non-steroidal anti-inflammatory drug
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Voltaren dolo forte drag 25 mg 10 pcs
Voltaren Dolo forte 25 mgDragées contain the active ingredient diclofenac potassium. This belongs to the group of non-steroidal anti-inflammatory drugs (prostaglandin synthesis inhibitors) and has an analgesic, fever-reducing and anti-inflammatory effect. The effect occurs within 30-60 minutes and lasts about 4-6 hours. Voltaren Dolo forte 25 mgDragées are suitable for short-term treatment, i. for the maximum 3-day treatment of: headaches, toothaches, menstrual pains, pain in the area of joints and ligaments, back pain, pain from injuries and to reduce fever in the case of influenza. Swissmedic-approved patient informationVoltaren Dolo forte 25 mg, dragees GSK Consumer Healthcare Schweiz AGWhat is Voltaren Dolo forte 25 mg, dragees and when is it used? Voltaren Dolo forte 25 mgDragées contain the active ingredient diclofenac potassium. This belongs to the group of non-steroidal anti-inflammatory drugs (prostaglandin synthesis inhibitors) and has an analgesic, fever-reducing and anti-inflammatory effect. The effect occurs within 30-60 minutes and lasts about 4-6 hours. Voltaren Dolo forte 25 mgDragées are suitable for short-term treatment, i. for the maximum 3-day treatment of: headaches, toothaches, menstrual pains, pain in the area of joints and ligaments, back pain, pain from injuries and to reduce fever in the case of influenza. When should Voltaren Dolo forte 25 mg coated tablets not be taken?if you are allergic to diclofenac or any of the excipients or after taking acetylsalicylic acid or others pain or rheumatism medicines, so-called non-steroidal anti-inflammatory drugs have had shortness of breath or allergic-like skin reactions, e.g. swelling of the face, lips, tongue, throat and/or extremities (signs of angioedema),if you are pregnant or breastfeeding (see also chapter «Can Voltaren Dolo forte 25 mg coated tablets be taken during pregnancy or breastfeeding?»),in active stomach and/or duodenal ulcers or stomach /intestinal bleeding or perforation (this may manifest as blackening of the stool, blood in the stool or vomiting of coffee grounds-like material),in chronic inflammatory bowel disease (Crohn's disease or ulcerative colitis), in severe impairment of liver or kidney function,in severe heart failure,for the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine),in children and adolescents under the age of 14. Voltaren Dolo forte 25 mg dragees have not been tested for use in children and adolescents under 14 years of age. For this reason, Voltaren Dolo forte 25 mg coated tablets should not be used in children and adolescents under the age of 14.When should Voltaren Dolo forte 25 mg be taken Dragées caution required? During treatment with Voltaren Dolo forte 25 mg dragées, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (stomach or intestinal perforations) can occur. appear. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine. Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. In the following situations, you may only take Voltaren Dolo forte 25 mg coated tablets if prescribed by a doctor and under medical supervision:if you are currently being treated by a doctor because of a serious illness treatment;if you have previously suffered from a stomach or duodenal ulcer;if you suffer from a heart or blood vessel disease (so-called cardiovascular diseases, including uncontrolled high blood pressure, heart failure, existing ischemic heart disease or peripheral arterial disease), have had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes [diabetes], high levels of fats [cholesterol, triglycerides] in the blood, smoking). Voltaren Dolo forte 25 mgDragées is usually not recommended in these situations. For certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found with high doses and/or long-term treatment. It is not known whether this increased risk also applies to Voltaren Dolo forte 25 mg coated tablets.It is important that you use the lowest effective dose for your pain relief and that you Voltaren Dolo forte 25 mg Take dragées for the shortest possible time to keep the risk of cardiovascular side effects as low as possible.if you have kidney disease, if you are taking medicines to treat high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. due to heavy sweating or diarrhea; Taking Voltaren Dolo forte 25 mg coated tablets may affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have a have liver problems;if you are being treated with anticoagulants (blood thinners, anticoagulants) or have a blood clotting disorder or any other blood disorder, including the rare disease hepatic porphyria; if you suffer from asthma;if you are taking anti-rheumatic medicines or other painkillers (e.g. acetylsalicylic acid, aspirin, ibuprofen) or other anti-inflammatory drugs (corticosteroids);if you are taking the following medicines: lithium or specific serotonin reuptake inhibitors (SSRI's, medicines used to treat depression), digoxin (medicines for heart problems), diuretics (medicines to increase urine output), medicines (e.g. metformin) for the treatment of diabetes/diabetes with the exception of insulin, methotrexate (used to treat arthritis and cancer), ciclosporin or tacrolimus (for organ transplants), trimethoprim (for urinary tract infections), quinolone antibiotics (used to treat infections), voriconazole (used to treat fungal infections), phenytoin (used to treat epileptic fits), or sulfinpyrazone (gout medicine). ).If you notice signs or symptoms while taking Voltaren Dolo forte 25 mg Dragées that indicate problems with the heart or blood vessels, such as chest pain, shortness of breath, weakness or slurred speech, contact your doctor immediately.Serious skin reactions have been reported in association with treatment with non-steroidal anti-inflammatory drugs. The highest risk of such reactions appears to be at the beginning of therapy. If a skin rash occurs, including fever, lesions of the mucous membranes, blisters or other signs of allergy, you should stop treatment with Voltaren Dolo forte 25 mg coated tablets and seek medical attention immediately, as these may be the first signs of a very serious skin reaction (see the section «What side effects can Voltaren Dolo forte 25 mg coated tablets have?»). Voltaren Dolo forte 25 mg coated tablets can reduce the symptoms of an infection (e.g. high fever) and thus make it more difficult to diagnose the infection. Information on the excipientsSucrose:Voltaren Dolo forte 25 mg Dragées contain sucrose (45,416 mg per coated tablet). Please only take Voltaren Dolo forte 25 mg Dragées after consulting your doctor if you know that you suffer from a sugar intolerance. This medicinal product contains less than 1 mmol sodium (23 mg) per coated tablet, i.e. essentially 'sodium-free'. it is almost «sodium-free». This medicine may affect your ability to react, drive and use any tools or machines. You should refrain from driving or using machines, especially if you experience dizziness or visual disturbances. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies oruse other medicines (including those you bought yourself!). Can Voltaren Dolo forte 25 mg coated tablets be taken during pregnancy or breastfeeding?PregnancyYou should take Voltaren Dolo forte Do not take 25 mg dragées unless it is clearly necessary and prescribed by a doctor. If taken during the first 6 months of pregnancy, the dose should be kept as low and the duration of treatment as short as possible. Taking nonsteroidal anti-inflammatory drugs (NSAIDs) after the 20th week of pregnancy may harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. If you are pregnant or planning a pregnancy, you should only take Voltaren Dolo forte 25 mg dragees after consulting your doctor. Voltaren Dolo forte 25 mg dragées should not be taken in the last third of pregnancy. BreastfeedingVoltaren Dolo forte 25 mg Dragées should not be taken while breastfeeding unless your doctor has expressly instructed you to do so permitted. Like other anti-inflammatory drugs, Voltaren Dolo forte 25 mg coated tablets can make it more difficult to get pregnant. After stopping the drug, this effect ends. If you are planning to become pregnant or are having trouble conceiving, talk to your doctor. How do you use Voltaren Dolo forte 25 mg coated tablets?How many Voltaren Dolo forte 25 mg coated tablets should you take?The recommended dosage must not be exceeded. The lowest effective dose should always be taken for the shortest possible time. Adults and adolescents from 14 years of age:1 dragée Voltaren Dolo forte 25 mg swallow up to 3 times a day with plenty of water, preferably with or after meals. A gap of at least 4 to 6 hours should be observed before the next dose. Maximum daily dose: Do not take more than 3 tablets of Voltaren Dolo forte 25 mg within 24 hours, unless prescribed by a doctor. How long should Voltaren Dolo forte 25 mg coated tablets be taken?Do not take Voltaren Dolo forte 25 mg coated tablets for more than 3 days and only to treat the complaints listed above. If the symptoms persist or worsen, consult your doctor so that the reason can be clarified. A serious illness can be the cause. If you have taken more Voltaren Dolo forte 25 mg coated tablets than you should?If you have accidentally taken more coated tablets, contact your doctor immediately Doctor. Children and adolescents under the age of 14:Voltaren Dolo forte 25 mg Dragées should not be used in children and adolescents under the age of 14. The use and safety of Voltaren Dolo forte 25 mg dragées in children and adolescents under the age of 14 has not yet been tested. Elderly patients:Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Voltaren Dolo forte 25 mg coated tablets have?After taking Voltaren Dolo forte 25 mg coated tablets, the following side effects can occur: Common side effects(in 1 to 10 out of 100 people treated):Stomach pain, stomach pain, diarrhoea, nausea, vomiting, Gas, indigestion, decreased appetite;Headache, drowsiness;Rash;Dizziness;Increased liver enzymes.Uncommon side effects(affects 1 to 10 users in 1000):Palpitation, sudden and oppressive Chest pain (signs of heart attack and heart attack)*;Shortness of breath, difficulty breathing when lying down, swelling of the feet or legs (signs of heart failure)*.Rare Side effects that occur(affects 1 to 10 users in 10,000):Unusual tiredness;Itchy rash;Uses in the gastrointestinal tract, blood in the stools or blackening of the stools, vomiting blood, bloody diarrhea;Allergic reaction including difficulty breathing or swallowing, swelling of the face, mouth, tongue or throat, often associated with a rash, collapse;Wheezing or shortness of breath, feeling suffocated (signs of asthma);Swelling in the arms, legs, and feet (oedema) ;Yellow skin or eyes (signs of liver inflammation or liver failure).Very rarelyOccurring side effects(less than 1 in 10,000 people treated):bleeding or unusual bruising;low white blood cells (resulting in a high fever or persistent sore throat, common infections), few red blood cells;Constipation, inflammation of the oral mucosa, inflammation and redness of the tongue, taste disturbances, upper abdominal cramps;Itching and reddening of the skin, hair loss;..
34.32 USD
Zentidol film-coated tablets 400 mg
Helvepharm AG What is ZentiDol and when is it used? ZentiDol contains the active ingredient ibuprofen. This has pain-relieving, antipyretic and anti-inflammatory properties. ZentiDol is suitable for short-term treatment, i.e. for a maximum of 3 days of treatment of: Pain in the area of joints and ligaments, Back pain, Headaches, Toothache, Pain during menstruation, Pain after injuries, Fever with flu-like illnesses. When should ZentiDol not be taken? ZentiDol must not be taken, if you are allergic to one of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other painkillers or anti-rheumatic drugs, so-called non-steroidal anti-inflammatory drugs, if you are pregnant or breastfeeding (see also chapter «Can ZentiDol be taken during pregnancy or breastfeeding?»), if you have active stomach and/or duodenal ulcers or stomach/intestinal bleeding, if you have chronic intestinal inflammation (Crohn's disease or ulcerative colitus), in the case of severe limitations in liver or kidney function, in the case of severe heart failure, for the treatment of pain after coronary bypass surgery on the heart (or use of a heart-lung machine), in children under 12 years of age: ZentiDol has not been tested for use in children under 12 years of age. When should you be careful when taking ZentiDol? During treatment with ZentiDol, mucous membrane ulcers, rarely bleeding or, in isolated cases, perforations (perforations of the stomach or intestines) can occur in the upper gastrointestinal tract. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used for the shortest possible duration of treatment. Contact your doctor if you have stomach pain and suspect a connection with taking the medicine. Elderly patients may react more sensitively to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. In the following situations, you may only take ZentiDol on prescription and under medical supervision: If you are currently receiving medical treatment for a serious illness; If you have previously suffered from a stomach or duodenal ulcer; If you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes, high blood fat levels [smoking]; for certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found in high doses and/or long-term treatment. It is not known whether this increased risk also applies to ZentiDol; If you have a heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or if you have increased fluid loss, e.g. due to heavy sweating; taking ZentiDol can affect the function of your kidneys which can lead to an increase in blood pressure and/or fluid retention (edema)ann; If you have a liver disease; If you are being treated with anticoagulants or suffer from a blood clotting disorder; If you suffer from asthma; If you are taking anti-rheumatic drugs or other painkillers (e.g. acetylsalicylic acid, aspirin); If you are taking medicines to treat diabetes (except insulin), medicines to increase urine output (diuretics), medicines to treat infections (quinolone antibiotics) or medicines containing one of the following substances: lithium, digoxin, methotrexate, baclofen, phenytoin, probenecid or sulfinpyrazone; Serious skin reactions have been reported in connection with treatment with non-steroidal anti-inflammatory drugs. The highest risk of such reactions appears to be at the beginning of therapy. If you experience a skin rash, including fever, lesions of the mucous membranes, blisters or other signs of allergy, you should stop treatment with ZentiDol and seek medical attention immediately, as these may be the first signs of a very serious skin reaction (see section «What side effects can ZentiDol have?»). Inform your doctor, pharmacist or druggist if you are being treated with medicines such as blood thinners, diuretics (water tablets), ACE inhibitors or β-blockers (medications for high blood pressure and heart failure), antibiotics, certain medicines for fungal infections (e.g. voriconazole or fluconazole), immunosuppressants (medications for transplant rejection), herbal Ginkgo biloba extract, medicines for high blood sugar, for AIDS, epilepsy and depression. Non-steroidal anti-inflammatory drugs such as ibuprofen and the medicines listed above can influence each other. If alcohol is consumed at the same time, side effects, particularly those affecting the gastrointestinal tract or the central nervous system, can be increased. Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking or applying other medicines (including those you have bought yourself!) externally. ZentiDol can impair your ability to react, drive and operate tools or machines! This is especially true if you take it with alcohol. Sodium This medicine contains less than 1 mmol sodium (23 mg) per film-coated tablet, i.e. it is essentially «sodium-free». Can ZentiDol be taken during pregnancy or while breast-feeding? Pregnancy If you are pregnant or planning to become pregnant, you should only take ZentiDol after consulting your doctor. You should not take ZentiDol unless it is clearly necessary and prescribed by a doctor. If taken in the first 6 months of pregnancy, the dose should be kept as low and the duration of treatment as short as possible. Taking non-steroidal anti-inflammatory drugs (NSAIDs) from the 20th week of pregnancy can harm your unborn child. If you need to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the heart of the unborn child. ZentiDol must not be taken in the last trimester of pregnancy. Breastfeeding ZentiDol should not be taken while breastfeeding unless your doctor has specifically given you permission to do so. How to use ZentiDol? Adults and adolescents aged 12 and over ZentiDol 200 mg Take 1-2 ZentiDol 200 mg film-coated tablets with plenty of liquid. Wait 4 to 6 hours before taking the next dose. Maximum daily dose : Do not take more than 6 ZentiDol 200 mg film-coated tablets (1200 mg ibuprofen) within 24 hours, unless prescribed by a doctor. ZentiDol 400 mg Take 1 ZentiDol 400 mg film-coated tablet with plenty of liquid. Wait 4 to 6 hours before taking the next dose. Maximum daily dose: Do not take more than 3 ZentiDol 400 mg film-coated tablets (1200 mg ibuprofen) within 24 hours, unless prescribed by a doctor. If you experience pain during your period, it is recommended that you start treatment with 2 ZentiDol 200 mg film-coated tablets or 1 ZentiDol 400 mg film-coated tablet at the first sign of symptoms. Do not use ZentiDol for longer than 3 days and only to treat the symptoms listed above. If the symptoms get worse despite taking ZentiDol or if the painful area becomes red or swollen, consult your doctor. A serious illness may be the cause. Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the cause can be clarified. Children under 12 years ZentiDol must not be used in children under 12 years. The use and safety of ZentiDol in children under 12 years has not yet been tested. Elderly patients Elderly patients may be more sensitive to the medicine than younger adults. It is especially important that elderly patients report any side effects to their doctor immediately. Follow the dosage stated in the package leaflet or prescribed by your doctor. If you have taken more ZentiDol than you should, or if children have accidentally taken the medicine, always contact a doctor for an assessment of the risk and advice on further treatment. Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and trembling eyes. At high doses, drowsiness, chest pain, palpitations, fainting, cramps (especially in children), weakness and dizziness, blood in the urine, chills and breathing problems have been reported. If you forget to take a dose, do not take more than the usual recommended amount at the next dose. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can ZentiDol have? The following side effects can occur when taking ZentiDol. They are listed according to their frequency: Common (affects 1 to 10 out of 100 users) Gastrointestinal complaints such as indigestion, diarrhea, nausea, vomiting, constipation, upper abdominal pain, flatulence, tarry stools, vomiting blood, gastrointestinal bleeding. Central nervous system side effects such as reduced reaction time (especially in combination with alcohol), headaches and dizziness. Acute skin rash. Uncommon (affects 1 to 10 in 1000 users) Inflammation of the nasal mucosa. Hypersensitivity reactions. Insomnia, feelings of anxiety. Visual disturbances (the visual disturbances are usually reversible when treatment is stopped). Ringing in the ears, hearing loss, dizziness. Asthma, spasm of the muscles of the respiratory tract and shortness of breath. In patients with heart failure there is a risk of acute pulmonary edema (water lung). Tiredness. Rare (affects 1 to 10 in 10,000 users) Aseptic meningitis (inflammation of the meninges). Angina, high fever, swelling of the lymph nodes in the neck area. Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia. Depression, confusion. "Tingling" of the skin, drowsiness. Irreversible visual impairment or visual impairment. Inflammation of the gastric mucosa, stomach and intestinal ulcers, ulcers of the oral mucosa, stomach and intestinal perforations. Hepatitis, jaundice, liver dysfunction. Hives, itching, bleeding into the skin, swelling of the skin and mucous membranes, sensitivity to light. Various kidney diseases such as kidney dysfunction with water retention in the tissue and even kidney failure. General swelling. Very rare (affects less than 1 in 10,000 users) Psychotic conditions. Heart failure, heart attack. High blood pressure. Pancreatitis. Liver failure. Severe allergic skin reactions with the formation of blisters and/or large-scale peeling of the skin. Isolated cases A severe 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 cells). Worsening of colitis or Crohn's disease. A red, scaly, widespread rash with bumps under the skin and blisters, mainly localized in the skin folds, on the trunk and upper extremities, accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). If these symptoms occur, stop taking ZentiDol and seek medical attention immediately. If you notice any side effects, contact your doctor or pharmacist. This applies in particular to side effects not listed in this leaflet. What else should you bear in mind? The medicine may only be used up to the date marked "EXP" on the packaging. Storage instructions Do not store above 25°C in the original packaging and out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed specialist information. What does ZentiDol contain? Active ingredients 1 ZentiDol 200 Film Tablet mg contains: 200mg Ibuprofen. 1 ZentiDol 400 Film Tablet mg Contains: 400 mg Ibuprofen. Aids Intragranular Excipients Microcrystalline Cellulose (E 460), Croscarmellose-Sodium (E 468), Hypromellose (E 464), Stearinsäure (E 570). Extragranular Excipients Croscarmellose-Sodium (E 468), hochdisperses Silicium dioxide (E 551), Magnesium stearate (E 470b). Filmüreview Hypromellose (E 464), Macrogol 300 (E 1521), Talcum (E 553b), Titanium Dioxide (E 171). The 200 mg film tablets also contain iron oxide yellow (E 172) as an excipient. Accession Number 68588 (Swissmedic). Where did you get ZentiDol? Which packages are available? In pharmacies and drug stores without prescription. ZentiDol 200mg : Packs of 20 Filmtabletten. ZentiDol 400mg : Packs of 10 Film Tablets. Reference Information Helvepharm AG, Frauenfeld This packaging was last tested by the Arzneimittelbehörde (Swissmedic) in November 2022. 30821 / 08.11.2023 SweetDoll ..
17.02 USD
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