Anti-rheumatics
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Algifor liquid caps 400 mg 10 pcs
AMZV What is Algifor Liquid caps 400 and when is it used? The soft gelatin capsule Algifor Liquid caps 400 contains the active ingredient ibuprofen. This has analgesic, antipyretic and anti-inflammatory properties.Algifor Liquid caps 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:pain in the area of joints and ligaments,back pain,headache,toothache,pain during the menstrual period,Pain after injury,Fever with a flu.When should Algifor Liquid caps 400 not be taken?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other painkillers or rheumatism drugs, so-called non-steroidal anti-inflammatory drugs.Im last trimester of pregnancy (see also chapter "Can Algifor Liquid caps 400 be taken during pregnancy or while breast-feeding?").If you have an active stomach and/or duodenal ulcer or stomach/intestinal bleeding that has occurred repeatedly in the past.If you have a history of bleeding or perforation (perforation) in the stomach or intestines in connection with previous therapy with so-called non-steroidal anti-inflammatory drugs.For chronic intestinal inflammation (Crohn's disease, ulcerative colitis).For severe impairment of liver or kidney function.For severe heart failure.For the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine).For varicella infection (chickenpox infection).In children under 12 years of age. Algifor Liquid caps 400 has not been tested for use in children under the age of 12.When should caution be taken when taking Algifor Liquid caps 400?During treatment with Algifor Liquid caps 400, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (gastrointestinal perforations) may occur. 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.Older people may be more sensitive to the medicine than younger adults. It is particularly important that older patients report any side effects to their doctor immediately.At the first sign of a sore throat, high fever, superficial mouth sores, flu-like symptoms, severe exhaustion, nose and skin bleeding, treatment with ibuprofen must be stopped immediately and the doctor consulted.In very rare cases, taking Algifor Liquid caps 400 can lead to severe headaches in connection with nausea and vomiting and neck stiffness. The treatment should then be stopped and a doctor consulted.You may only take Algifor Liquid caps 400 on prescription and under medical supervision in the following situations:if you are currently being treated by a doctor 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 vein thrombosis, or if you have risk factors (such as high blood pressure, diabetes (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 at high doses and/or long-term treatment. It is unclear whether this increased risk also applies to Algifor Liquid caps 400not known;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; taking Algifor Liquid caps 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (edema);if you have liver disease;if you are being treated with anticoagulants (blood thinners, anticoagulants) or have a blood clotting disorder;if you suffer from asthma;if you are taking antirheumatic medicines 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), medicines for AIDS (zidovudine), immunosuppressants (medicines used to treat transplant rejection (tacrolimus and cyclosporine), corticosteroids, antiplatelet medicines and selective S are taking erotonin reuptake inhibitors (SSRIs) or medicines containing any of the following: lithium, digoxin, methotrexate, baclofen, phenytoin, probenecid or sulfinpyrazone;if you have certain skin disorders (systemic lupus erythematosus (SLE) or mixed collagenosis). If you suffer from severe skin reactions such as exfoliative dermatitis, Stevens-Johnson syndrome or toxic epidermal necrolysis. The risk of such reactions appears to be highest at the start of therapy, since the majority of these reactions occurred within the first month of treatment. At the first sign of skin rashes, mucosal lesions or any other sign of hypersensitivity, Algifor Liquid caps 400 should be discontinued and your doctor consulted immediately;Acetylsalicylic acid or other painkillers should not be taken at the same time as ibuprofen, as the risk of side effects may increase.Inform your doctor if you have recently been treated for an abortion...
25.83 USD
Dolo-spedifen forte filmtabl 400 mg 10 pcs
What is Dolo-Spedifen forte 400 and when is it used? Dolo-Spedifen forte 400 contains the active ingredient ibuprofen in the form of ibuprofen arginate. This has pain-relieving, anti-inflammatory and antipyretic properties. The effect occurs after about 30 minutes and lasts about 6 hours. Dolo-Spedifen forte 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments; Back pain; Headache; Toothache; Pain during menstrual bleeding; Pain zen after injuries;Fever with flu-like illnesses.When should Dolo-Spedifen forte 400 not be taken?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other pain or rheumatism medicines, so-called non-steroidal anti-inflammatory drugs;if you are pregnant or breastfeeding (see also «Can Dolo-Spedifen forte 400 be taken during pregnancy or while breastfeeding?»);if you have active stomach and/or duodenal ulcers or gastrointestinal bleeding;if you have a history of gastrointestinal bleeding or perforation (perforation) in connection with previous therapy with so-called non-steroidal anti-inflammatory drugs;if you have chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in the case of cerebral hemorrhage;in the case of an increased tendency to bleed;in the case of severe impairment of liver or kidney function;in the case of severe heart failure;for the treatment of pain after a coronary bypass operation on the heart (or use of a heart-lung machine);in children under 12 years of age. Dolo-Spedifen forte 400 has not been tested for use in children under the age of 12. When is caution required when taking Dolo-Spedifen forte 400? During treatment with Dolo-Spedifen forte 400, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. 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.Older people 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.You may only take Dolo-Spedifen forte 400 with a prescription and under medical supervision in the following situations:if you are currently being treated by a doctor 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 a have had venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes, high levels of fat in your blood, 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 at high doses and/or long-term treatment. It is not known whether this increased risk also applies to Dolo-Spedifen forte 400;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; theTaking Dolo-Spedife forte 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;if you are being treated with medicines that inhibit blood clotting (blood thinners, anticoagulants) or have a blood clotting disorder;if you suffer from asthma;if you are taking medicines for Treatment of diabetes, medicines to increase urine output (water tablets), medicines to treat infections (quinolone antibiotics), for AIDS (zidovudine), immunosuppressants (tacrolimus, cyclosporine), corticosteroids, antiplatelet medicines such as acetylsalicylic acid, selective serotonin reuptake inhibitors (SSRIs), antifungal medicines (voriconazole, fluconazole), or medicines containing any of the following: lithium, digoxin, are taking methotrexate, mifepristone, baclofen, phenytoin, probenecid or sulfinpyrazone;if you have certain skin diseases (systemic lupus erythematosus (SLE) or mixed collagenosis);if you have an infection. Dolo-Spedifen forte 400 can mask signs of infection such as fever and pain. It is therefore possible that Dolo-Spedifen forte 400 may delay adequate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Serious skin reactions such as acute generalized pustular exanthema, scaly skin inflammation or Stevens-Johnson syndrome have been reported in connection with treatment with medicines containing ibuprofen. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of allergy, you should stop taking Dolo-Spedifen forte 400 and seek immediate medical attention, as these may be the first signs of a very serious skin reaction (see «What side effects can Dolo-Spedifen forte 400 have?»).Acetylsalicylic acid, other painkillers or Cox-2 inhibitors should not be taken at the same time as ibuprofen as the risk of side effects may be increased.Patients who experience visual disturbances during Dolo-Spedifen forte 400 therapy should discontinue treatment and consult a doctor immediately.Excipients of particular interestDolo-Spedifen forte 400 film-coated tablets contain:Sucrose: Please take Do not use this medicine until you have consulted your doctor if you know that you have an intolerance to sugar.Sodium: 83 mg sodium (main component of cooking/table salt) per 400 mg film-coated tablet. This corresponds to 4% of the recommended maximum daily dietary intake of sodium for an adult.This medicine may impair your ability to react, drive and use tools or machines.Inform your doctor, pharmacist or druggist if you suffer from any other illnesses, have allergies or are taking or using other medicines (including those you have bought yourself)!May do Thurs lo-Spedifen forte 400 taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take Dolo-Spedifen forte 400 after consulting your doctor. In the last third of pregnancyDolo-Spedifen forte 400 must not be taken afterwards.BreastfeedingDolo-Spedifen forte 400 should not be taken while breastfeeding unless your doctor has expressly permitted it.How do you use Dolo-Spedifen forte 400?Adults and adolescents from the age of 12D olo-Spedifen forte 400: Take 1 film-coated tablet with plenty of liquid. Before taking the next dose, wait 4 to 6 hours. In the case of pain during menstrual bleeding, it is recommended to start treatment with 1 film-coated tablet of Dolo-Spedifen forte 400 at the first sign of symptoms.Maximum daily dose Do not take more than 3 film-coated tablets of Dolo- Spedifen forte 400 within 24 hours, unless prescribed by a doctor.Do not use Dolo-Spedifen forte 400 for more than 3 days and only to treat the symptoms listed above.The lowest effective dose should be used for the shortest time necessary to relieve symptoms.If the symptoms increase despite taking Dolo-Spedifen forte 400 or if the pain is painful en area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. If you have an infection, consult a doctor immediately if the symptoms (e.g. fever and pain) persist or worsen (see «When should you be careful when taking Dolo-Spedifen forte 400?»).If you have taken more Dolo-Spedifen forte 400 than you should, or if children have accidentally taken the medicine, always consult a doctor to get 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 eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.Children under the age of 12Dolo-Spedifen forte 400 must not be used in children under the age of 12. The use and safety of Dolo-Spedifen forte 400 in children under the age of 12 has not yet been systematically tested. Stick to the dosage given in the package insert or prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Dolo-Spedifen forte 400 have?The following side effects can occur when taking Dolo-Spedifen forte 400, which may require medical treatment.Please tell your doctor or your doctor immediately if you experience one or more of the following symptoms and stop taking Dolo-Spedifen forte 400:Very common side effects, which may occur in more than 1 in 10 casesStomach and intestine problems such as indigestion, diarrheaCommon side effects, which occur in more than 1 in 100 cases but less than 1 in 10 casesGastro-intestinal complaints such as nausea, feeling of fullness, heartburn, pain in the upper abdomen, anorexia, constipation, flatulence, vomiting, erosive inflammation of the gastric mucosa, blood stoolCentral nervous side effects wie Impaired reactions (especially when combined with alcohol), drowsiness, headache and dizzinessDepression, anxiety, confusionVisual disturbances (the visual disturbances are usually reversible if treatment is stopped)Ringing in the ears, hearing lossAcute skin rashOccasional side effects, occurring in more than 1 in 1,000 cases but less than 1 in 100 casesAllergic reactions, swelling of the faceAsthma, spasm of the muscles of the airways and shortness of breathStomach ulcer, gastrointestinal bleeding, tarry stools, gastritisRare side effects, occurring in more than 1 in 10,000 cases but less than 1 in 1,000 casesChanges in the blood countSymptoms of lupus erythematosus (butterfly plexus), aseptic meningitis (meningitis) in patients suffering from an autoimmune disease"Tingling" of the skinIrreversible visual disturbance or visual impairmentPatients with heart failure are at risk of acute pulmonary edema (water lung)Perforation in the stomach and intestines, vomiting blood, ulcers in the oral mucosa, worsening of colitis or Crohn's diseaseLiver failure, liver dysfunctionBlood in the urineVarious kidney diseases such as kidney toxicity, kidney dysfunction with fluid retention in the tissueVery rare side effects occurring in less than 1 in 10'00 0 casesPsychotic statesSevere allergic skin reactions with formation of blisters and/or extensive detachment of the skin, photosensitivity reactions, worsening of skin reactionsAcute kidney failureSide effects with unknown frequency:AnemiaAnaphyl acute shockHeart failureArterial thrombosis, blood pressure disordersThroat irritationHepatitis, jaundice, liver injuryGeneral swellingSevere skin reaction: Known as DRESS syndrome. Symptoms of DRESS include a rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell). Known as acute generalized pustular exanthema (AGEP); at the start of treatment there is a red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk and upper extremities. Discontinue use of Dolo-Spedifen forte 400 if you develop these symptoms and seek medical treatment immediately (see also «When should you be careful when taking Dolo-Spedifen forte 400?»).If you notice any side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What else needs to be taken into account?The medicine may only be used up to the date marked «EXP» on the container.Storage instructionsStore at room temperature (15–25 °C) and out of the reach of children.Further informationYour doctor or pharmacist can provide you with further information or druggist or your doctor, pharmacist or druggist. These people have the executiveHonest professional information. What does Dolo-Spedifen forte 400 contain? Active ingredients 1 film-coated tablet contains 400 mg ibuprofen as ibuprofen arginate. Excipients Arginine, sodium bicarbonate, crospovidone, magnesium stearate, film coating: hypromellose, sucrose, titanium dioxide (E1 71), Macrogol 4000.Authorization number56720 (Swissmedic).Where can you get Dolo-Spedifen forte 400? Which packs are available? in pharmacies and drugstores, without medical prescription. packs of 10 film -coated tablets for 400 mg. registration owner Zambon Switzerland AG 6814 Cadempino This package insert was last in August 2020 checked (Swissmedic). ..
20.29 USD
Irfen dolo forte lactab 400 mg 10 pcs
What is Irfen Dolo and when is it used? Irfen Dolo contains the active ingredient ibuprofen. This has analgesic, fever-reducing and anti-inflammatory properties.Irfen Dolo is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:pain in the area of joints and ligaments,back pain,headache,toothache,pain during the menstrual period, Pain after injuries,Fever with flu-like illnesses.When must Irfen Dolo not be used?Irfen Dolo must not be taken if you are allergic to any of the ingredients or after taking acetylsalicylic acid or other painkillers or anti-inflammatory drugs, so-called non-steroidal anti-inflammatory drugs, shortness of breath or allergy-like had skin reactions,if you are pregnant or breastfeeding (see also chapter "Can Irfen Dolo be taken during pregnancy or while breastfeeding?"),if you have active stomach and/or or duodenal ulcers or gastrointestinal bleeding,in chronic intestinal inflammation (Crohn's disease, ulcerative colitis),in severe impairment of liver or kidney function,for severe cardiac insufficiency,for the treatment of pain after coronary bypass surgery on the heart (or use of a heart-lung machine),For children under the age of 12: Irfen Dolo has not been tested for use in children under the age of 12.When is at caution when taking Irfen Dolo? During treatment with Irfen Dolo, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (stomach or intestinal perforations) may occur. 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.Older people 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.You may only take Irfen Dolo on prescription and under medical supervision in the following situations:If you are currently being treated by a doctor 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 [diabetes], high blood fat levels [smoking]; high doses of certain similarly acting painkillers called COX-2 inhibitors have been used and/or long-term treatment has been found to be an increased risk of heart attack and stroke. It is not known whether this increased risk also applies to Irfen Dolo;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; taking Irfen Dolo can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;if you with anticoagulant medicineare being treated with medication (blood thinners, anticoagulants) or suffer from a blood clotting disorder;if you suffer from asthma;if you are taking rheumatism medicines or other painkillers (e.g. acetylsalicylic acid, aspirin); if you are taking medicines to treat diabetes (other than insulin), medicines to increase urine output (diuretics), medicines to treat infections (quinolone antibiotics) or medicines containing any of the following: lithium , digoxin, methotrexate, baclofen, phenytoin, probenecid or sulfinpyrazone.Serious skin reactions with reddening and blistering (exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis/Lyell's disease) have been reported with ibuprofen therapy. Syndrome).At the first sign of skin rashes, mucosal lesions or other signs of a hypersensitivity reaction, Irfen Dolo should be discontinued and your doctor, pharmacist or druggist should be consulted immediately.< li>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 (preparations for high blood pressure and heart failure) , antibiotics, certain antifungal agents (e.g. Voriconazole or Fluconazole), immunosuppressants (preparations against transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, against AIDS, epilepsy and depression. Nonsteroidal anti-inflammatory drugs, such as ibuprofen, and the drugs listed above can interact.Side effects, particularly those affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Inform your doctor, pharmacist or druggist if yousuffer from other diseasesHave allergies ortake other medicines (including those you bought yourself!) or use them externally.Irfen Dolo can improve your ability to react, your ability to drive and your ability , use tools or machines! This applies in particular to taking it with alcohol.Can Ifen Dolo be taken while pregnant or breastfeeding?PregnancyShould you be pregnant or planning a pregnancy, you should only take Irfen Dolo after consulting your doctor. Irfen Dolo should not be taken during the last third of pregnancy.BreastfeedingIrfen Dolo should not be taken while breastfeeding unless your doctor has given you express permission to do so. How do you use Irfen Dolo?Adults and adolescents from 12 years of ageIrfen Dolo 200 mg1-2 Lactab Irfen Dolo Take 200 mg with plenty of liquid. Leave an interval of 4 to 6 hours before taking the next dose. Maximum daily dose: Do not take more than 6 Lactab Irfen Dolo 200 mg (1200 mg ibuprofen) in a 24-hour period, unless prescribed by a doctor .Irfen Dolo forte 400 mgTake 1 Lactab Irfen Dolo forte 400 mg with plenty of liquid. An interval of 4 to 6 hours should be observed before the next intake. Maximum daily dose: Do not take more than 3 Lactab Irfen Dolo forte 400 mg (1200 mg ibuprofen) within 24 hours, unless prescribed by a doctor Prescription.In the case of pain during the menstrual period, it is recommended to start treatment with 2 Lactab Irfen Dolo 200 mg or 1 Lactab Irfen Dolo forte 400 mg at the first sign of symptoms.&Do not use Irfen Dolo for more than 3 days and only to treat the symptoms listed above.If the symptoms increase despite taking Irfen Dolo or if the painful area is red or swollen is, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. Children under 12 Irfen Dolo must not be used in children under 12 years of age. The use and safety of Irfen Dolo in children under the age of 12 has not yet been tested.Elderly patientsElderly 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.Follow the dosage provided in the package leaflet or as prescribed by your doctor. If you have taken more Irfen Dolo 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. These symptoms can include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.If you forget to take a dose, take it next dose, do not take more than the usual recommended amount.If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. Pharmacist.What side effects can Irfen Dolo have?The following side effects can occur when taking Irfen Dolo. They are listed according to their frequency:Common (affects 1 to 10 users in 100)Gastro-intestinal disorders such as indigestion, diarrhoea , nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizziness.Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.< /li>Hypersensitivity reactions.Insomnia, feeling anxious.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 airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung).Fatigue.Rare (affects 1 to 10 users in 10,000)Aseptic meningitis (inflammation of the brain).Angina, hoches Fever, swelling of the lymph nodes in the neck area.Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusional states."Tingling" of the Skin, drowsiness.Irreversible visual disturbance or poor eyesight.Inflammation of the gastric mucosa, stomach and intestinal ulcers, ulcers of the oral mucosa, stomach and intestinesbreakthroughs.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 accumulation of water in the tissue up to kidney failure.General swelling.Very rare (affects less than 1 in 10,000 users)< ul class="list-bullets">Psychotic conditions.Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Liver failure.Severe allergic skin reactions with formation of blisters and/or extensive detachment of the skin.Individual casesA severe skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include a rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).Aggravated colitis or Crohn's disease.A red, scaly , widespread rash with bumps under the skin and blisters located mainly in the skin folds, trunk and upper extremities, accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop taking Irfen Dolo if you experience these symptoms and see a doctor straight away.If you get any side effects, talk to your doctor or pharmacist or your doctor or pharmacist. This also applies in particular to side effects that are not listed in this leaflet.What else needs to be taken into account?The drug may only be used up to the end of the period marked "EXP" on the package Date are used.Storage instructionsDo not store above 30°C. Keep out of the reach of children.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Irfen Dolo contain?1 Lactab Irfen Dolo 200 mg contains: 200 mg ibuprofen as an active ingredient and excipients.< p>1 Lactab Irfen Dolo forte 400 mg contains: 400 mg ibuprofen as an active ingredient and excipients.Authorization number51547 (Swissmedic).Where can you get Irfen dolo? What packs are available? In pharmacies and drugstores without a doctor's prescription. Irfen Dolo 200 mg: packs of 20 Lactabs. Irfen Dolo forte 400 mg: Packs of 10 Lactab.Authorization holderMepha Pharma AG, Basel.This package leaflet was last checked by the drug authority (Swissmedic) in December 2020 .Internal version number: 9.2..
17.95 USD
Irfen dolo l forte lactab 400 mg 10 pcs
What is Irfen Dolo L forte 400 mg and when is it used? The Lactab Irfen Dolo L forte 400 mg contains the active ingredient ibuprofen as ibuprofen lysinate. It has pain-relieving, fever-reducing and anti-inflammatory properties. Ibuprofen lysinate shows the same properties as ibuprofen, but differs in its higher water solubility.Irfen Dolo L forte 400 mg is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:Pain in the area of joints and ligaments,Back pain,Headache,Toothache,< li>Pain during menstrual bleeding,Pain after injury,Fever with flu-like illnesses.When should Irfen Dolo L forte 400 mg not be taken be used?If you are allergic to any of the ingredients or after taking acetylsalicylic acid or other pain or rheumatism medicines, so-called non-steroidal anti-inflammatory drugs, shortness of breath or had allergy-like skin reactions;if you are pregnant or breastfeeding (see also chapter "Can Irfen Dolo L forte 400 mg be taken during pregnancy or while breastfeeding?");if active gastric and/or duodenal ulcers or gastrointestinal bleeding;in chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in severe impairment of liver or kidney function;for severe heart failure;for the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine);in the case of a varicella infection (chickenpox infection);in children under the age of 12. Irfen Dolo L forte 400 mg has not been tested for use in children under the age of 12.When is caution required when taking Irfen Dolo L forte 400 mg?During treatment with Irfen Dolo L forte 400 mg, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (perforations in 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, your doctor will prescribe the smallest effective dose for the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under "Infections".Certain painkillers called COX-2 inhibitors have been shown to be associated with an increased risk of heart attack and stroke with long-term treatment. This risk can also be slightly increased with Irfen Dolo L forte 400 mg at a high dose (2400 mg/day). However, at the usual dosage (maximum 1200 mg/day), no increase in this risk was found. If you have already had a heart attack, stroke or venous thrombosis, the use of Irfen Dolo L forte 400 mg in high doses is no longer recommended. Do not exceed the recommended dose or duration of treatment and in any case tell your doctor if you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes (diabetes), high blood fat levels, smoking). Your doctor will decide whether you can still use Irfen Dolo L forte 400 mg and which dose is right for you. Taking Irfen Dolo L forte 400 mg can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor or nursedoctor if you have heart or kidney disease, if you are taking medicines to treat high blood pressure (e.g. diuretics, ACE inhibitors) or if you have increased fluid loss, e.g. through heavy sweating.This medicine can impair your ability to react, your ability to drive and ability to use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of stomach or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients and patients who suffer or have suffered from asthma, chronic inflammation of the nasal mucosa (chronic cold), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagenosis).In connection with treatment with Irfen Dolo L forte 400 mg, serious skin reactions have been reported. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of allergy, you should stop treatment with Irfen Dolo L forte 400 mg and seek medical attention immediately, as these can be the first signs of a very serious skin reaction. The risk of such reactions appears to be highest at the start of therapy, since the majority of these reactions occurred within the first month of treatment. At the first sign of skin rashes, mucosal lesions or other signs of a hypersensitivity reaction, Irfen Dolo L forte 400 mg should be discontinued and your doctor consulted immediately.Irfen Dolo L forte 400 mg should not be used if you have chickenpox.InfectionsIrfen Dolo L forte 400 mg may mask signs of infections such as fever and pain. It is therefore possible that Irfen Dolo L forte 400 mg may delay adequate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Tell your doctor if you have recently received treatment for an abortion.Maximum daily dose: do not take more than 3 Lactabs in 24 hours unless prescribed by a doctor.Do not use Irfen Dolo L forte 400 mg for longer than 3 days and only for Treatment of the symptoms listed above.If the symptoms increase despite taking Irfen Dolo L forte 400 mg or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified.Children under 12 years of age: Irfen Dolo L forte 400 mg must not be used in children under 12 years of age. The use and safety of Irfen Dolo L forte 400 mg in children under the age of 12 has not yet been tested. Stick to the dosage given in the package insert or prescribed by the doctor.< /p>If you have taken more Irfen Dolo L forte 400 mg than you should, or if children have accidentally taken the medicine, always contact a doctor for an assessment of the risk and Get advice on further treatment.Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.If you forget to take a dosenext dose, do not take more than the usual recommended amount.If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist Your doctor, pharmacist or druggist.What side effects can Irfen Dolo L forte 400 mg have?The following side effects can occur when taking Irfen Dolo L forte 400 mg.They are listed according to their frequency:Common (affects 1 to 10 users in 100)Stomach and intestine problems such as indigestion, diarrhea, nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction (especially in combination with alcohol), headache and dizziness .Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.Hypersensitivity reactions.Insomnia, feeling anxious.Visual disturbances (the visual disturbances are usually reversible when treatment is stopped). li>Ringing in the ears, hearing loss, dizziness.Asthma, spasm of the muscles of the airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung).Fatigue.Rare (affects 1 to 10 users in 10,000) Aseptic meningitis.Angina, high fever, swelling of the lymph nodes in the neck.Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusional states."Tingling" of the skin, drowsiness.Irreversible visual disturbance or poor eyesight.< li>Inflammation of the gastric mucosa, stomach and intestinal ulcers, mouth ulcers, gastric and intestinal perforations.Hepatitis, jaundice, liver dysfunction.Hives, itching, bleeding in the skin, swelling of the skin and mucous membranes, sensitivity to light.Various diseases of the kidneys such as kidney dysfunction with accumulation of water in the tissue and even kidney failure.General swelling. Very rare (affects less than 1 in 10,000 users)Psychotic states.Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Liver failure.Severe allergic reactions of the skin with formation of blisters and/or extensive detachment of the skin.< /ul>Frequency not known (cannot be estimated from the available data)A serious skin reaction known as DRESS syndrome can occur . Symptoms of DRESS include rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).Worsening of colitis or Crohn's diseaseAt the start of treatment, a red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk, and upper extremities (acute generalized pustular ex anthem). Discontinue use of Irfen Dolo L forte 400 mg if you develop these symptoms and seek medical attention immediately.If you notice any side effectsn, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What else should be observed?The medicinal product may only be used up to the end of the period marked "EXP" on the container Date are used.Storage instructionsStore in the original packaging and at room temperature (15-25°C).Keep out of the reach of children.Further information Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for professionals.What does Irfen Dolo L forte 400 mg contain?Active substances1 Lactab Irfen Dolo L forte 400 mg ( divisible) contains 400 mg ibuprofen as ibuprofen lysinate.ExcipientsMicrocrystalline cellulose, croscarmellose sodium, talc, colloidal silica, magnesium stearate, hypromellose, macrogol 6000, glycerol 85% (E422). Authorization number61210 (Swissmedic).Where can you get Irfen Dolo L forte 400 mg? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Irfen Dolo L forte 400 mg (divisible): pack of 10 Lactab. Authorization holderMepha Pharma AG, Basel.This package leaflet was last checked by the drug authority (Swissmedic) in December 2020. Internal version number: 7.2..
18.30 USD
Saridon neo filmtablet 400 mg 10 pcs
What is Saridon neo 400 and when is it used? Saridon neo 400 contains the active ingredient ibuprofen. This has pain-relieving, fever-reducing and anti-inflammatory properties.Saridon neo 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of: Pain in the joints and ligaments;Back pain;Headache;Toothache;Pain during the menstrual period;Pain after injury;Fever with a flu.When should Saridon neo 400 not be used?Saridon neo 400 must not be takenif you are allergic to any of the ingredients or have shortness of breath after taking acetylsalicylic acid or other painkillers or anti-inflammatory drugs, so-called non-steroidal anti-inflammatory drugs , or had allergic-like skin reactions,If you are pregnant or breastfeeding (see also the chapter "Can Saridon neo 400 be taken during pregnancy or while breastfeeding?").If you a stomach and/or duodenal ulcer or gastrointestinal bleeding,in chronic intestinal inflammation (Crohn's disease, ulcerative colitis),in severe impairment of liver or kidney function,< /li>for 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. Saridon neo 400 has not been tested for use in children under the age of 12.When is caution required when taking Saridon neo 400?During treatment with Saridon neo 400, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (perforation in 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 over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under "Infection".Certain painkillers called COX-2 inhibitors have been shown to be associated with an increased risk of heart attack and stroke at high doses and/or long-term treatment. This risk can also be slightly increased with Saridon neo 400 at a high dose (2400 mg/day). However, at the usual dosage (maximum 1200 mg/day), no increase in this risk was found. If you have already had a heart attack, stroke or venous thrombosis, the use of Saridon neo 400 in high doses is no longer recommended. Do not exceed the recommended dose or duration of treatment and in any case tell your doctor if you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes (diabetes), high blood fat levels, smoking). Your doctor will decide whether you can still use Saridon neo 400 and which dose is right for you.Taking Saridon neo 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid accumulation (oedema). Tell your doctor if you have heart or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or if you lose more fluids, e.g. through heavy sweating.This medicine can the reactionimpair your ability to drive and use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of stomach or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients and patients who suffer or have suffered from asthma, chronic inflammation of the nasal mucosa (chronic cold), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases).In connection with the ibuprofen-containing medicines serious skin reactions reported. You should stop taking Saridon neo 400 and see a doctor straight away if you develop a skin rash, mucosal lesions, blisters or other signs of allergy, as these can be the first signs of a very serious skin reaction.The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of an allergy, you should stop taking Saridon neo 400 and seek medical treatment immediately, as these can be the first signs of a very serious skin reaction (see the section «What side effects can Saridon neo 400 have?»).Saridon neo 400 should not be used if you have chickenpox.InfectionsSaridon neo 400 can cause signs of infections such as cover up fever and pain. It is therefore possible that Saridon neo 400 may delay appropriate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Tell your doctor, pharmacist or druggist if you have recently been treated for an abortion.Tell your doctor, pharmacist or druggist if you are being treated with medicines such as blood thinners (e.g. low dose acetylsalicylic acid), diuretics (water tablets), ACE inhibitors or β-blockers (medicines for high blood pressure and heart failure), antibiotics, certain medicines for fungal infections (e.g. voriconazole or fluconazole), immunosuppressants (medicines for transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, anti-AIDS, epilepsy and depression. Non-steroidal anti-inflammatory drugs such as ibuprofen and the drugs listed above can interact. In particular, long-term treatment with Saridon neo 400 may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other painkillers should not be taken at the same time as ibuprofen, as the risk of side effects can increase. Concomitant consumption of alcohol can cause side effects, particularly those affecting the gastrointestinal tract or the central nervous system , be intensified.Long-term use of painkillers can cause headaches. Do not treat them with an increased dose of the drug, but inform your doctor.Elderly patientsElderly patients are more likely to experience side effects after using non-steroidal anti-inflammatory drugs, in particular bleeding and perforation in the stomach and intestines. Therefore, particularly careful medical supervision is required in elderly patients.Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!) or using them externally!Can Saridon neo 400 be taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take Saridon neo 400 after consulting your doctor or your doctor. Saridon neo 400 must not be taken during the last third of pregnancy.BreastfeedingSaridon neo 400 should not be taken while breastfeeding unless your doctor has expressly instructed you to do so permitted. How do you use Saridon neo 400? Adults and adolescents over the age of 12 Take 1 film-coated tablet of Saridon neo 400 with plenty of liquid. A gap of 6 hours must be observed before the next dose.Maximum daily dose: Do not take more than 3 film-coated tablets of Saridon neo 400 within 24 hours, unless prescribed by a doctor. In the case of pain during the menstrual period, it is recommended to start treatment at the first sign of the symptoms. Do not use Saridon neo 400 for longer than 3 days and only to treat the symptoms listed above.If the symptoms increase despite taking Saridon neo 400 or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. Children under the age of 12 Saridon neo 400 must not be used in children under the age of 12. The use and safety of Saridon neo 400 in children under the age of 12 have not yet been systematically tested.Elderly patientsElderly patients can react more sensitively to the drug than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.If you have taken more Saridon neo 400 than you should, always consult 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 eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported. If you forget to take a dose, do not take more than the usual recommended amount for the next dose. Follow 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 Saridon neo 400 have?The following side effects can occur when taking Saridon neo 400. They are listed according to their frequency:Common (affects 1 to 10 users in 100)Gastro-intestinal disorders such as indigestion, diarrhoea , nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizziness.Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.Hypersensitivity reactions.Insomnia, feeling anxious.Visual disturbances (the visual disturbances are usually reversible if treatment is stopped), ringing in the ears, hearing loss, dizziness.< li>Asthma, spasm of the muscles of the airways and shortness of breath, There is a risk of acute pulmonary edema (water lung) in patients with heart failure.Fatigue.Rare (affects 1 up to 10 out of 10,000 users)Aseptic meningitis (inflammation of the meninges).Angina, high fever, swelling of the lymph nodes in the neck area.< /li>Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusion."Tingling" of the skin, drowsiness.< li>Irreversible visual impairment or poor eyesight.Inflammation of the gastric mucosa, gastric and intestinal ulcers, ulcers of the oral mucosa, gastric and intestinal perforations.Hepatitis, jaundice, liver dysfunction.< li>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 accumulation in the tissue and even kidney failure.General swelling .Very rare (affects less than 1 in 10,000 users)Psychotic states.< li>Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Aggravation of colitis or Crohn's disease.Liver failure.Severe allergic skin reactions with formation of blisters and/or extensive detachment of the skin.Individual cases A severe skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).worsening of colitis or Crohn's disease.A red, scaly, widespread rash with bumps under the skin and blisters, mostly located in the skin folds on the trunk and upper extremities (acute generalized exanthematous pustulosis). Stop taking Saridon neo 400 if you experience these symptoms and see a doctor straight away.Frequency unknown..
21.56 USD
Tonopan forte drag 25 mg 10 pcs
What is Tonopan forte 25 mg coated tablets and when is it used? Tonopan forte 25 mg coated tablets 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. Tonopan forte 25 mg coated tablets are suitable for short-term treatment, i.e. for a maximum of 3 days of treatment of: headache, toothache, menstrual pain , pain in the area of joints and ligaments, back pain, pain from injuries and to reduce fever with flu-like illnesses.When should Tonopan forte 25 mg dragées not be taken?If you are allergic to diclofenac or any of the excipients, or have had shortness of breath or allergy-like skin reactions, e.g. swelling of the face, lips, tongue, throat and /or on the extremities (signs of angioedema),if you are pregnant or breastfeeding (see also the chapter "Can Tonopan forte 25 mg coated tablets be taken during pregnancy or while breastfeeding?"),if you have an active stomach and/or duodenal ulcer or gastrointestinal bleeding or perforation (this may manifest itself as blackening of the stool, blood in the stool or vomiting of coffee grounds-like material),for chronic intestinal inflammation (Crohn's disease or ulcerative colitis),for severe impairment of liver or kidney function,for severe heart failure,for the treatment of pain after a coronary bypass operation on the heart (or Use of a heart-lung machine),in children and adolescents under the age of 14. Tonopan forte 25 mg coated tablets have not been tested for use in children and adolescents under 14 years of age. For this reason, Tonopan forte 25 mg dragees must not be used in children and adolescents under the age of 14.When is caution required when taking Tonopan forte 25 mg dragees?< p>During treatment with Tonopan forte 25 mg coated tablets, ulcers in the mucous membranes of the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. 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.Older people may be more sensitive to the medicine than younger adults. It is particularly important that older patients report any side effects to their doctor immediately.In the following situations, you may only take Tonopan forte 25 mg coated tablets if prescribed by a doctor and under medical supervision: if you are currently being treated by a doctor for a serious illness;if you have previously suffered from a stomach or duodenal ulcer;if you have a heart or blood vessel disease (known as cardiovascular disease, including uncontrolled high blood pressure, heart failure, existing ischemic heart disease or peripheral arterial disease), have ever 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 in the blood [cholesterol, triglycerides], smoking). tonopan forte 25 mg dragées 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 Tonopan forte 25 mg coated tablets. It is important that you use the lowest effective dose to relieve your pain and that you take Tonopan forte 25 mg coated tablets for the shortest time necessary to reduce the risks to keep cardiovascular side effects as low as possible.if you have kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating or during Diarrhea; taking Tonopan forte 25 mg coated tablets can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;< li>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 have asthma;if you are taking anti-rheumatic drugs 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 to treat depression), digoxin (medicine for heart problems), diuretics (medicines to increase urine output), medicines (e.g. metformin) to treat 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 (to treat infections), voriconazole (to treat fungal infections), phenytoin (to treat epileptic seizures), or sulfinpyrazone (gout medicine).If you notice signs or symptoms while taking Tonopan forte 25 mg coated tablets that indicate problems with the heart or blood vessels, such as chest pain, shortness of breath, weakness or slurred speech, contact your doctor immediately.In very rare cases, anti-inflammatory drugs (including Tonopan forte 25 mg coated tablets) can cause serious skin reactions (e.g. skin rash). At the first sign of a skin reaction, treatment with Tonopan forte 25 mg coated tablets should be discontinued and medical attention sought immediately. Tonopan forte 25 mg coated tablets can reduce the symptoms of an infection (e.g. high fever) and thus the diagnosis of the Complicate infection.Information on the excipientsSucrose:Tonopan forte 25 mg coated tablets contain sucrose (45,416 mg per coated tablet). Please only take Tonopan forte 25 mg dragées after consulting your doctor if you know that you suffer from sugar intolerance. This medicine contains less than 1 mmol sodium (23 mg ) per dragee, i.e. it is almost "sodium-free".This medicine may impair your ability to react, the ability to drive and the ability to use tools or machines. In particular, if you experience dizziness or visual disturbances, you should refrain from driving or using machines.Inform your doctor, pharmacist or druggist if yousuffer from other diseases,Have allergies oruse other medicines (including those you bought yourself!)!Can Tonopan forte 25 mg coated tablets be taken during pregnancy or while breastfeeding?< /h3>PregnancyIf you are pregnant or planning a pregnancy, you should only take Tonopan forte 25 mg coated tablets after consulting your doctor. Tonopan forte 25 mg dragees should not be taken during the last third of pregnancy.BreastfeedingTonopan forte 25 mg dragees should not be taken while breastfeeding, unless your doctor has told you expressly allowed you to do so.Like other anti-inflammatory drugs, Tonopan forte 25 mg coated tablets can make it more difficult to become pregnant. After stopping the drug, this effect ends. If you are planning to become pregnant or are having difficulties conceiving, talk to your doctor.How do you use Tonopan forte 25 mg coated tablets?How many Tonopan forte 25 mg dragées should be taken?The recommended dosage must not be exceeded.The lowest effective dose should always be taken for the shortest possible time. Adults and adolescents from the age of 14: Swallow 1 dragée Tonopan forte 25 mg up to 3 times a day with plenty of water, preferably with or after eating. Before the next dose an interval of at least 4 to 6 hours must be observed. Maximum daily dose: Do not take more than 3 tablets Tonopan forte 25 mg within 24 hours, unless prescribed by a doctor. How long should Tonopan forte 25 mg dragees be taken?Do not take Tonopan forte 25 mg dragees for longer than 3 days and only to treat the symptoms 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 Tonopan forte 25 mg coated tablets than you should?If you have accidentally taken more coated tablets, contact your doctor immediately Doctor, to your doctor. Children and adolescents under the age of 14: Tonopan forte 25 mg coated tablets should not be used in children and adolescents under the age of 14. The use and safety of Tonopan forte 25 mg dragées in children and adolescents under the age of 14 has not yet been tested.Elderly patients:Elderly patients can react more sensitively to the drug than younger ones Adult. It is particularly important that elderly patients report any side effects to their doctor immediately.Follow the dosage provided 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 Tonopan forte 25 mg coated tablets have? The following side effects may occur after taking Tonopan forte 25 mg coated tablets: Common side effects (in 1 to 10 out of 100 patients): Abdominal pain, stomach pain, diarrhea, nausea, vomiting, gas, indigestion, decreased appetite;Headache, lightheadedness;Rash;Dizziness;Increased liver enzyme levels.Uncommon side effects (affects 1 to 10 patients in 1000):palpitations, 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 (affects 1 to 10 patients in 10,000):Unusual tiredness; Itchy rash;Upper gastrointestinal tract, blood in stools or blackening of stools, vomiting blood, bloody diarrhea;Allergic reaction including Difficulty breathing or swallowing, swelling of the face, mouth, tongue or throat often with a rash, collapse;Wheezing or shortness of breath, feeling choked (signs of asthma);Swelling of the arms, legs and feet (oedema);Yellow skin or eyes (signs of liver inflammation or liver failure).Very rare side effects (less than 1 in 10,000 patients):Bleeding or unusual bruising;Low white blood cells (causing a high fever or persistent sore throat, frequent infections), low red blood cells;Constipation, sore mouth, sore and red tongue, taste disturbance, upper abdominal cramps;Itching and reddening of the skin, hair loss;Tingling or rigidity of the hands or feet, tremors;blurred vision, ringing in the ears, hearing problems;Mood swings, trouble sleeping, confusion;If you notice any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.* This frequency can occur when taking a high daily dose (150 mg) over a longer period of time.What is other things to note?Shelf lifeThe medicinal product may only be used up to the date marked «EXP» on the container.Storage instructions Store at 15-30°C. Keep out of the reach of children. Further information Your doctor, pharmacist or druggist can provide you with further information Your doctor, pharmacist or druggist. These people have the detailed technical information.What does Tonopan forte 25 mg dragee contain?Active substance1 Tonopan forte 25 mg dragee contains 25 mg diclofenac Potassium.ExcipientsSucrose, tricalcium phosphate, corn starch, sodium starch glycolate (type A), colloidal anhydrous silicon dioxide, povidone, magnesium stearate, talc, macrogol 8000, microcrystalline cellulose, iron oxide (E 172 ), titanium dioxide (E 171).Approval number66826 (Swissmedic).Where can you get Tonopan forte 25 mg coated tablets? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Packs of 10 dragées Tonopan forte 25 mg. Approval inhaberinGSK Consumer Healthcare Schweiz AG, Risch.This leaflet was last checked by the drug authority (Swissmedic) in June 2020...
28.51 USD
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