cbr\u003e • if you have had two or more distinct episodes of ulcers or bleeding in your stomach or intestines (including blood in your vomit or during bowel movements or black, tarry stools);\u003cbr\u003e • if you have severe liver or kidney problems;\u003cbr\u003e • if you suffer from severe heart failure;\u003cbr\u003e • if you have any disease that increases the risk of bleeding;\u003cbr\u003e • if you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or drink very little;\u003cbr\u003e • during the third trimester of pregnancy.\u003cbr\u003e\u003cbr\u003e Do not use BRUFENKIDS FEVER AND PAIN in children under 3 months of age or weighing less than 5 kg.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor before taking BRUFENKIDS FEVER AND PAIN if: \u003cbr\u003e• have systemic lupus erythematosus (SLE, known as lupus) or mixed connective tissue disease, diseases that affect the connective tissue causing joint or muscle pain, skin changes, and problems with other organs;\u003cbr\u003e • have had stomach or intestinal diseases, such as ulcers, Crohn's disease, ulcerative colitis;\u003cbr\u003e • has reduced kidney function;\u003cbr\u003e • has liver problems;\u003cbr\u003e • has blood clotting problems;\u003cbr\u003e • have or have had allergies (e.g. hay fever);\u003cbr\u003e • has inflammation of the nose (chronic rhinitis) or nasal polyps;\u003cbr\u003e • is elderly, as he or she is more likely to develop adverse events from this medicine;\u003cbr\u003e • have chickenpox, as pain and inflammation medicines (NSAIDs) can make the skin lesions caused by it worse. In such cases your doctor may advise you not to use this medicine;\u003cbr\u003e • suffers from asthma or respiratory diseases that have lasted for a long time (chronic); \u003cbr\u003e• if you are a child or teenager or elderly and are dehydrated as you are more likely to have kidney problems.\u003cbr\u003e • have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHeart attack and stroke\u003c\/b\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking BRUFENKIDS FEVER AND PAIN if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack); \u003cbr\u003e• high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop BRUFENKIDS FEVER AND PAIN immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSkin reactions\u003c\/b\u003e\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using BRUFENKIDS FEVER AND PAIN and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e BRUFENKIDS FEVER AND PAIN may hide the symptoms of infections such as fever and pain. It is therefore possible that BRUFENKIDS FEVER AND PAIN may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePLEASE NOTE\u003c\/b\u003e , because during treatment with all pain and inflammation medicines (NSAIDs):\u003cbr\u003e • at any time, with or without warning symptoms, even in patients with no previous serious stomach or intestinal (gastrointestinal) problems, bleeding, ulceration or perforation of the stomach or intestine, which can be fatal, has been reported; \u003cbr\u003e• although very rarely, serious skin reactions, some of them fatal, manifesting as redness, blistering and peeling (e.g. exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis), have been reported. Patients appear to be at highest risk in the early stages of therapy: these reactions occur in the majority of cases within the first month of treatment;\u003cbr\u003e • eye changes may occur if BRUFENKIDS FEVER AND PAIN is used for prolonged treatments. During therapy, periodic eye checks are necessary;\u003cbr\u003e • especially if used for prolonged periods and at high doses, headache may occur; in this case, do not increase the dose of BRUFENKIDS FEVER AND PAIN to relieve the pain.\u003cbr\u003e   \u003cbr\u003eThe risk of side effects can be reduced by using the lowest effective dose and for the shortest duration of treatment necessary to control the symptoms. Do not take more than the recommended dose of BRUFENKIDS FEVER AND PAIN and do not take it for long periods; always follow your doctor's instructions carefully.\u003cbr\u003e\u003cbr\u003e STOP treatment and contact your doctor if:\u003cbr\u003e • note any symptoms affecting your stomach and intestines (gastrointestinal), especially if they involve bleeding;\u003cbr\u003e • a skin rash, mucosal lesions or any other sign of an allergic reaction appears (e.g. redness, itching, swelling of the face and throat, sudden drop in blood pressure).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSerious side effects\u003c\/b\u003e \u003cbr\u003eStop taking BRUFENKIDS FEVER AND PAIN and contact your doctor \u003cu\u003eimmediately\u003c\/u\u003e if you experience any of the following conditions:\u003cbr\u003e • serious stomach problems, heartburn or abdominal pain due to stomach or duodenal ulcer (peptic ulcers), sudden severe pain in the pit of the stomach or belly (gastrointestinal perforation). These side effects are uncommon;\u003cbr\u003e • vomiting containing blood (haematemesis) or black stools (melena), associated with bleeding from the stomach or intestine (gastrointestinal haemorrhages) or abnormal tiredness with reduced urine output (due to invisible bleeding). These conditions are common side effects; \u003cbr\u003e• allergic reactions, even serious ones, which manifest themselves with the more or less sudden appearance of skin lesions, for example changes in colour in patches or widespread (rash, purpura), hives, itching, swelling (angioedema) of the face, eyes, lips, swelling of the tongue and throat with possible difficulty in breathing and swallowing. An increase in heart rate and a sudden drop in blood pressure may also occur (anaphylactic reaction, anaphylaxis or severe shock);\u003cbr\u003e • severe skin rashes with redness, peeling and\/or blistering (e.g. erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, exfoliative and bullous dermatitis).\u003cbr\u003e Such conditions occur very rarely;\u003cbr\u003e • difficulty breathing (asthma, bronchospasm, dyspnoea or apnoea). These conditions are uncommon side effects; \u003cbr\u003e• systemic lupus erythematosus (SLE, commonly known as lupus), a disease that affects connective tissue, causing joint or muscle pain, skin changes, and problems with other organs. This condition occurs rarely;\u003cbr\u003e • worsening of infections such as the onset of necrotizing fasciitis which manifests itself with fever, chills, weakness, sweating, diarrhoea, vomiting, redness, pain, swelling, bruising in an area of ​​the body due to tissue necrosis (death of tissue cells);\u003cbr\u003e • inflammation of the meninges (aseptic meningitis) which manifests itself with: very high fever, sudden headache, inability to bend the head, nausea, vomiting, confusion, drowsiness and sensitivity to light. This condition occurs rarely;\u003cbr\u003e • serious skin reaction known as DRESS syndrome. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell); \u003cbr\u003e• a widespread, red, scaly rash with pustules under the skin and blisters mainly located on the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using BRUFENKIDS FEVER AND PAIN if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2;\u003cbr\u003e • non-raised, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes.\u003cbr\u003e These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects\u003c\/b\u003e\u003cbr\u003e Tell your doctor if you notice: \u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon side effects\u003c\/b\u003e (may affect up to 1 in 10 people)\u003cbr\u003e • nausea, vomiting, diarrhoea, intestinal gas (flatulence), difficulty in evacuating (constipation), indigestion (dyspepsia), abdominal pain;\u003cbr\u003e • headache, dizziness;\u003cbr\u003e • fatigue;\u003cbr\u003e • rash.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects\u003c\/b\u003e (may affect up to 1 in 100 people)\u003cbr\u003e • inflammation of the nose (rhinitis);\u003cbr\u003e • gastritis, mouth ulcers;\u003cbr\u003e • dizziness, drowsiness, difficulty falling asleep (insomnia), anxiety, changes in sensation (paraesthesia);\u003cbr\u003e • ringing in the ears (tinnitus), impaired hearing, vision disturbances;\u003cbr\u003e • appearance of skin lesions following exposure to the sun (photosensitivity);\u003cbr\u003e • changes in liver function, yellowing of the eyes or skin (jaundice), dark urine, pale stools, itching or pain in the abdomen, possible signs of inflammation of the liver (hepatitis);\u003cbr\u003e • hypersensitivity reactions (hives, itching); \u003cbr\u003e• kidney problems such as nephrotic syndrome, inflammation of the kidney (tubulointerstitial nephritis), changes in function (renal failure).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects\u003c\/b\u003e (may affect up to 1 in 1,000 people)\u003cbr\u003e • decrease in the number of white blood cells (leukopenia) or certain types of white blood cells (neutropenia, agranulocytosis), decrease in the number of platelets (thrombocytopenia), decrease in the number of red blood cells due to destruction (haemolytic anaemia) or problems with the bone marrow (aplastic anaemia);\u003cbr\u003e • depression, confusion;\u003cbr\u003e • alteration of vision due for example to inflammation of the optic nerve (optic neuritis) or to toxic optic neuropathy;\u003cbr\u003e • swelling (edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects\u003c\/b\u003e (may affect up to 1 in 10,000 people)\u003cbr\u003e • reduced liver function, inflammation of the pancreas (pancreatitis); \u003cbr\u003e• feeling of heart in the throat (palpitations), heart attack, reduced heart function (failure), high blood pressure (hypertension);\u003cbr\u003e • breathing problems due to swelling in the lungs;\u003cbr\u003e • kidney damage (acute renal failure, papillary necrosis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects with unknown frequency\u003c\/b\u003e (frequency cannot be estimated from the available data)\u003cbr\u003e • burning sensation in the mouth or throat, pain or burning (heartburn) in the pit of the stomach, inflammation of the lining of the mouth with ulcers (ulcerative stomatitis), worsening of inflammation of the colon (colitis) or Crohn's disease;\u003cbr\u003e • worsening of skin infections caused by chickenpox;\u003cbr\u003e • stroke;\u003cbr\u003e • hallucinations, malaise, reduced appetite.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"VIATRIS ITALIA SRL","offers":[{"title":"Default Title","offer_id":50220816335182,"sku":"036061024","price":10.4,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0009297_4f9a7a2b-1eb9-48ea-a46c-e1881d6fff51.jpg?v=1768749395"},{"product_id":"paidofen-orale-sosp-150-ml-100-mg-5-ml-gusto-fragola-senza-zucchero","title":"PAIDOFEN CHILDREN 100 MG\/5 ML ORAL SUSPENSION STRAWBERRY FLAVOUR SUGAR FREE 1 BOTTLE OF 150 ML WITH DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003ePAIDOFEN Children 100mg\/5ml oral suspension strawberry flavour sugar free\u003cbr\u003e PAIDOFEN Children 100mg\/5ml oral suspension orange flavour sugar free\u003cbr\u003e\u003c\/b\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e PAIDOFEN contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e This medicine is indicated for the treatment of symptoms of fever and mild to moderate pain in children aged 3 months to 12 years.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop Paidofen immediately and contact your doctor or medical emergency immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not take\/give your child PAIDOFEN:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if the child is less than 3 months old or weighs less than 5.6 kg (See the section \"How to use PAIDOFEN\");\u003cbr\u003e - if you are allergic to medicines such as acetylsalicylic acid or to other similar medicines (analgesics, antipyretics, non-steroidal anti-inflammatory drugs), especially if you have had nose problems such as nasal polyps and asthma (See section \"Warnings and precautions\");\u003cbr\u003e - if you suffer from stomach ulcer (active peptic ulcer);\u003cbr\u003e - if you suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - if you suffer from severe heart disease (heart failure); \u003cbr\u003e- if you have suffered in the past from blood loss (haemorrhage), perforation of the stomach or intestine or if you have suffered recurrent stomach bleeding or ulcers (two or more distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you are being treated with other anti-inflammatory medicines (NSAIDs, including specific COX-2 inhibitors) (See the sections \"Warnings and precautions\" and \"Other medicines and PAIDOFEN\");\u003cbr\u003e - If you have any disease that increases the risk of bleeding;\u003cbr\u003e - In case of unclear blood disorders;\u003cbr\u003e - If you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or if you drink very little.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePregnancy, breastfeeding and fertility\u003c\/u\u003e\u003cbr\u003e • Do not take Paidofen during the last 3 months of pregnancy, as it may harm the unborn baby or cause problems during delivery:\u003cbr\u003e - It can cause kidney and heart problems in the unborn baby.\u003cbr\u003e - May affect the bleeding tendency of mother and baby \u003cbr\u003e- and cause labor to be delayed or take longer than expected.\u003cbr\u003e\u003cbr\u003e You should not take Paidofen during the first 6 months of pregnancy unless strictly necessary and advised by your doctor. If treatment is necessary during this period or while trying to become pregnant, the lowest possible dose should be used for the shortest possible time.\u003cbr\u003e\u003cbr\u003e If taken for more than a few days from 20 weeks of pregnancy onwards, Paidofen may cause kidney problems in the unborn baby which may cause low levels of amniotic fluid surrounding the baby (oligohydramnios) or narrowing of a blood vessel (ductus arteriosus) in the baby’s heart. If you need treatment for more than a few days, your doctor may recommend additional monitoring.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking or administering PAIDOFEN to your child if:\u003cbr\u003e   \u003cbr\u003e• you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), polyps in the nose or angioedema)\u003cbr\u003e • are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and PAIDOFEN\"); \u003cbr\u003e• have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and PAIDOFEN\"). Bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with PAIDOFEN and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section \"Possible side effects\");\u003cbr\u003e • if you are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and PAIDOFEN\"); \u003cbr\u003e• have heart disease (uncontrolled hypertension, congestive heart failure, established ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think your child may be at risk of these conditions (for example, if you have high blood pressure, high levels of sugar (diabetes) or fat in the blood, or if you smoke). Medicines like PAIDOFEN may be associated with a small increased risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e • have an infection – see section “Infections below”.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e \u003cbr\u003ePaidofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Paidofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e \u003cbr\u003eSerious skin reactions have been reported in association with Paidofen treatment. Stop taking Paidofen and contact a doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy as these may be the first signs of a very serious skin reaction. See section 4. Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with Ibuprofen treatment. Stop using Paidofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e   \u003cbr\u003eUndesirable effects may be minimised by using the lowest effective dose for the shortest duration of treatment necessary to control symptoms. Use PAIDOFEN with caution and tell your doctor if you or your child:\u003cbr\u003e - have had stomach or intestinal problems in the past such as ulcers, perforations or bleeding. If your child is being treated with other medicines that can cause stomach and intestinal problems, your doctor may prescribe medicines that protect the stomach (misoprostol or proton pump inhibitors) (See the section \"Other medicines and PAIDOFEN\");\u003cbr\u003e - suffer from asthma. PAIDOFEN may cause breathing problems in this case;\u003cbr\u003e - has problems with blood clotting; \u003cbr\u003e- suffer from kidney disease, heart disease, high blood pressure or are being treated with medicines called diuretics. In these cases, serious kidney problems may occur (critical reduction of kidney function, nephrotoxicity or fluid retention);\u003cbr\u003e - suffers from liver disease;\u003cbr\u003e - is dehydrated (for example due to fever, vomiting or diarrhoea). In this case, your child will need to be rehydrated before starting and during treatment.\u003cbr\u003e\u003cbr\u003e In case of prolonged treatments with PAIDOFEN you must pay particular attention and inform your doctor immediately if the following appear:\u003cbr\u003e - signs or symptoms of ulcers or bleeding in your stomach or intestines; - signs or symptoms of liver problems;\u003cbr\u003e - signs or symptoms of kidney damage;\u003cbr\u003e - vision disturbances (blurred or reduced vision, areas of complete or partial blindness, alterations in color perception); \u003cbr\u003e- signs or symptoms of meningitis, a serious inflammation of the meninges. Symptoms may include fever, neck tension, headache, vomiting and disorientation. Ibuprofen can rarely cause aseptic meningitis; this inflammation is more common in people with systemic lupus erythematosus or other collagen diseases (See the section \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e \u003cb\u003eElderly people\u003c\/b\u003e\u003cbr\u003e This medicine is intended for children, however it may be used in the elderly.\u003cbr\u003e If you are elderly, you may be more likely to experience some side effects such as bleeding and perforation of the stomach or intestine, even serious ones, following treatment with medicines such as PAIDOFEN.\u003cbr\u003e These effects may occur especially at high doses of PAIDOFEN or if you have suffered in the past from ulcers, haemorrhages and perforations of the stomach or intestine (See the section \"Possible side effects\"). \u003cbr\u003eIf you are elderly, take the lowest possible dose of this medicine. In elderly people, the use of medicines that protect the stomach (misoprostol or proton pump inhibitors) is recommended.\u003cbr\u003e Tell your doctor if you have stomach or intestinal problems, especially if you have had ulcers, bleeding or perforation of the stomach or intestine in the past.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If your child experiences any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment with PAIDOFEN and contact your doctor: \u003cbr\u003e- non-raised, target-shaped or circular reddish patches on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e - Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome).\u003cbr\u003e - A widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis) \u003cbr\u003e- allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), abnormal heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma;\u003cbr\u003e - aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more common if the child suffers from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e The following additional side effects may occur:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia);\u003cbr\u003e • skin rashes;\u003cbr\u003e • vision disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing problems; \u003cbr\u003e• cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting;\u003cbr\u003e • hair loss (alopecia);\u003cbr\u003e • the skin becomes sensitive to light;\u003cbr\u003e • severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis); \u003cbr\u003e• simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice);\u003cbr\u003e • severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood;\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotising fasciitis) associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease);\u003cbr\u003e • inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis);\u003cbr\u003e • inflammation of the esophagus (esophagitis); \u003cbr\u003e• a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using Paidofen if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e • Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"D.M.G. ITALIA SRL","offers":[{"title":"Default Title","offer_id":50220816499022,"sku":"041952019","price":6.17,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0004580.png?v=1768749405"},{"product_id":"ibuprofene-zentiva-italia-12-cpr-riv-200-mg","title":"IBUPROFENE ZEN 200 MG FILM-COATED TABLETS, 12 TABLETS IN PVC\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eIBUPROFENE ZENTIVA ITALIA 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e Equivalent medicine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e IBUPROFENE ZENTIVA ITALIA 200 mg contains ibuprofen, a medicine that belongs to a class of medicines called NSAIDs (non-steroidal anti-inflammatory drugs) which work by reducing pain, inflammation and fever.\u003cbr\u003e   \u003cbr\u003eIBUPROFENE ZENTIVA ITALIA 200 mg is used in \u003cb\u003eadults, adolescents and children aged 6 years and over\u003c\/b\u003e to provide relief in the case of:\u003cbr\u003e - mild to moderate pain (such as headache, including migraine, toothache, and fever).\u003cbr\u003e IBUPROFENE ZENTIVA ITALIA 200 mg is used in \u003cb\u003eadults and adolescents from 12 years of age\u003c\/b\u003e to provide relief in case of:\u003cbr\u003e - menstrual cramps (primary dysmenorrhea).\u003cbr\u003e\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after 3 days (in children and adolescents) or after 7 days (in adults).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take IBUPROFENE ZENTIVA ITALIA 200 mg\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6). If you are allergic to other non-steroidal anti-inflammatory drugs; \u003cbr\u003e- if you have suffered from allergic reactions such as asthma, runny nose (rhinitis), itchy skin rashes (hives) or swelling of the lips, face, tongue or throat (angioedema) after taking medicines containing acetylsalicylic acid or other painkillers or anti-inflammatory medicines (NSAIDs);\u003cbr\u003e - if you have suffered from a lesion (ulcer) or bleeding in the stomach or intestine in relation to previous use of painkillers or anti-inflammatory medicines (NSAIDs);\u003cbr\u003e - if you suffer from a lesion (ulcer) or bleeding in the stomach or intestine or have suffered from two or more episodes of this type in the past;\u003cbr\u003e - if you suffer or have suffered from ulcerative colitis, Crohn's disease, peptic ulcer or recurrent gastrointestinal bleeding (defined as two or more distinct episodes of confirmed ulceration or haemorrhage);\u003cbr\u003e - if you suffer or have suffered from congenital porphyrin metabolite disorder (e.g. acute intermittent porphyria); \u003cbr\u003e- chronic alcoholism (14 to 20 drinks\/week or more);\u003cbr\u003e - if you suffer from severe liver problems (liver failure), kidney problems (renal failure) or heart problems (cardiac failure) or an alteration of the coronary arteries, the vessels that carry blood to the heart (coronary heart disease);\u003cbr\u003e - if you are in the last three months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from a large loss of fluid from the body (dehydration) caused by vomiting, diarrhoea or insufficient fluid consumption;\u003cbr\u003e - if you have active bleeding (including in the brain);\u003cbr\u003e - if you suffer from a disease of unknown origin that causes abnormal formation of blood cells (dyshematopoiesis);\u003cbr\u003e - if he is under 6 years old.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with treatment with IBUPROFENE ZENTIVA ITALIA. Stop using IBUPROFENE ZENTIVA ITALIA and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003e Stop taking IBUPROFENE ZENTIVA ITALIA immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e Talk to your doctor or pharmacist before taking IBUPROFENE ZENTIVA ITALIA 200 mg if:\u003cbr\u003e - have heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or are a smoker;\u003cbr\u003e - suffers from congestive heart failure; \u003cbr\u003e- have an autoimmune disease called systemic lupus erythematosus (SLE) or other diseases that affect the immune system; - have an inherited disorder of haemoglobin, a substance that carries oxygen in the blood (acute intermittent porphyria);\u003cbr\u003e - is significantly dehydrated (caused by vomiting, diarrhea, or insufficient fluid intake);\u003cbr\u003e - suffer from chronic inflammatory bowel diseases such as inflammation of the intestine with ulcers (ulcerative colitis), inflammation of the digestive tract (Crohn's disease) or other diseases of the stomach and intestines; \u003cbr\u003e- have suffered from an ulcer (ulcer) of the stomach or intestine, especially if it was complicated by perforation or accompanied by bleeding. Report to your doctor immediately any unusual symptoms of the stomach or intestine (especially bleeding or ulceration) especially if these symptoms occur at the beginning of treatment. These symptoms are more likely to occur if you are elderly. See section \"Possible side effects\";\u003cbr\u003e - suffer from disorders of blood cell formation (haematopoiesis disorder);\u003cbr\u003e - suffers from problems related to the normal blood clotting mechanism;\u003cbr\u003e - suffer from allergies, a disease affecting the mucous membranes of the nose (hay fever), asthma, chronic swelling of the nasal passages (adenoids) or chronic obstructive airway diseases (asthma);\u003cbr\u003e - have liver, kidney, heart problems or high blood pressure (especially if you are elderly); \u003cbr\u003e- recently underwent surgery;\u003cbr\u003e - is in the first six months of pregnancy;\u003cbr\u003e - is breastfeeding;\u003cbr\u003e - have blurred vision or other eye symptoms, skin rash, weight gain or fluid retention (edema);\u003cbr\u003e - have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Respiratory disorders\u003cbr\u003e Special precautions should be taken in asthmatic patients or those with a previous history of asthma, bronchial disease, chronic rhinitis or respiratory disease, since ibuprofen may trigger bronchospasm, urticaria or angioedema in these patients.\u003cbr\u003e\u003cbr\u003e Allergic reactions \u003cbr\u003eSevere acute hypersensitivity reactions (e.g. anaphylactic shock) have been observed rarely. At the first signs of a hypersensitivity reaction after taking Ibuprofen Zentiva Italia, therapy should be discontinued. Medically necessary measures, depending on the symptoms, should be initiated by specialist personnel. Caution is required in patients who have suffered from allergic reactions or hypersensitivity to other substances, as they may have an increased risk of drug reactions, hypersensitivity to ibuprofen. Caution is required in patients suffering from hay fever, nasal polyps or chronic obstructive respiratory tract infections as the risk of allergic reactions increases. These may occur in asthma attacks (so-called analgesic asthma), Quincke's edema or urticaria.\u003cbr\u003e\u003cbr\u003e Heart, kidney or liver problems \u003cbr\u003ePrecautions should be taken in patients with renal, hepatic or cardiac insufficiency, as the use of NSAIDs may deteriorate renal function. Habitual concomitant ingestion of several painkillers further increases this risk. In these patients the dose should be as low as possible and for the shortest period of time (see section \"Do not take Ibuprofen Zentiva Italia\").\u003cbr\u003e\u003cbr\u003e Effects on the kidneys \u003cbr\u003eAt the beginning of treatment, ibuprofen, like other NSAIDs, should be administered with caution. in patients with significant dehydration (there is a risk of renal failure especially in dehydrated children, adolescents and the elderly). As with other NSAIDs, prolonged administration of ibuprofen has caused renal papillary necrosis and other pathological renal changes. Cases of renal toxicity in patients in whom prostaglandins have a compensatory function maintenance of renal perfusion. In these patients, administration of NSAIDs may cause a dose-dependent decrease in prostaglandin formation and, secondarily, renal blood flow, which may precipitate overt renal decompensation. Most patients at risk for this reaction are those with renal dysfunction, heart failure, liver disease, those taking diuretics and ACE inhibitors and elderly patients. \u003cbr\u003eDiscontinuation of NSAID therapy is generally followed by recovery to the pre-treatment state.\u003cbr\u003e\u003cbr\u003e Aseptic meningitis\u003cbr\u003e On rare occasions, aseptic meningitis has been observed in patients receiving ibuprofen. Although it is more likely to occur in patients with systemic lupus erythematosus and connective tissue diseases, cases of aseptic meningitis have been reported in patients without underlying chronic conditions.\u003cbr\u003e\u003cbr\u003e Hematological effects\u003cbr\u003e Ibuprofen, like other NSAIDs, may inhibit platelet aggregation and prolong bleeding time in normal patients.\u003cbr\u003e\u003cbr\u003e Exceptionally, chickenpox can cause serious complications, severe skin or soft tissue infections. To date, a role of NSAIDs in worsening these infections cannot be ruled out. Therefore, it is recommended to avoid the use of Ibuprofen Zentiva Italia in case of chickenpox.\u003cbr\u003e\u003cbr\u003e Elderly population \u003cbr\u003eElderly patients have a higher frequency of adverse reactions to NSAIDs, particularly gastrointestinal bleeding and perforation, which may be fatal.\u003cbr\u003e\u003cbr\u003e Gastrointestinal bleeding, ulceration and perforation: \u003cbr\u003eIbuprofen should be administered with caution to patients with a history of peptic ulcer or other gastrointestinal disease as these conditions may be exacerbated. Cases of life-threatening gastrointestinal bleeding, ulceration and perforation have been reported with all NSAIDs at various stages of treatment, with or without warning symptoms or a history of serious gastrointestinal events. The risk of bleeding, ulceration or perforation is greater with higher doses of ibuprofen, in patients with a history of peptic ulcer, particularly if associated with bleeding or perforation, and in the elderly. In these patients, treatment should be initiated at the lowest effective dose. Concomitant administration of protective agents (e.g. misoprostol or proton pump inhibitors) should be considered in these patients, as well as in those who need to take concomitant low-dose aspirin, or other drugs likely to increase gastrointestinal risk. Precaution should be taken in patients who need to take concomitant medications which could increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants (such as warfarin), selective serotonin reuptake inhibitors or antiplatelet agents such as acetylsalicylic acid. If gastrointestinal bleeding or ulceration occurs in patients receiving Ibuprofene Zentiva Italia, the treatment should be withdrawn. Concomitant administration of Ibuprofene Zentiva Italia with other NSAIDs, including cyclooxygenase-2 selective inhibitors, should be avoided due to the increased risk of ulceration or bleeding. Patients with a history of gastrointestinal disease, particularly the elderly, should report unusual abdominal symptoms (especially gastrointestinal bleeding) in the early stages of treatment. \u003cbr\u003e\u003cbr\u003eInfections\u003cbr\u003e Ibuprofene Zentiva Italia may hide the symptoms of infections such as fever and pain. It is therefore possible that Ibuprofene Zentiva Italia may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e Medicines such as IBUPROFENE ZENTIVA ITALIA 200 mg may be associated with a small increased risk of blood clot formation (arteriovenous thrombotic events) such as heart attack (\"myocardial infarction\") or stroke (loss of blood flow to the brain): this risk is more likely with high doses and prolonged treatment.\u003cbr\u003e Ibuprofen may temporarily increase the tendency to bleed.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions have been reported in association with treatment with IBUPROFENE ZENTIVA ITALIA. Stop taking IBUPROFENE ZENTIVA ITALIA and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and Adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Infections and infestations\u003cbr\u003e Exacerbations of inflammation related to skin infections (e.g. development of necrotizing fasciitis) coinciding with the use of NSAIDs. If signs of infection occur or worsen during the use of ibuprofen, the patient should be advised to consult a doctor immediately.\u003cbr\u003e  \u003cbr\u003eSkin and subcutaneous tissue disorders\u003cbr\u003e In exceptional cases, serious skin infections and soft tissue complications may occur during chickenpox infection (see also infections and infestations).\u003cbr\u003e\u003cbr\u003e Cardiovascular and cerebrovascular effects\u003cbr\u003e Clinical trials suggest that administration of ibuprofen, particularly at high doses (2400 mg daily) and in long-term treatment, may be associated with a small increased risk of arterial thrombotic events (for example myocardial infarction or stroke) (see \"Warnings and precautions\").\u003cbr\u003e\u003cbr\u003e Gastrointestinal diseases \u003cbr\u003eThe most frequently observed adverse reactions are gastrointestinal in nature. Nausea, dyspepsia, vomiting, haematemesis, flatulence, abdominal pain, diarrhoea, constipation, melaena, aphthous stomatitis, gastrointestinal bleeding, exacerbation of colitis and Crohn's disease have been reported following the administration of these medicinal products. Less frequently, cases of gastritis, duodenal and gastric ulcer and gastrointestinal perforation have been observed.\u003cbr\u003e\u003cbr\u003e Side effects are more likely to occur with higher doses and longer duration of treatment. Side effects are listed below according to how often they occur.\u003cbr\u003e\u003cbr\u003e The following side effects are important and require immediate attention if they occur.\u003cbr\u003e \u003cb\u003eSTOP\u003c\/b\u003e taking IBUPROFENE ZENTIVA ITALIA 200 mg and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e  \u003cbr\u003e\u003cb\u003e\u003cu\u003eVery common (affects more than 1 in 10 people)\u003c\/u\u003e :\u003c\/b\u003e • digestive tract disorders, such as heartburn (pyrosis), difficult digestion (dyspepsia), abdominal pain, nausea, vomiting, excessive production of gas in the stomach (flatulence), diarrhoea, constipation.\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eCommon (affects 1 to 10 people in 100)\u003c\/u\u003e :\u003c\/b\u003e\u003cbr\u003e • intestinal inflammation and worsening of inflammation of the colon, part of the intestine (colitis) and digestive tract (Crohn's disease)\u003cbr\u003e • complication of diverticula, small pockets that form in the terminal part of the intestine (perforation or fistula) \u003cbr\u003e• lesions of the stomach and intestines (gastrointestinal ulcers), sometimes with loss of blood, which may cause anaemia (reduction of haemoglobin in the blood, a substance that carries oxygen in the blood), melaena (black stools), haematemesis (presence of blood in the vomit), ulcerative stomatitis (inflammation of the mucosa of the mouth), colitis. Generally these effects increase with increasing the dose of ibuprofen or if you are taking certain other medicines (See section \"Other medicines and IBUPROFENE ZENTIVA ITALIA 200 mg\"). Elderly people are more prone to bleeding and perforation of the digestive tract. These effects can also be fatal.\u003cbr\u003e • heachache\u003cbr\u003e • drowsiness\u003cbr\u003e • dizziness\u003cbr\u003e • dizziness\u003cbr\u003e • fatigue\u003cbr\u003e • agitation\u003cbr\u003e • insomnia\u003cbr\u003e • irritability.\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eUncommon (affects 1 to 10 people in 1000)\u003c\/u\u003e :\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis) \u003cbr\u003e• kidney problems (nephrotic syndrome), development of edema (swelling due to fluid accumulation), swelling of the legs, inflammation of the kidneys (interstitial nephritis), reduction in kidney function (renal failure)\u003cbr\u003e • increased sensitivity of the skin to the sun (photosensitivity)\u003cbr\u003e • vision disorders\u003cbr\u003e • insomnia\u003cbr\u003e • anxiety\u003cbr\u003e • paresthesia\u003cbr\u003e • hearing impairment\u003cbr\u003e • profuse secretion from the nasal passages (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm)\u003cbr\u003e • allergic reactions, such as skin rashes (exanthema and urticaria), itching, redness of the skin due to broken capillaries (purpura), asthma attacks sometimes accompanied by low blood pressure (hypotension)\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eRare (affects 1 to 10 people in 10,000)\u003c\/u\u003e :\u003c\/b\u003e • depression\u003cbr\u003e • state of confusion\u003cbr\u003e • hallucinations (perception of things that do not exist in reality)\u003cbr\u003e • optic neuritis\u003cbr\u003e • toxic optic neuropathy\u003cbr\u003e • SLE, systemic lupus erythematosus (disease affecting the immune system) \u003cbr\u003e• lazy eye (toxic amblyopia) increased blood urea nitrogen (a substance present in the blood, the increase of which may indicate a kidney or liver disorder)\u003cbr\u003e • increased levels of liver enzymes (substances present in the blood, the increase of which may indicate a liver disorder)\u003cbr\u003e • decrease in hemoglobin (a substance that carries oxygen in the blood)\u003cbr\u003e • decreased hematocrit (volume of blood occupied by red blood cells, a type of blood cell)\u003cbr\u003e • reduction of the aggregation activity of platelets (cells present in the blood, involved in the coagulation process) and prolongation of bleeding time\u003cbr\u003e • decrease in calcium in the blood\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cu\u003eVery rare (affects less than 1 in 10,000 people)\u003c\/u\u003e :\u003c\/b\u003e\u003cbr\u003e • perception of heartbeat (palpitations)\u003cbr\u003e • reduced ability of the heart to pump blood around the body (heart failure)\u003cbr\u003e • heart attack (myocardial infarction) \u003cbr\u003e• fluid build-up in the lungs (acute pulmonary edema)\u003cbr\u003e • swelling due to fluid accumulation (edema)\u003cbr\u003e • kidney disease (papillary necrosis)\u003cbr\u003e • high blood pressure (hypertension)\u003cbr\u003e • disorders of red blood cell formation (with symptoms such as: fever, sore throat, lesions on the surface of the mouth, flu-like symptoms, severe tiredness, nose and skin bleeding)\u003cbr\u003e • noises in the ear (tinnitus)\u003cbr\u003e • esophagitis (inflammation of the esophagus, the tube that carries food to the stomach), pancreatitis (inflammation of the pancreas (gland that has the function of digesting certain substances and regulating blood sugar levels))\u003cbr\u003e • narrowing of the intestine (intestinal stenosis)\u003cbr\u003e • acute inflammation of the liver (acute hepatitis)\u003cbr\u003e • yellowing of the skin or whites of the eyes (jaundice)\u003cbr\u003e • liver dysfunction or failure (reduced liver function)\u003cbr\u003e • liver damage\u003cbr\u003e • pancreatitis \u003cbr\u003e• aseptic meningitis (inflammation without infection of the meninges which are membranes that cover the brain)\u003cbr\u003e • Non-raised, target-shaped or circular reddish patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis)\u003cbr\u003e • severe hypersensitivity reactions with swelling of the face, tongue, throat, narrowing of the airways, difficulty breathing (dyspnoea), increased heart rate (tachycardia), reduction in blood pressure up to life-threatening shock \u003cbr\u003e• kidney damage. This effect occurs in particular if you\/the child have previously suffered from kidney, heart or liver problems, if you are taking diuretic medicines or ACE inhibitors (See section \"Other medicines and IBUPROFENE ZENTIVA ITALIA 200 mg\") or if you are elderly. This effect usually disappears when the therapy is stopped.\u003cbr\u003e • hair loss (alopecia)\u003cbr\u003e • reduction in the number of: red blood cells (anaemia), white blood cells (leukopenia), platelets (thrombocytopenia), all blood cells (pancytopenia). These conditions may cause fever, sore throat, ulcers on the surface of the mouth, flu-like symptoms, severe tiredness, nosebleeds and skin bleeding\u003cbr\u003e\u003cbr\u003e Not known (frequency cannot be estimated from the available data): \u003cbr\u003e• A widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using IBUPROFENE ZENTIVA ITALIA if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e • Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome. A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ZENTIVA ITALIA SRL","offers":[{"title":"Default Title","offer_id":50220816531790,"sku":"042324020","price":3.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0004302_b49b9432-90c4-4b14-8510-bc32ac325bc0.png?v=1768749404"},{"product_id":"benatia-bb-orale-sosp-150-ml-100-mg-5-ml-gusto-arancia-senzazucchero","title":"BENATIA CHILDREN 100MG\/5ML ORAL SUSPENSION ORANGE FLAVOUR SUGAR FREE 1 PET BOTTLE OF 150ML WITH PE DOSING SYRINGE","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eBENATIA Children 100mg\/5ml oral suspension strawberry flavour sugar free\u003cbr\u003e BENATIA Children 100mg\/5ml oral suspension orange flavour sugar free\u003cbr\u003e\u003c\/b\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eBENATIA contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action allows to reduce pain, fever and inflammation. BENATIA is indicated in children from 3 months to 12 years for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earaches).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not give your child BENATIA:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - you experience or have experienced in the past allergic reactions such as shortness of breath, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, particularly if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs); \u003cbr\u003e- suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e - suffer from a serious heart disease (heart failure);\u003cbr\u003e - suffer or have suffered from bleeding in the stomach and\/or intestine (gastrointestinal haemorrhage) or perforation following previous treatments with NSAIDs;\u003cbr\u003e - suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you are taking other non-steroidal anti-inflammatory drugs (NSAIDs, including selective COX-2 inhibitors) (see section \"Other medicines and BENATIA\");\u003cbr\u003e - if you have any disease that increases the risk of bleeding;\u003cbr\u003e - in case of unclear blood disorders;\u003cbr\u003e - if you are severely dehydrated, for example if you have had severe vomiting, diarrhoea or if you drink very little;\u003cbr\u003e - is less than 3 months old or weighs less than 5.6 kg; \u003cbr\u003e- is in the last trimester of pregnancy (see section \"Pregnancy and breast-feeding\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before giving BENATIA to your child.\u003cbr\u003e • you suffer or have suffered from allergy to medicines used to treat fever, pain and inflammation (non-steroidal anti-inflammatory drugs) and if you suffer from difficulty breathing (asthma), seasonal allergies (hay fever), polyps in the nose, if you have severe breathing or chest problems, e.g. chronic obstructive pulmonary disease, swelling of the face, lips and throat (angioedema);\u003cbr\u003e • are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and BENATIA\"); \u003cbr\u003e• have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and BENATIA\"). Bleeding, ulceration and perforation of the stomach or intestine, which can be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop treatment with BENATIA and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section \"Possible side effects\");\u003cbr\u003e • if you are taking medicines that may increase the risk of ulcers or bleeding, such as medicines used to treat inflammation and some immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and BENATIA\"); \u003cbr\u003e• have heart disease (uncontrolled hypertension, congestive heart failure, known ischaemic heart disease, peripheral arterial disease) or have had reduced blood flow to the brain (stroke), or if you think your child may be at risk of these conditions (for example, if you have high blood pressure, high levels of sugar (diabetes) or fat in your blood, or if you smoke). Medicines like BENATIA may be associated with a small increase in the risk of heart attack or reduced blood flow to the brain: the risk is more likely at high doses and during prolonged treatment. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) since fluid retention, high blood pressure and swelling (oedema) have been reported in association with NSAID therapy;\u003cbr\u003e • have an infection (see section \"Infections\" below); \u003cbr\u003e• have chickenpox, in which case it is advisable to avoid using BENATIA.\u003cbr\u003e\u003cbr\u003e The use of BENATIA requires adequate precautions, especially if the child:\u003cbr\u003e • suffer or have suffered from asthma as it could make breathing difficulties worse;\u003cbr\u003e • suffers from clotting problems or high blood pressure;\u003cbr\u003e • suffers from kidney, heart or liver disease, if he\/she takes drugs that increase urine production (diuretics), or if he\/she has undergone major surgery resulting in loss of fluids, since in these cases your doctor will advise you to perform periodic blood and urine tests on your child;\u003cbr\u003e • has undergone major surgery; \u003cbr\u003e• suffers from certain congenital diseases affecting blood formation (for example acute intermittent porphyria); is dehydrated (for example due to fever, vomiting or diarrhoea), in this case rehydrate him before starting and during treatment to avoid the risk of altering kidney function.\u003cbr\u003e\u003cbr\u003e During prolonged treatments with BENATIA, you must pay particular attention and immediately inform your doctor if the following occur:\u003cbr\u003e • signs or symptoms of ulceration or bleeding in the stomach and intestines (e.g. black, foul-smelling stools, vomiting blood);\u003cbr\u003e • signs or symptoms of liver damage (e.g. hepatitis and jaundice);\u003cbr\u003e • signs or symptoms of kidney damage (e.g. increased urine production, blood in the urine);\u003cbr\u003e • visual disturbances (blurred or reduced vision, areas of complete or partial blindness, alteration of color perception); \u003cbr\u003e• symptoms such as frequent or daily headaches despite regular use of headache medicines, as they may be caused by excessive use of these medicines;\u003cbr\u003e • symptoms such as headache, disorientation, nausea, vomiting, stiff neck and fever as these could be symptoms due to aseptic meningitis (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions have been reported in association with treatment with BENATIA. Stop taking BENATIA and consult your doctor immediately if you experience a rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction.\u003cbr\u003e See paragraph 4.\u003cbr\u003e\u003cbr\u003e Infections   \u003cbr\u003eBENATIA may hide the symptoms of infections such as fever and pain. It is therefore possible that BENATIA may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e \u003cb\u003eIf your child experiences any of the following serious side effects, stop taking the tablets and tell your doctor immediately or go to the nearest hospital:\u003c\/b\u003e \u003cbr\u003e• severe skin and mucous membrane disorders characterized by rashes, redness, itching and blisters (bullous and exfoliative dermatitis including erythema multiforme, Stevens-Johnson syndrome and toxic epidermal necrolysis);\u003cbr\u003e • allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), abnormal heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, severe shock and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck and fever (more frequent if the child suffers from systemic lupus erythematosus or other collagen diseases). Further side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness and convulsions;\u003cbr\u003e • stomach pain, nausea and difficulty in digesting (dyspepsia); \u003cbr\u003e• skin rashes;\u003cbr\u003e • vision disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, mood swings, hearing problems;\u003cbr\u003e • cerebrovascular hemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • perception of one's heartbeat (palpitations);\u003cbr\u003e • diarrhea, flatulence, dry mouth, constipation and vomiting;\u003cbr\u003e • hair loss (alopecia);\u003cbr\u003e • the skin becomes sensitive to light;\u003cbr\u003e • severe kidney disease including tubular necrosis, glomerular nephritis, blood in the urine and increased urine output;\u003cbr\u003e • decrease in hematocrit levels.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e \u003cbr\u003e• reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nosebleeds and hemorrhages;\u003cbr\u003e • signs or symptoms of ulceration or bleeding of the stomach and intestines, black and foul-smelling stools, vomiting blood;\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis);\u003cbr\u003e • simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (liver necrosis), liver disease (liver failure, liver dysfunction, hepatitis, jaundice);\u003cbr\u003e • severe kidney disease (acute renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood and swelling (edema);\u003cbr\u003e • decrease in hemoglobin levels in the blood; \u003cbr\u003e• heart attack (myocardial infarction);\u003cbr\u003e • serious skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammation (e.g. necrotizing fasciitis) associated with the use of some non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (edema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock); \u003cbr\u003e• respiratory tract disorders including asthma, obstruction of the larynx, shortness of breath (bronchospasm), temporary cessation of breathing (apnoea) and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the esophagus (esophagitis);\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • the skin becomes sensitive to light.\u003cbr\u003e   \u003cbr\u003eStop using BENATIA if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2.\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"DYMALIFE PHARMACEUTICAL SRL","offers":[{"title":"Default Title","offer_id":50220816564558,"sku":"043186028","price":9.52,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0010385.png?v=1768749406"},{"product_id":"ibuprofene-pensavital-12-cpr-riv-400-mg","title":"IBUPROFENE PENSA 400 MG FILM-COATED TABLETS 12 TABLETS IN AI\/PVC\/PVDC BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eIBUPROFENE PENSAVITAL 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e IBUPROFENE PENSAVITAL belongs to a group of medicines called NSAIDs (nonsteroidal anti-inflammatory drugs) which work by reducing pain, inflammation and fever.\u003cbr\u003e\u003cbr\u003e IBUPROFENE PENSAVITAL 400 mg is used for the symptomatic treatment of mild to moderate pain such as headache, dental pain, menstrual pain and fever (less than 3 days).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take IBUPROFENE PENSAVITAL if:\u003c\/b\u003e\u003cbr\u003e - are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6). Symptoms of an allergic reaction may include swelling of the eyelids, lips, tongue or throat \u003cbr\u003e- if you have ever had an allergic reaction (such as bronchospasm (tightening of the lung muscles which can cause asthma and shortness of breath), asthma attacks, runny nose, swelling of the airways, skin reactions or sudden swelling) after taking acetylsalicylic acid or other similar painkillers (NSAIDs) you suffer from unexplained blood formation disorders\u003cbr\u003e - have recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least 2 different episodes of confirmed ulcers or bleeding) have a history of gastrointestinal bleeding or perforation associated with previous NSAID treatment have any active bleeding (including cerebral bleeding)\u003cbr\u003e - suffer from severe liver, kidney or heart impairment\u003cbr\u003e - has severe dehydration (caused by vomiting, diarrhea or insufficient fluid intake)\u003cbr\u003e - suffers from chronic alcoholism (14 to 20 drinks\/week or more) \u003cbr\u003e- is a child under 12 years of age or adolescents weighing less than 40 kg\u003cbr\u003e - is in the last three months of pregnancy\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking IBUPROFENE PENSAVITAL.\u003cbr\u003e\u003cbr\u003e Undesirable effects can be minimised by using the lowest effective dose to control symptoms for the shortest possible treatment period.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking IBUPROFENE PENSAVITAL if:\u003cbr\u003e - suffer from systemic lupus erythematosus (SLE, sometimes known as lupus) or connective tissue disease (an autoimmune disease affecting the connective tissue) have or have had gastrointestinal diseases (such as ulcerative colitis, Crohn's disease) as your condition may get worse\u003cbr\u003e - suffer from certain hereditary blood formation diseases (e.g. acute intermittent porphyria)\u003cbr\u003e - has reduced liver and kidney function \u003cbr\u003e- recently underwent major surgery\u003cbr\u003e - suffer from hay fever, nasal polyps or chronic obstructive respiratory disease, because there is an increased risk of allergic reactions. Allergic reactions may present as asthma attacks (so-called analgesic asthma), Quincke's edema (rapid swelling) or urticaria\u003cbr\u003e - he is dehydrated\u003cbr\u003e - have an infection – see “Infections” section below.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eEffects on the gastrointestinal tract\u003c\/u\u003e\u003cbr\u003e The combined use of IBUPROFENE PENSAVITAL with another nonsteroidal anti-inflammatory drug (NSAID), so-called COX-2 inhibitor (cyclooxygenase-2 inhibitor), should be avoided.\u003cbr\u003e\u003cbr\u003e \u003cem\u003eGastrointestinal tract bleeding, ulcers and perforations\u003c\/em\u003e \u003cbr\u003eGastrointestinal bleeding, ulcers and perforation, sometimes fatal, have been reported with all NSAIDs. These have occurred at any time during therapy, with or without antecedent warning symptoms or a history of serious gastrointestinal events.\u003cbr\u003e\u003cbr\u003e The risk of gastrointestinal bleeding, ulcers and perforation is higher with increasing doses of NSAIDs and is higher in patients with a history of ulcers, especially with complications of bleeding or perforation (see section 2 \"Do not take IBUPROFENE PENSAVITAL\") and in elderly patients. These patients should start treatment at the lowest available dose. \u003cbr\u003eFor these patients, as well as for patients requiring additional treatment with low-dose acetylsalicylic acid or other medicinal products likely to increase the risk of gastrointestinal disorders, combination treatment with protective medicinal products (e.g. misoprostol or proton pump inhibitors) should be considered.\u003cbr\u003e\u003cbr\u003e If you have a history of gastrointestinal side effects, especially if you are elderly, you should contact a doctor if you experience any unusual abdominal symptoms (especially gastrointestinal bleeding), particularly at the start of therapy.\u003cbr\u003e   \u003cbr\u003eCaution is advised if you are also taking other medicines which may increase the risk of ulcers or bleeding, e.g. oral corticosteroids, anticoagulants (blood thinners) such as warfarin, selective serotonin reuptake inhibitors (used to treat psychiatric disorders including depression) or platelet aggregation inhibitors such as acetylsalicylic acid (see section 2 \"Other medicines and IBUPROFENE PENSAVITAL\").\u003cbr\u003e\u003cbr\u003e Treatment should be stopped and a doctor should be consulted if you develop gastrointestinal bleeding or ulcers during treatment with IBUPROFENE PENSAVITAL. Effects on the cardiovascular system Anti-inflammatory\/pain-relieving medicines such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when used in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e   \u003cbr\u003eYou should discuss your treatment with your doctor or pharmacist before taking IBUPROFENE PENSAVITAL if:\u003cbr\u003e - have heart problems including heart failure and angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral artery disease (poor blood circulation in the legs or feet due to narrow or blocked arteries) or any type of stroke (including 'mini-stroke' or transient ischaemic attack 'TIA').\u003cbr\u003e - have high blood pressure, diabetes, or high cholesterol, have a family history of heart disease or stroke, or are a smoker.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRenal effects\u003c\/u\u003e\u003cbr\u003e Caution should be exercised when initiating treatment with ibuprofen in patients with significant dehydration. There is a risk of renal impairment especially in dehydrated children, adolescents and the elderly. \u003cbr\u003eAs with other NSAIDs, long-term administration of ibuprofen has caused renal papillary necrosis and other pathological renal changes. Renal toxicity has also been observed in patients in whom renal prostaglandins have a compensatory role in the maintenance of renal perfusion. In these patients, administration of an NSAID may cause a dose-dependent reduction in prostaglandin formation and, secondarily, in renal blood flow, which may result in renal failure. Patients at greatest risk of this reaction are those with impaired renal function, heart failure, hepatic dysfunction, those taking diuretics and ACE inhibitors, and the elderly. Discontinuation of NSAID therapy is usually followed by recovery to the pre-treatment state.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using IBUPROFENE PENSAVITAL and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e During chickenpox infection (varicella infection), it is advisable to avoid the use of IBUPROFENE PENSAVITAL.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e \u003cbr\u003eIBUPROFENE PENSAVITAL may hide signs of infection such as fever and pain. It is therefore possible that IBUPROFENE PENSAVITAL may delay appropriate treatment of the infection, which may lead to an increased risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, consult a doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRespiratory disorders and hypersensitivity reactions\u003c\/u\u003e\u003cbr\u003e Very rarely, severe acute hypersensitivity reactions (e.g. anaphylactic shock) have been observed.\u003cbr\u003e At the first signs of a hypersensitivity reaction after taking\/administering IBUPROFENE PENSAVITAL, treatment should be stopped and a doctor should be consulted. The necessary medical measures, in line with the symptoms, should be initiated by the healthcare professional.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eHematological effects\u003c\/u\u003e \u003cbr\u003eIbuprofen may temporarily inhibit platelet function (platelet aggregation). Patients with blood clotting disorders should therefore be carefully monitored.\u003cbr\u003e\u003cbr\u003e During prolonged use of IBUPROFENE PENSAVITAL, regular monitoring of liver function tests, renal function and blood count is necessary.\u003cbr\u003e\u003cbr\u003e If IBUPROFENE PENSAVITAL is taken before surgery, it is necessary to consult\/inform your doctor or dentist.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSLE and mixed connective tissue disease\u003c\/u\u003e\u003cbr\u003e In patients with systemic lupus erythematosus (SLE) and mixed connective tissue disorders there may be an increased risk of aseptic meningitis (see below and section 4.8).\u003cbr\u003e\u003cbr\u003e \u003cu\u003eAseptic meningitis\u003c\/u\u003e \u003cbr\u003eAseptic meningitis has been observed on rare occasions in patients receiving ibuprofen. Although it is probably more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has been reported in patients without underlying chronic disease.\u003cbr\u003e\u003cbr\u003e Patients who report eye complaints during treatment with ibuprofen should discontinue therapy and undergo ophthalmological examinations.\u003cbr\u003e\u003cbr\u003e When using NSAIDs, adverse reactions, particularly those affecting the gastrointestinal tract or the central nervous system, may be increased by concomitant consumption of alcohol.\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop taking IBUPROFENE PENSAVITAL immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eElderly people\u003c\/b\u003e\u003cbr\u003e In elderly patients, side effects occur more frequently after the use of nonsteroidal anti-inflammatory drugs, especially gastrointestinal bleeding and perforation, which in some cases can be life-threatening. For this reason, particularly close medical surveillance is necessary in elderly patients.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e There is a risk of renal impairment in dehydrated adolescents.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e The pattern of adverse events reported for ibuprofen is similar to that for other NSAIDs.\u003cbr\u003e   \u003cbr\u003e\u003cu\u003eGastrointestinal disorders\u003c\/u\u003e : The most commonly observed side effects affect the digestive tract. Stomach\/duodenal ulcers (peptic ulcers), perforation or bleeding, sometimes fatal, may occur, especially in elderly patients (see section 2: \"Warnings and precautions\"). Nausea, vomiting, diarrhoea, flatulence, constipation, indigestion, abdominal pain, tarry stools, vomiting blood, sores (ulceration) in the mouth and throat area (ulcerative stomatitis), worsening of colitis and Crohn's disease (see section 2: \"Warnings and precautions\") have been reported after use. Less commonly, inflammation of the stomach lining (gastritis) has been observed. In particular, the risk of developing gastrointestinal bleeding depends on the dose level and duration of treatment.\u003cbr\u003e   \u003cbr\u003e\u003cu\u003eImmune system disorders\u003c\/u\u003e : Hypersensitivity reactions have been reported following treatment with NSAIDs. These may consist of (a) non-specific allergic reaction and anaphylaxis, (b) respiratory tract reactivity including asthma, aggravated asthma, bronchospasm or dyspnoea, or (c) assorted skin disorders including rashes of various types, pruritus, urticaria, purpura, angioedema and, very rarely, erythema multiforme, bullous dermatosis (including Stevens-Johnson syndrome and toxic epidermal necrolysis).\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections and infestations\u003c\/u\u003e : Rhinitis and aseptic meningitis (especially in patients with existing autoimmune diseases, such as systemic lupus erythematosus and mixed connective tissue disease) with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation (see section 4.4). \u003cbr\u003eExacerbation of infection-related inflammation has been reported to coincide with the use of NSAIDs. If signs of infection appear or worsen during the use of ibuprofen, the patient is therefore advised to seek immediate medical attention.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin and subcutaneous tissue disorders\u003c\/u\u003e : In exceptional cases, serious skin infections and soft tissue complications may occur during a chickenpox infection (see also \"Infections and infestations\").\u003cbr\u003e\u003cbr\u003e \u003cu\u003eCardiac and vascular disorders\u003c\/u\u003e : Oedema, hypertension and cardiac failure have been reported in association with NSAID treatment. Clinical trials suggest that use of ibuprofen, particularly at high doses (2400 mg\/day), may be associated with a small increased risk of arterial thrombotic events such as myocardial infarction or stroke (see section 4.4).\u003cbr\u003e\u003cbr\u003e Stop using ibuprofen and see your doctor immediately if you notice any of the following symptoms: \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e • Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome).\u003cbr\u003e • Widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003e\u003cem\u003e\u003cu\u003eOther side effects that may occur:\u003c\/u\u003e\u003c\/em\u003e\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cem\u003eCommon (may affect up to 1 in 10 people):\u003c\/em\u003e\u003cbr\u003e - Headache, dizziness \u003cbr\u003e- Gastrointestinal side effects (indigestion, diarrhea, nausea, vomiting, abdominal pain, flatulence, constipation, black stools, stomach and intestinal bleeding, vomiting blood)\u003cbr\u003e - Skin rash\u003cbr\u003e - Tiredness\u003cbr\u003e\u003cbr\u003e \u003cem\u003eUncommon (may affect up to 1 in 100 people):\u003c\/em\u003e\u003cbr\u003e - Rhinitis\u003cbr\u003e - Hypersensitivity\u003cbr\u003e - Insomnia, anxiety\u003cbr\u003e - Paresthesia\u003cbr\u003e - Drowsiness\u003cbr\u003e - Visual disturbances, hearing impairment\u003cbr\u003e - Dizziness\u003cbr\u003e - Tinnitus\u003cbr\u003e - Bronchial spasm, asthma\u003cbr\u003e - Dyspnea\u003cbr\u003e - Mouth ulceration\u003cbr\u003e - Stomach ulcer, intestinal ulcer, ruptured gastric ulcer, inflammation of the stomach lining\u003cbr\u003e - Hepatitis, jaundice, abnormal liver function\u003cbr\u003e - Itching, small bruises on the skin and mucous membranes\u003cbr\u003e - Photosensitivity\u003cbr\u003e - Nephrotoxicity in various forms e.g. tubulointerstitial nephritis, nephrotic syndrome and renal failure\u003cbr\u003e\u003cbr\u003e \u003cem\u003eRare (may affect up to 1 in 1000 people):\u003c\/em\u003e\u003cbr\u003e - Nonbacterial meningitis\u003cbr\u003e\u003cbr\u003e - Leukopenia\u003cbr\u003e - Thrombocytopenia\u003cbr\u003e - Aplastic anemia\u003cbr\u003e - Neutropenia \u003cbr\u003e- Agranulocytosis\u003cbr\u003e - Hemolytic anemia\u003cbr\u003e - Anaphylactic reaction\u003cbr\u003e - Depression, confusion\u003cbr\u003e - Optic neuritis\u003cbr\u003e - Toxic optic neuropathy\u003cbr\u003e - Edema\u003cbr\u003e\u003cbr\u003e \u003cem\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/em\u003e\u003cbr\u003e - Heart failure, myocardial infarction\u003cbr\u003e - Hypertension\u003cbr\u003e - Inflammation of the pancreas, liver failure\u003cbr\u003e - Severe forms of skin reactions (e.g. erythema multiforme, bullous reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis)\u003cbr\u003e\u003cbr\u003e \u003cem\u003eNot known (frequency cannot be estimated from the available data):\u003c\/em\u003e\u003cbr\u003e - Worsening of ulcers of the large intestine (colitis) and Crohn's disease (bowel disease)\u003cbr\u003e - Drug reaction with eosinophilia and systemic symptoms (DRESS syndrome)\u003cbr\u003e - Acute generalized exanthematous pustulosis (AGEP)\u003cbr\u003e - Chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"TOWA PHARMACEUTICAL SPA","offers":[{"title":"Default Title","offer_id":50220873580878,"sku":"049714013","price":7.44,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0009289_71326bbe-a660-4f40-9b26-61b1eee0a15b.png?v=1768749600"},{"product_id":"naprosyn-gel-50-g-10","title":"NAPROSYN \"10% GEL\" TUBE 50 G\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNaprosyn 100 mg\/g gel\u003c\/b\u003e\u003cbr\u003e Naproxen\u003cbr\u003e\u003cbr\u003e \u003cbr\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Naprosyn contains the active substance naproxen.\u003cbr\u003e Naproxen belongs to a class of medicines called nonsteroidal anti-inflammatory\/antirheumatic drugs that have numerous actions, with an important role in pain control.\u003cbr\u003e\u003cbr\u003e Naprosyn gel is used for local treatment of:\u003cbr\u003e • muscle pain (myalgia);\u003cbr\u003e • back pain (lumbago);\u003cbr\u003e • neck pain (stiff neck);\u003cbr\u003e • inflammation of the muscles (fibromyositis);\u003cbr\u003e • joint inflammation (bursitis, tendonitis, tenosynovitis, periarthritis);\u003cbr\u003e • trauma (bruises, muscle tears, sprains, hematomas, edema and traumatic infiltrates);\u003cbr\u003e • inflammation of the veins (phlebitis).\u003cbr\u003e\u003cbr\u003e Naprosyn gel is also used as a support for:\u003cbr\u003e • orthopedic therapies;\u003cbr\u003e • rehabilitation therapies.\u003cbr\u003e\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse after a short time of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use Naprosyn\u003c\/b\u003e \u003cbr\u003e• if you are allergic to naproxen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you are allergic to substances closely chemically related to naproxen;\u003cbr\u003e • if you are in the last 3 months of pregnancy.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Naprosyn:\u003cbr\u003e • if you are suffering or have suffered from any allergies;\u003cbr\u003e • if you are allergic to medicines such as aspirin (acetylsalicylic acid) or other non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e\u003cbr\u003e If you have any wounds, avoid applying the gel.\u003cbr\u003e Prolonged use of medicines such as Naprosyn gel may cause allergies (sensitization phenomena). In this case, stop treatment immediately.\u003cbr\u003e To avoid possible allergies, including those to light (photosensitization), do not expose yourself to direct sunlight, including solarium, during treatment and for two weeks after. \u003cbr\u003eIf the medicine is applied to a large area and for a prolonged period of time, the appearance of side effects on the whole body cannot be ruled out.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Side effects that may occur with the use of Naprosyn gel are:\u003cbr\u003e • redness of the skin (erythema);\u003cbr\u003e • inflammation of the skin (contact dermatitis);\u003cbr\u003e • itching;\u003cbr\u003e • skin irritation;\u003cbr\u003e • sensation of heat or burning;\u003cbr\u003e • bullous eruptions of varying severity;\u003cbr\u003e • possible abnormal and exaggerated reactions of the skin to light (photosensitivity).\u003cbr\u003e\u003cbr\u003e The use, especially if prolonged, of products to be applied on the skin can give rise to sensitization phenomena (allergy to one or more components). In this case, stop the treatment and contact your doctor who will provide an appropriate therapy.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECORDATI SPA","offers":[{"title":"Default Title","offer_id":50221833486670,"sku":"023177102","price":9.52,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0001011_253bff19-be6b-408b-9bd8-2d521ecd1c37.jpg?v=1768753316"},{"product_id":"algofen-24-cpr-riv-200-mg","title":"ALGOFEN \"200 MG COATED TABLETS\" 24 TABLETS\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eALGOFEN 200 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e ALGOFEN contains the active ingredient ibuprofen which belongs to the class of medicines called Non-Steroidal Anti-Inflammatory Drugs (or NSAIDs) which work by reducing pain and inflammation.\u003cbr\u003e\u003cbr\u003e This medicine is used to treat pain of various origins such as: headache, toothache, nerve pain (neuralgia), bone and joint pain (osteoarticular), muscle pain and menstrual pain.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use ALGOFEN\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you are allergic to acetylsalicylic acid or other medicines used to reduce pain (analgesics) and fever (antipyretics) or to non-steroidal anti-inflammatory drugs (NSAIDs), in particular when the allergy is associated with swelling of the nasal mucosa (nasal polyposis) or asthma, and presents with an asthmatic reaction (bronchospasm), urticaria or severe cold (acute rhinitis) (see section \"Warnings and precautions\");\u003cbr\u003e - if you have suffered from ulcers or bleeding in the stomach or intestines after taking other medicines;\u003cbr\u003e - if you suffer from ulcers or bleeding in the stomach or small intestine (duodenum);\u003cbr\u003e - if you have suffered from two or more episodes of this type in the past;\u003cbr\u003e - if you have a disorder in the production of blood cells, the cause of which is not known;\u003cbr\u003e - if you have bleeding in the brain (cerebrovascular haemorrhage) or other types of bleeding;\u003cbr\u003e - if you suffer from a disease that may lead to an increased tendency to bleed; \u003cbr\u003e- if you have severe liver or kidney problems;\u003cbr\u003e - if he is very dehydrated (this condition may be due to vomiting, diarrhoea or insufficient fluid intake);\u003cbr\u003e - if you are in the last three months of pregnancy (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e - in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using ALGOFEN.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e   \u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop ALGOFEN immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using ALGOFEN and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking ALGOFEN if: \u003cbr\u003e- have heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or are a smoker;\u003cbr\u003e - suffer from asthma (difficulty breathing) or other allergies;\u003cbr\u003e - have seasonal colds on an allergic basis (allergic rhinitis), swelling of the nasal mucosa (e.g. nasal polyps);\u003cbr\u003e - have chronic obstructive pulmonary disease or chronic respiratory tract infections; \u003cbr\u003e- have liver or kidney problems, unless you have a severe form of liver or kidney failure because in these cases you should not take ALGOFEN (see section 2 \"Do not use ALGOFEN\"). If you are in any doubt, ask your doctor;\u003cbr\u003e - has hepatic porphyria;\u003cbr\u003e - are using medicines that increase urine production (diuretics) or other medicines that may affect the way your kidneys work;\u003cbr\u003e - has reduced body fluid volume (for example before or after major surgery);\u003cbr\u003e - is due to undergo or has undergone major surgery;\u003cbr\u003e - are taking other NSAID medicines, including the specific type of NSAIDs called COX-2 inhibitors. In this case, taking ALGOFEN should be avoided; \u003cbr\u003e- are taking other medicines used against inflammation belonging to the corticosteroid family, or medicines used to prevent blood clotting (such as warfarin), or aspirin, or medicines against depression called selective serotonin reuptake inhibitors or SSRIs;\u003cbr\u003e - suffer from chronic inflammatory bowel diseases such as inflammation of the colon with ulcers (ulcerative colitis), inflammation of the digestive tract (Crohn's disease);\u003cbr\u003e - you are elderly, because you may be more susceptible to side effects, which may be serious or life-threatening (see \"Elderly\" and \"Ulcers, perforations and bleeding in the stomach or intestines\");\u003cbr\u003e - if you have stomach or intestinal problems, unless you have one or more conditions for which you should not take ALGOFEN (see section \"Do not use ALGOFEN\");\u003cbr\u003e - is in the first six months of pregnancy (see \"Pregnancy, breastfeeding and fertility\"); \u003cbr\u003e- the patient is a teenager with dehydration problems, because in this case the medicine can cause kidney problems;\u003cbr\u003e - have an autoimmune disease e.g. lupus erythematosus or connective tissue disease;\u003cbr\u003e - have an infection (see section \"Infections\" below).\u003cbr\u003e\u003cbr\u003e \u003cem\u003eEffects on the heart and brain\u003c\/em\u003e\u003cbr\u003e Medicines containing ibuprofen, such as ALGOFEN, are associated with a slightly higher risk of heart attack (myocardial infarction) or stroke. The risk is higher if you take high doses of ibuprofen and long-term treatment. Do not exceed the recommended doses or duration of treatment indicated.\u003cbr\u003e\u003cbr\u003e \u003cem\u003eElderly people\u003c\/em\u003e\u003cbr\u003e Older people may be more susceptible to side effects, especially bleeding and perforation of the digestive tract, which can be fatal. \u003cbr\u003eUlcers, perforations and bleeding in the stomach or intestines If you have had a gastric or intestinal ulcer, particularly if it was complicated by perforation or accompanied by bleeding, you should pay attention to any unusual symptoms in the abdomen and report them to your doctor immediately, especially if these symptoms occur at the start of treatment. In fact, the risk of bleeding or ulceration of the digestive tract is greater in this case, particularly in elderly patients. If bleeding or ulceration of the digestive tract occurs, treatment should be stopped.\u003cbr\u003e\u003cbr\u003e Bleeding, ulceration, or perforation in the stomach or intestines may occur without any warning signs, even in patients who have never had these problems before.\u003cbr\u003e They can also be fatal.\u003cbr\u003e   \u003cbr\u003eThe risk of ulcers, perforations or bleeding in the stomach or intestines generally increases with higher doses of ibuprofen. The risk also increases if certain other medicines are taken at the same time as ibuprofen (see \"Other medicines and ALGOFEN\").\u003cbr\u003e\u003cbr\u003e \u003cem\u003eSkin reactions\u003c\/em\u003e\u003cbr\u003e Severe skin reactions have been reported in association with treatment with ALGOFEN.\u003cbr\u003e Stop taking ALGOFEN and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e \u003cem\u003eInfections\u003c\/em\u003e \u003cbr\u003eALGOFEN may hide the symptoms of infections such as fever and pain. It is therefore possible that ALGOFEN may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e ALGOFEN may decrease the chances of becoming pregnant. Tell your doctor if you are planning to become pregnant or have fertility problems (see \"Pregnancy, breast-feeding and fertility\").\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should not be used in children under 12 years of age (see section 2 \"Do not use ALGOFEN\").\u003cbr\u003e In dehydrated adolescents there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e \u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e Side effects depend on the dose and may vary from patient to patient.\u003cbr\u003e\u003cbr\u003e Stop using ibuprofen and see your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes and increased eosinophils (a type of white blood cell) (DRESS syndrome); \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Medicines containing ibuprofen for long-term treatment may be associated with a slightly increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e Fluid retention (oedema), high blood pressure and heart problems (heart failure) have been reported in association with NSAIDs.\u003cbr\u003e\u003cbr\u003e The most commonly observed adverse events are stomach and\/or intestinal. Ulcers of the stomach or upper intestine (peptic ulcer), perforation or bleeding from the stomach and\/or intestine may occur, which may be fatal, particularly in the elderly.\u003cbr\u003e In particular, the risk of bleeding from the stomach and\/or intestine depends on the dose and duration of treatment.\u003cbr\u003e   \u003cbr\u003eIn addition to the side effects listed below, the following have been reported after administration of ALGOFEN: black stools (melaena), presence of blood in vomit (ulcer of the digestive tract with bleeding).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery common side effects (may affect more than 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - nausea, flatulence, diarrhea, constipation, vomiting;\u003cbr\u003e - difficulty digesting (dyspepsia);\u003cbr\u003e - abdominal pain;\u003cbr\u003e - heartburn.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - skin rash;\u003cbr\u003e - headache, drowsiness, dizziness, vertigo, fatigue, agitation, insomnia, irritability;\u003cbr\u003e - gastric and duodenal ulcers, sometimes with bleeding and perforation, occult blood loss which may lead to anemia, black tarry stools, vomiting blood, mouth ulcers, inflammation of the colon, worsening of inflammatory bowel disease, inflammation of the intestinal wall;\u003cbr\u003e - vision problems.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eUncommon side effects (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e - allergic reactions including skin rash, hives, itching and asthma attacks;\u003cbr\u003e - skin irritation associated with bleeding (purpura);\u003cbr\u003e - skin sensitivity to light;\u003cbr\u003e - alteration of sensitivity in some parts of the body (paraesthesia);\u003cbr\u003e - difficulty breathing (bronchospasm);\u003cbr\u003e - sneezing, stuffy or runny nose (rhinitis);\u003cbr\u003e - inflammation of the stomach (gastritis);\u003cbr\u003e - liver problems, inflammation of the liver (hepatitis) and yellowing of the skin, mucous membranes and eyes (jaundice);\u003cbr\u003e - formation of edema particularly in patients with high blood pressure or kidney problems (renal failure, nephrotic syndrome, interstitial nephritis) which may be accompanied by acute kidney failure.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e - cerebrovascular accident (stroke, cerebral hemorrhage); \u003cbr\u003e- ringing and buzzing in the ears (tinnitus);\u003cbr\u003e - hearing impairment;\u003cbr\u003e - worsening of inflammation of the colon (colitis);\u003cbr\u003e - worsening of a chronic inflammatory disease of the digestive system (Crohn's disease);\u003cbr\u003e - kidney failure;\u003cbr\u003e - damage to kidney tissue (papillary necrosis) (particularly in long-term therapy);\u003cbr\u003e - increased concentration of uric acid in the blood;\u003cbr\u003e - aseptic meningitis (infection of the meninges, membranes of the brain);\u003cbr\u003e - a disease affecting the skin, joints and kidneys (lupus erythematosus syndrome);\u003cbr\u003e - depression, confusion, hallucinations, mental changes (psychotic reactions);\u003cbr\u003e - increased blood urea nitrogen, transaminases and alkaline phosphatase, decreased hemoglobin and hematocrit values, inhibition of platelet aggregation, prolongation of bleeding time, decreased serum calcium, increased serum uric acid, all observed with a blood test; \u003cbr\u003e- decreased vision.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e - worsening of inflammation associated with infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e - reduction in the number of platelets in the blood (thrombocytopenia);\u003cbr\u003e - anemia;\u003cbr\u003e - reduction in the number of white blood cells in the blood (leukopenia, agranulocytosis);\u003cbr\u003e - reduction in the number of all cells present in the blood (pancytopenia);\u003cbr\u003e - presence of blood in the urine (hematuria);\u003cbr\u003e - severe allergic reaction (anaphylactic reaction);\u003cbr\u003e - swelling of the face, lips, mouth, tongue or throat, which may cause difficulty swallowing or breathing (angioedema);\u003cbr\u003e - changes in tests to evaluate liver function;\u003cbr\u003e - acute hepatitis;\u003cbr\u003e - liver damage, particularly in long-term therapy and liver failure; \u003cbr\u003e- skin and mucous membrane reactions, including severe ones (erythema multiforme, exfoliative dermatitis, bullous reactions including Stevens-Johnson syndrome and toxic epidermal necrolysis);\u003cbr\u003e - rapid or irregular heartbeat (palpitations);\u003cbr\u003e - inflammation of the esophagus, narrowing of the intestine;\u003cbr\u003e - serious skin infections, with soft tissue complications, may occur if you have chickenpox;\u003cbr\u003e - fluid build-up in the lungs, symptoms include shortness of breath, which can be very severe and usually worsens when lying down (pulmonary edema);\u003cbr\u003e - swelling (edema);\u003cbr\u003e - heart attack;\u003cbr\u003e - high blood pressure (hypertension);\u003cbr\u003e - heart failure;\u003cbr\u003e - inflammation of the pancreas;\u003cbr\u003e - unusual hair loss (alopecia);\u003cbr\u003e - menstrual disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSide effects with unknown frequency (frequency cannot be estimated from the available data):\u003c\/b\u003e \u003cbr\u003e- a widespread, red, scaly rash with pustules under the skin and vesicles located mainly in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using ALGOFEN if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2;\u003cbr\u003e - muscle stiffness (musculoskeletal stiffness);\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"SIT LABORATORIO FARMAC. SRL","offers":[{"title":"Default Title","offer_id":50221848756558,"sku":"023766037","price":7.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0009729.png?v=1768753381"},{"product_id":"viamal-trauma-gel-50-g","title":"VIAMAL TRAUMA GEL TUBE 50 G","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eVIAMAL Trauma gel\u003cbr\u003e Diethylammonium salicylate 100 mg - Sodium heparin 0.368 mg - Menthol 2 mg\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Viamal Trauma is a medicine for local use, containing three active ingredients: diethylammonium salicylate, sodium heparin and menthol.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eDiethylammonium salicylate\u003c\/u\u003e has an anti-inflammatory and analgesic action. In addition, by softening the skin, it facilitates the absorption of the other two active ingredients. \u003cbr\u003eHeparin prevents blood clotting, rapidly reducing blood effusions and fluid accumulations in the superficial layers of the skin. In this way, heparin reduces swelling and tightness, and pain is relieved.\u003cbr\u003e Menthol enhances the effect of heparin, and has a mild local anesthetic action and a pleasant refreshing action.\u003cbr\u003e Viamal Trauma is in gel form, and is rapidly absorbed through the skin and penetrates deeply into the tissues.\u003cbr\u003e\u003cbr\u003e Viamal Trauma is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003echildren over 6 years of age\u003c\/b\u003e for joint and muscle pain, as a support in the local treatment of trauma such as: bruises, sprains, hematomas (accumulation of blood in the tissues), muscle tears.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you\/your child does not feel better or if you\/your child feels worse after 3 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use\/give the child Viamal Trauma\u003c\/b\u003e \u003cbr\u003e- if you and\/or the child are allergic to diethylammonium salicylate, sodium heparin and menthol or any of the other ingredients of this medicine (listed in section 6)\u003cbr\u003e - if you and\/or the child have kidney damage caused by previous illnesses and the surface area of ​​the body to be treated is large\u003cbr\u003e - if you and\/or the child are also using other local preparations based on salicylates (anti-inflammatories), unless otherwise indicated by the doctor\u003cbr\u003e - if you and\/or your child have flu or chickenpox\u003cbr\u003e - if you are pregnant or breast-feeding (see section “Pregnancy and breast-feeding”)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not\u003c\/b\u003e give Viamal Trauma:\u003cbr\u003e - infants and children under 6 years of age\u003cbr\u003e - children who have suffered from epilepsy or febrile convulsions in the past.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using\/giving your child Viamal Trauma \u003cbr\u003eDo not exceed 3 days of treatment as you\/your child may experience side effects in the brain due to the accumulation of terpene substances, such as menthol and pine oil, contained in this medicine.\u003cbr\u003e Do not use a dose higher than recommended to avoid a higher risk of adverse reactions to the medicine and disorders associated with overdose.\u003cbr\u003e Do not use on damaged skin (wounds, burns, irritated skin).\u003cbr\u003e Avoid sun exposure of the treated area.\u003cbr\u003e Do not use occlusive dressings (gauze strips or other materials) or heat applications, as this may increase absorption through the skin.\u003cbr\u003e Avoid contact with eyes and mucous membranes.\u003cbr\u003e This medicine is flammable, so do not bring it near flames.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003eDo not give Viamal Trauma to infants, children under 6 years of age and children who have suffered from epilepsy or febrile convulsions in the past (see the section “Do not use\/give the child Viamal Trauma”) as neurological disorders may occur.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eImproper use\u003c\/b\u003e\u003cbr\u003e In case of accidental oral intake, incorrect administration in infants or children under six years of age or in children with a history of epilepsy or febrile convulsions, neurological disorders may occur. In case of improper use, contact your doctor immediately or go to the nearest hospital.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e If you experience the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and consult your doctor \u003cb\u003eimmediately\u003c\/b\u003e :\u003cbr\u003e • allergic reactions\u003cbr\u003e • prolonged vomiting\u003cbr\u003e • deep drowsiness\u003cbr\u003e \u003cbr\u003e\u003cb\u003eSide effects with unknown frequency\u003c\/b\u003e (frequency cannot be estimated from the available data)\u003cbr\u003e • burns at the application site.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eAdditional side effects in children\u003c\/b\u003e\u003cbr\u003e \u003cem\u003eEffects on the nervous system\u003c\/em\u003e\u003cbr\u003e • convulsions. This effect may occur in children when the dose and duration of treatment recommended by the doctor are not respected.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"POLIFARMA BENESSERE SRL","offers":[{"title":"Default Title","offer_id":50221862879566,"sku":"025208024","price":10.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000671_e4fee3d5-526c-4ffc-bd69-080e2d3f4634.jpg?v=1768753479"},{"product_id":"nurofen-12-cpr-riv-200-mg-1","title":"NUROFEN 200 MG COATED TABLETS 12 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNUROFEN 200 mg coated tablets\u003cbr\u003e NUROFEN 400 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) which work by reducing pain and swelling caused by inflammation and fever.\u003cbr\u003e   \u003cbr\u003eNurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003e Nurofen is also indicated as an adjuvant for the symptomatic treatment of fever and influenza.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema) and chest pain. Stop Nurofen immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e\u003cbr\u003e • are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e• have previously experienced allergic reactions such as difficulty breathing (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or hives after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e • suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e • suffer from severe heart disease (severe heart failure);\u003cbr\u003e • have suffered from stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e • suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e • is in the last trimester of pregnancy;\u003cbr\u003e • is due to have or has had heart surgery.\u003cbr\u003e\u003cbr\u003e Do not give Nurofen to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Nurofen if: \u003cbr\u003e• you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen\"); \u003cbr\u003e• are elderly and\/or have had stomach and intestinal problems (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of stomach-protective medicines (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen\"). Bleeding, ulceration and perforation of the stomach or intestine, which may be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop taking Nurofen and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • are taking medicines which may increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines which may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen\");\u003cbr\u003e • suffer from high blood pressure and\/or severe heart disease (heart failure) as fluid retention, high blood pressure and swelling have been reported in association with NSAID therapy; \u003cbr\u003e• suffer from reduced liver and\/or kidney function, as the habitual use of painkillers such as Nurofen can lead to serious permanent kidney problems (with possible onset of kidney failure). Your doctor will advise you to carry out periodic tests during treatment;\u003cbr\u003e • suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e • suffers from clotting problems; \u003cbr\u003e• suffer from a chronic autoimmune disease that causes problems in various parts of the body, especially the skin (systemic lupus erythematosus) or mixed connective tissue disease, as the risk of aseptic meningitis increases; manifests the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or is suspected, you should stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptoms;\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs containing ibuprofen may cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e • have an infection – see section “Infections” below.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Nurofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eDo not\u003c\/b\u003e give this medicine to children under 12 years of age.\u003cbr\u003e Caution is advised in dehydrated adolescents (12-18 years) as there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • Widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • stomach disturbances, such as heartburn, stomach pain and nausea\u003cbr\u003e • heachache\u003cbr\u003e • dizziness\u003cbr\u003e • skin rashes\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, flatulence, constipation\u003cbr\u003e • increased transaminases, increased alkaline phosphatase, decreased haematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e • brain attack or stroke\u003cbr\u003e • liver damage (hepatotoxicity)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, perforation and bleeding of the stomach and intestines, black stools and vomiting blood\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis)\u003cbr\u003e • severe heart disease (heart failure), swelling and high blood pressure (hypertension) \u003cbr\u003e• severe kidney disease (renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (haematuria), inflammation of the kidney (nephritis), a set of signs and symptoms such as loss of protein in the urine, decreased levels of protein in the blood, accumulation of fluid in the body resulting in swelling, increased levels of lipids or fats in the blood, hypercoagulability of the blood, related to kidney disease (nephrotic syndrome)\u003cbr\u003e • liver damage especially following long-term treatments, hepatitis, jaundice \u003cbr\u003e• reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nose and skin bleeding, bruising on the skin (hematomas)\u003cbr\u003e • aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more common if you have systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e • decrease in hemoglobin levels in the blood\u003cbr\u003e • visual disturbances\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e • respiratory tract disorders including asthma, worsening of asthma, shortness of breath (bronchospasm) and difficulty breathing (dyspnoea) \u003cbr\u003e• worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • inflammation of the pancreas (pancreatitis)\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e • the skin becomes sensitive to light\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day) may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50221871300942,"sku":"025634015","price":5.68,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000700.jpg?v=1768753517"},{"product_id":"nurofen-12-cpr-riv-400-mg","title":"NUROFEN 400 MG COATED TABLETS 12 PVC\/ALUMINIUM TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eNUROFEN 200 mg coated tablets\u003cbr\u003e NUROFEN 400 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Nurofen contains ibuprofen which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) which work by reducing pain and swelling caused by inflammation and fever.\u003cbr\u003e   \u003cbr\u003eNurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003e Nurofen is also indicated as an adjuvant for the symptomatic treatment of fever and influenza.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema) and chest pain. Stop Nurofen immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e\u003cbr\u003e • are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e• have previously experienced allergic reactions such as difficulty breathing (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or hives after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e • suffer from severe kidney or liver disease (renal or hepatic failure);\u003cbr\u003e • suffer from severe heart disease (severe heart failure);\u003cbr\u003e • have suffered from stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e • suffer or have suffered from active or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e • is in the last trimester of pregnancy;\u003cbr\u003e • is due to have or has had heart surgery.\u003cbr\u003e\u003cbr\u003e Do not give Nurofen to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Nurofen if: \u003cbr\u003e• you are taking other medicines used to treat pain, to lower fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section \"Other medicines and Nurofen\"); \u003cbr\u003e• are elderly and\/or have had stomach and intestinal problems (history of ulcer), especially if complicated by bleeding or perforation as an increase in gastrointestinal bleeding and perforation may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of stomach-protective medicines (misoprostol or proton pump inhibitors). This should also be considered if you are taking low dose aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section \"Other medicines and Nurofen\"). Bleeding, ulceration and perforation of the stomach or intestine, which may be fatal, may occur at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. Therefore, tell your doctor about any uncommon gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, stop taking Nurofen and contact your doctor; \u003cbr\u003e• suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • are taking medicines which may increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines which may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section \"Other medicines and Nurofen\");\u003cbr\u003e • suffer from high blood pressure and\/or severe heart disease (heart failure) as fluid retention, high blood pressure and swelling have been reported in association with NSAID therapy; \u003cbr\u003e• suffer from reduced liver and\/or kidney function, as the habitual use of painkillers such as Nurofen can lead to serious permanent kidney problems (with possible onset of kidney failure). Your doctor will advise you to carry out periodic tests during treatment;\u003cbr\u003e • suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e • suffers from clotting problems; \u003cbr\u003e• suffer from a chronic autoimmune disease that causes problems in various parts of the body, especially the skin (systemic lupus erythematosus) or mixed connective tissue disease, as the risk of aseptic meningitis increases; manifests the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or is suspected, you should stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptoms;\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs containing ibuprofen may cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e • have an infection – see section “Infections” below.\u003cbr\u003e   \u003cbr\u003eAnti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Nurofen may hide the symptoms of infections such as fever and pain. It is therefore possible that Nurofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eDo not\u003c\/b\u003e give this medicine to children under 12 years of age.\u003cbr\u003e Caution is advised in dehydrated adolescents (12-18 years) as there is a risk of impaired renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e If you experience any of the following side effects \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • allergic reactions, including serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart beat (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma; \u003cbr\u003e• flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • Widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Additional side effects include:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • stomach disturbances, such as heartburn, stomach pain and nausea\u003cbr\u003e • heachache\u003cbr\u003e • dizziness\u003cbr\u003e • skin rashes\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, flatulence, constipation\u003cbr\u003e • increased transaminases, increased alkaline phosphatase, decreased haematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e • brain attack or stroke\u003cbr\u003e • liver damage (hepatotoxicity)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, perforation and bleeding of the stomach and intestines, black stools and vomiting blood\u003cbr\u003e • lesions with bleeding from the mouth, heartburn (gastritis)\u003cbr\u003e • severe heart disease (heart failure), swelling and high blood pressure (hypertension) \u003cbr\u003e• severe kidney disease (renal failure, papillary necrosis) particularly following long-term treatment, associated with an increase in the concentration of urea in the blood (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (haematuria), inflammation of the kidney (nephritis), a set of signs and symptoms such as loss of protein in the urine, decreased levels of protein in the blood, accumulation of fluid in the body resulting in swelling, increased levels of lipids or fats in the blood, hypercoagulability of the blood, related to kidney disease (nephrotic syndrome)\u003cbr\u003e • liver damage especially following long-term treatments, hepatitis, jaundice \u003cbr\u003e• reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe tiredness, nose and skin bleeding, bruising on the skin (hematomas)\u003cbr\u003e • aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more common if you have systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e • decrease in hemoglobin levels in the blood\u003cbr\u003e • visual disturbances\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e • respiratory tract disorders including asthma, worsening of asthma, shortness of breath (bronchospasm) and difficulty breathing (dyspnoea) \u003cbr\u003e• worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e • a serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • inflammation of the pancreas (pancreatitis)\u003cbr\u003e • a widespread, red, scaly rash with pustules under the skin and blisters mainly located in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalised exanthematous pustulosis). Stop using Nurofen if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e • the skin becomes sensitive to light\u003cbr\u003e\u003cbr\u003e Use of ibuprofen, especially at high doses (2400 mg\/day) may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"RECKITT BENCKISER H.(IT.) SPA","offers":[{"title":"Default Title","offer_id":50221871792462,"sku":"025634128","price":9.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000701.png?v=1768753518"},{"product_id":"ibuprofene-sandoz-24-cpr-riv-200-mg","title":"IBUPROFENE SAN 200 MG FILM-COATED TABLETS BLISTER OF 24 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eIbuprofen Sandoz 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Equivalent medicine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e This medicine contains the active substance ibuprofen which belongs to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs) which work by reducing pain (analgesic action) and lowering fever.\u003cbr\u003e\u003cbr\u003e Ibuprofene Sandoz is indicated for the treatment of pain of various kinds: menstrual pain, headache, toothache, pain in one or more nerves (neuralgia), bone, joint and muscle pain (osteo-articular and muscular).\u003cbr\u003e\u003cbr\u003e The medicine is also indicated as an adjunctive therapy in the treatment of fever and flu symptoms.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e \u003cbr\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Ibuprofen Sandoz\u003c\/b\u003e\u003cbr\u003e - if you are allergic to the active substance, or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to acetylsalicylic acid or other medicines used to reduce pain (analgesics), fever (antipyretics) such as non-steroidal anti-inflammatory drugs (NSAIDs), in particular when the allergy is associated with swelling of the nasal mucosa (nasal polyposis), angioedema and asthma, and presents with an asthmatic reaction (bronchospasm), urticaria or severe cold (acute rhinitis) (see section \"Warnings and precautions\");\u003cbr\u003e - if you suffer from severe liver or kidney problems;\u003cbr\u003e - if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e - if you have had bleeding (haemorrhage) from the stomach and\/or intestine or perforation after previous treatments with other medicines; \u003cbr\u003e- if you suffer or have suffered from bleeding or ulcers that occur repeatedly (two or more distinct episodes of proven ulceration or bleeding);\u003cbr\u003e - if you have had a severe ulcer in your stomach or upper intestine;\u003cbr\u003e - if you have an ongoing ulcer;\u003cbr\u003e - if you have bleeding in the brain (cerebrovascular haemorrhage) or other types of bleeding;\u003cbr\u003e - if you have a disorder in the production of blood cells, the cause of which is not known;\u003cbr\u003e - if you are in the last 3 months of pregnancy (See section \"Pregnancy and breast-feeding\");\u003cbr\u003e - if the patient is a child under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003e What you need to know before taking Ibuprofen Sandoz\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. \u003cbr\u003eStop taking Ibuprofen Sandoz immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e Take special care with Ibuprofene Sandoz:\u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Ibuprofen Sandoz and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving medicines such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment. \u003cbr\u003eDo not take this medicine if you are already taking other medicines (See section \"Other medicines and Ibuprofen Sandoz\").\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Ibuprofene Sandoz if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Take this medicine with caution:\u003cbr\u003e - if you suffer or have suffered in the past from intestinal disorders (ulcerative colitis, Crohn's disease); \u003cbr\u003e- if you suffer from heart problems (mild to moderate heart failure, congestive heart failure, established ischaemic heart disease, cardiac decompensation). In this case, your doctor should monitor you frequently, especially if you take the medicine for prolonged periods of time;\u003cbr\u003e - if you have hepatic porphyria;\u003cbr\u003e - if you have chronic obstructive pulmonary disease or chronic respiratory tract infections;\u003cbr\u003e - if you are taking medicines that may increase the risk of bleeding, ulceration and perforation such as acetylsalicylic acid (e.g. aspirin) and other NSAIDs, corticosteroids given by mouth, injection or rectally (e.g. cortisone), anticoagulants (e.g. warfarin), selective serotonin reuptake inhibitors (antidepressants) (see section \"Other medicines and Ibuprofene Sandoz\"); \u003cbr\u003e- if you have liver, kidney or heart problems unless you have severe liver, kidney or heart failure because in these cases you should not take Ibuprofene Sandoz (see section 2 \"Do not take Ibuprofene Sandoz\");\u003cbr\u003e - if you have reduced kidney function or if you suffer from liver problems (liver dysfunction). In these cases, your doctor should monitor you frequently, especially if you take the medicine for long periods of time;\u003cbr\u003e - if you suffer from breathing problems (asthma), if you have seasonal colds on an allergic basis (allergic rhinitis), swelling of the nasal mucosa (e.g. nasal polyps), other allergic diseases or if you have had difficulty breathing (bronchospasm) in the past, even following the use of other medicines similar to Ibuprofene Sandoz (aspirin or other NSAIDs); \u003cbr\u003e- if the patient is a child or an adolescent with problems of dehydration, because in this case the medicine can cause kidney problems;\u003cbr\u003e - if you are using medicines that increase urine production (diuretics) or other medicines that may affect the way your kidneys work;\u003cbr\u003e - if you have low body fluid volume (for example before or after major surgery);\u003cbr\u003e - if you are undergoing or have undergone major surgery;\u003cbr\u003e - if you have stomach or intestinal problems, unless you have one or more conditions for which you should not take Ibuprofene Sandoz (see section \"Do not take Ibuprofene Sandoz\");\u003cbr\u003e - if she is a woman and is planning a pregnancy;\u003cbr\u003e - if you are a woman and have fertility problems or are undergoing investigations into fertility, because you should stop treatment with Ibuprofene Sandoz;\u003cbr\u003e - if you have an autoimmune disease e.g. lupus erythematosus or connective tissue disease.\u003cbr\u003e   \u003cbr\u003eIn these cases, your doctor will monitor you closely and periodically reassess the need for treatment with Ibuprofene Sandoz. In addition, your doctor may perform periodic tests (such as monitoring of kidney function) to assess your condition during treatment with Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e Ibuprofene Sandoz may hide the symptoms of infections such as fever and pain. It is therefore possible that Ibuprofene Sandoz may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop treatment and inform your doctor if during treatment with Ibuprofen Sandoz you develop:\u003c\/b\u003e\u003cbr\u003e • gastrointestinal bleeding or ulceration \u003cbr\u003e• mucosal lesions or any other signs of allergic reaction\u003cbr\u003e • fluid retention and swelling from fluid accumulation (edema)\u003cbr\u003e • signs and symptoms of liver problems or if liver function parameters are not normal (visible in blood tests)\u003cbr\u003e • unusual symptoms in the stomach and intestines especially at the beginning of treatment with Ibuprofene Sandoz\u003cbr\u003e • fever, sore throat, superficial mouth ulcers, flu-like symptoms, profound tiredness, unexplained bruising and bleeding because you may have a reduction in white blood cells (agranulocytosis)\u003cbr\u003e • tension in the back of the neck, headache, nausea, vomiting, fever, disorientation because you may be suffering from aseptic meningitis. Patients with autoimmune diseases (Systemic Lupus Erythematosus, connective tissue disease) seem to be more predisposed to developing aseptic meningitis \u003cbr\u003e• symptoms of an infection (e.g. headache, fever) or if you notice a worsening of an infection as Ibuprofene Sandoz may hide the signs and symptoms of infection.\u003cbr\u003e\u003cbr\u003e In these cases, the doctor will evaluate whether to continue or stop treatment with Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003e Serious skin reactions have been reported in association with treatment with Ibuprofen Sandoz. Stop taking Ibuprofen Sandoz and consult your doctor immediately if you experience a skin rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther important information:\u003c\/b\u003e \u003cbr\u003e- Gastrointestinal bleeding, ulceration or perforation, which may be fatal, may occur during treatment with NSAIDs, including ibuprofen, and may occur at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. You should take the lowest effective dose of ibuprofen to reduce the risk of gastrointestinal toxicity and your doctor may prescribe medicines (e.g. misoprostol or proton pump inhibitors) to protect the gastrointestinal mucosa.\u003cbr\u003e - Undesirable effects can be reduced by using the lowest effective dose for the shortest possible time (see section 3 \"How to take Ibuprofene Sandoz\"). \u003cbr\u003e- Avoid using ibuprofen during treatment with other NSAIDs administered by mouth, injection and rectal administration, including selective cyclooxygenase-2 inhibitors, because it increases the possibility of you experiencing side effects.\u003cbr\u003e\u003cbr\u003e Cases of aseptic meningitis have been reported during treatment with ibuprofen, although they are more likely in patients with lupus erythematosus or connective tissue diseases.\u003cbr\u003e\u003cbr\u003e During treatment with this medicine, eye problems (eye changes) may occur. Therefore, in case of prolonged treatments, it is recommended to undergo periodic eye (ophthalmological) checks.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Ibuprofene Sandoz is contraindicated in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eElderly patients\u003c\/b\u003e \u003cbr\u003eElderly patients are more likely to experience adverse reactions, especially stomach or intestinal bleeding and perforation, which are usually more severe and can be fatal.\u003cbr\u003e If you are elderly, you should take the lowest dose of Ibuprofen Sandoz. As a precaution, your doctor may check your kidney function and prescribe medicines that act by protecting the gastrointestinal mucosa, such as misoprostol or proton pump inhibitors.\u003cbr\u003e Tell your doctor about any unusual stomach and intestinal symptoms, especially when you first start taking this medicine.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms. \u003cbr\u003eSide effects depend on the dose and may vary from patient to patient.\u003cbr\u003e\u003cbr\u003e Stop taking Ibuprofen Sandoz and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome); \u003cbr\u003e• widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e\u003cbr\u003e The most commonly observed adverse events are stomach and\/or intestinal. Ulcers of the stomach or upper intestine (peptic ulcer), perforation or bleeding from the stomach and\/or intestine may occur, which may be fatal, particularly in the elderly.\u003cbr\u003e In particular, the risk of bleeding from the stomach and\/or intestine depends on the dose and duration of treatment.\u003cbr\u003e\u003cbr\u003e In addition to the side effects listed below, dark bloody stools (melaena) and bloody vomiting (haematemesis) due to bleeding from the stomach, oesophagus and duodenum have been reported after administration of Ibuprofen Sandoz.\u003cbr\u003e   \u003cbr\u003eMedicines such as Ibuprofen Sandoz may be associated with a small increased risk of heart attack (myocardial infarction) or stroke (see section \"Warnings and precautions\").\u003cbr\u003e\u003cbr\u003e The following side effects may occur, which generally resolve with discontinuation of treatment:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e - difficulty digesting (dyspepsia)\u003cbr\u003e - abdominal pain\u003cbr\u003e - nausea\u003cbr\u003e - vomit\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - allergic reactions including skin rash, hives, itching and asthma attacks\u003cbr\u003e - heachache\u003cbr\u003e - dizziness\u003cbr\u003e - insomnia\u003cbr\u003e - agitation\u003cbr\u003e - irritability\u003cbr\u003e - fatigue\u003cbr\u003e - skin rash\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e - ringing and buzzing in the ears (tinnitus)\u003cbr\u003e - hearing impairment\u003cbr\u003e - ulcer of the stomach or upper part of the intestine (peptic ulcer) \u003cbr\u003e- perforation or bleeding from the stomach and\/or intestines\u003cbr\u003e - inflammation of the oral mucosa with ulceration (ulcerative stomatitis)\u003cbr\u003e - inflammation of the stomach (gastritis)\u003cbr\u003e - worsening of inflammation of the colon (colitis)\u003cbr\u003e - worsening of a chronic inflammatory disease of the digestive system (Crohn's disease)\u003cbr\u003e - kidney failure\u003cbr\u003e - damage to kidney tissue (papillary necrosis) (particularly in long-term therapy)\u003cbr\u003e - increased concentration of uric acid in the blood\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e - worsening of inflammation associated with infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e - reduction in the number of platelets in the blood (thrombocytopenia)\u003cbr\u003e - anemia\u003cbr\u003e - reduction in the number of white blood cells in the blood (leukopenia, agranulocytosis)\u003cbr\u003e - reduction in the number of all cells present in the blood (pancytopenia)\u003cbr\u003e - severe allergic reaction (anaphylactic reaction) \u003cbr\u003e- swelling due to fluid accumulation (angioedema)\u003cbr\u003e - aseptic meningitis (infection of the meninges, membranes of the brain)\u003cbr\u003e - changes in tests to assess liver function\u003cbr\u003e - liver problems, e.g. inflammation of the liver (hepatitis) and yellowing of the skin, mucous membranes and eyes (jaundice)\u003cbr\u003e - liver damage, especially in long-term therapy\u003cbr\u003e - skin and mucous membrane reactions, even severe (bullous dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e - mental changes (psychotic reactions)\u003cbr\u003e - depression\u003cbr\u003e - vision problems\u003cbr\u003e - irregular heartbeat (palpitations)\u003cbr\u003e - swelling (edema)\u003cbr\u003e - heart failure\u003cbr\u003e - heart attack\u003cbr\u003e - high blood pressure (hypertension)\u003cbr\u003e - inflammation of the esophagus (esophagitis)\u003cbr\u003e - inflammation of the pancreas (pancreatitis)\u003cbr\u003e - narrowing of the intestine (diaphragmatic intestinal stenosis) \u003cbr\u003e- gas emission (flatulence)\u003cbr\u003e - diarrhea\u003cbr\u003e - constipation (constipation)\u003cbr\u003e - formation of edema particularly in patients with high blood pressure or kidney problems (renal failure, nephrotic syndrome, interstitial nephritis) which may be accompanied by acute kidney failure\u003cbr\u003e - the skin becomes sensitive to light\u003cbr\u003e - a widespread, red, scaly rash with pustules under the skin and vesicles located mainly in the skin folds, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell). \u003cbr\u003eOther adverse effects have been reported: bronchospasm or dyspnea, apnea, epigastric pain, heartburn, rhinitis, anxiety, confusional state, hallucinations, paraesthesia, somnolence, optic neuritis, optic neuropathy, vertigo, photosensitivity reactions, malaise.\u003cbr\u003e Stop using Ibuprofen Sandoz if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"SANDOZ SPA","offers":[{"title":"Default Title","offer_id":50221872677198,"sku":"025636059","price":7.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0010672_37f0cef9-ed09-478c-98eb-67c86f65a455.png?v=1768753522"},{"product_id":"moment-10-cps-molli-200-mg","title":"MOMENT \"200 MG SOFT CAPSULES\"10 CAPSULES\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENT 200 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Moment contains ibuprofen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e\u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for:\u003cbr\u003e - treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain); \u003cbr\u003e- reduction of feverish and flu symptoms.\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDon't take Moment\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other antirheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used to treat joint or muscle pain (see section \"Other medicines and Moment\");\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breast-feeding (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you suffer from stomach and intestinal diseases (for example, active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines; \u003cbr\u003e- if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - in the presence of serious heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e What you need to know before taking Moment\u003cbr\u003e Signs of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop Moment immediately and contact your doctor or emergency services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e Skin reactions \u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment.\u003cbr\u003e Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs; \u003cbr\u003e- if you suffer from asthma, a runny nose (chronic rhinitis), the presence of polyps in the nose (nasal polyposis) or inflammation of the mucosa of the paranasal sinuses (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), redness of the skin with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or to treat inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you are elderly or have had an ulcer, especially if the ulcer has also manifested itself with bleeding or perforation (see section \"Do not take Moment\"), since the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and if necessary contact your doctor to obtain a prescription for a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility must also be taken into account if you take low doses of acetylsalicylic acid or medicines that can increase the risk of stomach and\/or intestinal diseases (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 \"Possible side effects\"); \u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report to your doctor any unusual intestinal symptoms (especially bleeding) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding in the stomach and\/or intestines, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or anti-blood coagulation agents (e.g. acetylsalicylic acid). See also the section \"Other medicines and Moment\". If gastrointestinal bleeding or ulceration occurs in patients taking Moment, the treatment should be discontinued; \u003cbr\u003e- if you have high blood pressure and the medicines you are taking do not lower it and\/or you have heart or blood circulation problems in the brain or other areas of the body or you think you may be at risk of these diseases (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs. NSAIDs may reduce the effect of medicines to lower blood pressure (see section \"Other medicines and Moment\");\u003cbr\u003e - if you have lost a significant amount of fluid or develop swelling, heart problems or high blood pressure; \u003cbr\u003e- if you have impaired kidney function, heart or liver function, or if you are elderly or are taking medicines for high blood pressure as you may be more susceptible to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from a bleeding disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section \"Other medicines and Moment\"); \u003cbr\u003e- if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, which is present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of \"aseptic meningitis\" have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients without concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section \"Other medicines and Moment\"). - if you intend to become pregnant (see section \"Pregnancy, breast-feeding and fertility\");\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility tests (see section \"Pregnancy, breast-feeding and fertility\"); \u003cbr\u003e- if you have an infection – see section “Infections” below.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain-relieving drugs such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries) or any type of stroke (including 'mini-stroke' or 'TIA', transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Medicines like Moment can: \u003cbr\u003e- be associated with the onset of even serious kidney disease (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore the doctor will monitor the function of your kidneys;\u003cbr\u003e - cause eye disorders, therefore it is recommended in case of prolonged treatments, to carry out periodic eye checks. If vision disorders occur, stop treatment with Moment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment may hide the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTeenagers\u003c\/b\u003e \u003cbr\u003eIf the teenager is dehydrated there is a risk that he or she will develop kidney disease.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the medicine can be minimised if you use the lowest recommended dose and if you use the medicine only for as long as necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003e If you develop an ulcer or bleeding in the stomach and\/or intestine or lesions of the skin and\/or mucous membranes, you should stop treatment with Moment and contact your doctor. These side effects are usually more frequent in the elderly.\u003cbr\u003e\u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, although rarely.\u003cbr\u003e   \u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucosal lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, hives, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • flaking skin;\u003cbr\u003e • flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis); \u003cbr\u003e• widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disorders;\u003cbr\u003e • liver disease (liver dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003e If you experience any of the allergic reactions listed above, go to the hospital as it is necessary to have the equipment, drugs and personnel suitable for emergency treatment immediately available, as in rare cases serious side effects, sometimes with fatal outcomes, have been reported following the use of ibuprofen, even in the absence of a known allergy.\u003cbr\u003e   \u003cbr\u003eThe risk of manifesting these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paraesthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary interruption of breathing (apnea);\u003cbr\u003e • vision disorders;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • dizziness;\u003cbr\u003e • liver disorders (altered liver function); \u003cbr\u003e• inflammation of the liver (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney disease (impaired kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, hives, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnoea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity).\u003cbr\u003e\u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations; \u003cbr\u003e• inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section \"Warnings and precautions\"), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase); \u003cbr\u003e• abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e\u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling your heart beating (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension; \u003cbr\u003e• serious allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heartbeat, severe allergic reaction that occurs quickly and can cause death (anaphylaxis), severe rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • serious skin infections and soft tissue disease can occur during chickenpox infection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomit;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stool;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease); \u003cbr\u003e• increased risk of sudden reduction in blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS Syndrome): A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell).\u003cbr\u003e a widespread, red, scaly rash with pustules under the skin and blisters mainly located on the skin sores, trunk and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis) Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50221874250062,"sku":"025669197","price":7.12,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000344.jpg?v=1768753528"},{"product_id":"momendol-12-cpr-riv-220-mg","title":"MOMENDOL \"220 MG FILM-COATED TABLETS\"12 COATED TABLETS\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENDOL 220 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Naproxen sodium\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Momendol belongs to the class of nonsteroidal analgesic-anti-inflammatory-antirheumatic drugs, that is, medicines that fight pain, inflammation, fever and are useful in the symptomatic treatment of rheumatic diseases. \u003cbr\u003eMomendol is used for the short-term symptomatic treatment of mild to moderate pain, such as muscle and joint pain (e.g. back pain, stiff neck), headache, toothache and menstrual pain.\u003cbr\u003e Momendol can also be used to treat fever.\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 7 days of treatment for pain, and after 3 days of treatment for fever.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take MOMENDOL:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to naproxen sodium or any of the other ingredients of this medicine (listed in section 6), or to other chemically related substances;\u003cbr\u003e • if you suffer from allergic reactions, such as asthma, urticaria, rhinitis, nasal polyps, angioedema and allergic reactions induced by acetylsalicylic acid, analgesics, anti-inflammatory and\/or antirheumatic drugs; \u003cbr\u003e• if you have had a history of gastrointestinal bleeding or perforation, active or previous recurrent peptic ulcer, chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease), severe liver failure, severe heart failure, severe renal failure (creatinine clearance \u0026lt;30 ml\/min), angioedema, during intensive therapy with diuretics, in subjects with active haemorrhage and at risk of haemorrhage during therapy with anticoagulants (See \"Other medicines and MOMENDOL\" and \"Warnings and precautions\");\u003cbr\u003e • during pregnancy, starting from the third trimester and during breastfeeding (See \"Pregnancy, breastfeeding and fertility\");\u003cbr\u003e • the medicine cannot be administered to children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Momendol: \u003cbr\u003e• since there is a close correlation between dosage and the appearance of severe gastrointestinal side effects. Therefore, the minimum effective dosage should always be used;\u003cbr\u003e • medicines such as MOMENDOL may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke. Any risk is more likely with high doses and prolonged treatment. Do not exceed the recommended dose or duration of treatment (7 days for pain and 3 days for the treatment of fever); \u003cbr\u003e• when MOMENDOL is used in hypertensive patients and\/or in patients with reduced cardiac and\/or renal function. During treatment with MOMENDOL, diuresis and renal function should be well monitored, particularly in the elderly, in patients with cardiac insufficiency or chronic renal insufficiency and in patients treated with diuretics, following major surgical interventions involving large blood loss;\u003cbr\u003e • if you have heart problems, or a history of stroke or think you may be at risk of these conditions (for example if you have high blood pressure, diabetes or high cholesterol or if you smoke) you should discuss your treatment with your doctor or pharmacist;\u003cbr\u003e • when MOMENDOL is used in patients with severe heart failure, worsening of the conditions may occur; \u003cbr\u003e• when MOMENDOL is used in patients with a history of gastrointestinal diseases or liver failure and in patients with current or previous allergic reactions, as in these subjects the product may cause bronchospasm, asthma, or other allergic phenomena. In these cases, particular caution is recommended;\u003cbr\u003e • MOMENDOL must be discontinued at the first appearance of skin rash, mucosal lesions or any other sign of allergy and\/or hypersensitivity;\u003cbr\u003e • if visual disturbances occur, treatment with MOMENDOL must be discontinued;\u003cbr\u003e • since naproxen, like any other anti-inflammatory drug, can mask concomitant symptoms of infectious diseases;\u003cbr\u003e • since in isolated cases, in temporal connection with the use of anti-inflammatory drugs, an aggravation of inflammation on an infectious basis has been reported; \u003cbr\u003e• if used in elderly patients, who generally have some degree of impairment of renal, hepatic and cardiac functions, since this group of patients is more exposed to the risk of developing side effects related to the use of anti-inflammatory drugs. The prolonged use of anti-inflammatory drugs in the elderly is not recommended;\u003cbr\u003e • since naproxen inhibits platelet aggregation and may prolong bleeding time. Patients with coagulation disorders or taking medicinal products that interfere with coagulation should be carefully monitored while taking MOMENDOL;\u003cbr\u003e • when MOMENDOL is used by habitual consumers of high daily doses of alcohol there is a high risk of stomach bleeding; \u003cbr\u003e• the use of the product should be avoided in cases of pain of gastrointestinal origin. It is in fact known that bleeding in the stomach or intestine may occur in patients taking anti-inflammatory drugs;\u003cbr\u003e • in asthmatic patients, the product is generally contraindicated;\u003cbr\u003e • when MOMENDOL is used in combination with other drugs that require caution, see \"Other medicines and MOMENDOL\";\u003cbr\u003e • serious skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with Momendol. If you notice any symptoms of these serious skin reactions, described in section 4, stop taking Momendol and contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e If you are under 16 years of age, it is recommended to contact your doctor.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e \u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most commonly observed adverse effects are gastrointestinal in nature.\u003cbr\u003e The following adverse effects have been reported with NSAIDs and naproxen:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - Headache, drowsiness, dizziness;\u003cbr\u003e - Nausea, dyspepsia, vomiting, heartburn, gastralgia, flatulence.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e - Allergic reaction (including facial swelling and angioedema);\u003cbr\u003e - Sleep disturbances, excitement;\u003cbr\u003e - Vision disturbances;\u003cbr\u003e - Tinnitus, hearing disorders;\u003cbr\u003e - Contusion;\u003cbr\u003e - Diarrhea, constipation;\u003cbr\u003e - Skin rash\/itching;\u003cbr\u003e - Abnormal kidney function;\u003cbr\u003e - Chills, edema (including peripheral edema).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e \u003cbr\u003e- Peptic ulcer, perforation or gastrointestinal bleeding, sometimes fatal, may occur especially in the elderly, haematemesis, ulcerative stomatitis, aggravated colitis and aggravated Crohn's disease.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e - Hemolytic or aplastic anemia, thrombocytopenia, granulocytopenia;\u003cbr\u003e - Meningitis-like reaction;\u003cbr\u003e - Tachycardia, edema, hypertension and cardiac failure have been observed in association with treatment with NSAIDs;\u003cbr\u003e - Dyspnea, asthma;\u003cbr\u003e - Colitis, stomatitis. Less frequently, gastritis has been observed;\u003cbr\u003e - Jaundice, hepatitis, reduced liver function;\u003cbr\u003e - Photosensitivity, alopecia, bullous disorder including Stevens-Johnson syndrome and toxic epidermal necrolysis;\u003cbr\u003e - Increased blood pressure.\u003cbr\u003e\u003cbr\u003e Stop taking Momendol and contact your doctor immediately if you notice any of the following side effects:\u003cbr\u003e   \u003cbr\u003e\u003cem\u003eNot known:\u003c\/em\u003e frequency cannot be estimated from the available data\u003cbr\u003e - Extensive skin rash, high body temperature, increased liver enzymes, blood abnormalities (eosinophilia), swollen lymph nodes and involvement of other organs (Drug Reaction with Eosinophilia and Systemic Symptoms, also known as DRESS). See also section 2;\u003cbr\u003e - A distinctive allergic skin reaction known as a fixed drug eruption, which usually recurs at the same site or sites with new exposure to the medicine and may appear as round or oval patches with redness and swelling of the skin, a rash with blisters (hives), or an itchy sensation.\u003cbr\u003e\u003cbr\u003e As with other anti-inflammatory drugs, anaphylactic or anaphylactoid allergic reactions may occur in patients with or without previous exposure to drugs of the same class.\u003cbr\u003e   \u003cbr\u003eThe characteristic symptoms of an anaphylactic reaction are: sudden severe hypotension, acceleration or slowing of the heartbeat, unusual tiredness or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, hives with or without angioedema, redness of the skin, nausea, vomiting, crampy abdominal pain, diarrhea.\u003cbr\u003e Medicines like MOMENDOL may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50221879787854,"sku":"025829084","price":8.8,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005708.png?v=1768753551"},{"product_id":"momendol-gel-50-g-10","title":"MOMENDOL \"10% GEL\"50 G TUBE\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENDOL 10% gel\u003cbr\u003e Naproxen\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Momendol gel belongs to the class of nonsteroidal anti-inflammatory analgesics for topical use. Momendol gel is used for the local treatment of muscle and joint pain, such as: muscle pain (myalgia), back pain, stiff neck, inflammation of a synovial bursa near a joint or tendon (bursitis), tendon inflammation (tendinitis), inflammation of the synovial sheath surrounding tendons (tenosynovitis), inflammation of the tissue around a joint (periarthritis), muscle strains, bruises and hematomas.\u003cbr\u003e Momendol gel can also be used as an adjuvant in rehabilitation following trauma and\/or orthopedic surgery. \u003cbr\u003eContact your doctor if you do not feel better or if you feel worse after 7 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use MOMENDOL GEL\u003c\/b\u003e\u003cbr\u003e - if you are allergic to naproxen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - during the third trimester of pregnancy (see \"Pregnancy, breast-feeding\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using Momendol gel:\u003cbr\u003e - if you have allergic reactions such as asthma, urticaria, rhinitis, nasal polyps, angioedema, and anaphylactic reactions induced by acetylsalicylic acid and\/or other nonsteroidal anti-inflammatory drugs;\u003cbr\u003e - if you are using other medicines that require caution, see the next paragraph \"Other medicines and Momendol gel\".\u003cbr\u003e\u003cbr\u003e The product must not be applied to eyes, mucous membranes, wounds and\/or skin lesions. \u003cbr\u003eTo avoid any possible hypersensitivity or photosensitivity reactions, do not expose yourself to direct sunlight, including solariums and tanning lamps or beds, during treatment and for two weeks after (see \"Possible side effects\").\u003cbr\u003e Discontinue treatment if skin rash or irritation occurs.\u003cbr\u003e This medicine contains a fragrance with D-Limonene. D-Limonene may cause allergic reactions.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, Momendol gel can cause side effects, although not everybody gets them.\u003cbr\u003e Frequency not known (frequency cannot be estimated from the available data):\u003cbr\u003e • redness of the skin (erythema),\u003cbr\u003e • itching,\u003cbr\u003e • skin irritation,\u003cbr\u003e • sensation of heat or burning,\u003cbr\u003e • skin rash in the area of ​​application of the gel (contact dermatitis),\u003cbr\u003e • formation of blisters (bullous eruption),\u003cbr\u003e • photosensitivity reaction, \u003cbr\u003e• hypersensitivity reaction,\u003cbr\u003e • heat at the application site.\u003cbr\u003e\u003cbr\u003e Prolonged use of topical medications may cause hypersensitivity phenomena. In this case, stop treatment, see your doctor and report what happened.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50221880279374,"sku":"025829197","price":9.84,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0000341.jpg?v=1768753553"},{"product_id":"momendol-12-cps-molli-220-mg","title":"MOMENDOL 220 MG SOFT CAPSULE 12 CAPSULES IN PVC\/PCTFE\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENDOL 220 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Naproxen sodium\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eMomendol contains naproxen, a medicine that belongs to the class of analgesics-anti-inflammatory, i.e. drugs that fight pain and inflammation.\u003cbr\u003e Momendol is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 16 years and over\u003c\/b\u003e for the short-term treatment of:\u003cbr\u003e - mild to moderate pain such as headache, joint and muscle pain (e.g. backache, stiff neck), toothache and menstrual pain;\u003cbr\u003e - fever.\u003cbr\u003e\u003cbr\u003e Talk to your doctor if you do not feel better or if you feel worse.\u003cbr\u003e Do not prolong treatment with Momendol for:\u003cbr\u003e - more than 7 days for pain;\u003cbr\u003e - more than 3 days for fever.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Momendol\u003c\/b\u003e\u003cbr\u003e - if you are allergic to naproxen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to substances closely related to naproxen from a chemical point of view; \u003cbr\u003e- if you suffer from allergic diseases, such as asthma, hives, runny nose (rhinitis), polyps in the nose, swelling of the skin and mucous membranes (angioedema);\u003cbr\u003e - if you have had allergic reactions caused by acetylsalicylic acid, painkillers, anti-inflammatories or drugs used to treat rheumatism;\u003cbr\u003e - if you have suffered from gastrointestinal or other bleeding, such as cerebrovascular;\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines;\u003cbr\u003e - if you have had two or more distinct episodes of stomach ulcers or bleeding in the past;\u003cbr\u003e - if you have suffered from inflammation of the stomach lining (e.g. congestive gastropathy, atrophic gastritis);\u003cbr\u003e - if you have an active stomach or duodenal ulcer;\u003cbr\u003e - if you suffer from inflammatory bowel diseases (e.g. ulcerative colitis and Crohn's disease);\u003cbr\u003e - if you are under 16 years of age; \u003cbr\u003e- if you are pregnant or breast-feeding (see section \"Pregnancy and breast-feeding\");\u003cbr\u003e - if you have serious heart disease;\u003cbr\u003e - if you have severe liver or kidney disease;\u003cbr\u003e - if you are taking diuretics (medicines to treat high blood pressure) in high doses (see section \"Other medicines and Momendol\");\u003cbr\u003e - if you are currently bleeding or are taking anticoagulant medicines (medicines that thin the blood) and are at risk of bleeding.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e In general, adverse effects may be minimized by using the lowest effective dose, and for the shortest duration of treatment necessary to control symptoms, especially in elderly patients.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eTalk to your doctor or pharmacist before taking Momendol:\u003c\/b\u003e \u003cbr\u003e- if you are taking other anti-inflammatory medicines (including selective COX-2 inhibitors and some NSAIDs) as they may cause a small increase in the risk of heart attack (myocardial infarction) or failure of blood flow to the brain (stroke) (see section \"Other medicines and Momendol\");\u003cbr\u003e - if you suffer from high blood pressure and\/or have non-serious heart disease, since fluid retention, increased blood pressure and swelling have been reported following treatment with NSAIDs;\u003cbr\u003e - if you suspect you have an infection;\u003cbr\u003e - if you are elderly, have known non-serious kidney, liver or heart problems or are taking an anti-inflammatory medicine for a long time; in these cases your doctor will advise you to start treatment with the lowest dose and possibly use concomitant medicines that protect the stomach;\u003cbr\u003e - if you habitually drink high doses of alcohol;\u003cbr\u003e - if you want to take Momendol because you have stomach pain; \u003cbr\u003e- if you have suffered from non-serious stomach and\/or intestinal problems in the past due to a medicine;\u003cbr\u003e - if you are taking medicines against inflammation (oral corticosteroids), medicines that thin the blood (anticoagulants such as warfarin) or medicines against depression (selective serotonin reuptake inhibitors);\u003cbr\u003e - if you are taking Aspirin\/acetylsalicylic acid to prevent blood clots;\u003cbr\u003e - serious skin reactions, including exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with Momendol. If you notice any of the symptoms of these serious skin reactions, described in section 4, stop taking Momendol and contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop taking Momendol and contact your doctor or pharmacist if while taking Momendol:\u003c\/b\u003e\u003cbr\u003e - vision problems appear; \u003cbr\u003e- have an infection or notice a worsening of an infection;\u003cbr\u003e - in the event of an injury you notice a prolongation of the time it takes for the bleeding to stop;\u003cbr\u003e - a sudden, intense pain appears in your stomach;\u003cbr\u003e - especially in the first few days of treatment, you experience any unusual symptoms in your stomach and\/or intestines (especially bleeding);\u003cbr\u003e - particularly in the first month of treatment, you experience changes in the skin or mucous membranes or any other sign of hypersensitivity which could be signs of serious allergic reactions (exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis).\u003cbr\u003e\u003cbr\u003e Your doctor will monitor your kidney function:\u003cbr\u003e - if he is elderly;\u003cbr\u003e - if you suffer from diseases that compromise kidney function and diuresis (the process that allows the formation of urine);\u003cbr\u003e - if you are taking diuretics (medicines used to treat high blood pressure and which increase the amount of urine); \u003cbr\u003e- if you have recently undergone surgery involving hypovolaemia (decrease in blood volume).\u003cbr\u003e\u003cbr\u003e During treatment with Momendol, your doctor will monitor you carefully:\u003cbr\u003e - if you have any diseases that alter blood clotting;\u003cbr\u003e - if you are taking any medicines that may affect blood clotting.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Momendol can be used in adolescents aged 16 years and over.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e The use of Momendol can cause side effects that are generally mild or moderate (nausea, vomiting, diarrhea, flatulence, constipation, dyspepsia (difficulty digesting), abdominal pain), or more serious, allergic-type reactions.\u003cbr\u003e   \u003cbr\u003eIf you develop an ulcer, or if you experience bleeding in the stomach with melaena (passage of blackish stools), haematemesis (vomiting blood) and\/or in the intestine or lesions of the skin and\/or mucous membranes, you must stop treatment with Momendol and contact your doctor.\u003cbr\u003e Furthermore, if you experience any of the following symptoms, \u003cb\u003eSTOP using Momendol immediately\u003c\/b\u003e and contact your doctor or the nearest hospital where you will be given appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions\u003cbr\u003e • mucosal lesions\u003cbr\u003e • signs of allergic reaction (erythema, itching, urticaria)\u003cbr\u003e • flaking skin\u003cbr\u003e • severe skin rash or peeling of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome)\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestines, which can be fatal, particularly in the elderly\u003cbr\u003e • visual disturbances\u003cbr\u003e • edema, hypertension and heart failure.\u003cbr\u003e   \u003cbr\u003eThe risk of experiencing these symptoms is higher in the early stages of therapy. In most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms.\u003cbr\u003e\u003cbr\u003e You may also experience other side effects, listed below according to frequency:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • nausea\u003cbr\u003e • difficulty digesting (dyspepsia)\u003cbr\u003e • vomit\u003cbr\u003e • heartburn (pyrosis)\u003cbr\u003e • stomach pain (gastralgia)\u003cbr\u003e • emission of gas (flatulence)\u003cbr\u003e • headache (cephalea)\u003cbr\u003e • drowsiness\u003cbr\u003e • dizziness\u003cbr\u003e • dizziness\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • diarrhea\u003cbr\u003e • constipation\u003cbr\u003e • sleep disturbances, insomnia and drowsiness\u003cbr\u003e • excitement\u003cbr\u003e • vision disorders\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • hearing disorders \u003cbr\u003e• allergic reactions with swelling and angioedema\u003cbr\u003e • chills\u003cbr\u003e • skin rash\u003cbr\u003e • itching\u003cbr\u003e • swelling (edema)\u003cbr\u003e • bruises (ecchymosis)\u003cbr\u003e • reduced kidney function\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • stomach or intestinal ulcer\u003cbr\u003e • stomach or intestinal bleeding\u003cbr\u003e • perforation of the stomach or intestine\u003cbr\u003e • blood in vomit (hematemesis)\u003cbr\u003e • lesions inside the mouth (ulcerative stomatitis)\u003cbr\u003e • worsening of colitis\u003cbr\u003e • worsening of a chronic inflammatory bowel disease (Crohn's disease)\u003cbr\u003e • kidney inflammation (glomerulonephritis)\u003cbr\u003e • weakness and muscle pain (myalgia)\u003cbr\u003e • fever\u003cbr\u003e • increase and decrease in blood glucose\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation inside the mouth (stomatitis), aphthous ulcers\u003cbr\u003e • inflammatory disease of the colon and intestine (colitis), pancreas (pancreatitis) and esophagus (esophagitis) \u003cbr\u003e• yellowish coloration of the skin (jaundice)\u003cbr\u003e • inflammation of the liver (hepatitis)\u003cbr\u003e • reduced liver function\u003cbr\u003e • decrease in hemoglobin, the substance that carries oxygen in the blood (aplastic or hemolytic anemia)\u003cbr\u003e • reduction in the number of platelets in the blood (thrombocytopenia)\u003cbr\u003e • decreased number of white blood cells (granulocytopenia, leukopenia) up to complete absence (agranulocytosis)\u003cbr\u003e • increase in blood cells called eosinophils (eosinophilia)\u003cbr\u003e • difficulty breathing (dyspnea, asthma), eosinophilic pneumonia, alveolitis\u003cbr\u003e • sensitivity to light (photosensitivity)\u003cbr\u003e • reduction in the quantity of hair and fur (alopecia)\u003cbr\u003e • skin rash with blisters (vesicular rash) or with nodules, pustules or reddish spots\u003cbr\u003e • red rosette-shaped patches on the skin (erythema multiforme)\u003cbr\u003e • redness and blisters (fixed erythema)\u003cbr\u003e inflammatory reaction with formation of small purple papules (lichen planus) • sweating \u003cbr\u003e• systemic lupus erythematosus (chronic autoimmune disease)\u003cbr\u003e • rapid heartbeat (tachycardia)\u003cbr\u003e • swelling (edema) and inflammation of the vessels (vasculitis)\u003cbr\u003e • high blood pressure (hypertension)\u003cbr\u003e • heart failure (serious heart disease)\u003cbr\u003e • renal failure\u003cbr\u003e • inflammation or damage to the kidneys with loss of proteins and blood in the urine\u003cbr\u003e • increased potassium in the blood\u003cbr\u003e • increased creatinine in the blood\u003cbr\u003e • symptoms such as fever, drowsiness, headache, sensitivity to light in patients with immune system diseases (meningitis-like symptoms) and convulsions\u003cbr\u003e • cognitive disorders\u003cbr\u003e • thirst and malaise\u003cbr\u003e • depression and difficulty concentrating and thinking\u003cbr\u003e • inflammation of the anterior part of the optic nerve (papillitis)\u003cbr\u003e • inflammation of the back of the optic nerve (retrobulbar optic neuritis)\u003cbr\u003e • swelling of the papilla at the back of the eye (papilledema)\u003cbr\u003e • hearing loss.\u003cbr\u003e   \u003cbr\u003eNot known: frequency cannot be estimated from the available data\u003cbr\u003e\u003cbr\u003e Stop taking Momendol and contact your doctor immediately if you notice any of the following side effects:\u003cbr\u003e\u003cbr\u003e -Extensive skin rash, high body temperature, increased liver enzymes, blood abnormalities (eosinophilia), swollen lymph nodes and involvement of other organs (Drug Reaction with Eosinophilia and Systemic Symptoms, also known as DRESS). See also section 2.\u003cbr\u003e\u003cbr\u003e -A distinctive allergic skin reaction known as a fixed drug eruption, which usually recurs at the same site or sites with new exposure to the medicine and may appear as round or oval patches of red, swollen skin, a rash with blisters (hives), or an itchy sensation.\u003cbr\u003e\u003cbr\u003e • inflammation of the stomach (gastritis)\u003cbr\u003e   \u003cbr\u003eOther side effects that have been reported with other medicines similar to Momendol and which may therefore also be potential side effects of Momendol:\u003cbr\u003e • allergic reactions, even serious ones.\u003cbr\u003e The characteristic symptoms of a serious allergic reaction are: sudden severe low blood pressure, rapid or slow heartbeat, unusual tiredness or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, hives with or without swelling of the skin, redness of the skin, nausea, vomiting, abdominal pain with cramps, diarrhoea.\u003cbr\u003e Medicines similar to Momendol may be associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50221880541518,"sku":"025829223","price":9.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0007976.png?v=1768753555"},{"product_id":"flomax-20-bust-grat-350-mg","title":"FLOMAX 350 MG GRANULES FOR ORAL SUSPENSION 20 PE\/AI\/PAPER SACHETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eFLOMAX 350 mg granules for oral suspension\u003cbr\u003e FLOMAX 700 mg tablets\u003c\/b\u003e\u003cbr\u003e Morniflumate\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eThis medicine contains the active substance morniflumate and belongs to a class of medicines called NSAIDs (nonsteroidal anti-inflammatory drugs) which act against pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e FLOMAX is used:\u003cbr\u003e in \u003cb\u003eADULTS and adolescents aged 15 years and over\u003c\/b\u003e , to treat pain of various origins and natures, even those accompanied by fever, in particular in cases of inflammation of the ear (otitis), paranasal sinuses (sinusitis), tonsils (tonsillitis), throat (pharyngitis, laryngitis).\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 5 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take FLOMAX:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to the active substance or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you have had allergy or asthma after taking other NSAIDs such as acetylsalicylic acid known as aspirin; \u003cbr\u003e• if you have an ulcer in your stomach and\/or duodenum (gastroduodenal);\u003cbr\u003e • if you have had two or more distinct episodes of ulcers or bleeding in your stomach or intestines (including blood in your vomit or during bowel movements or black, tarry stools);\u003cbr\u003e • if you have had even one episode of ulcer, perforation or bleeding in the stomach or intestine caused by taking medicines;\u003cbr\u003e • if you have serious liver, kidney or heart problems;\u003cbr\u003e • after the sixth month of pregnancy.\u003cbr\u003e\u003cbr\u003e FLOMAX is contraindicated in children and adolescents under 15 years of age and in adolescents with a history of rectal inflammation (rectitis), rectal bleeding or ulcer.\u003cbr\u003e\u003cbr\u003e Do not take FLOMAX granules for oral suspension if you suffer from phenylketonuria.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking FLOMAX if:\u003cbr\u003e\u003cbr\u003e • is taking other NSAIDs; \u003cbr\u003e• have had stomach or intestinal problems, such as ulcers or bleeding, stomach hernia (hiatal hernia), Crohn's disease, ulcerative colitis;\u003cbr\u003e • are taking medicines that may increase the risk of ulcers and bleeding (see section \"Other medicines and FLOMAX\");\u003cbr\u003e • are elderly or feel very weak (debilitated) or have a low body weight, as they are more likely to develop side effects;\u003cbr\u003e • has asthma associated with chronic inflammation of the nose or nasal passages as a whole (sinusitis) and\/or nasal polyps;\u003cbr\u003e • have chickenpox, as NSAIDs may make the skin lesions caused by it worse;\u003cbr\u003e • you must undergo urine tests to detect the presence of drugs such as marijuana and hashish, as this medicine may give positive results even in the absence of these substances.\u003cbr\u003e\u003cbr\u003e In particular, consult your doctor with caution if:\u003cbr\u003e • has reduced kidney function; \u003cbr\u003e• recently had surgery that caused a large amount of blood loss;\u003cbr\u003e • has liver problems;\u003cbr\u003e • have or have had heart or blood circulation problems, such as stroke, heart attack or heart failure, or are at risk of these conditions (for example if you have high blood pressure, diabetes or raised triglycerides or smoke), as medicines such as FLOMAX may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e IN ALL THESE CASES, THE DOCTOR WILL EVALUATE THE NEED TO CARRY OUT CHECK-UP TESTS.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePLEASE NOTE\u003c\/u\u003e , as during treatment with all NSAIDs:\u003cbr\u003e • at any time, with or without warning symptoms, even in patients without previous serious stomach or intestinal (gastrointestinal) problems, bleeding, ulceration or perforation of the stomach or intestine, which can be fatal, has been reported (see section 4.8); \u003cbr\u003e• although very rare, serious skin reactions, some of them fatal, manifesting as redness, blistering and peeling (e.g. exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis), have been reported. Patients appear to be at highest risk early in the course of therapy: these reactions occur in the majority of cases within the first month of treatment (see section 4.8);\u003cbr\u003e • signs of infection can be masked.\u003cbr\u003e\u003cbr\u003e The risk of having side effects increases with high doses and prolonged treatments. Do not exceed the dose of FLOMAX and do not take it for long periods; always carefully follow the doctor's instructions.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSTOP\u003c\/u\u003e treatment and contact your doctor if:\u003cbr\u003e • note any symptoms affecting your stomach and intestines (gastrointestinal), especially if they involve bleeding; \u003cbr\u003e• a skin rash, mucosal lesions or any other sign of an allergic reaction appears (e.g. redness, itching, swelling of the face and throat, sudden drop in blood pressure).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Do not give this medicine to children and adolescents under 15 years of age.\u003cbr\u003e\u003cbr\u003e FLOMAX should be administered in cases of real need and under the direct supervision of a doctor since adolescents are more likely to develop side effects to this medicine.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Stop taking FLOMAX \u003cu\u003eimmediately\u003c\/u\u003e and contact your doctor if you experience any of the following conditions: \u003cbr\u003e• serious allergic reactions such as: swelling (angioedema) of the face, eyes, lips, throat with difficulty breathing, sudden drop in blood pressure (anaphylactic shock);\u003cbr\u003e • severe breathing difficulties (asthma attacks);\u003cbr\u003e • severe stomach problems, heartburn or abdominal pain due to stomach or duodenal (peptic) ulcer or abdominal ulcer;\u003cbr\u003e • sudden, severe pain in the pit of the stomach (perforation of the ulcer);\u003cbr\u003e • vomiting containing blood (haematemesis) or black stools (melena), associated with bleeding from the stomach or intestine (gastrointestinal) or abnormal tiredness with reduced urine output (due to invisible bleeding);\u003cbr\u003e • severe skin rashes with redness, blistering and peeling (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects with unknown frequency (frequency cannot be estimated from the available data)\u003c\/b\u003e \u003cbr\u003e• worsening of skin infections caused by chickenpox;\u003cbr\u003e • decrease in platelets (thrombocytopenia), decrease in white blood cells (leukopenia);\u003cbr\u003e • headache and dizziness;\u003cbr\u003e • heart attack (myocardial infarction) or stroke, swelling (edema), high blood pressure (hypertension), inability of the heart to supply adequate blood to the body (heart failure), low blood pressure (hypotension), inflammation of the blood vessels (vasculitis);\u003cbr\u003e • nausea, vomiting, diarrhoea, intestinal gas (flatulence), constipation (constipation), indigestion (dyspepsia), abdominal pain, inflammation of the mucosa of the mouth with ulcers (ulcerative stomatitis), worsening of inflammation of the colon (colitis) and Crohn's disease, gastritis; \u003cbr\u003e• more or less sudden appearance of skin lesions, even following exposure to the sun (photosensitization dermatitis), for example spotty or widespread changes in color (rashes, purpura, erythema multiforme and dermatitis), urticaria, itching;\u003cbr\u003e • changes in kidney function (renal failure) which can cause swelling (edema), loss of proteins in the urine, decreased proteins in the blood (nephrotic syndrome), inflammation of the kidney (interstitial nephritis), presence of blood in the urine (haematuria);\u003cbr\u003e • changes in liver tests;\u003cbr\u003e • alterations in tests (false positive) that detect the presence of drugs such as marijuana and hashish; further tests are necessary to confirm the positive result;\u003cbr\u003e • fluoride intoxication (fluorosis), especially if FLOMAX is taken in high doses and for several years.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"CHIESI FARMACEUTICI SPA","offers":[{"title":"Default Title","offer_id":50221895319886,"sku":"027244072","price":10.84,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0005998_c1a230e4-0489-45fe-98f6-89d70e908cc4.png?v=1768753598"},{"product_id":"momenactcompi-10-cps-molli-25-mg","title":"MOMENACTCOMPI' 25 MG SOFT CAPSULES 10 CAPSULES IN PVC-PVDC\/AL BLISTER","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eMOMENACTCOMPÌ 25 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ketoprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e MOMENACTCOMPÌ contains the active substance ketoprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) with pain-relieving and anti-inflammatory properties. \u003cbr\u003eMOMENACTCOMPÌ is used in adults and adolescents over 15 years of age for the treatment of pain of various origins or natures (headache, toothache, neuralgia, menstrual pain, bone and joint (osteoarticular) and muscular pain).\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after three days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take MOMENACTCOMPÌ\u003c\/b\u003e\u003cbr\u003e - If you are allergic to the active substance or to any of the other ingredients of this medicine, such as peanuts or soya (listed in section 6)\u003cbr\u003e - If you are allergic or have had hypersensitivity reactions in the past (such as asthma, bronchial constriction, rhinitis, urticaria, etc.) to acetylsalicylic acid or other anti-inflammatory drugs (called NSAIDs)\u003cbr\u003e - If you are undergoing intensive diuretic therapy\u003cbr\u003e - If you suffer from a severe form of liver failure (liver cirrhosis, severe hepatitis) \u003cbr\u003e- If you suffer from certain blood disorders (leukopenia and thrombocytopenia)\u003cbr\u003e - If you have any bleeding (active bleeding)\u003cbr\u003e - If you are prone to bleeding (hemorrhagic diathesis)\u003cbr\u003e - If you suffer from blood clotting problems (haemostatic disorders)\u003cbr\u003e - If you have severe heart failure\u003cbr\u003e - If you suffer from a disease characterized by severe stomach ulcers called active peptic ulcers, or have suffered in the past from bleeding in the stomach and intestines (gastrointestinal haemorrhage), ulceration or perforation\u003cbr\u003e - If the person who is to take the medicine is a child under 15 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking MOMENACTCOMPÌ.\u003cbr\u003e You can minimise side effects by using the lowest effective dose for the shortest duration of treatment needed to control your symptoms. \u003cbr\u003eTell your doctor or pharmacist if you are taking other anti-inflammatory drugs, as you should avoid concomitant use with other drugs called NSAIDs.\u003cbr\u003e Talk to your doctor or nurse if you have an infection – see section “Infections” below.\u003cbr\u003e During treatment with MOMENACTCOMPÌ, cases of gastrointestinal bleeding, ulceration and perforation, which can be fatal, may occur at any time without warning symptoms or a previous history of serious gastrointestinal events. Therefore, if cases of gastrointestinal bleeding (bleeding from the stomach or intestine) should occur, stop treatment with MOMENACTCOMPÌ and contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eTake special care if:\u003c\/u\u003e\u003cbr\u003e • you are an elderly person or if you are a patient suffering from ulcer, especially if complicated by haemorrhage or perforation, the risk of gastrointestinal bleeding, ulceration or perforation is higher with large doses of MOMENACTCOMPÌ; \u003cbr\u003e• is using concomitantly low doses of aspirin or other drugs that can increase the risk of gastrointestinal events. As it may be necessary to take drugs called \"gastro-protectors\" (misoprostol or proton pump inhibitors).\u003cbr\u003e If you have any doubts, consult your doctor or pharmacist;\u003cbr\u003e • you suffer from stomach or intestinal problems, particularly if you are elderly, you should report any abdominal symptoms to your doctor, particularly in the early stages of your treatment;\u003cbr\u003e • if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (cortisone), anticoagulants (drugs to thin the blood, such as warfarin), serotonin reuptake inhibitors (\"antidepressant\" drugs) or antiplatelet agents (drugs to reduce blood clotting) you should exercise caution; \u003cbr\u003e• a patient with a history of gastrointestinal disease (ulcerative colitis, Crohn's disease) should take NSAIDs with caution, as these conditions may be more severe;\u003cbr\u003e • suffer from an active stomach (peptic) ulcer;\u003cbr\u003e • have ever had asthmatic or allergic reactions after taking other types of non-steroidal anti-inflammatory drugs (such as, for example, acetylsalicylic acid and its derivatives).\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cu\u003eThe doctor will have to carefully monitor you and have you undergo appropriate tests if one of these conditions concerns you:\u003c\/u\u003e\u003cbr\u003e • if you suffer from certain blood disorders (leukopenia and thrombocytopenia);\u003cbr\u003e • if you suffer from serious heart problems (such as high blood pressure and\/or congestive heart failure);\u003cbr\u003e • if you suffer from severely reduced kidney or liver function;\u003cbr\u003e • if you have a predisposition to bleeding;\u003cbr\u003e • if you suffer from diabetes mellitus; \u003cbr\u003e• if you are undergoing concomitant treatment with agents that promote hyperkalaemia (e.g. potassium supplements);\u003cbr\u003e • if you are an elderly person the possibility of adverse reactions to NSAIDs is greater, especially gastrointestinal bleeding and perforation, which can be fatal.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eThis medicine may cause:\u003c\/u\u003e\u003cbr\u003e • serious heart and blood circulation problems (arterial thrombotic events, heart attack or stroke), especially at high doses and for prolonged treatments;\u003cbr\u003e • skin and mucous membrane diseases, even life-threatening, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis which may manifest with lesions of the skin and mucous membranes. This may occur especially in the first month of treatment (See the section \"Possible side effects\").\u003cbr\u003e • vision problems such as blurred vision (See section \"Possible side effects\").\u003cbr\u003e   \u003cbr\u003eYou should also consult your doctor if you are a heavy smoker, if you have had previous strokes, if you have diabetes, if you have high levels of cholesterol in your blood.\u003cbr\u003e\u003cbr\u003e If after three days of treatment you do not notice a decrease in pain, you should consult your doctor.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e MOMENACTCOMPÌ may hide the symptoms of infections such as fever and pain. It is therefore possible that MOMENACTCOMPÌ may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should not be taken by children and adolescents under 15 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e \u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e Stop using MOMENACTCOMPÌ and contact your doctor immediately if you experience:\u003cbr\u003e • swelling due to fluid retention (edema)\u003cbr\u003e • severe increase in blood pressure (hypertension) and reduced heart function (heart failure)\u003cbr\u003e • presence of stools with digested blood (because it could be a symptom of perforation or haemorrhage of the intestine, potentially fatal if you are an elderly patient)\u003cbr\u003e • severe abdominal pain (which may be a symptom of pancreatitis)\u003cbr\u003e • vomiting mixed with blood (as this could be a symptom of perforation or bleeding of the stomach, potentially fatal especially if you are an elderly patient)\u003cbr\u003e • worsening of colitis (inflammation of the colon) and Crohn's disease, which is sometimes fatal, particularly in the elderly. \u003cbr\u003eMOMENACTCOMPÌ as well as other nonsteroidal anti-inflammatory drugs (NSAIDs) are associated with a small increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e The most commonly observed adverse events with MOMENACTCOMPÌ are:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people):\u003cbr\u003e • stomach ulcers (peptic)\u003cbr\u003e • perforation or bleeding of the stomach and intestines (gastrointestinal), sometimes fatal, particularly in the elderly\u003cbr\u003e • digestive difficulties (dyspepsia)\u003cbr\u003e • abdominal pain\u003cbr\u003e • nausea, vomiting.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people):\u003cbr\u003e • diarrhea\u003cbr\u003e • excessive production of gas in the intestine (flatulence)\u003cbr\u003e • constipation\u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e • skin rash, itching\u003cbr\u003e • headache, dizziness, vertigo, drowsiness\u003cbr\u003e • fatigue.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1000 people): \u003cbr\u003e• inflammation of the mouth with the presence of painful lesions (ulcerative stomatitis)\u003cbr\u003e • stomach ulcer\u003cbr\u003e • inflammation of the colon (colitis)\u003cbr\u003e • asthma attacks\u003cbr\u003e • tingling of the limbs (paraesthesia)\u003cbr\u003e • blurred vision\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • inflammation of the liver (hepatitis), yellowing of the skin and the part of the eye that should be white (jaundice)\u003cbr\u003e • alteration of liver function tests (increased transaminase levels, increased serum bilirubin)\u003cbr\u003e • reduction in red blood cells (anemia) caused by bleeding\u003cbr\u003e • reduction of some white blood cells (leukopenia)\u003cbr\u003e • weight gain.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known\u003c\/b\u003e (frequency cannot be estimated from the available data):\u003cbr\u003e • increased sensitivity to light (photosensitivity reactions), rare in case of systemic administration\u003cbr\u003e • skin problems (skin rash)\u003cbr\u003e • hair loss\u003cbr\u003e • urticaria \u003cbr\u003e• swelling of the face and throat (angioedema)\u003cbr\u003e • erythema, bullous skin reactions (including Stevens-Johnson syndrome) and toxic epidermal necrolysis (serious skin disease with severe scaling, potentially fatal), pustule formation\u003cbr\u003e • feeling of tightness in the chest with difficulty breathing (bronchospasm) particularly in patients with known hypersensitivity to acetylsalicylic acid (ASA and other NSAIDs), rhinitis, difficulty breathing (dyspnoea)\u003cbr\u003e • aseptic meningitis (inflammation of the meninges not caused by bacteria)\u003cbr\u003e • convulsions\u003cbr\u003e • taste alterations (dysgeusia)\u003cbr\u003e • abnormal tests to check kidney function, acute kidney failure, interstitial tubular nephritis, loss of nutrients from the body (such as proteins) through the urine (nephrotic syndrome) \u003cbr\u003e• reduction in the number of granulocytes resulting in an increased risk of infections (agranulocytosis), reduction in the number of platelets in the blood (thrombocytopenia), reduced production of blood cells by the marrow (bone marrow aplasia), destruction of red blood cells (haemolytic anaemia)\u003cbr\u003e • anaphylactic reactions (including shock)\u003cbr\u003e • depression, hallucinations, confusion, mood changes\u003cbr\u003e • heart failure, atrial fibrillation, palpitations and tachycardia\u003cbr\u003e • hypertension, vasodilation, inflammation of blood vessels (vasculitis including leukocytoclastic vasculitis)\u003cbr\u003e • hyponatremia (reduction of sodium levels in the blood), hyperkalemia (increase of potassium levels in the blood).\u003cbr\u003e\u003cbr\u003e Clinical trial and epidemiological data suggest that use of some NSAIDs (particularly at high doses and in long-term treatment) may be associated with a small increased risk of arterial thromboembolic events (for example myocardial infarction or stroke).\u003cbr\u003e \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ANGELINI PHARMA ITALIA SPA","offers":[{"title":"Default Title","offer_id":50221895876942,"sku":"027366032","price":6.8,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0009279.png?v=1768753601"},{"product_id":"antalgil-10-cpr-200-mg","title":"ANTALGIL 200 MG TABLETS 10 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eANTALGIL 200 mg tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat is it and what is it for?\u003c\/b\u003e\u003cbr\u003e Antalgil contains the active ingredient ibuprofen, which belongs to the category of non-steroidal anti-inflammatory antirheumatic drugs.\u003cbr\u003e\u003cbr\u003e Antalgil is used for the symptomatic treatment of pain of various origins and nature (headache, toothache, neuralgia, menstrual pain, osteoarticular and muscular pain).\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take ANTALGIL:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen, to other chemically similar substances (in particular to acetylsalicylic acid or other antirheumatics), or to any of the other ingredients of this medicine (listed in section 6); \u003cbr\u003e- if you have a history of gastrointestinal bleeding or perforation following previous treatments or a history of recurrent peptic ulcer\/haemorrhage (two or more distinct episodes of stomach ulcer or bleeding);\u003cbr\u003e - if you suffer from active gastroduodenal ulcer or other stomach diseases;\u003cbr\u003e - if you suffer from severe heart failure;\u003cbr\u003e - if you are in the last trimester of pregnancy or if you are breastfeeding;\u003cbr\u003e - if you suffer from severe kidney or liver failure;\u003cbr\u003e\u003cbr\u003e Antalgil is contraindicated in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking ANTALGIL.\u003cbr\u003e\u003cbr\u003e The use of ANTALGIL is contraindicated during pregnancy and breastfeeding, or if you are planning to become pregnant. Stop taking Antalgil if you have fertility problems or are undergoing fertility tests (see section \"Pregnancy, breastfeeding, and fertility\").\u003cbr\u003e   \u003cbr\u003eDo not take Antalgil with other NSAIDs (Non-Steroidal Anti-Inflammatory Drugs). You can reduce side effects by using the lowest effective dose for the shortest duration necessary to control symptoms (see section \"Other medicines and Antalgil\"). Do not take multiple painkillers at the same time, as this may cause permanent kidney damage and the risk of kidney failure (analgesic nephropathy).\u003cbr\u003e\u003cbr\u003e Signs of an allergic reaction to ibuprofen have been reported, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop taking ANTALGIL immediately and contact your doctor or emergency medical services immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eElderly people\u003c\/u\u003e : \u003cbr\u003eElderly patients have an increased frequency of adverse reactions to NSAIDs, especially bleeding and perforation of the stomach and intestines, which can be fatal. If you belong to this group of patients and treatment is considered necessary, use the lowest dose for the shortest duration necessary to control symptoms. If you experience no benefit or if you experience adverse reactions, contact your doctor, who will regularly review your treatment and\/or discontinue it.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eGastrointestinal bleeding, ulceration and perforation\u003c\/u\u003e : \u003cbr\u003eGastrointestinal bleeding, ulceration, and perforation, which can be fatal, have been reported at any time during treatment with all NSAIDs, with or without warning symptoms or a previous history of serious gastrointestinal events. If you are elderly or have a history of ulcers, particularly if complicated by haemorrhage or perforation (see the section \"Do not take Antalgil\"), the risk of gastrointestinal bleeding, ulceration, or perforation is higher with higher doses of NSAIDs. If you belong to these patient groups, you should start treatment with the lowest available dose. If you belong to these patient groups or if you take low-dose aspirin or other drugs that may increase the risk of gastrointestinal events (see the section \"Other medicines and Antalgil\"), take a stomach-protective medication at the same time (gastroprotectives: misoprostol or proton pump inhibitors). If you have a history of gastrointestinal toxicity, particularly if you are elderly, report any unusual gastrointestinal symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment. \u003cbr\u003eCaution should be exercised if you are taking concomitant medications that could increase the risk of ulcers or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin reuptake inhibitors or antiplatelet agents such as aspirin (see section \"Other medicines and ANTALGIL\").\u003cbr\u003e If gastrointestinal bleeding or ulceration occurs while taking Antalgil, treatment should be discontinued.\u003cbr\u003e If you have a history of gastrointestinal disease (ulcerative colitis, Crohn's disease), you should take NSAIDs with caution as these conditions may be exacerbated (see section \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e \u003cu\u003eCardiovascular and cerebrovascular effects\u003c\/u\u003e :\u003cbr\u003e If you have a history of hypertension and\/or heart failure, you should exercise caution as fluid retention, hypertension and edema have been reported in association with NSAID therapy. \u003cbr\u003eAnti-inflammatory\/painkiller medications such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking ANTALGIL if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have had a heart attack, coronary artery bypass surgery, peripheral artery disease (poor circulation in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a \"mini-stroke\" or \"TIA\" - transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003e Exercise caution if you are being treated with diuretics, ACE inhibitors and angiotensin II antagonists (see section \"Other medicines and ANTALGIL\"). \u003cbr\u003eIf you have uncontrolled high blood pressure (hypertension), congestive heart failure, ischemic heart disease, peripheral arterial disease, and\/or cerebrovascular disease, you should take ibuprofen only after careful consideration by your doctor. Your doctor will also consider similar measures before initiating longer-term treatment if you have risk factors for cardiovascular events (e.g., hypertension, hyperlipidemia, diabetes mellitus, and smoking).\u003cbr\u003e\u003cbr\u003e \u003cu\u003eKidney effects\u003c\/u\u003e :\u003cbr\u003e If you have mild or moderate reduction in kidney function, your doctor will tell you to take the lowest possible dose for the shortest duration necessary to control your symptoms, and your kidney function should be monitored. \u003cbr\u003eIbuprofen can cause sodium, potassium, and fluid retention in patients with no history of kidney disease due to its effects on renal perfusion. This can cause edema or even lead to heart failure or hypertension if predisposed.\u003cbr\u003e Prolonged use of ibuprofen, as with other NSAIDs, can cause kidney disease with blood in the urine (acute interstitial nephritis with hematuria), protein in the urine (proteinuria), and nephrotic syndrome. People with kidney problems, heart failure, liver problems, diuretics, and ACE inhibitors, and those who are elderly, are at increased risk of developing kidney problems. These problems resolve with discontinuation of treatment.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eLiver failure\u003c\/u\u003e : \u003cbr\u003eIf you have mild or moderate reduction in liver function, your doctor will tell you to take the lowest possible dose for the shortest duration necessary to control your symptoms and will monitor your liver function.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e :\u003cbr\u003e Serious skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using ANTALGIL and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e : \u003cbr\u003eAntalgil may mask the symptoms of infections, such as fever and pain. Therefore, Antalgil may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eOther precautions\u003c\/u\u003e :\u003cbr\u003e If you suffer or have suffered from bronchial asthma, chronic rhinitis, sinusitis, nasal polyps, adenoids, or allergic diseases, symptoms such as bronchospasm, urticaria, or angioedema may worsen. If you have asthma, use this medication with caution and only after consulting your doctor.\u003cbr\u003e\u003cbr\u003e Ibuprofen may mask the signs or symptoms of infection (fever, pain, and swelling). \u003cbr\u003eDuring treatment with ibuprofen, some cases with symptoms of aseptic meningitis, such as stiff neck, headache, nausea, vomiting, fever or disorientation have been observed in patients with existing autoimmune disorders (such as systemic lupus erythematosus, mixed connective tissue disease).\u003cbr\u003e\u003cbr\u003e If you have a blood clotting disorder or are taking anticoagulant drugs, you should be monitored closely by your doctor, as ibuprofen can prolong bleeding time and slow clotting.\u003cbr\u003e\u003cbr\u003e Report to your doctor any signs or symptoms of gastrointestinal ulcer or bleeding, blurred vision or other eye symptoms, skin rash, weight gain, or swelling.\u003cbr\u003e\u003cbr\u003e If you are a high-risk patient, you will need to have your liver and kidney function monitored periodically and have blood tests performed if you are on long-term treatment with ibuprofen.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003eThe use of Antalgil is not indicated in children under 12 years of age.\u003cbr\u003e In dehydrated adolescents there is a risk of altered renal function.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStop using Ibuprofen and see your doctor immediately if you notice any of these symptoms:\u003c\/b\u003e\u003cbr\u003e - Flat, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, and ulcers of the mouth, throat, nose, genitals, and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e - Widespread skin rash, high body temperature and swollen lymph nodes (DRESS syndrome). \u003cbr\u003e- Widespread, red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003e Side effects are mostly dose-dependent. In particular, the risk of gastrointestinal bleeding depends on the dosage and duration of treatment.\u003cbr\u003e Ibuprofen, particularly at high doses (2400 mg daily) and in long-term treatment, may be associated with a modest increased risk of arterial thrombotic events (for example, myocardial infarction or stroke).\u003cbr\u003e\u003cbr\u003e Oedema (accumulation of fluid in the tissues resulting in swelling), hypertension (increased blood pressure), heart failure and chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome, have been reported in association with treatment with NSAIDs.\u003cbr\u003e   \u003cbr\u003eThe following side effects are listed in order of frequency of occurrence:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery common (may affect more than 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - Gastrointestinal disorders, such as heartburn, dyspepsia (difficulty in digestion), abdominal pain, nausea, vomiting, diarrhoea, flatulence (bloating), constipation (constipation).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e - Headache (headache), drowsiness, dizziness, tiredness, insomnia, irritability.\u003cbr\u003e - Gastrointestinal ulcers, sometimes with haemorrhage and perforation (see section \"Warnings and precautions\"), occult blood loss (not visible to the naked eye), which may lead to anaemia, melaena, haematemesis (loss of blood from the stomach, esophagus and intestine), ulcerative stomatitis, colitis, worsening of inflammatory bowel disease, complications of colonic diverticula (perforation, fistula).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e - Visual disturbances \u003cbr\u003e- Rhinitis, bronchospasm\u003cbr\u003e - Gastritis\u003cbr\u003e - Development of edema especially in patients with arterial hypertension or renal failure, nephrotic syndrome, interstitial nephritis which may be associated with renal failure\u003cbr\u003e - Photosensitivity\u003cbr\u003e - Hypersensitivity reactions such as urticaria, pruritus, purpura and rash as well as asthma attacks (sometimes with hypotension)\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e - Increased azotemia, serum transaminases and alkaline phosphatase, decreased hemoglobin and hematocrit values, inhibition of platelet aggregation, prolongation of bleeding time, decreased serum calcium, increased serum uric acid.\u003cbr\u003e - Weakening of vision in one eye, also known as \"lazy eye\" (toxic amblyopia).\u003cbr\u003e - Lupus erythematosus syndrome (i.e. a syndrome similar to systemic lupus erythematosus which however regresses when the drug is stopped).\u003cbr\u003e - Depression, confusion, hallucinations.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e - Palpitations, heart failure, myocardial infarction, acute pulmonary edema, edema.\u003cbr\u003e - Hematopoietic disorders (anemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis). Early symptoms or signs may include fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nosebleeds, and skin bleeding.\u003cbr\u003e - Aseptic (non-infectious) meningitis\u003cbr\u003e - Tinnitus\u003cbr\u003e - Esophagitis, pancreatitis, intestinal stenosis\u003cbr\u003e - Renal papillary necrosis in long-term use (see section \"Warnings and precautions\").\u003cbr\u003e - Bullous reactions, severe forms of skin reactions (erythema multiforme, exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis), alopecia, necrotizing fasciitis, i.e. a significant and serious skin infection with tissue destruction.\u003cbr\u003e - Hypertension \u003cbr\u003e- Severe hypersensitivity reactions. Symptoms may include facial swelling, swelling of the tongue and internal larynx, swelling with airway constriction, dyspnea, tachycardia, and a drop in blood pressure to the point of shock and potentially life-threatening.\u003cbr\u003e - Liver dysfunction, liver damage, especially with long-term use, liver failure, acute hepatitis, jaundice.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e - A serious skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell). \u003cbr\u003e- A widespread, red, scaly rash with pustules under the skin and blisters, mainly located in the skin folds, trunk, and upper limbs, accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop using Antalgil if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eAdditional side effects in children and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated adolescents there is a risk of altered renal function.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you experience any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"VIM G.OTTAVIANI SPA","offers":[{"title":"Default Title","offer_id":50221895942478,"sku":"027432020","price":5.6,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0006771.png?v=1768753602"},{"product_id":"flector-5-cerotti-medicati-180-mg","title":"FLECTOR \"180 MG MEDICATED PATCH\"5 MEDICATED PATCHES\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eFLECTOR 180 mg medicated plaster\u003c\/b\u003e\u003cbr\u003e Diclofenac hydroxyethylpyrrolidine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e FLECTOR contains the active substance diclofenac hydroxyethylpyrrolidine and belongs to a group of medicines that reduce pain and inflammation called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e\u003cbr\u003e FLECTOR patch is applied to the skin and acts against pain and inflammation of joints, muscles, tendons and ligaments, due to trauma or rheumatic diseases.\u003cbr\u003e\u003cbr\u003e Talk to your doctor if, when using FLECTOR, you do not feel better or if you feel worse after a short period of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use FLECTOR:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to diclofenac hydroxyethylpyrrolidine, acetylsalicylic acid or other NSAIDs; \u003cbr\u003e• if you are allergic to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • during the last three months of pregnancy (see “Pregnancy, breastfeeding and fertility”);\u003cbr\u003e • if you have a stomach or duodenal (peptic) ulcer;\u003cbr\u003e • if the skin where you want to apply the patch is damaged or has lesions (exudative dermatitis, eczema, infections, burns or wounds);\u003cbr\u003e • if you have had asthma, hives or inflammation of the nose (acute rhinitis) after using medicines containing acetylsalicylic acid or other NSAIDs.\u003cbr\u003e\u003cbr\u003e Do not use FLECTOR in children and adolescents \u003cu\u003eunder\u003c\/u\u003e 16 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using FLECTOR if:\u003cbr\u003e • has respiratory problems such as asthma, inflammation of the nose due to allergies (allergic rhinitis), nasal polyps, bronchial diseases;\u003cbr\u003e • have heart, liver or kidney problems;\u003cbr\u003e • have had a stomach or duodenal (peptic) ulcer; \u003cbr\u003e• has suffered from inflammatory bowel disease;\u003cbr\u003e • is predisposed to blood loss (hemorrhagic diathesis);\u003cbr\u003e • is elderly, as he or she is more likely to experience side effects.\u003cbr\u003e\u003cbr\u003e Do not expose yourself to direct sunlight or the light of sunlamps (tanning lamps) for at least one day after removing the patch; this will reduce the risk of experiencing an adverse reaction to light (photosensitivity).\u003cbr\u003e\u003cbr\u003e Like other local (topical) medicines, especially in case of prolonged therapy, FLECTOR can cause redness and itching (sensitization phenomena). Stop the treatment and contact your doctor or pharmacist if using this patch you experience skin reactions at the application site.\u003cbr\u003e   \u003cbr\u003eSide effects can be minimised by using the lowest effective dose for the shortest duration necessary. Do not exceed the dose of FLECTOR, do not apply it to large areas of skin and do not take it for long periods.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, FLECTOR can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • Skin rashes and redness (eczema, erythema), inflammation of the skin (dermatitis, including allergic and contact dermatitis), itching at the site where you applied the patch.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • Inflammation of the skin with blistering (bullous dermatitis).\u003cbr\u003e • Dry skin.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e \u003cbr\u003e• Symptoms due to allergic reactions: hives, swelling (angioedema) of the face, eyes, lips and throat with difficulty breathing.\u003cbr\u003e • skin lesions after exposure to the sun (photosensitivity reaction).\u003cbr\u003e • Asthma.\u003cbr\u003e • Inflammation of the skin with the presence of pus (rash with pustules).\u003cbr\u003e\u003cbr\u003e Because \u003cu\u003eFLECTOR plaster\u003c\/u\u003e is applied directly to the affected area, the risk of having side effects that affect the whole body (systemic), such as stomach or intestinal problems, is lower than when taking diclofenac by mouth. If medicated plasters are not used correctly, are used on large areas of skin and for a very long time, these effects can still occur.\u003cbr\u003e   \u003cbr\u003eIf medicated plasters are used in combination with other medicines containing diclofenac, the likelihood of skin reactions, including after exposure to the sun, such as blistering, erythema and eczema, increases. In rare cases, even serious reactions may occur, such as skin rashes with redness, blistering and peeling (e.g. Stevens-Johnson syndrome, Lyell syndrome).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"IBSA FARMACEUTICI ITALIA SRL","offers":[{"title":"Default Title","offer_id":50221898891598,"sku":"027757032","price":14.32,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0003851.jpg?v=1768753609"},{"product_id":"flector-10-cerotti-medicati-180-mg","title":"FLECTOR \"180 MG MEDICATED PATCH\"10 MEDICATED PATCHES\"","description":"\u003cb\u003eName\u003c\/b\u003e \u003cbr\u003e\u003cb\u003eFLECTOR 180 mg medicated plaster\u003c\/b\u003e\u003cbr\u003e Diclofenac hydroxyethylpyrrolidine\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e FLECTOR contains the active substance diclofenac hydroxyethylpyrrolidine and belongs to a group of medicines that reduce pain and inflammation called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e\u003cbr\u003e FLECTOR patch is applied to the skin and acts against pain and inflammation of joints, muscles, tendons and ligaments, due to trauma or rheumatic diseases.\u003cbr\u003e\u003cbr\u003e Talk to your doctor if, when using FLECTOR, you do not feel better or if you feel worse after a short period of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use FLECTOR:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to diclofenac hydroxyethylpyrrolidine, acetylsalicylic acid or other NSAIDs;\u003cbr\u003e • if you are allergic to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • during the last three months of pregnancy (see “Pregnancy, breastfeeding and fertility”); \u003cbr\u003e• if you have a stomach or duodenal (peptic) ulcer;\u003cbr\u003e • if the skin where you want to apply the patch is damaged or has lesions (exudative dermatitis, eczema, infections, burns or wounds);\u003cbr\u003e • if you have had asthma, hives or inflammation of the nose (acute rhinitis) after using medicines containing acetylsalicylic acid or other NSAIDs.\u003cbr\u003e\u003cbr\u003e Do not use FLECTOR in children and adolescents \u003cu\u003eunder\u003c\/u\u003e 16 years of age.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before using FLECTOR if:\u003cbr\u003e • has respiratory problems such as asthma, inflammation of the nose due to allergies (allergic rhinitis), nasal polyps, bronchial diseases;\u003cbr\u003e • have heart, liver or kidney problems;\u003cbr\u003e • have had a stomach or duodenal (peptic) ulcer;\u003cbr\u003e • has suffered from inflammatory bowel disease;\u003cbr\u003e • is predisposed to blood loss (hemorrhagic diathesis);\u003cbr\u003e • is elderly, as he or she is more likely to experience side effects.\u003cbr\u003e   \u003cbr\u003eDo not expose yourself to direct sunlight or the light of sunlamps (tanning lamps) for at least one day after removing the patch; this will reduce the risk of experiencing an adverse reaction to light (photosensitivity).\u003cbr\u003e\u003cbr\u003e Like other local (topical) medicines, especially in case of prolonged therapy, FLECTOR can cause redness and itching (sensitization phenomena). Stop the treatment and contact your doctor or pharmacist if using this patch you experience skin reactions at the application site.\u003cbr\u003e\u003cbr\u003e Side effects can be minimised by using the lowest effective dose for the shortest duration necessary. Do not exceed the dose of FLECTOR, do not apply it to large areas of skin and do not take it for long periods.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, FLECTOR can cause side effects, although not everybody gets them.\u003cbr\u003e   \u003cbr\u003e\u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • Skin rashes and redness (eczema, erythema), inflammation of the skin (dermatitis, including allergic and contact dermatitis), itching at the site where you applied the patch.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • Inflammation of the skin with blistering (bullous dermatitis).\u003cbr\u003e • Dry skin.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • Symptoms due to allergic reactions: hives, swelling (angioedema) of the face, eyes, lips and throat with difficulty breathing.\u003cbr\u003e • skin lesions after exposure to the sun (photosensitivity reaction).\u003cbr\u003e • Asthma.\u003cbr\u003e • Inflammation of the skin with the presence of pus (rash with pustules).\u003cbr\u003e   \u003cbr\u003eBecause \u003cu\u003eFLECTOR plaster\u003c\/u\u003e is applied directly to the affected area, the risk of having side effects that affect the whole body (systemic), such as stomach or intestinal problems, is lower than when taking diclofenac by mouth. If medicated plasters are not used correctly, are used on large areas of skin and for a very long time, these effects can still occur.\u003cbr\u003e\u003cbr\u003e If medicated plasters are used in combination with other medicines containing diclofenac, the likelihood of skin reactions, including after exposure to the sun, such as blistering, erythema and eczema, increases. In rare cases, even serious reactions may occur, such as skin rashes with redness, blistering and peeling (e.g. Stevens-Johnson syndrome, Lyell syndrome).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e \u003cbr\u003eIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"IBSA FARMACEUTICI ITALIA SRL","offers":[{"title":"Default Title","offer_id":50221899153742,"sku":"027757044","price":19.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0003852.jpg?v=1768753610"},{"product_id":"flumarin-20-bust-grat-350-mg","title":"FLUMARIN 350 MG GRANULES FOR ORAL SUSPENSION 20 BIPARTITE SACHETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eFLUMARIN 350 mg granules for oral suspension\u003c\/b\u003e\u003cbr\u003e Morniflumate\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e This medicine contains the active substance morniflumate and belongs to a class of medicines called NSAIDs (nonsteroidal anti-inflammatory drugs) which act against pain, fever and inflammation.\u003cbr\u003e\u003cbr\u003e FLUMARIN is used: \u003cbr\u003ein \u003cb\u003eADULTS and ADOLESCENTS aged 15 years and over\u003c\/b\u003e to treat pain of various origins and natures, even those accompanied by fever, in particular in cases of inflammation of the ear (otitis), paranasal sinuses (sinusitis), tonsils (tonsillitis), throat (pharyngitis, laryngitis).\u003cbr\u003e\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 5 days of treatment.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take FLUMARIN:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to the active substance or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you have had allergy or asthma after taking other NSAIDs such as acetylsalicylic acid known as aspirin;\u003cbr\u003e • if you have an ulcer in your stomach and\/or duodenum (gastroduodenal);\u003cbr\u003e • if you have had two or more distinct episodes of ulcers or bleeding in your stomach or intestines (including blood in your vomit or during bowel movements or black, tarry stools); \u003cbr\u003e• if you have had even one episode of ulcer, perforation or bleeding in the stomach or intestine caused by taking medicines;\u003cbr\u003e • if you have serious liver, kidney or heart problems;\u003cbr\u003e • after the sixth month of pregnancy;\u003cbr\u003e • if you are breastfeeding.\u003cbr\u003e\u003cbr\u003e FLUMARIN is contraindicated in children and adolescents under 15 years of age and in adolescents with a history of rectal inflammation (rectitis), rectal bleeding or ulcer.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eDo not take FLUMARIN granules for oral suspension if you suffer from phenylketonuria\u003c\/u\u003e .\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking FLUMARIN if:\u003cbr\u003e • is taking other NSAIDs;\u003cbr\u003e • have had stomach or intestinal diseases, for example ulcer or bleeding, stomach hernia (hiatal), Crohn's disease, ulcerative colitis; are taking medicines that may increase the risk of ulcers and bleeding (see section \"Other medicines and Flumarin\"); \u003cbr\u003e• are elderly or feel very weak (debilitated) or have a low body weight, as you are more likely to develop side effects from this medicine;\u003cbr\u003e • has asthma associated with chronic inflammation of the nose or nasal passages as a whole (sinusitis) and\/or nasal polyps;\u003cbr\u003e • have chickenpox, as NSAIDs may make the skin lesions caused by it worse;\u003cbr\u003e • you must undergo urine tests to detect the presence of drugs such as marijuana and hashish, as this medicine may give positive results even in the absence of these substances.\u003cbr\u003e\u003cbr\u003e In particular, consult your doctor as a precaution if:\u003cbr\u003e • has reduced kidney function;\u003cbr\u003e • have recently undergone surgery which caused significant blood loss;\u003cbr\u003e • has liver problems; \u003cbr\u003e• have problems with your heart or blood vessels, such as stroke, heart attack or heart failure, or think you may be at risk of these conditions (for example if you have high blood pressure, diabetes or high cholesterol or smoke), as medicines like FLUMARIN may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e IN ALL THESE CASES, YOUR DOCTOR WILL EVALUATE THE NEED TO UNDERGO CHECK-UP TESTS.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePLEASE NOTE\u003c\/u\u003e , as during treatment with all NSAIDs:\u003cbr\u003e • at any time, with or without warning symptoms, even in patients with no previous serious stomach or intestinal (gastrointestinal) problems, bleeding, ulceration or perforation of the stomach or intestine, which can be fatal, has been reported; \u003cbr\u003e• although very rarely, serious skin reactions, some of them fatal, manifesting as redness, blistering and peeling (e.g. exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis), have been reported. Patients appear to be at highest risk in the early stages of therapy: these reactions occur in the majority of cases within the first month of treatment;\u003cbr\u003e • signs of infection can be masked.\u003cbr\u003e\u003cbr\u003e The risk of having side effects increases with high doses and prolonged treatments. Do not exceed the dose of FLUMARIN and do not take it for long periods; always carefully follow the doctor's instructions.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSTOP\u003c\/u\u003e treatment and contact your doctor if:\u003cbr\u003e • note any symptoms affecting your stomach and intestines (gastrointestinal), especially if they involve bleeding; \u003cbr\u003e• a skin rash, mucosal lesions or any other sign of an allergic reaction appears (e.g. redness, itching, swelling of the face and throat, sudden drop in blood pressure).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Do not give this medicine to children and adolescents under 15 years of age.\u003cbr\u003e FLUMARIN should be administered in cases of real need and under the direct supervision of a doctor since adolescents are more likely to develop adverse events to this medicine.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Stop taking FLUMARIN \u003cu\u003eimmediately\u003c\/u\u003e and contact your doctor if you experience any of the following conditions: \u003cbr\u003e• serious allergic reactions such as: swelling (angioedema) of the face, eyes, lips, throat with difficulty breathing, sudden drop in blood pressure (anaphylactic shock);\u003cbr\u003e • severe breathing difficulties (asthma attacks);\u003cbr\u003e • severe stomach problems, heartburn or abdominal pain due to stomach or duodenal (peptic) ulcer or abdominal ulcer;\u003cbr\u003e • sudden, severe pain in the pit of the stomach (perforation of the ulcer);\u003cbr\u003e • vomiting containing blood (haematemesis) or black stools (melena), associated with bleeding from the stomach or intestine (gastrointestinal) or abnormal tiredness with reduced urine output (due to invisible bleeding);\u003cbr\u003e • severe skin rashes with redness, blistering and peeling (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eOther side effects\u003c\/b\u003e\u003cbr\u003e • worsening of skin infections caused by chickenpox; \u003cbr\u003e• decrease in platelets (thrombocytopenia), decrease in white blood cells (leukopenia);\u003cbr\u003e • headache and dizziness;\u003cbr\u003e • heart attack (myocardial infarction) or stroke, swelling (edema), high blood pressure (hypertension), reduced heart function (failure), low blood pressure (hypotension), inflammation of the blood vessels (vasculitis);\u003cbr\u003e • nausea, vomiting, diarrhoea, intestinal gas (flatulence), difficulty in evacuating (constipation), indigestion (dyspepsia), abdominal pain, inflammation of the mucosa of the mouth with ulcers (ulcerative stomatitis), worsening of inflammation of the colon (colitis) and Crohn's disease, gastritis;\u003cbr\u003e • more or less sudden appearance of skin lesions, even following exposure to the sun (photosensitization dermatitis), for example spotty or widespread changes in color (rashes, purpura, erythema multiforme and dermatitis), urticaria, itching; \u003cbr\u003e• changes in kidney function (renal failure) which can cause swelling (edema), loss of proteins in the urine, decreased proteins in the blood (nephrotic syndrome), inflammation of the kidney (interstitial nephritis), presence of blood in the urine (haematuria);\u003cbr\u003e • changes in liver tests;\u003cbr\u003e • alterations in tests (false positives) that detect the presence of drugs such as marijuana and hashish (tests for THC);\u003cbr\u003e • fluoride intoxication (fluorosis), especially if FLUMARIN is taken in high doses and for several years.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e . \u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.","brand":"I.B.N. SAVIO SRL","offers":[{"title":"Default Title","offer_id":50221905183054,"sku":"028332082","price":11.36,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0010593.png?v=1768753657"},{"product_id":"ketodol-20-cpr-25-mg-200-mg","title":"KETODOL 25 MG + 200 MG TABLETS 20 TABLETS","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eKETODOL 25 mg + 200 mg tablets\u003c\/b\u003e\u003cbr\u003e ketoprofen and sucralfate\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Ketodol belongs to a category of drugs called NSAIDs (nonsteroidal anti-inflammatory drugs).\u003cbr\u003e Ketodol contains the active ingredients ketoprofen and sucralfate. Ketoprofen is contained in the central core of the tablet and has an analgesic – anti-inflammatory effect; sucralfate is contained in the coating of the tablet and has a protective effect on the internal surface of the stomach (gastric mucosa).\u003cbr\u003e First, sucralfate is released, which protects the gastric mucosa, and immediately after, ketoprofen, which carries out its analgesic and anti-inflammatory activity.\u003cbr\u003e\u003cbr\u003e Ketodol is used in case of pain of various origins and nature:\u003cbr\u003e • heachache;\u003cbr\u003e • toothache; \u003cbr\u003e• nerve pain (neuralgia);\u003cbr\u003e • bone, joint and muscle pain;\u003cbr\u003e • menstrual cramps.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not take Ketodol\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ketoprofen or sucralfate or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you have had allergic reactions in the past such as severe breathing difficulties (bronchospasm), asthmatic attacks, internal inflammation of the nose (rhinitis), allergic skin reactions (urticaria) or if substances with the same mechanism of action as Ketodol (for example acetylsalicylic acid or other NSAIDs) have previously caused allergic-type reactions. In fact, particularly serious allergic reactions (anaphylactic), rarely fatal, have been observed in these patients (see “Possible side effects”); \u003cbr\u003e• in the third trimester of pregnancy, during breastfeeding (see “Pregnancy, breastfeeding and fertility”) and in children and adolescents under 15 years of age;\u003cbr\u003e • if you suffer from a severe reduction in the heart's ability to supply an adequate amount of blood to the body (heart failure);\u003cbr\u003e • if you suffer from open sores developing on the inner lining of the stomach (active peptic ulcer) or have suffered in the past from bleeding, ulceration or perforation of the stomach and intestines;\u003cbr\u003e • if you have suffered in the past from bleeding or perforation in the stomach and intestine due to previous therapy with NSAIDs;\u003cbr\u003e • in case of easy bleeding tendency;\u003cbr\u003e • in case of severe liver failure;\u003cbr\u003e • in case of severe kidney failure;\u003cbr\u003e • if you have acute kidney damage (renal hypoperfusion);\u003cbr\u003e • if you are taking medicines that cause increased urine output (intensive diuretic therapy); \u003cbr\u003e• in case of chronic digestive difficulties;\u003cbr\u003e • if you suffer from stomach inflammation (gastritis);\u003cbr\u003e • in case of low number of white blood cells and platelets (leukopenia and thrombocytopenia);\u003cbr\u003e • in case of hereditary alterations in the formation of hemoglobin (porphyria);\u003cbr\u003e • if you suffer from chronic inflammation of the liver (liver cirrhosis);\u003cbr\u003e • if you are taking antibiotics such as tetracyclines, as these may be ineffective.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Talk to your doctor or pharmacist before taking Ketodol. To avoid any hypersensitivity or allergy reactions to the sun, it is recommended not to expose yourself to the sun during use.\u003cbr\u003e\u003cbr\u003e Stop taking ketoprofen:\u003cbr\u003e • if you notice bleeding or if you have severe pain (ulceration) in your stomach or intestines;\u003cbr\u003e • at the first appearance of skin allergies (rash), mucosal lesions or any other sign of hypersensitivity or allergic reaction; \u003cbr\u003e• in case of significant increase in the values ​​of some liver parameters and transaminases (which are used to evaluate liver function);\u003cbr\u003e • if you experience vision problems, such as blurred vision.\u003cbr\u003e\u003cbr\u003e Ask your doctor or pharmacist for advice before using KETODOL if:\u003cbr\u003e • suffer from a disease of the intestine (ulcerative colitis, Crohn's disease) as these conditions could worsen;\u003cbr\u003e • suffer from asthma associated with chronic rhinitis, chronic sinusitis and\/or nasal polyps, because the use of this medicine may contribute to triggering asthma attacks or bronchospasms;\u003cbr\u003e • has problems with kidney function since the medicine is eliminated mainly through the kidneys;\u003cbr\u003e • have an infection – see section \u0026lt;\u003cinfezioni\u003e \u0026gt; below;\u003cbr\u003e • is in intensive care and especially if he receives enteral nutrition, or if he has predisposing factors such as delayed gastric emptying; \u003cbr\u003e• take other medications that may increase the risk of gastrointestinal events, ulceration or bleeding such as:\u003cbr\u003e • oral corticosteroids,\u003cbr\u003e • warfarin (anticoagulant),\u003cbr\u003e • drugs for depression (SSRI antidepressants),\u003cbr\u003e • anti-platelet agents such as aspirin (see “Other medicines and Ketodol”).\u003cbr\u003e\u003cbr\u003e In these cases, the concomitant use of stomach-protective drugs (misoprostol or proton pump inhibitors) is useful.\u003cbr\u003e\u003cbr\u003e Infections\u003cbr\u003e KETODOL may hide the symptoms of infections such as fever and pain. It is therefore possible that KETODOL may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or get worse, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e Contact your doctor: \u003cbr\u003e• in case of any abdominal symptoms (especially gastrointestinal bleeding), particularly in the initial stages of treatment;\u003cbr\u003e • for adequate monitoring and appropriate instructions, if you suffer from high blood pressure and\/or congestive heart failure, if you have suffered from liver disease in the past or if you have abnormal liver function values;\u003cbr\u003e • if you have certain risk factors associated with cardiovascular disease (high blood pressure, high cholesterol, diabetes mellitus, smoking) before starting long-term treatment;\u003cbr\u003e • before taking this medicine, if you have hereditary problems of intolerance to some sugars;\u003cbr\u003e • for adequate monitoring of potassium levels in the blood, if you suffer from diabetes, kidney failure or if you are being treated with medicines that increase the concentration of potassium in the blood.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eElderly patients\u003c\/u\u003e \u003cbr\u003eUse the medicine with caution because it may cause an increase in side effects, especially bleeding and perforation in the stomach and intestines, which can also be fatal (see “How to use Ketodol”).\u003cbr\u003e Start treatment with the lowest possible dose, because the risk of gastrointestinal bleeding, ulceration, perforation is greater with increased doses of NSAIDs.\u003cbr\u003e\u003cbr\u003e At the beginning of treatment, renal function must be carefully monitored in patients with heart failure, chronic inflammation of the liver (cirrhosis) and severe kidney disease (nephrosis), in subjects treated with diuretics or suffering from chronic renal failure, especially if elderly. In these patients, the use of ketoprofen may cause a reduction in blood flow to the kidneys and lead to renal failure.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e \u003cbr\u003eDo not give the medicine to children and adolescents up to 15 years of age because the safety and efficacy of the medicine have not been established for these age groups.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e Undesirable effects may be minimised by using the lowest effective dose for the shortest duration possible.\u003cbr\u003e \u003cb\u003eSerious side effects\u003c\/b\u003e\u003cbr\u003e The following side effects are serious or may become serious. If you experience any of the following symptoms, stop taking Ketodol and contact your doctor immediately:\u003cbr\u003e • serious skin reactions (some of them fatal) such as:\u003cbr\u003e - death of skin cells, accompanied by malaise, chills, muscle aches and fever (toxic epidermal necrolysis);\u003cbr\u003e - skin rashes with blistering (Stevens-Johnson syndrome); \u003cbr\u003e• severe skin reaction characterized by redness and swelling together with pustule formation (acute generalized exanthematous pustulosis);\u003cbr\u003e • severe inflammation with redness of the skin (exfoliative dermatitis);\u003cbr\u003e • constant stomach pain, which gets worse on an empty stomach (gastric ulcers);\u003cbr\u003e • vomiting blood, blood in the stool (gastrointestinal bleeding);\u003cbr\u003e • swelling of the throat (larynx edema and\/or glottis edema), difficulty breathing (dyspnoea), intense awareness of the heartbeat (palpitation) or increased heart rate (tachycardia).\u003cbr\u003e\u003cbr\u003e Other side effects are listed below:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects\u003c\/b\u003e (may affect up to 1 in 10 people) include:\u003cbr\u003e • Nausea, vomiting, heartburn, indigestion, abdominal pain, stomach pain.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects\u003c\/b\u003e (may affect up to 1 in 100 people) include:\u003cbr\u003e • Headache, dizziness, drowsiness. \u003cbr\u003e• Diarrhea, constipation (constipation), flatulence (gas), inflammation of the stomach (gastritis).\u003cbr\u003e • Skin irritation, itching.\u003cbr\u003e • Swelling (accumulation of fluid under the skin), feeling tired.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eRare side effects\u003c\/b\u003e (may affect up to 1 in 1000 people) include:\u003cbr\u003e • Anemia due to hemorrhage, low white blood cell count (seen in blood test).\u003cbr\u003e • Lack of sensation and tingling sensation in some parts of the body, involuntary muscle movements.\u003cbr\u003e • Blurred vision.\u003cbr\u003e • Ringing in the ears, loss of balance (vertigo).\u003cbr\u003e • Wheezing and difficulty breathing (asthma).\u003cbr\u003e • Oral ulcerations, colitis.\u003cbr\u003e • Inflammation of the liver (hepatitis), increased transaminases and bilirubin (seen in blood tests), yellowing of the skin (jaundice).\u003cbr\u003e • Generalized weakness.\u003cbr\u003e • Weight gain.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects\u003c\/b\u003e (may affect up to 1 in 10,000 people) include: \u003cbr\u003e• Presence of a mass of foreign material in the stomach (bezoar).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSide effects with unknown frequency\u003c\/b\u003e (frequency cannot be estimated from the available data):\u003cbr\u003e • Significant reduction in white blood cells, reduction in the number of platelets, inability of the bone marrow to produce the normal amount of blood cells, anemia due to destruction of red blood cells (seen in blood tests).\u003cbr\u003e • Allergic hypersensitivity reactions (including anaphylactic shock).\u003cbr\u003e • Reduction of sodium levels in the blood (hyponatremia) and increase of potassium levels in the blood (hyperkalemia).\u003cbr\u003e • Depression, hallucinations, confusion, mood changes, insomnia.\u003cbr\u003e • Disease of the membranes of the brain and spinal cord of viral origin (aseptic meningitis), involuntary muscle contraction (convulsions), alteration of the sense of taste. \u003cbr\u003e• Poor heart function, atrial fibrillation (a form of arrhythmia that causes the heartbeat to be irregular).\u003cbr\u003e • Increased blood pressure (hypertension), enlarged blood vessels, inflammation of blood vessels (vasculitis).\u003cbr\u003e • Severe respiratory distress (bronchospasm) particularly in patients with known hypersensitivity to acetylsalicylic acid and NSAIDs.\u003cbr\u003e • Internal inflammation of the nose (rhinitis).\u003cbr\u003e • Worsening of colitis and Crohn's disease, inflammation of the pancreas (pancreatitis).\u003cbr\u003e • Allergic reactions to the sun (photosensitivity), hair loss (alopecia), urticaria, even widespread with swelling, blistering eruptions, inflammation and redness of the skin (dermatitis, eczema, erythema).\u003cbr\u003e • Difficulty urinating, decreased kidney function, inflammation of the kidneys, kidney damage (nephrotoxic syndrome), abnormal kidney function tests (seen in blood tests).\u003cbr\u003e • Arterial thrombotic events (e.g. heart attack or stroke).  \u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/infezioni\u003e","brand":"EG SPA","offers":[{"title":"Default Title","offer_id":50221909344590,"sku":"028561037","price":10.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0011601.png?v=1768753673"},{"product_id":"gladio-crema-derm-50-g-1-5-g-100-g","title":"GLADIO \"1.5% CREAM\"50 G TUBE\"","description":"\u003cb\u003eName\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eGLADIO 1.5 g\/100 g cream\u003c\/b\u003e\u003cbr\u003e Aceclofenac\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e \u003cbr\u003eGLADIO contains the active ingredient aceclofenac which belongs to the category of non-steroidal anti-inflammatory drugs (NSAIDs) and antirheumatic drugs (drugs used for diseases affecting the bones, cartilage and muscles).\u003cbr\u003e\u003cbr\u003e This medicine is indicated for the local treatment of painful and inflammatory (inflammatory) conditions of a rheumatic or traumatic nature of the joints, muscles, tendons and ligaments such as tendonitis (inflammation of the tendons), tenosynovitis (inflammation of the membrane covering the tendon), sprains, contusions, periarthritis (inflammatory diseases involving the fibrous tissues surrounding a joint), dislocations (displacement of the joint surfaces relative to each other), lumbago (back pain), stiff neck, bursitis (inflammation of the fluid-filled sacs that form a cushion between the bones and tendons and\/or muscles surrounding a joint), strains and sequelae of trauma.\u003cbr\u003e   \u003cbr\u003eTalk to your doctor if you do not feel better or if you feel worse.\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e \u003cb\u003eDo not use GLADIO\u003c\/b\u003e\u003cbr\u003e - if you are allergic to aceclofenac, to other NSAIDs (including acetylsalicylic acid) or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you have experienced in the past, after taking acetylsalicylic acid, diclofenac or other NSAIDs, an aggravation of asthma attacks, acute rhinitis (inflammation of the nasal mucosa) or urticaria (redness of the skin with intense itching);\u003cbr\u003e - if you have or have had in the past hypersensitivity (allergy) reactions to diclofenac, even if cross-allergenicity with this medicine has not been demonstrated;\u003cbr\u003e - if you are in the last 3 months of pregnancy and are breastfeeding (see \"Pregnancy, breastfeeding and fertility\").\u003cbr\u003e\u003cbr\u003e GLADIO is contraindicated in pediatric age (see \"Children and adolescents\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings and precautions\u003c\/b\u003e \u003cbr\u003eTalk to your doctor or pharmacist before using GLADIO.\u003cbr\u003e\u003cbr\u003e Use GLADIO cream for external use only.\u003cbr\u003e During treatment with GLADIO you should avoid:\u003cbr\u003e - Inappropriate exposure of the treated area to sunlight without adequate protection to prevent photosensitivity reactions (reaction of the immune system to sunlight).\u003cbr\u003e - Applying the cream to open sores or wounds.\u003cbr\u003e - Contact with eyes, mucous membranes or any other application site with ongoing skin lesions.\u003cbr\u003e\u003cbr\u003e Stop treatment with GLADIO and contact your doctor for appropriate therapeutic treatment if you experience symptoms of local irritation.\u003cbr\u003e\u003cbr\u003e Prolonged use of dermatological products may give rise to sensitization (allergy) phenomena.\u003cbr\u003e   \u003cbr\u003eAs with other NSAIDs, allergic reactions, including anaphylactic\/anaphylactoid reactions (rapid-onset allergic reactions), may also occur without previous exposure to aceclofenac (see section 4 \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e Serious skin reactions, some of them fatal, including exfoliative dermatitis (skin irritation with peeling), Stevens-Johnson syndrome (a serious illness involving lesions of the skin and mucous membranes), and toxic epidermal necrolysis (a serious skin disease in which the skin peels off in sheets), have been reported very rarely in association with the use of NSAIDs (see section 4 \"Possible side effects\"). The risk appears to be highest in the early stages of therapy, the onset of the reaction occurring in the majority of cases within the first month of treatment.\u003cbr\u003e   \u003cbr\u003eStop taking GLADIO at the first appearance of skin rash, mucosal lesions or any other sign of hypersensitivity (allergy).\u003cbr\u003e\u003cbr\u003e Avoid using GLADIO if you have chickenpox; in some cases chickenpox can cause serious infectious complications of the skin and soft tissues and the role of NSAIDs in the worsening of these infections cannot be excluded (see paragraph 4 \"Possible side effects\").\u003cbr\u003e\u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e There are currently no data available regarding the safety and efficacy of aceclofenac in children up to 14 years of age, therefore its administration is not recommended (see \"Do not use GLADIO\").\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Possible side effects that may occur following the intake of GLADIO are:\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e \u003cbr\u003eMild or moderate skin irritation accompanied by redness and mild itching which disappear when treatment is stopped.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eUncommon side effects (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - Photosensitivity (increased sensitivity to light) if treated areas of skin have been exposed to strong sunlight without adequate protection (see \"Warnings and precautions\").\u003cbr\u003e - Erythema (skin irritation).\u003cbr\u003e - Itching.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e Bullous reactions (including Stevens-Johnson syndrome and toxic epidermal necrolysis).\u003cbr\u003e\u003cbr\u003e Exceptionally, serious skin and soft tissue infectious complications have been reported in association with NSAID treatment during chickenpox (see \"Warnings and precautions\").\u003cbr\u003e\u003cbr\u003e Following the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e .\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.","brand":"ABIOGEN PHARMA SPA","offers":[{"title":"Default Title","offer_id":50221943947598,"sku":"031220054","price":10.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE004-H0001648_d2e5eb72-e074-420f-aa42-93786e3a49ea.jpg?v=1768753779"}],"url":"https:\/\/farmaspeed.it\/en-eu\/collections\/sistema-muscolo-scheletrico.oembed?page=6","provider":"Farmaspeed","version":"1.0","type":"link"}