ibuprofen
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Algifor dolo forte susp 400 mg/10ml 10 bags 10 ml
Algifor Dolo forte Susp 400 mg / 10 ml 10 ml 10 Btl Algifor Dolo forte Susp 400 mg / 10 ml 10 ml 10 Btl is a suspension used for the relief of pain and fever. It contains the active ingredient ibuprofen, which is a non-steroidal anti-inflammatory drug (NSAID) that works by blocking the production of certain substances in the body that cause pain and inflammation. Key Features: Contains 400 mg of ibuprofen per 10 ml of suspension Comes in a pack of 10 bottles, each containing 10 ml of suspension Suspension form allows for easy administration, even for children Can be used for the relief of various types of pain, such as headache, menstrual cramps, dental pain, and musculoskeletal pain Also indicated for the treatment of fever Directions for Use: Shake the bottle well before use. Use the measuring cup provided to measure the correct dose of suspension. The dose will depend on the age and weight of the patient, and should be taken with food or milk to minimize the risk of stomach irritation. Do not exceed the recommended dose or use for more than 3 days for fever or 5 days for pain, unless otherwise directed by a healthcare professional. Warning and Precautions: Do not take with other NSAID-containing products or if you are allergic to ibuprofen Consult a healthcare professional before using if you have a history of stomach ulcers or bleeding disorders Avoid use in late pregnancy as it may affect the baby's circulation Do not give to children under 6 months of age without medical advice Algifor Dolo forte Susp 400 mg / 10 ml 10 ml 10 Btl provides effective relief from pain and fever in a convenient suspension form that is easy to administer. However, it is important to follow the directions for use and precautions to ensure maximum safety and efficacy. If symptoms persist or worsen, seek advice from a healthcare professional...
42.30 USD
Algifor dolo junior susp 100mg/5ml bottle 200ml
Algifor Dolo Junior Susp 100 mg / 5ml Fl 200 ml Algifor Dolo Junior Suspension is a medicine specially designed to relieve pain and reduce fever in children aged 2 to 12 years old. This medicine comes in a 200 ml bottle and contains 100 mg of ibuprofen per 5 ml of liquid suspension. The active ingredient in Algifor Dolo Junior Suspension is ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). Ibuprofen works by reducing the activity of certain chemicals in the body that cause pain and inflammation, making it an effective pain reliever and fever reducer for children. This suspension is easy to administer, as it can be taken by mouth without the need for swallowing tablets or capsules. The liquid suspension is also available in a pleasant strawberry flavor, making it more appealing to children. Dosage instructions should be carefully followed, as dosages vary according to the age and weight of the child. The suspension should be used only under the supervision of a healthcare professional or a parent or guardian. It is important to note that this medicine should not be used for more than 3 days in a row without consulting a healthcare professional. It is also recommended to monitor the child's temperature, as prolonged high fever may indicate a more serious underlying condition requiring medical attention. In summary, Algifor Dolo Junior Suspension is a reliable and safe medicine for children with mild to moderate pain and fever. It provides fast and effective relief, is easy to administer, and is available in a pleasant flavor. Always consult a healthcare professional before using any medicine on children. ..
28.17 USD
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...
32.19 USD
Algifor-l filmtablet 200 mg 20 pcs
The Algifor-L 200 film-coated tablet contains the active ingredient ibuprofen in the form of 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. Algifor-L 200 is suitable for short-term treatment, i. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments, Back pain, Headache, Toothache, Pain during of menstrual bleeding, Pain after injury, Fever with flu-like illnesses. Swissmedic-approved patient information Algifor-L® 200 film-coated tabletsVERFORA SAWhat is Algifor-L 200 and when is it used?..
27.93 USD
Algifor-l forte filmtabl 400 mg 10 pcs
The Algifor-L forte 400 film-coated tablet contains the active ingredient ibuprofen in the form of 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. Algifor-L forte 400 is suitable for short-term treatment, i. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments, Back pain, Headache, Toothache, Pain during of menstrual bleeding, Pain after injury, Fever with flu-like illnesses. Swissmedic-approved patient information Algifor-L® forte 400 film-coated tabletsVERFORA SAWhat is Algifor-L forte 400 and when is it used?The Algifor-L forte 400 film-coated tablet 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. Algifor-L forte 400 is suitable for short-term treatment, i. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments,Back pain,Headache,Toothache,Pain during of the menstrual period,Pain after injury,Fever with flu-like illnesses.When may Algifor-L forte 400 not be used?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 medicines, so-called non-steroidal anti-inflammatory drugs;if you are pregnant or breastfeeding (see also chapter "Can Algifor-L forte 400 be taken during pregnancy or while breastfeeding?");if you have an active stomach and/or duodenal ulcers or gastrointestinal bleeding;in chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in severe impairment of liver or kidney function;in severe cardiac insufficiency;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. Algifor-L forte 400 has not been tested for use in children under the age of 12.When should caution be taken when taking Algifor-L forte 400?During treatment with Algifor-L forte 400, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (stomach or intestinal perforations) may 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». For certain painkillers, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found with long-term treatment. This risk can also be slightly increased with Algifor-L forte 400 at a high dose (2400 mg/day). However, no increase in this risk was found at the usual dosage (maximum 1200 mg/day). If you have already had a heart attack, stroke or venous thrombosis, the use of Algifor-L forte 400 in high doses is no longer recommended. Do not exceed the recommended dose or duration of treatment and always tell your doctor if you have had a heart attack, stroke or thrombosis in a vein, or if you have risk factors (such as high blood pressure, diabetes (sugar diabetes), high blood fat levels, Smoking). Your doctor will decide whether you can still use Algifor-L forte 400 and which dose is suitable for you. Taking Algifor-L forte 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor 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 lose more fluids, e.g. through heavy sweating. This medicine can affect your ability to react, drive and use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of gastric or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients suffering from asthma, chronic inflammation of the nasal mucosa (chronic runny nose), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases). 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 you develop a skin rash, including fever, mucous membrane lesions, blisters or any other sign of allergy, you should stop using Algifor-L forte 400 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 Algifor-L forte 400 have?»). Algifor-L forte 400 should not be used if you have chickenpox. InfectionsAlgifor-L forte 400 can mask signs of infections such as fever and pain. It is therefore possible that Algifor-L forte 400 delays adequate treatment of the infection, which can 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. Tell your doctor 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 against fungal infections (e.g. voriconazole or fluconazole), immunosuppressants (preparations against transplant rejection), herbal extract from Ginkgo biloba, medicines for high blood sugar, against AIDS, epilepsy and depression. Nonsteroidal anti-inflammatory drugs such as ibuprofen and the medicines listed above can interact. In particular, long-term treatment with Algifor-L forte 400 may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other pain relievers should not be taken at the same time as ibuprofen as the risk of side effects may be increased. Side effects, particularly affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Prolonged use of painkillers can cause headaches. Do not treat them with an increased dose of the drug, but inform your doctor, pharmacist or your doctor, pharmacist. Elderly patientsElderly patients are more likely to experience side effects after using non-steroidal anti-inflammatory drugs, especially 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 Algifor-L forte 400 be used during pregnancy or breastfeeding?PregnancyYou should If you are pregnant or planning a pregnancy, you should only take Algifor-L forte 400 after consulting your doctor. You should not take Algifor-L forte 400 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. Algifor-L forte 400 must not be taken in the last third of pregnancy. BreastfeedingAlgifor-L forte 400 should not be taken while breastfeeding unless your doctor has given you express permission to do so. How do you use Algifor-L forte 400?Algifor-L forte 400 film-coated tablets should be taken with or after meals. The film-coated tablets should be swallowed with a glass of water or other liquid. The film-coated tablets are to be swallowed whole and should not be chewed, broken, crushed or sucked to prevent mouth discomfort and throat irritation. The lowest effective dose should be used for the shortest time necessary to relieve symptoms. If you have an infection, consult a doctor immediately if symptoms (e.g. fever and pain) persist or worsen (see «When should you take Algifor-L forte 400 with caution?»). Adults and adolescents from 12 years of age: take 1 film-coated tablet with plenty of liquid. A gap of 4 to 6 hours should be observed before the next dose. In the case of pain during the menstrual period, it is recommended to start treatment with 1 Algifor-L forte 400 tablet at the first sign of the symptoms. Maximum daily dose: Do not take more than 3 film-coated tablets in a 24-hour period, unless prescribed by a doctor. Do not use Algifor-L forte 400 for more than 3 days and only to treat the symptoms listed above. If the symptoms increase despite taking Algifor-L forte 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. The tablets are not suitable for half-dose dosing by splitting. Children under the age of 12: Algifor-L forte 400 must not be used in children under the age of 12. The use and safety of Algifor-L forte 400 in children under the age of 12 has not yet been tested. Follow the dosage given in the package leaflet or as prescribed by your doctor. If you have taken more Algifor-L forte 400 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 to get. 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, do not take more than the usual recommended amount next time. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Algifor-L forte 400 have?The following side effects can occur when taking Algifor-L forte 400. They are listed by frequency: Common (affects 1 to 10 users in 100)gastrointestinal disorders such as indigestion, diarrhea, nausea, vomiting, constipation, upper abdominal pain, Flatulence, tarry stool, vomiting blood, gastrointestinal bleedingCentral nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizzinessAcute skin rashUncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosaHypersensitivity reactionsInsomnia , feeling anxiousVisual disturbances (the visual disturbances are usually reversible if treatment is stopped)Ringing in the ears, hearing loss, dizzinessAsthma, spasms of the muscles of the airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung)FatigueRare (affects 1 to 10 users in 10,000)Aseptic meningitis (meningitis)Angina, high fever, swelling of the lymph nodes in the neck areaAllergic reactions, symptoms of lupus erythematosus (butterfly plexus) , anemiaDepression, confusional states"Tingling" of the skin, drowsinessIrreversible visual disturbance or poor eyesightInflammation of the stomach lining, stomach and intestinal ulcers, ulcers of the oral mucosa, gastric and intestinal perforationsHepatitis, jaundice, liver dysfunctionHives, itching, bleeding in the skin, swelling of the skin and mucous membranes, sensitivity to light Various kidney disorders such as kidney dysfunction with fluid retention in the tissues and kidney failureGeneral swellingVery rare (affects less than 1 in 10' 000 users)Psychotic statesHeart failure, heart attackHigh blood pressureInflammation of the pancreasLiver failureSevere allergic skin reactions with blistering and/or widespread detachment of the skin.Frequency not known (can be estimated from the available data cannot be estimated)A serious 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).worsening of colitis or Crohn's diseasea 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 rash). Stop using Algifor-L forte 400 if you develop these symptoms and seek medical attention immediately.If you get any side effects, talk to your doctor or pharmacist or druggists or 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 considered?The medicinal product may only be used up to the date marked «EXP» on the container. Storage instructionsStore the medicine at room temperature (15-25 °C) and out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Algifor-L forte 400 contain?1 film-coated tablet Algifor-L forte 400 contains: Active ingredients400 mg ibuprofen as ibuprofen lysinate ExcipientsMicrocrystalline cellulose, crospovidone, magnesium stearate, polyvinyl alcohol, titanium dioxide, talc, macrogol 3350, soy lecithin Approval number55766 (Swissmedic). Where can you get Algifor-L forte 400? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Algifor-L forte 400: pack of 10 film-coated tablets. Authorization holderVERFORA SA, 1752 Villars-sur-Glâne. This leaflet was last checked by the Medicines Agency (Swissmedic) in November 2022. ..
27.93 USD
Dismenol formel l filmtabl 200 mg 20 pcs
Inhaltsverzeichnis Was ist Dismenol Formel L und wann wird es angewendet? Wann darf Dismenol Formel L nicht angewendet werden? Wann ist bei der Einnahme von Dismenol Formel L Vorsicht geboten? Darf Dismenol Formel L während einer Schwangerschaft oder in der Stillzeit eingenommen werden? Wie verwenden Sie Dismenol Formel L? Welche Nebenwirkungen kann Dismenol Formel L haben? Was ist ferner zu beachten? Was ist in Dismenol Formel L enthalten? Zulassungsnummer Wo erhalten Sie Dismenol Formel L? Welche Packungen sind erhältlich? Zulassungsinhaberin COMPENDIUM Swissmedic-genehmigte Patienteninformation Dismenol® Formel L Merz Pharma (Schweiz) AG AMZV Was ist Dismenol Formel L und wann wird es angewendet? Dismenol Formel L enthält den Wirkstoff Ibuprofen als Ibuprofenlysinat. Dieser hat schmerzlindernde, fiebersenkende und entzündungshemmende Eigenschaften. Ibuprofenlysinat zeigt die gleichen Eigenschaften wie Ibuprofen, unterscheidet sich aber durch seine höhere Wasserlöslichkeit.Dismenol Formel L eignet sich zur Kurzzeitbehandlung, d.h. zur maximal 3 Tage dauernden Behandlung von:Schmerzen im Bereich von Gelenken und Bändern;Rückenschmerzen;Kopfschmerzen;Zahnschmerzen;Schmerzen während der Monatsblutung;Schmerzen nach Verletzungen;Fieber bei grippalen Erkrankungen. Wann darf Dismenol Formel L nicht angewendet werden? Wenn Sie auf einen der Inhaltsstoffe allergisch reagieren oder nach der Einnahme von Acetylsalicylsäure oder anderen Schmerz- oder Rheumamitteln, sogenannten nicht-steroidalen entzündungshemmenden Arzneimittel, Atemnot oder allergieähnliche Hautreaktionen hatten.Wenn Sie schwanger sind oder stillen (siehe auch Kapitel «Darf Dismenol Formel L während einer Schwangerschaft oder in der Stillzeit eingenommen werden?»).Bei aktiven Magen- und/oder Zwölffingerdarmgeschwüren oder Magen-Darm-Blutungen.Bei chronischen Darmentzündungen (Morbus Crohn, Colitis ulcerosa).Bei schwerer Einschränkung der Leber- oder Nierenfunktion.Bei schwerer Herzleistungsschwäche.Zur Behandlung von Schmerzen nach einer koronaren Bypassoperation am Herzen (resp. Einsatz einer Herz-Lungen-Maschine).Bei einer Varizelleninfektion (Windpockeninfektion).Bei Kindern unter 12 Jahren. Dismenol Formel L wurde für die Anwendung bei Kindern unter 12 Jahren nicht geprüft. Wann ist bei der Einnahme von Dismenol Formel L Vorsicht geboten? Während der Behandlung mit Dismenol Formel L können im oberen Magen-Darm-Trakt Schleimhautgeschwüre, selten Blutungen oder in Einzelfällen Perforationen (Magen-, Darmdurchbrüche) auftreten. Diese Komplikationen können während der Behandlung jederzeit auch ohne Warnsymptome auftreten. Um dieses Risiko zu verringern, verschreibt Ihr Arzt oder Ihre Ärztin Ihnen die kleinste wirksame Dosis während der kürzest möglichen Therapiedauer. Wenden Sie sich an Ihren Arzt oder Ihre Ärztin, wenn Sie Magenschmerzen haben und einen Zusammenhang mit der Einnahme des Arzneimittels vermuten.Für gewisse Schmerzmittel, die sogenannten COX-2-Hemmer, wurde unter hohen Dosierungen und/oder Langzeitbehandlung ein erhöhtes Risiko für Herzinfarkt und Schlaganfall festgestellt. Auch bei Dismenol Formel L kann bei einer hohen Dosis (2400 mg/Tag) dieses Risiko geringfügig erhöht sein. Bei üblicher Dosierung (maximal 1200 mg/Tag) wurde jedoch keine Erhöhung dieses Risikos festgestellt. Falls Sie bereits einen Herzinfarkt, Schlaganfall oder eine Venenthrombose hatten, wird die Anwendung von Dismenol Formel L in hohen Dosen nicht mehr empfohlen. Überschreiten Sie nicht die empfohlene Dosis oder Behandlungsdauer und informieren Sie in jedem Fall Ihren Arzt oder Ihre Ärztin, falls Sie bereits einen Herzinfarkt, Schlaganfall oder eine Venenthrombose hatten, oder falls Sie Risikofaktoren haben (wie hoher Blutdruck, Diabetes (Zuckerkrankheit), hohe Blutfettwerte, Rauchen). Ihr Arzt oder Ihre Ärztin wird entscheiden, ob Sie Dismenol Formel L trotzdem anwenden können und welche Dosis für Sie geeignet ist.Die Einnahme von Dismenol Formel L kann die Funktion Ihrer Nieren beeinträchtigen, was zu einer Erhöhung des Blutdrucks und/oder zu Flüssigkeitsansammlungen (Ödemen) führen kann. Informieren Sie Ihren Arzt oder Ihre Ärztin, wenn Sie herzkrank oder nierenkrank sind, falls Sie Arzneimittel gegen Bluthochdruck (z.B. harntreibende Mittel, ACE-Hemmer) einnehmen oder bei einem erhöhten Flüssigkeitsverlust, z.B. durch starkes Schwitzen.Dieses Arzneimittel kann die Reaktionsfähigkeit, die Fahrtüchtigkeit und Fähigkeit Werkzeuge oder Maschinen zu bedienen, beeinträchtigen! Das gilt besonders für die Einnahme zusammen mit Alkohol.Vorsicht ist angezeigt bei Patientinnen und Patienten mit einer Vorgeschichte an Magen- oder Zwölffingerdarmgeschwür, bei eingeschränkter Leber-, Nieren- oder Herzfunktion, bei Störungen der Blutgerinnung sowie bei Patientinnen und Patienten, die an Asthma, einer chronischen Entzündung der Nasenschleimhaut (chronischer Schnupfen), allergischen Erkrankungen oder an bestimmten rheumatischen Erkrankungen (Lupus erythematodes oder Kollagenosen) leiden oder litten.Unter Schmerzmittel-Therapie wurde sehr selten über schwerwiegende Hautreaktionen mit Rötung und Blasenbildung berichtet (exfoliative Dermatitis, Stevens-Johnson-Syndrom und toxische epidermale Nekrolyse/Lyell-Syndrom). Das höchste Risiko für derartige Reaktionen scheint zu Beginn der Therapie zu bestehen, da diese Reaktionen in der Mehrzahl der Fälle im ersten Behandlungsmonat auftraten. Beim ersten Zeichen von Hautausschlägen, Schleimhautläsionen oder sonstigen Anzeichen einer Überempfindlichkeitsreaktion sollte Dismenol Formel Labgesetzt und umgehend der Arzt oder die Ärztin konsultiert werden.Dismenol Formel L sollte nicht angewendet werden, wenn Sie an Windpocken erkrankt sind.Informieren Sie Ihren Arzt oder Ihre Ärztin, falls Sie vor kurzem wegen einem Schwangerschaftsabbruch behandelt wurden.Informieren Sie Ihren Arzt oder Ihre Ärztin, falls Sie mit Arzneimitteln behandelt werden, wie Blutverdünnungsmitteln (z.B. niedrig dosierte Acetylsalicylsäure), Diuretika (harntreibende Mittel), ACE-Hemmern oder β-Blockern (Präparate gegen hohen Blutdruck und Herzinsuffizienz), Antibiotika, bestimmte Mittel gegen Pilzinfektionen (z.B. Voriconazol oder Fluconazol), Immunsuppressiva (Präparate gegen Transplantatabstossungen), pflanzlicher Ginkgo biloba Extrakt, Arzneimittel gegen erhöhten Blutzucker, gegen Aids, Epilepsie und Depressionen. Nichtsteroidale Antirheumatika, wie Ibuprofen, und die oben aufgeführten Arzneimittel können sich gegenseitig beeinflussen. Insbesondere kann es sein, dass die herzschützende Wirkung von niedrig dosierter Acetylsalicylsäure bei einer Langzeitbehandlung mit Dismenol Formel L reduziert wird.Acetylsalicylsäure oder andere Schmerzmittel sollten nicht gleichzeitig mit Ibuprofen eingenommen werden, da das Risiko von Nebenwirkungen erhöht werden kann.Bei gleichzeitigem Alkoholkonsum können Nebenwirkungen, insbesondere die den Magen-Darm-Trakt oder das zentrale Nervensystem betreffen, verstärkt werden.Bei längerer Verwendung von Schmerzmitteln können Kopfschmerzen auftreten. Behandeln Sie diese nicht mit einer erhöhten Dosis des Arzneimittels sondern informieren Sie Ihren Arzt oder Ihre Ärztin.Ältere PatientenBei älteren Patienten treten häufiger Nebenwirkungen nach Anwendung von nicht-steroidalen Entzündungshemmern auf, insbesondere Blutungen und Durchbrüche im Magen- und Darmbereich. Daher ist bei älteren Patienten eine besonders sorgfältige ärztliche Überwachung erforderlich.Informieren Sie Ihren Arzt oder Apotheker oder Drogisten bzw. Ihre Ärztin oder Apothekerin, oder Drogistin wenn Sie an anderen Krankheiten leiden, Allergien haben oder andere Arzneimittel (auch selbstgekaufte!) einnehmen oder äusserlich anwenden. Darf Dismenol Formel L während einer Schwangerschaft oder in der Stillzeit eingenommen werden? SchwangerschaftSollten Sie schwanger sein oder eine Schwangerschaft planen, sollten Sie Dismenol Formel L nur nach Rücksprache mit Ihrem Arzt bzw. Ihrer Ärztin einnehmen. Im letzten Drittel der Schwangerschaft darf Dismenol Formel L nicht eingenommen werden.StillzeitDismenol Formel L sollte während der Stillzeit nicht eingenommen werden, ausser Ihr Arzt bzw. Ihre Ärztin hat es Ihnen ausdrücklich erlaubt. Wie verwenden Sie Dismenol Formel L? DosierungErwachsene und Kinder über 12 Jahren1–2 Tabletten mit reichlich Flüssigkeit einnehmen. Vor der nächsten Einnahme ist ein Abstand von 4–6 Stunden einzuhalten.Maximale Tagesdosis: Nehmen Sie nicht mehr als 6 Tabletten innerhalb von 24 Stunden ein, ausser auf ärztliche Verschreibung.Bei Schmerzen während der Monatsblutung wird empfohlen, die Behandlung bereits bei den ersten Anzeichen der Beschwerden mit 2 Tabletten zu beginnen.Verwenden Sie Dismenol Formel L nicht länger als 3 Tage und nur zur Behandlung der oben aufgeführten Beschwerden. Falls die Beschwerden trotz Einnahme von Dismenol Formel L zunehmen oder falls die schmerzende Stelle rot oder geschwollen wird, konsultieren Sie Ihren Arzt oder Ihre Ärztin. Eine ernsthafte Krankheit kann die Ursache sein. Auch wenn die Beschwerden innert 3 Tagen nicht bessern, sollten Sie Ihren Arzt, Ihre Ärztin konsultieren, damit der Grund abgeklärt werden kann.Hinweis: Die Filmtabletten sind nicht zur Dosierung der halben Dosis durch Teilen geeignet.Kinder unter 12 JahrenDismenol Formel L darf bei Kindern unter 12 Jahren nicht angewendet werden. Die Anwendung und Sicherheit von Dismenol Formel L bei Kindern unter 12 Jahren ist bisher nicht systematisch geprüft worden.Halten Sie sich an die in dieser Packungsbeilage angegebene oder vom Arzt oder der Ärztin verschriebene Dosierung. Wenn Sie glauben, das Arzneimittel wirke zu schwach oder zu stark, so sprechen Sie mit Ihrem Arzt, Apotheker oder Drogisten bzw. Ihrer Ärztin, Apothekerin oder Drogistin. Welche Nebenwirkungen kann Dismenol Formel L haben? Folgende Nebenwirkungen können bei der Einnahme von Dismenol Formel Lauftreten. Sie sind nach ihrer Häufigkeit aufgelistet:Häufige Nebenwirkungen die in mehr als 1 von 100 Fällen aber weniger als 1 von 10 Fällen auftreten könnenMagen-Darm-Beschwerden wie Verdauungsbeschwerden, Diarrhö, Übelkeit, Erbrechen, Verstopfung, Schmerzen im Oberbauch, Blähungen, Teerstuhl, Erbrechen von Blut, gastrointestinale Blutungen.Zentralnervöse Nebenwirkungen wie Einschränkung des Reaktionsvermögens (besonders im Zusammenwirken mit Alkohol), Kopfschmerzen und Schwindel.Akuter Hautausschlag.Gelegentliche Nebenwirkungen die in mehr als 1 von 1'000 Fällen aber weniger als 1 von 100 Fällen auftreten könnenEntzündung der Nasenschleimhaut.Überempfindlichkeitsreaktionen.Schlaflosigkeit, Angstgefühle.Sehstörungen (die Sehstörungen sind normalerweise reversibel, wenn die Behandlung abgebrochen wird)Ohrensausen, Schwerhörigkeit, Schwindel.Asthma, Verkrampfung der Muskeln der Atemwege und Atemnot, Bei Patienten mit Herzinsuffizienz besteht die Gefahr eines akuten Lungenödems (Wasserlunge).Müdigkeit.Seltene Nebenwirkungen die in mehr als 1 von 10'000 Fällen aber weniger als 1 von 1'000 Fällen auftreten könnenAseptische Meningitis (Hirnhautentzündung)Angina, hohes Fieber, Anschwellen der Lymphknoten im HalsbereichAllergische Reaktionen, Symptome eines Lupus erythematodes (Schmetterlingsgeflecht), Blutarmut.Depressionen, Verwirrtheitszustände«Kribbeln» der Haut, SchläfrigkeitIrreversible Sehstörung oder Sehschwäche,Entzündung der Magenschleimhaut, Magen- und Darmgeschwüre, Geschwüre der Mundschleimhaut, Magen- und DarmdurchbrücheHepatitis, Gelbsucht, LeberfunktionsstörungenNesselsucht, Juckreiz, Einblutungen in die Haut, Schwellungen der Haut und Schleimhäute, LichtempfindlichkeitVerschiedene Erkrankungen der Nieren wie Nierenfunktionsstörungen mit Wasseransammlungen im Gewebe bis hin zu Nierenversagen.Allgemeine SchwellungenSehr seltene Nebenwirkungen die in weniger als 1 von 10'000 Fällen auftreten könnenPsychotische ZuständeHerzversagen, HerzinfarktBluthochdruckBauchspeicheldrüsenentzündungVerschlimmerung einer Kolitis oder eines Morbus CrohnLeberversagenSchwere allergische Reaktionen der Haut mit Bildung von Blasen und/oder grossflächiger Ablösung der Haut.Wenn Sie Nebenwirkungen bemerken, die hier nicht beschrieben sind, sollten Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin informieren. Was ist ferner zu beachten? Arzneimittel ausser Reichweite von Kindern aufbewahren und bei Raumtemperatur (15–25 °C) lagern.Das Arzneimittel darf nur bis zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.Weitere Auskünfte erteilt Ihnen Ihr Arzt, Apotheker oder Drogist bzw. Ihre Ärztin, Apothekerin oder Drogistin. Diese Personen verfügen über die ausführliche Fachinformation. Was ist in Dismenol Formel L enthalten? 1 Filmtablette enthält: 200 mg Ibuprofen als Ibuprofenlysinat, Hilfsstoffe zur Tablettenherstellung. Zulassungsnummer 57054 (Swissmedic). Wo erhalten Sie Dismenol Formel L? Welche Packungen sind erhältlich? In Apotheken und Drogerien ohne ärztliche Verschreibung.Packungen zu 10 Filmtabletten.Packungen zu 20 Filmtabletten. Zulassungsinhaberin Merz Pharma (Schweiz) AG, 4123 Allschwil. Diese Packungsbeilage wurde im September 2016 letztmals durch die Arzneimittelbehörde (Swissmedic) geprüft. 18515 / 15.05.2018 ..
29.11 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). ..
24.97 USD
Ibu sandoz filmtablet 400 mg 10 pcs
Ibu Sandoz contains the active ingredient ibuprofen. It has pain-relieving, fever-reducing and anti-inflammatory properties. Ibu Sandoz is suitable for short-term treatment, i. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments; Back pain; Headache; Toothache; Pain during of menstrual bleeding; Pain after injury; Fever with flu-like illnesses. Swissmedic-approved patient information Ibu Sandoz® 400Sandoz Pharmaceuticals AGWhat is Ibu Sandoz and when is it used ? Ibu Sandoz contains the active ingredient ibuprofen. It has pain-relieving, fever-reducing and anti-inflammatory properties. Ibu Sandoz is suitable for short-term treatment, i. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments;Back pain;Headache;Toothache;Pain during of the menstrual period;Pain after injuries;Fever with flu-like illnesses.When can Ibu Sandoz not to be taken? Ibu Sandoz must 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 medicines called non-steroidal anti-inflammatory drugs,if you are pregnant are or are breastfeeding (see also the chapter "Can Ibu Sandoz be taken while pregnant or breastfeeding?"),if you suffer from 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,in severe heart failure,for the treatment of pain after coronary heart bypass surgery (or use of a heart-lung machine),in children under 12 years of age. Ibu Sandoz has not been tested for use in children under the age of 12.When should you be careful when taking Ibu Sandoz? During treatment with Ibu Sandoz, 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 or if you have an infection - see below under 'Infection'. For certain painkillers, 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. This risk can also be slightly increased with Ibu Sandoz 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 high doses of Ibu Sandoz is no longer recommended. Do not exceed the recommended dose or duration of treatment and always tell your doctor if you have had a heart attack, stroke or thrombosis in a vein, or if you have risk factors (such as high blood pressure, diabetes (sugar diabetes), high blood fat levels, Smoking. Your doctor will decide if you can still use Ibu Sandoz and what dose is right for you.Taking Ibu Sandoz can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor 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 lose more fluids, e.g. through heavy sweating. This medicine may impair your ability to react, the ability to drive and the ability to use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of gastric or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients suffering from asthma, chronic inflammation of the nasal mucosa (chronic runny nose), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases). Serious skin reactions have been reported in association with medicines containing ibuprofen. You should stop taking Ibu Sandoz and see a doctor straight away if you develop a rash, mucosal lesions, blisters or any other sign 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 any other sign of allergy, you should stop taking Ibu Sandoz 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 Ibu Sandoz have? »). Ibu Sandoz should not be used if you have chickenpox. InfectionsIbu Sandoz may mask signs of infections such as fever and pain. It is therefore possible that Ibu Sandoz 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, 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 (preparations for high blood pressure). and heart failure), antibiotics, certain antifungal medicines (e.g. voriconazole or fluconazole), immunosuppressants (preparations against transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, AIDS, epilepsy and depression. Nonsteroidal anti-inflammatory drugs such as ibuprofen and the medicines listed above can interact. In particular, long-term treatment with Ibu Sandoz may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other pain relievers should not be taken at the same time as ibuprofen as the risk of side effects may be increased. Side effects, particularly those affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Prolonged 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, especially bleeding and perforation in the stomach and intestines. Therefore, particularly careful medical supervision is required in elderly patients. This medicinal product contains less than 1 mmol sodium (23 mg) per film-coated tablet, i.e. essentially 'sodium-free'. it is almost «sodium-free». Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally.Can Ibu Sandoz be taken during pregnancy or breastfeeding?PregnancyIf you are pregnant or planning to become pregnant, you should only take Ibu Sandoz after consulting your doctor. Ibu Sandoz should not be taken during the last trimester of pregnancy. BreastfeedingIbu Sandoz should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use Ibu Sandoz?Adults and adolescents aged 12 and over Take 1 film-coated tablet Ibu Sandoz with plenty of liquid. The film-coated tablets can be swallowed whole or divided to halve the dose or for ease of administration. A gap of 6 to 8 hours should be observed before the next dose. Maximum daily doseDo not take more than 3 film-coated tablets of Ibu Sandoz in a 24-hour period, 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 Ibu Sandoz for more than 3 days and only to treat the conditions listed above. If symptoms worsen despite taking Ibu Sandoz, 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 yearsIbu Sandoz should not be used in children under 12 years of age. The use and safety of Ibu Sandoz in children under the age of 12 has not been systematically evaluated. 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. If you have taken more Ibu Sandoz than you should, always consult a doctor for an assessment of the risk and advice on further treatment. 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, do not take more than the usual recommended amount next time. 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 Ibu Sandoz have?The following side effects can occur when taking Ibu Sandoz. They are listed by frequency: Common (affects 1 to 10 users in 100)gastrointestinal disorders such as indigestion, diarrhea, nausea, vomiting, constipation, upper abdominal pain, 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...
17.50 USD
Irfen dolo filmtabl 200 mg
Inhaltsverzeichnis Was ist Irfen Dolo und wann wird es angewendet? Wann darf Irfen Dolo nicht angewendet werden? Wann ist bei der Einnahme von Irfen Dolo Vorsicht geboten? Darf Irfen Dolo während einer Schwangerschaft oder in der Stillzeit eingenommen werden? Wie verwenden Sie Irfen Dolo? Welche Nebenwirkungen kann Irfen Dolo haben? Was ist ferner zu beachten? Was ist in Irfen Dolo enthalten? Zulassungsnummer Wo erhalten Sie Irfen Dolo? Welche Packungen sind erhältlich? Zulassungsinhaberin COMPENDIUM Swissmedic-genehmigte Patienteninformation Irfen Dolo 200 mg, Filmtabletten / Irfen Dolo forte 400 mg, Filmtabletten Mepha Pharma AG Was ist Irfen Dolo und wann wird es angewendet? Irfen Dolo enthält den Wirkstoff Ibuprofen. Dieser hat schmerzlindernde, fiebersenkende und entzündungshemmende Eigenschaften.Irfen Dolo eignet sich zur Kurzzeitbehandlung, d.h. zur maximal 3 Tage dauernden Behandlung von:Schmerzen im Bereich von Gelenken und Bändern,Rückenschmerzen,Kopfschmerzen,Zahnschmerzen,Schmerzen während der Monatsblutung,Schmerzen nach Verletzungen,Fieber bei grippalen Erkrankungen. Wann darf Irfen Dolo nicht angewendet werden? Irfen Dolo darf nicht eingenommen werden,wenn Sie auf einen der Inhaltsstoffe allergisch reagieren oder nach der Einnahme von Acetylsalicylsäure oder anderen Schmerz- oder Rheumamitteln, sogenannten nicht-steroidalen entzündungshemmenden Arzneimitteln, Atemnot, allergieähnliche Hautreaktionen hatten,wenn Sie schwanger sind oder stillen (siehe auch Kapitel «Darf Irfen Dolo während einer Schwangerschaft oder in der Stillzeit eingenommen werden?»),bei aktiven Magen- und/oder Zwölffingerdarmgeschwüren oder Magen-/Darm-Blutungen,bei chronischen Darmentzündungen (Morbus Crohn, Colitus ulcerosa),bei schweren Einschränkungen der Leber- oder Nierenfunktion,bei schwerer Herzleistungsschwäche,zur Behandlung von Schmerzen nach einer koronaren Bypassoperation am Herzen (resp. Einsatz einer Herz-Lungen-Maschine).Bei Kindern unter 12 Jahren: Irfen Dolo wurde für die Anwendung bei Kindern unter 12 Jahren nicht geprüft. Wann ist bei der Einnahme von Irfen Dolo Vorsicht geboten? Während der Behandlung mit Irfen Dolo können im oberen Magen-Darm-Trakt Schleimhautgeschwüre, selten Blutungen oder in Einzelfällen Perforationen (Magen-, Darmdurchbrüche) auftreten. Diese Komplikationen können während der Behandlung jederzeit auch ohne Warnsymptome auftreten. Um dieses Risiko zu verringern, sollte die kleinste wirksame Dosis während der kürzesten möglichen Therapiedauer angewendet werden. Wenden Sie sich an Ihren Arzt oder Ihre Ärztin, wenn Sie Magenschmerzen haben und einen Zusammenhang mit der Einnahme des Arzneimittels vermuten.Ältere Patienten können empfindlicher auf das Arzneimittel reagieren als jüngere Erwachsene. Es ist besonders wichtig, dass ältere Patienten eventuelle Nebenwirkungen sofort Ihrem Arzt bzw. Ihrer Ärztin melden.In folgenden Situationen dürfen Sie Irfen Dolo nur auf ärztliche Verschreibung und unter ärztlicher Überwachung einnehmen:Wenn Sie gegenwärtig wegen einer ernsthaften Krankheit in ärztlicher Behandlung sind;wenn Sie früher an einem Magen- oder Zwölffingerdarmgeschwür erkrankt sind;wenn Sie bereits einen Herzinfarkt, Schlaganfall oder eine Venenthrombose hatten, oder falls Sie Risikofaktoren haben (wie hoher Blutdruck, Diabetes [Zuckerkrankheit], hohe Blutfettwerte [Rauchen]; für gewisse ähnlich wirkende Schmerzmittel, die so genannten COX-2-Hemmer, wurde unter hohen Dosierungen und/oder Langzeitbehandlung ein erhöhtes Risiko für Herzinfarkt und Schlaganfall festgestellt. Ob dieses erhöhte Risiko auch für Irfen Dolo zutrifft, ist nicht bekannt;wenn Sie eine Herzkrankheit oder ein Nierenleiden haben, falls Sie Arzneimittel gegen Bluthochdruck (z.B. harntreibende Mittel, ACE-Hemmer) einnehmen oder bei einem erhöhten Flüssigkeitsverlust, z.B. durch starkes Schwitzen; die Einnahme von Irfen Dolo kann die Funktion Ihrer Nieren beeinträchtigen, was zu einer Erhöhung des Blutdrucks und/oder zu Flüssigkeitsansammlungen (Ödemen) führen kann;wenn Sie ein Leberleiden haben;wenn Sie mit gerinnungshemmenden Arzneimitteln (Blutverdünner, Antikoagulantien) behandelt werden oder an einer Störung der Blutgerinnung leiden;wenn Sie an Asthma leiden;wenn Sie Rheumamittel oder andere Schmerzmittel (z.B. Acetylsalicylsäure, Aspirin) einnehmen;wenn Sie Arzneimittel zur Behandlung der Zuckerkrankheit (mit Ausnahme von Insulin), Arzneimittel zur Erhöhung der Urinausscheidung (harntreibende Mittel), Arzneimittel zur Behandlung von Infektionen (Chinolon-Antibiotika) oder Arzneimittel mit einer der folgenden Substanzen: Lithium, Digoxin, Methotrexat, Baclofen, Phenytoin, Probenecid oder Sulfinpyrazon einnehmen.Im Zusammenhang mit der Behandlung mit nicht-steroidalen Antirheumatika wurden schwerwiegende Hautreaktionen berichtet. Das höchste Risiko für derartige Reaktionen scheint zu Beginn der Therapie zu bestehen. Bei Auftreten von Hautausschlag, einschliesslich Fieber, Läsionen der Schleimhäute, Blasen oder sonstigen Anzeichen einer Allergie, sollten Sie die Behandlung mit Irfen Dolo einstellen und sich unverzüglich in medizinische Behandlung begeben, da dies die ersten Anzeichen einer sehr schwerwiegenden Hautreaktion sein können (siehe Rubrik «Welche Nebenwirkungen kann Irfen Dolo haben?»).Informieren Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin, falls Sie mit Arzneimitteln behandelt werden, wie Blutverdünnungsmitteln, Diuretika (harntreibende Mittel), ACE-Hemmern oder β-Blockern (Präparate gegen hohen Blutdruck und Herzinsuffizienz), Antibiotika, bestimmte Mittel gegen Pilzinfektionen (z.B. Voriconazol oder Fluconazol), Immunsuppressiva (Präparate gegen Transplantatabstossungen), pflanzlicher Ginkgo biloba Extrakt, Arzneimittel gegen erhöhten Blutzucker, gegen Aids, Epilepsie und Depressionen. Nichtsteroidale Antirheumatika, wie Ibuprofen, und die oben aufgeführten Arzneimittel können sich gegenseitig beeinflussen.Bei gleichzeitigem Alkoholkonsum können Nebenwirkungen, insbesondere die den Magen-Darm-Trakt oder das zentrale Nervensystem betreffen, verstärkt werden.Informieren Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin, wenn Siean anderen Krankheiten leiden,Allergien haben oderandere Arzneimittel (auch selbst gekaufte!) einnehmen oder äusserlich anwenden.Irfen Dolo kann die Reaktionsfähigkeit, die Fahrtüchtigkeit und die Fähigkeit, Werkzeuge oder Maschinen zu bedienen, beeinträchtigen! Das gilt besonders für die Einnahme zusammen mit Alkohol.Dieses Arzneimittel enthält weniger als 1 mmol Natrium (23 mg) pro Filmtablette, d.h. es ist nahezu «natriumfrei». Darf Irfen Dolo während einer Schwangerschaft oder in der Stillzeit eingenommen werden? SchwangerschaftSollten Sie schwanger sein oder eine Schwangerschaft planen, sollten Sie Irfen Dolo nur nach Rücksprache mit Ihrem Arzt bzw. Ihrer Ärztin einnehmen. Sie sollten Irfen Dolo nicht einnehmen, es sei denn, es ist eindeutig notwendig und wird von einem Arzt / einer Ärztin verordnet. Bei Einnahme in den ersten 6 Monaten der Schwangerschaft sollte die Dosis so niedrig und die Behandlungsdauer so kurz wie möglich gehalten werden.Die Einnahme von nichtsteroidalen Antirheumatika (NSAR) ab der 20. Schwangerschaftswoche kann Ihrem ungeborenen Kind Schaden zufügen. Wenn Sie NSAR für mehr als 2 Tage einnehmen müssen, muss Ihr Arzt bzw. Ihre Ärztin möglicherweise die Fruchtwassermenge im Mutterleib und das Herz des ungeborenen Kindes überwachen.Im letzten Drittel der Schwangerschaft darf Irfen Dolo nicht eingenommen werden.StillzeitIrfen Dolo sollte während der Stillzeit nicht eingenommen werden, ausser Ihr Arzt bzw. Ihre Ärztin hat es Ihnen ausdrücklich erlaubt. Wie verwenden Sie Irfen Dolo? Erwachsene und Jugendliche ab 12 JahrenIrfen Dolo 200 mg1–2 Filmtabletten Irfen Dolo 200 mg mit reichlich Flüssigkeit unzerkaut einnehmen. Vor der nächsten Einnahme ist ein Abstand von 4 bis 6 Stunden einzuhalten.Maximale Tagesdosis: Nehmen Sie nicht mehr als 6 Filmtabletten Irfen Dolo 200 mg (1200 mg Ibuprofen) innerhalb von 24 Stunden ein, ausser auf ärztliche Verschreibung.Irfen Dolo forte 400 mg1 Filmtablette Irfen Dolo forte 400 mg mit reichlich Flüssigkeit unzerkaut einnehmen. Die Filmtabletten können zur Halbierung der Dosis oder zur Erleichterung der Einnahme geteilt werden.Vor der nächsten Einnahme ist ein Abstand von 4 bis 6 Stunden einzuhalten.Maximale Tagesdosis: Nehmen Sie nicht mehr als 3 Filmtabletten Irfen Dolo forte 400 mg (1200 mg Ibuprofen) innerhalb von 24 Stunden ein, ausser auf ärztliche Verschreibung.Bei Schmerzen während der Monatsblutung wird empfohlen, die Behandlung bereits bei ersten Anzeichen der Beschwerden mit 2 Filmtabletten Irfen Dolo 200 mg oder 1 Filmtablette Irfen Dolo forte 400 mg zu beginnen.Verwenden Sie Irfen Dolo nicht länger als 3 Tage und nur zur Behandlung der oben aufgeführten Beschwerden.Falls die Beschwerden trotz Einnahme von Irfen Dolo zunehmen oder falls die schmerzende Stelle rot oder geschwollen wird, konsultieren Sie Ihren Arzt bzw. Ihre Ärztin. Eine ernsthafte Krankheit kann die Ursache sein.Auch wenn die Beschwerden nicht spätestens innert 3 Tagen bessern, sollten Sie Ihren Arzt bzw. Ihre Ärztin konsultieren, damit der Grund abgeklärt werden kann.Kinder unter 12 JahrenIrfen Dolo darf bei Kindern unter 12 Jahren nicht angewendet werden. Die Anwendung und Sicherheit von Irfen Dolo bei Kindern unter 12 Jahren ist bisher nicht geprüft worden.Ältere PatientenÄltere Patienten können empfindlicher auf das Arzneimittel reagieren als jüngere Erwachsene. Es ist besonders wichtig, dass ältere Patienten eventuelle Nebenwirkungen sofort Ihrem Arzt bzw. Ihrer Ärztin melden.Halten Sie sich an die in der Packungsbeilage angegebene oder vom Arzt bzw. von der Ärztin verschriebene Dosierung.Falls Sie mehr Irfen Dolo eingenommen haben, als Sie sollten, oder falls Kinder aus Versehen das Arzneimittel eingenommen haben, wenden Sie sich immer an einen Arzt oder an eine Ärztin, um eine Einschätzung des Risikos und Rat zur weiteren Behandlung zu bekommen.Die Symptome können Übelkeit, Magenschmerzen, Erbrechen (möglicherweise mit Blut), Kopfschmerzen, Ohrensausen, Verwirrung und Augenzittern umfassen. Bei hohen Dosen wurde über Schläfrigkeit, Brustschmerzen, Herzklopfen, Ohnmacht, Krämpfe (vor allem bei Kindern), Schwäche und Schwindelgefühle, Blut im Urin, Frieren und Atemprobleme berichtet.Falls Sie die Einnahme einmal vergessen haben, nehmen Sie bei der nächsten Gabe nicht mehr als die übliche empfohlene Menge ein.Wenn Sie glauben, das Arzneimittel wirke zu schwach oder zu stark, so sprechen Sie mit Ihrem Arzt, Apotheker oder Drogisten bzw. mit Ihrer Ärztin, Apothekerin oder Drogistin. Welche Nebenwirkungen kann Irfen Dolo haben? Folgende Nebenwirkungen können bei der Einnahme von Irfen Dolo auftreten. Sie sind nach ihrer Häufigkeit aufgelistet:Häufig (betrifft 1 bis 10 von 100 Anwendern)Magen-Darm-Beschwerden wie Verdauungsbeschwerden, Diarrhö, Übelkeit, Erbrechen, Verstopfung, Schmerzen im Oberbauch, Blähungen, Teerstuhl, Erbrechen von Blut, gastrointestinale Blutungen.Zentralnervöse Nebenwirkungen wie Einschränkung des Reaktionsvermögens (besonders im Zusammenwirken mit Alkohol), Kopfschmerzen und Schwindel.Akuter Hautausschlag.Gelegentlich (betrifft 1 bis 10 von 1000 Anwendern)Entzündung der Nasenschleimhaut.Überempfindlichkeitsreaktionen.Schlaflosigkeit, Angstgefühle.Sehstörungen (die Sehstörungen sind normalerweise reversibel, wenn die Behandlung abgebrochen wird).Ohrensausen, Schwerhörigkeit, Schwindel.Asthma, Verkrampfung der Muskeln der Atemwege und Atemnot, Bei Patienten mit Herzinsuffizienz besteht die Gefahr eines akuten Lungenödems (Wasserlunge).Müdigkeit.Selten (betrifft 1 bis 10 von 10'000 Anwendern)Aseptische Meningitis (Hirnhautentzündung).Angina, hohes Fieber, Anschwellen der Lymphknoten im Halsbereich.Allergische Reaktionen, Symptome eines Lupus erythematodes (Schmetterlingsgeflecht), Blutarmut.Depressionen, Verwirrtheitszustände.«Kribbeln» der Haut, Schläfrigkeit.Irreversible Sehstörung oder Sehschwäche.Entzündung der Magenschleimhaut, Magen- und Darmgeschwüre, Geschwüre der Mundschleimhaut, Magen- und Darmdurchbrüche.Hepatitis, Gelbsucht, Leberfunktionsstörungen.Nesselsucht, Juckreiz, Einblutungen in die Haut, Schwellungen der Haut und Schleimhäute, Lichtempfindlichkeit.Verschiedene Erkrankungen der Nieren wie Nierenfunktionsstörungen mit Wasseransammlungen im Gewebe bis hin zu Nierenversagen.Allgemeine Schwellungen.Sehr selten (betrifft weniger als 1 von 10'000 Anwendern)Psychotische Zustände.Herzversagen, Herzinfarkt.Bluthochdruck.Bauchspeicheldrüsenentzündung.Leberversagen.Schwere allergische Reaktionen der Haut mit Bildung von Blasen und/oder grossflächiger Ablösung der Haut.EinzelfälleEs kann zu einer schweren Hautreaktion, bekannt als DRESS-Syndrom, kommen. Die Symptome von DRESS umfassen Hautausschlag, Fieber, geschwollene Lymphknoten und eine Zunahme von Eosinophilen (einer Form der weissen Blutkörperchen).Verschlimmerung einer Kolitis oder eines Morbus Crohn.Ein roter, schuppiger, weit verbreiteter Hautausschlag mit Beulen unter der Haut und Blasen, die hauptsächlich in den Hautfalten, am Rumpf und an den oberen Extremitäten lokalisiert sind, begleitet von Fieber zu Beginn der Behandlung (akute generalisierte exanthematöse Pustulose). Beenden Sie die Einnahme von Irfen Dolo, wenn diese Symptome auftreten, und suchen Sie sofort einen Arzt oder eine Ärztin auf.Wenn Sie Nebenwirkungen bemerken, wenden Sie sich an Ihren Arzt oder Apotheker bzw. Ihre Ärztin oder Apothekerin. Dies gilt insbesondere auch für Nebenwirkungen, die nicht in dieser Packungsbeilage angegeben sind. Was ist ferner zu beachten? Das Arzneimittel darf nur bis zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.LagerungshinweisIn der Originalverpackung und nicht über 30°C lagern.Ausser Reichweite von Kindern aufbewahren.Weitere Auskünfte erteilt Ihnen Ihr Arzt, Apotheker oder Drogist bzw. Ihre Ärztin, Apothekerin oder Drogistin. Diese Personen verfügen über die ausführliche Fachinformation. Was ist in Irfen Dolo enthalten? Wirkstoffe1 Filmtablette Irfen Dolo 200 mg enthält: 200 mg Ibuprofen als Wirkstoff.1 Filmtablette Irfen Dolo forte 400 mg enthält: 400 mg Ibuprofen als Wirkstoff.HilfsstoffeTablettenkern: vorverkleisterte Stärke, Croscarmellose-Natrium, Hypromellose, Stearinsäure, hochdisperses Siliciumdioxid.Tablettenfilm: Hypromellose, Macrogol 8000, Titandioxid (E171). Zulassungsnummer 67372 (Swissmedic). Wo erhalten Sie Irfen Dolo? Welche Packungen sind erhältlich? In Apotheken und Drogerien ohne ärztliche Verschreibung.Irfen Dolo 200 mg: Packungen zu 20 Filmtabletten.Irfen Dolo forte 400 mg (mit Bruchrille, teilbar): Packungen zu 10 Filmtabletten. Zulassungsinhaberin Mepha Pharma AG, Basel. Diese Packungsbeilage wurde im November 2022 letztmals durch die Arzneimittelbehörde (Swissmedic) geprüft. Interne Versionsnummer: 3.1 31280 / 18.01.2024 ..
22.05 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,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...
22.05 USD
Nurofen drag 200 mg 20 pcs
Nurofen Drag 200 mg of 20 pcs Nurofen Drag 200 mg of 20 pcs is a fast-acting pain reliever that swiftly alleviates pain and inflammation. The drug comes in tablet form and can be ingested without water. This medication is designed to provide relief for a variety of pain types, including headaches, menstrual cramps, dental pain, muscle pain, and fever. The active ingredient in Nurofen Drag tablets is ibuprofen, which is a non-steroidal anti-inflammatory drug (NSAID) that operates by reducing the production of the hormone called prostaglandin that causes inflammation and pain. The dosage is a 200 mg tablet per dose, with a maximum of four doses per day. The medication is for adults and children aged 12 and up who weigh at least 40 kg. Nurofen Drag 200 mg of 20 pcs is designed to be swiftly absorbed by the body, with effects that last for up to 8 hours. Since the tablet dissolves in the mouth, it enables active time relief during on-the-go activities like school, work, or commuting. The active formula is powerful, effective, and safe when used as directed, making it a reliable choice for pain relief. In summary, Nurofen Drag 200 mg of 20 pcs is a powerful, fast-acting, swallow-free pain relief medication that helps alleviate various types of pain, including headaches, menstrual cramps, dental pain, muscle pain, and fever. With a time-tested, active ingredient, Ibuprofen, and a tablet form that dissolves in the mouth, this medication provides swift pain relief for adults and children aged 12 and up who weigh at least 40 kg. ..
26.04 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,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.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.Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusion."Tingling" of the skin, drowsiness.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.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.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..
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