Anti-inflammatory
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Akileine dermo akilortho cream for prosthesis tb 75 ml
AKILEINE Dermo Akilortho Cream for Denture Tb 75 ml product description AKILEINE Dermo Akilortho Cream for Denture Tb 75 ml Do you wear dentures and experience discomfort or pain due to the friction caused by the denture rubbing against your gums? AKILEINE Dermo Akilortho cream for denture Tb 75 ml can help alleviate these issues. The cream contains natural active ingredients such as arnica, sage, and ginger which provide anti-inflammatory and analgesic properties. These ingredients also have antiseptic and antioxidant properties which help to protect and heal the delicate gum tissue. The cream is easy to apply and does not leave any residue or greasy feeling in your mouth. Simply apply a small amount of cream on the areas of your gums where the denture rubs against and massage gently. Repeat as needed throughout the day. AKILEINE Dermo Akilortho cream for denture Tb 75 ml is suitable for anyone who wears dentures and experiences discomfort or pain. It is also suitable for those who have sensitive gums or allergies to certain chemicals or ingredients commonly found in other denture creams. Don't let denture discomfort or pain ruin your day. Try AKILEINE Dermo Akilortho cream for denture Tb 75 ml today and experience the relief and comfort you deserve...
21.28 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
Alka seltzer effervescent tablets 10 x 2 pcs
Alka-Seltzer contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and anti-inflammatory properties. Alka-Seltzer is suitable for short-term treatment, i. for the maximum 3-day treatment of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic treatment of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's prescription and only as a second-line drug (see «When should caution be taken when taking Alka-Seltzer?»). Swissmedic-approved patient informationAlka-Seltzer®, effervescent tablets Bayer (Schweiz) AG What is ALKA-SELTZER and when is it used?Alka-Seltzer contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and anti-inflammatory properties. Alka-Seltzer is suitable for short-term treatment, i. for the maximum 3-day treatment of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic treatment of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's prescription and only as a second-line drug (see «When should caution be taken when taking Alka-Seltzer?»). What should be considered?Alka-Seltzer should not be used for more than 3 days, unless prescribed by a doctor. Painkillers should not be taken regularly over a long period of time without medical supervision. Long-lasting pain requires a medical check-up. The dosage specified or prescribed by the doctor must not be exceeded. It's also important to remember that long-term use of painkillers can itself contribute to headache persistence. Long-term use of painkillers, especially when taking a combination of several painkillers, can lead to permanent kidney damage with the risk of kidney failure. When should ALKA-SELTZER not be used?You should not use Alka-Seltzer in the following cases: If you are allergic to any of the ingredients or have had shortness of breath or an allergy-like skin reaction after taking acetylsalicylic acid, other salicylates or other pain or rheumatism medicines called non-steroidal anti-inflammatory drugs. in the case of active stomach and/or duodenal ulcers or stomach/intestinal bleeding,In the case of chronic intestinal inflammation (Crohn's disease, ulcerative colitis).If you have a pathologically increased tendency to bleed.Severely impaired liver or kidney function.Severe heart failure.For the treatment of pain after coronary bypass surgery on the heart (or use of a heart-lung machine).If you have to take methotrexate at a dose of more than 15 mg per week at the same time.In children under 12 years of age.When is caution required when using ALKA-SELTZER?During treatment with Alka-Seltzer, ulcers in the mucous membranes of the upper gastrointestinal tract, rarely bleeding or in individual cases perforations (gastrointestinal breakthroughs) 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. Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. You should only take Alka-Seltzer 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 had a stomach or duodenal ulcer.If you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors ) or in case of increased fluid loss, e.g. through heavy sweating; taking Alka-Seltzer can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema).If you have liver problems. If you are being treated with anticoagulants (blood thinners, anticoagulants) or suffer from a blood clotting disorder;If you suffer from asthma;If you are taking antirheumatic medicines or other painkillers.For asthma, hives, nasal polyps, hay fever or other allergies, for a rare hereditary disease of the red blood cells, the so-called "glucose-6-phosphate dehydrogenase deficiency" and for treatment with anticoagulants (“blood thinners”, anticoagulants) or blood pressure lowering agents (antihypertensives) should only be taken according to the doctor’s strict instructions. Patients who have to eat a low-salt diet on medical advice (e.g. kidney disease, severe heart failure) should only use Alka-Seltzer effervescent tablets in exceptional cases because of their high sodium content. Adolescents from the age of 12 with fever, flu, chickenpox or other viral diseases may only take Alka-Seltzer on the doctor's instructions and only as a second-line remedy. If these diseases lead to disorders of consciousness with vomiting or after they have disappeared, the doctor should be consulted immediately. The simultaneous and prolonged use of Alka-Seltzer can increase the effect of cortisone preparations, anticonvulsants (antiepileptics), blood thinners, digoxin and lithium preparations against depression. There may be an increase in the undesirable effects of these medicines. The effect of gout medicines (Probenecid and Sulfinpyrazone), water tablets (diuretics) and medicines for high blood pressure can be reduced. The use of anti-rheumatic drugs or methotrexate (which is taken for chronic polyarthritis, for example; see also the section "When should Alka-Seltzer not be used?") may result in an increase in the undesirable effects. Alka-Seltzer can increase the risk of bleeding if you take cortisone preparations, alcohol or drugs from the group of so-called serotonin reuptake inhibitors for depression. If Alka-Seltzer and antidiabetics (e.g. insulin, sulfonylureas) are taken at the same time, the blood sugar level can drop. Even in small doses, acetylsalicylic acid reduces the excretion of uric acid. This can trigger gout in patients who already have low uric acid excretion. Caution is required in conditions with an increased risk of bleeding (e.g. menstrual bleeding or injuries). There may be an increased tendency to bleed, especially during and after surgical interventions (including minor interventions such as tooth extraction). Your doctor or dentist should be asked or informed about taking it before surgery. 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, mucosal lesions, blisters or any other sign of allergy, you should stop using Alka-Seltzer and seek medical attention immediately, as these may be the first signs of a very serious skin reaction (see section «What side effects can Alka-Seltzer have?» ). Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!).Can ALKA-SELTZER be taken while pregnant or breastfeeding?PregnancyYou should not take Alka-Seltzer, es 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 can harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. If you are pregnant or planning to become pregnant, you should only take Alka-Seltzer after consulting your doctor. Alka-Seltzer should not be taken during the last trimester of pregnancy. BreastfeedingAlka-Seltzer should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use ALKA-SELTZER?Adults and young people aged 12 and over and weighing more than 40 kg: 1-2 effervescent tablets A daily dose of 8 tablets must not be exceeded for adults. Alka-Seltzer must always be dissolved in water. The intake can be repeated about every 4 hours up to 4 doses within 24 hours. It should not be taken on an empty stomach. Adolescents from the age of 12 may only take Alka-Seltzer if prescribed by a doctor and only as a second-line drug. Alka-Seltzer should not be used in children under 12 years of age. In the event of uncontrolled intake (overdose), consult a doctor immediately. Ringing in the ears and/or sweating can be an indication of an overdose. Follow the dosage given in this 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 ALKA-SELTZER have?Stomach problems can occur as side effects. In rare cases, hypersensitivity reactions such as swelling of the skin and mucous membranes (e.g. blocked nose), skin rashes, asthma, shortness of breath and gastrointestinal ulcers and gastrointestinal bleeding, bruising, nosebleeds or bleeding gums may occur. Serious bleeding, which in isolated cases can be potentially life-threatening, has also been reported very rarely. Changes in the intestinal wall have been reported. If signs of a hypersensitivity reaction occur, the drug should be discontinued and the doctor consulted. If the stool turns black or there is blood in the vomit during treatment, the drug should be discontinued and the doctor consulted immediately. Rarely, dizziness, headaches, blurred vision and confusion occur. Frequency not known: 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). If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What else is to be done note? Store at room temperature (15 - 25°C) and protect from moisture. The medicinal product should be kept out of the reach of children! The medicinal product may only be used up to the date marked «EXP» on the container. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does ALKA-SELTZER contain?Active ingredients1 effervescent tablet contains 324 mg acetylsalicylic acid ExcipientsFlavourings, sodium saccharate, preservative: sodium benzoate (E 211) and other excipients. Approval number08671 (Swissmedic) Where can you get ALKA-SELTZER? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 20 effervescent tablets. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Swissmedic) in February 2023. ..
37.16 USD
Aromasan ginger ether/oil organic 15 ml
Elevate your well-being with Aromasan's organic ginger ether/oil. Carefully crafted with nature's finest ingredients, this 15 ml bottle is a powerhouse of wellness benefits. Use it in aromatherapy to invigorate your senses or dilute it for topical application to soothe muscles and joints. Ginger is renowned for its anti-inflammatory properties and digestive support, making it a versatile addition to your natural remedies collection. Treat yourself to the soothing essence of organic ginger and experience the holistic benefits of phytotherapy with Aromasan...
60.04 USD
Aromasan wintergreen ether/oil 30 ml
Aromasan Wintergreen Äth/Oil 30 mL If you're looking for a natural remedy for muscle pain and inflammation, look no further than Aromasan Wintergreen Äth/Oil 30 mL. Wintergreen essential oil, or Gaultheria procumbens, has been used for centuries to alleviate pain and reduce inflammation naturally. This oil is derived from the leaves of the wintergreen plant and has a minty scent that can help invigorate the mind and body. Benefits of Aromasan Wintergreen Äth/Oil Reduces muscle pain and inflammation Improves circulation Relieves tension and stress Alleviates headaches and migraines How to Use Aromasan Wintergreen Äth/Oil Wintergreen essential oil should never be used undiluted on the skin as it can cause irritation. To use this oil, dilute it with a carrier oil such as coconut or jojoba oil. Aromasan Wintergreen Äth/Oil can be used topically or in aromatherapy. To use topically, mix a few drops with a carrier oil and apply to the affected area. For aromatherapy, add a few drops to a diffuser or humidifier to fill your room with the scent. Why Choose Aromasan Wintergreen Äth/Oil Aromasan Wintergreen Äth/Oil is made from high-quality, pure wintergreen essential oil that is rigorously tested for purity and potency. This product is free from additives, fillers, and synthetic fragrances, making it a natural alternative to conventional pain relief medications. Plus, the convenient 30 mL bottle makes it easy to take with you on the go. Order Aromasan Wintergreen Äth/Oil Today If you're looking for a natural remedy for muscle pain and inflammation, Aromasan Wintergreen Äth/Oil 30 mL is the perfect solution. Order yours today and experience the natural healing power of wintergreen essential oil. ..
34.31 USD
Aspirin chewable 500 mg 20 pcs
Aspirin contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and anti-inflammatory properties. Aspirin chewable tablets are suitable for short-term treatment, i. for the maximum 3-day treatment of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic treatment of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's prescription and only as a second-line drug (see "When should you be careful when taking aspirin?"). Swissmedic-approved patient informationAspirin® chewable tabletsBayer (Schweiz) AGWhat is aspirin and when is it used?Aspirin contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and anti-inflammatory properties. Aspirin chewable tablets are suitable for short-term treatment, i. for the maximum 3-day treatment of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic treatment of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's prescription and only as a second-line drug (see "When should you be careful when taking aspirin?"). What should be considered?Aspirin should not be used for more than 3 days unless prescribed by a doctor. Painkillers should not be taken regularly over a long period of time without medical supervision. Long-lasting pain requires a medical check-up. The dosage specified or prescribed by the doctor must not be exceeded. It's also important to remember that long-term use of painkillers can itself contribute to headache persistence. Long-term use of painkillers, especially when taking several painkillers in combination, can lead to permanent kidney damage with the risk of kidney failure. When shouldn't aspirin be taken/used?You shouldn't use aspirin in the following cases: If you are allergic to any of the ingredients or have had shortness of breath or an allergy-like skin reaction after taking acetylsalicylic acid, other salicylates or other pain or rheumatism medicines called non-steroidal anti-inflammatory drugs. If you suffer from a stomach and/or duodenal ulcer or have gastrointestinal bleeding.If you have chronic intestinal inflammation (Crohn's disease, ulcerative colitis).If you have a have a pathologically increased tendency to bleed.Severely impaired liver or kidney function.Severe heart failure.For the treatment of pain after coronary bypass surgery on the Heart (or use of a heart-lung machine).If you have to take methotrexate at a dose of more than 15 mg per week at the same time.If you are pregnant or breastfeeding (See also the section «Can aspirin be taken during pregnancy or breastfeeding?»).For children under the age of 12.When is caution required when taking / using aspirin? During treatment with aspirin, 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. Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. You may only take aspirin 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 heart disease or have kidney disease or increased fluid loss, e.g. due to heavy sweating, diarrhea or after major surgery; taking aspirin can affect how your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema).If you have liver problems.If you have asthma, hives, nasal polyps, hay fever or other allergies, if you have a rare hereditary disease of the red blood cells, the so-called "glucose-6-phosphate dehydrogenase deficiency" and if you are being treated with anticoagulants ("blood thinners", Anticoagulants) or blood pressure lowering agents (antihypertensives) should only be taken according to the strict instructions of the doctor. Adolescents from the age of 12 with fever, flu, chickenpox or other viral diseases may only take aspirin as directed by their doctor and only as a second-line drug. If these diseases lead to disorders of consciousness with vomiting or after they have disappeared, the doctor should be consulted immediately. The effect of cortisone preparations, antispasmodics (antiepileptics), blood thinners, digoxin and lithium preparations against depression can be increased with simultaneous and prolonged use of aspirin. There may be an increase in the undesirable effects of these medicines. The effect of gout medicines (Probenecid and Sulfinpyrazone), water tablets (diuretics) and medicines for high blood pressure can be reduced. The use of anti-rheumatic drugs or methotrexate (which is taken, for example, for chronic polyarthritis; see also the section “When should aspirin not be used?”) may result in an increase in the undesirable effects. Aspirin can increase the risk of bleeding if you take cortisone preparations, alcohol or drugs from the group of so-called serotonin reuptake inhibitors for depression. If you take aspirin and antidiabetics (e.g. insulin, sulfonylureas) at the same time, the blood sugar level can drop. Even in small doses, acetylsalicylic acid reduces the excretion of uric acid. This can trigger gout in patients who already have low uric acid excretion. In conditions with an increased risk of bleeding (e.g. menstrual bleeding or injuries), caution is required, especially during and after surgical interventions (including minor interventions such as tooth extractions) there may be an increased tendency to bleed. Your doctor or dentist should be asked or informed about taking it before surgery. This medicinal product contains 16.5 mg aspartame per tablet. Aspartame is a source of phenylalanine. It can be harmful if you have phenylketonuria (PKU), a rare inherited disorder in which phenylalanine builds up because the body can't break it down enough. This medicinal product contains less than 1 mmol sodium (23 mg) per tablet, i.e. essentially 'sodium-free'. it is almost «sodium-free». This medicine contains the azo dye sunset yellow FCF (E110). E 110 can cause allergic reactions. This medicine contains fructose. Fructose can damage teeth. This medicine contains sulfur dioxide (E 220). In rare cases, E 220 can cause severe hypersensitivity reactions and bronchial spasms (bronchospasms). This medicinal product contains small amounts of ethanol (alcohol) in the flavour. The small amount of alcohol in this medicine has no noticeable effects. 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 taking aspirin and seek medical attention immediately, as these can be the first signs of a very serious skin reaction (see section What Aspirin can have side effects?» ). Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!).Can aspirin be taken/used while pregnant or breastfeeding?PregnancyYou should not take aspirin unless , it is clearly necessary and prescribed by a doctor. If taken during the first 6 months of pregnancy, the dose should be kept as low and the duration of treatment as short as possible. Taking nonsteroidal anti-inflammatory drugs (NSAIDs) after the 20th week of pregnancy may harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. If you are pregnant or planning to become pregnant, you should only take aspirin after consulting your doctor. Aspirin should not be taken during the last trimester of pregnancy. BreastfeedingAspirin should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use aspirin?Adults and adolescents aged 12 and over and heavier than 40 kg: 1-2 chewable tablets, if necessary every 4th day - Repeat for 8 hours. Up to a maximum of 6 chewable tablets daily. Chew the aspirin tablets in your mouth and swallow with or without water. It should not be taken on an empty stomach. Adolescents 12 years and older may only take aspirin with a doctor's prescription and only as a second-line drug. Children under the age of 12: Aspirin chewable tablets are not suitable for children under the age of 12 because of the high active ingredient content. In the event of uncontrolled intake (overdose), consult a doctor immediately. Ringing in the ears and/or sweating can be an indication of an overdose. Follow the dosage given in this 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 aspirin have?Very common (affects more than 1 in 10 people)Micro bleeding ( 70%). Common (affects 1 to 10 users in 100)Stomach disorders. Uncommon (affects 1 to 10 users in 1000)Asthma, shortness of breath, upper abdominal discomfort, nausea, vomiting, diarrhoea. Rare (affects 1 to 10 users in 10,000)Coagulation deficiency (lack of blood platelets), lack of white blood cells, lack of blood cells (aplastic anaemia), iron deficiency , increased risk of bleeding (e.g. gastrointestinal bleeding, bruising, nosebleeds, bleeding gums, bleeding in the urine and genital organs, bleeding during operations, bleeding in the brain). Hypersensitivity reactions, such as swelling of the skin and mucous membranes (e.g. blocked nose), skin rashes (Steven Johnson syndrome, toxic epidermal necrolysis), nettle fever, hay fever, spasms of the airways, Quincke's edema (facial swelling), drop in blood pressure. Stomach/intestinal ulcers. Dizziness, headache, tinnitus (ringing in the ears), hearing loss, visual disturbances, confusional states. Hypoglycaemia, disturbance of the acid-base balance. Liver dysfunction. Kidney dysfunction. Very rare (affects less than 1 in 10,000 people treated)Severe bleeding, which in isolated cases can be life-threatening, has also been reported very rarely. Elevated transaminases (liver values). Reye's syndrome (disease affecting the brain and liver in children). If signs of a hypersensitivity reaction occur, the drug should be discontinued and your doctor consulted. If the stool turns black or there is blood in the vomit during treatment, the drug should be discontinued and the doctor consulted immediately. Frequency not known (cannot be estimated from the available data)Changes in the intestinal wall, especially with long-term use, as well as anemia and acute kidney failure have been reported. Frequency not known: 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). If you get any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?Shelf lifeThe medicinal product may only be used up to the date marked on the container with « EXP» can be used. Storage instructionsStore at room temperature (15-25°C), protected from moisture and out of the reach of children. Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does aspirin contain?Active ingredients1 chewable tablet contains 500 mg acetylsalicylic acid ExcipientsMannitol (E 421), corn starch, calcium stearate, sunset yellow FCF (E110), heavy basic magnesium carbonate, pregelatinized starch, citric acid, ascorbic acid, carmellose sodium, sodium carbonate , Aromatics: orange, tangerine (contains ethanol), and dry flavor (contains fructose and sulfur dioxide (E220)), aspartame (E951). Approval number49526 (Swissmedic). Where can you get aspirin? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 10 and 20 chewable tablets. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Swissmedic) in February 2023. ..
27.69 USD
Aspirin instant tabl 500 mg 6 bags 2 pieces
Aspirin 500 contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and anti-inflammatory properties. Aspirin 500 effervescent tablets are used in adults and adolescents aged 12 and over and weighing more than 40 kg for the symptomatic treatment of acute headaches. Aspirin 500 effervescent tablets are suitable for short-term treatment, i. for a maximum of 3 days of treatment. Adolescents from the age of 12 only with a doctor's prescription and only as a second-line drug (see "When should you be careful when taking Aspirin 500?") Swissmedic-approved patient informationAspirin® 500, effervescent tabletsBayer (Schweiz) AGWhat is Aspirin 500 and when is it used?..
24.97 USD
Assan thermo cream tb 100 g
Assan thermo cream has anti-inflammatory and analgesic properties as well as circulation-enhancing and warming properties and accelerates the regression of swelling. Assan thermo cream does not smear or grease. Assan thermo cream is suitable as a supportive measure for the local treatment of rheumatic complaints of the musculoskeletal system, including muscular pain such as muscle tension, stiff neck and lumbago.T Swissmedic-approved patient informationAssan® thermo CremePermamed AGWhat is Assan thermo Creme and when is it used?Assan thermo cream has anti-inflammatory and pain-relieving properties as well as circulation-enhancing and warming properties and accelerates the regression of swelling. Assan thermo cream does not smear or grease. Assan thermo cream is suitable as a supportive measure for the local treatment of rheumatic complaints of the musculoskeletal system, including muscular pain such as muscle tension, stiff neck and lumbago.T When should Assan thermo cream not be used?Assan thermo cream should not be used if you are hypersensitive to any of the ingredients or to other pain-relieving and anti-inflammatory substances.Do not apply Assan thermo cream to the eyes, mucous membranes, open wounds or damaged skin.Assan thermo cream should not be combined with bathing therapies.With known heparin-induced/associated thrombocytopenia (HIT, lack of blood platelets caused by heparin) Assan thermo cream must not be used. When is caution required when using Assan thermo cream?Assan thermo cream should not be applied to large areas over a long period of time, unless expressly prescribed by a doctor. Tell your doctor, pharmacist or druggist if you have already used similar products (rheumatism ointments) and these have led to allergic reactionssuffer from other diseases,have allergies orothers Taking medicines (including those you bought yourself!) or using them externallyCan Assan thermo cream be used during pregnancy or while breastfeeding?Assan thermo cream should not be used during pregnancy or while breastfeeding, unless specifically prescribed by a doctor. How do you use Assan thermo cream?Adults:Unless otherwise prescribed by the doctor, Assan thermo cream Apply 2-3 times a day in a 5-10 cm long strand to the affected areas and the surrounding skin and massage in. The order center should be free of pharmaceuticals and cosmetics. Tell your doctor if symptoms worsen or have not improved after 2 weeks. Wash your hands thoroughly after rubbing in Assan thermo cream. Children:The use and safety of Assan thermo cream in children has not yet been tested. 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 Assan thermo cream have?In rare cases, skin irritations are possible due to the circulation-enhancing and warming properties. Rarely local allergic reactions. In these cases, treatment with Assan thermo cream should be discontinued. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Shelf lifeThe medicinal product may only be used up to the date marked on the container with « EXP» can be used. Storage instructionsStore Assan thermo cream at room temperature (15-25 °C). Do not ingest and keep out of the reach of children. Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Assan thermo cream contain?Active ingredients1 g of Assan thermo cream contains the following active ingredients: 35 mg flufenamic acid, 100 mg hydroxyethyl salicylate, 5 mg benzyl nicotinate, 300 IU heparin sodium ExcipientsGlyceryl stearate/PEG-100 stearate, isopropyl palmitate, dimeticone, PEG-2 stearate, PEG-20 methyl glucose sesquistearate, liquid paraffin, methyl glucose sesquistearate, rosemary oil , carbomer 980, pentadecalactone 10%, sodium edetate, caustic soda 30%, purified water. Approval number44615 (Swissmedic). Where can you get Assan thermo cream? What packs are available? Assan thermo Creme 50 g and 100 g is available in pharmacies and drugstores without a doctor's prescription. Authorization holderPermamed AG, 4143 Dornach. This leaflet was last checked by the drug authority (Swissmedic) in April 2019. ..
58.07 USD
Dermacalm d cream tb 20 g
Dermacalm-d is a cooling cream that has a local anti-inflammatory and anti-allergic effect on the skin damage listed below: Skin irritation or mild allergic reactions (with or without itching) caused by contact with detergents, cosmetics, plants, animals or metals (jewellery); Insect bites; Sunburn; Minor burns without open skin. Dermacalm-d has an anti-itching, anti-inflammatory and anti-allergic effect and supports the structure of the damaged skin. The properties of Dermacalm-d are due to hydrocortisone acetate, the most important ingredient in the cream. Hydrocortisone is a naturally occurring hormone in the human body that has an anti-inflammatory effect. If it is applied to the skin, it develops a predominantly local effect. Dermacalm-d also contains dexpanthenol, which is quickly converted into pantothenic acid, a vitamin, by the skin's cells. The pantothenic acid can promote healing of the skin. Swissmedic-approved patient informationDermacalm-d®, cream Bayer (Schweiz) AG What is Dermacalm-d and when is it used?Dermacalm-d is a cooling cream that has a local anti-inflammatory and anti-allergic effect on the skin damage listed below: Skin irritation or mild allergic reactions (with or without itching) caused by contact with detergents, cosmetics, plants, animals or metal (jewellery);Insect bites;Sunburn;Minor burns without open skin.Dermacalm-d has an anti-itching, anti-inflammatory and anti-allergic effect and supports the structure of the damaged skin. The properties of Dermacalm-d are due to hydrocortisone acetate, the most important ingredient in the cream. Hydrocortisone is a naturally occurring hormone in the human body that has an anti-inflammatory effect. If it is applied to the skin, it develops a predominantly local effect. Dermacalm-d also contains dexpanthenol, which is quickly converted into pantothenic acid, a vitamin, by the skin's cells. The pantothenic acid can promote healing of the skin. What do you need to know?To clean an inflamed or irritated area of skin, use only water as soap may make the irritation worse. Avoid all contact with the substance or material that caused the infection. When not to use Dermacalm-d?Do not use Dermacalm-d if you are allergic to any of its ingredients. Dermacalm-d must not come into contact with the eyes; avoid applying it to the eyelids as well. The cream should not be used if you suffer from fungal infections (e.g. athlete's foot), a viral infection (e.g. cold sores, shingles) or skin reactions following a vaccination; Likewise, application to open wounds and purulent inflammation (e.g. boils, abscesses, acne) should be avoided. When is caution required when using Dermacalm-d?Children under 2 years of age may only use Dermacalm-d under medical supervision. Dermacalm-d should not be applied to large areas of skin or under an impermeable bandage. The cream should not be used for a long time. If there is no improvement after two weeks, you should see a doctor. If symptoms worsen, you should stop treatment and consult your doctor. If your symptoms come back within 2 weeks of stopping treatment, do not use the cream again without consulting a doctor first, unless your doctor has instructed you to do so. If your symptoms return after they have disappeared, you should seek medical advice before repeating the treatment if the redness extends beyond the originally treated area and the skin burns. Inform your doctor, pharmacist or druggist if you suffer from any other illnesses,have allergies orother medicines ( also take bought ones) or use them externally!Can Dermacalm-d be used during pregnancy or while breastfeeding?If you are pregnant or want to become pregnant, you may only use Dermacalm-d after consulting your doctor. Dermacalm-d should not be used while breastfeeding. How do you use Dermacalm-d?Apply a thin layer of the cream 1-2 times a day and let it absorb by massaging it in gently. Unless otherwise prescribed by the doctor, a treatment with Dermacalm-d should be carried out for a maximum of 2 weeks and not over a large area. In children under the age of 2, Dermacalm-d may only be used under medical supervision. 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 Dermacalm-d have?Undesirable effects such as slight burning, itching or increased reddening of the skin can be signs of a hypersensitivity reaction to one or more components of the cream. Hydrocortisone can also cause skin dehydration. With long-term or too frequent use, the risk of the skin becoming increasingly brittle or other skin changes occurring cannot be ruled out. Withdrawal reaction after the end of treatment: After continuous use over a long period of time, a withdrawal reaction may occur after the end of treatment. You may experience one or more of the following symptoms: reddening of the skin that may extend beyond the treated area, burning or stinging sensation, severe itching, peeling skin, open blisters weeping. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Dermacalm-d is to be kept out of the reach of children and at room temperature (15-25 °C) to keep. The medicinal product may only be used up to the date marked “EXP” on the container. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Dermacalm-d contain?1 g cream contains the active ingredients hydrocortisone acetate (5 mg) and dexpanthenol (50 mg) as well as the following auxiliary substances: DL-pantolactone, Cetyl alcohol, paraffin, wool grease (E913), polyoxyl 40 stearate, chlorhexidine dihydrochloride (preservative), water. Approval number51464 (Swissmedic). Where can you get Dermacalm-d? What packs are available?In pharmacies and drugstores without a doctor's prescription. Tubes of 20 g. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Swissmedic) in December 2021. ..
32.90 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
Dolobene gel 50g
What is Dolobene Gel and when is it used? Dolobene Gel is a combination of active ingredients with the following properties: Heparin counteracts blood clotting and improves the regression of bruises. Dexpanthenol protects and cares for the skin. Dimethyl sulfoxide (DMSO) increases the absorption of other substances by the skin and has an anti-inflammatory and pain-relieving effect. Dolobene Gel used for complaints related to venous leg disorders such as pain and swelling; with blunt (not open) sports injuries and accidents such as bruises, bruises, contusions, strains, sprains and pain in the muscles, tendons, ligaments and joints.On medical prescription, this preparation is also used against superficial inflammation in venous leg disorders, tennis elbow, tendinitis, tendonitis, bursitis and stiff arms and shoulders.What should be considered?Follow the advice of your doctor that goes beyond the actual dosage recommendations, e.g. gymnastics or wearing support stockings.When must Dolobene Gel not be used?Dolobene must not be used in the case of DMSO and/or heparin hypersensitivity, asthmatics, pregnant women, breastfeeding women, children and adolescents, severe liver and/or kidney dysfunction, circulatory weaknesses and lupus ery thematodes, an autoimmune disease of the vascular system.When is caution required when using Dolobene Gel?Immediately before and after applying Dolobene Gel, no other medicines and agents should be applied to the affected area of the skin.Dolobene Gel must not be applied to open wounds, previously damaged skin or mucous membranes. Massage should not be used in the case of venous diseases that can be traced back to the presence of a blood clot (so-called thromboembolism). If symptoms persist or worsen, consult a doctor. Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking or using other medicines (including those you bought yourself!) or use them externally. Can Dolobene Gel be used during pregnancy or breastfeeding? If you are pregnant, it or if you are breastfeeding, you should avoid taking medicines as a precaution or ask your doctor, pharmacist or druggist for advice. Since at least one of the active substances contained in Dolobene crosses the placenta, you should not use the preparation during pregnancy or while breastfeeding. How do you use Dolobene Gel? Adults The gel Apply 1-2 times a day to the affected area. Dolobene gel should not be massaged in, but only applied lightly and then distributed. Using under bandages: After application, do not cover with airtight bandages. When used under air-permeable bandages, you should apply the gel as thick as a knife back and allow it to soak in before applying the bandage. Observe the dosage given in the package insert or 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 Dolobene Gel have?The following side effects can occur when using Dolobene Gel:DMSO can in rare cases lead to allergic skin symptoms such as reddening of the skin, itching and burningn lead. These symptoms can also be caused by the vasodilating effect of DMSO and generally disappear during further treatment.After using Dolobene Gel, a temporary garlic-like bad breath can occasionally occur. This odor is due to dimethyl sulphide (DMS), a metabolite of DMSO. A change in taste perception disappears again after a few minutes. Stomach and intestine complaints such as nausea, vomiting, diarrhea or constipation can occur. In individual cases, allergic reactions with itching, wheal formation (nettle rash) and sometimes asymmetrical swelling on the face, skin and mucous membranes can occur. In these cases, a doctor must be consulted immediately.If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container.Do not store above 25°C. Don't ingest. Do not freeze or store in the refrigerator. Keep out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information. What does Dolobene Gel contain? 1 g of gel contains: Active ingredients: heparin sodium 500 IU, dimethyl sulfoxide (DMSO) 150 mg, dexpanthenol 25 mg. Excipients: propylene glycol, aromatics and other excipients. Approval number..
17.86 USD
Elixan eucalyptus 80/85 oil 10 ml
Characteristics of Elixan Eucalyptus oil 80/85 10 mlStorage temp min/max 15/25 degrees CelsiusAmount in pack : 1 mlWeight: 49g Length: 36mm Width: 36mm Height: 77mm Buy Elixan Eucalyptus oil 80/85 10 ml online from Switzerland..
16.72 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
Ichtholan ointment 10% tb 40 g
Ichtholan Zugsalbe contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, anti-inflammatory and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseases ICHTHOLAN 20% ointment for deeper inflammatory skin diseases, such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands. ICHTHOLAN 50% Ointment for the maturation of boils Swissmedic-approved patient information ICHTHOLAN® 10%, 20%, 50% traction ointmentMerz Pharma (Switzerland) AGWhat is Ichtholan 10%, 20%, 50% traction ointment and when is it used? Ichtholan traction ointment contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, anti-inflammatory and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseasesICHTHOLAN 20% ointment for deeper inflammatory skin diseases such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands.ICHTHOLAN 50% Pulling ointment for the maturation of boilsWhen may Ichtholan 10 %, 20%, 50% traction ointment not to be used? Known hypersensitivity to Ichthammolum (ammonium bituminosulfonate), or one of the excipients according to the composition. The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. When is caution required when using Ichtholan 10%, 20%, 50% traction ointment?In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation is passed on by smear infection and eventually a hard-to-control furunculosis (the recurrence of boils) develops. Careful bandaging technique is therefore necessary (see «How do you use Ichtholan Zugsalbe?»). If a local deterioration occurs or if there is no healing within 2-3 weeks, a doctor or pharmacist should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. During treatment with Ichtholan traction ointment in the genital and anal area, the fats and emulsifiers contained as auxiliary substances and the simultaneous use of latex condoms can lead to a reduction in the tear strength and thus to an impairment of the safety of the condoms. The use of other ointments or creams can impair the effect of Ichtholan Zugsalbe. Ichtholan can increase the solubility of other active ingredients and thus enhance their absorption into the skin. Ichtholan contains butylated hydroxytoluene and wool wax, which can cause localized skin reactions (e.g. contact dermatitis). Butylated hydroxytoluene can also cause irritation to the eyes and mucous membranes. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Ichtholan 10%, 20%, 50% traction ointment be used during pregnancy or breastfeeding?PregnancyThere are insufficient data for the use of Ichtholan Zugsalbe during pregnancy. If you are pregnant or would like to become pregnant, only use Ichtholan Zugsalbe on the prescription of your doctor. A large area application during pregnancy will Generally discouraged. BreastfeedingIt is not known whether the active ingredient in Ichtholan is excreted in human milk. Breastfeeding women should only use Ichtholan Zugsalbe if prescribed by their doctor. Ichtholan traction ointment should not be used on the breasts while breastfeeding. How do you use Ichtholan 10%, 20%, 50% Draw Balm?Ichtholan 10% Draw BalmIf unless otherwise prescribed by the doctor, Ichtholan 10% Zugsalbe is applied thinly to the inflamed skin regions once a day and distributed well. The treatment can be carried out until the inflammation of the skin has subsided. Ichtholan 20% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 20% traction ointment is applied thickly to the skin regions to be treated and covered over a large area with a bandage . For this purpose, a cotton swab can be placed on the applied ointment, for example, and this can be covered over a large area with a plaster. The dressing is changed daily. Every time the bandage is changed, the ointment residues on the skin must be washed off with warm water and soap before you start treating again with Ichtholan 20% Zugointment. The duration of treatment depends on the response. ICHTHOLAN 50% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 50% traction ointment is applied to the skin region to be treated as thick as a knife back and covered over a large area with a bandage . The bandage should be changed after 3 days at the latest. The duration of use depends on the success of the treatment. Whenever the bandage is changed, the ointment residue should be washed off with lukewarm water and soap before treating again with 50% Zugointment. In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation will be passed on by smear infection and furunculosis (the repeated occurrence of boils) may develop that is difficult to influence. Therefore, a careful bandaging technique is necessary: Meticulous cleanliness, cleaning and disinfection of the surrounding healthy skinPut on a well-covering, non-slipping and non-abrasive bandagePossibly bathing with disinfectant additives.The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. 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 Ichtholan 10%, 20%, 50% Zugointment have?The following side effects can occur when using Ichtholan Zugointment: Rarely (affects 1 to 10 users in 10,000)Intolerance reactions of the skin that manifest themselves as itching, burning or reddening of the skin; allergic skin reactions (contact dermatitis). Very rare (affects less than 1 in 10,000 people)severe skin reactions, e.g. blistering (under an airtight bandage). If these symptoms occur, a doctor should be consulted. If you get any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Tubes should be closed well after opening. Any ointment stains can be easily removed from the laundry by first using an organic solvent (e.g. petrol) and then washing with a detergent. Storage instructionsMedicines should be kept out of the reach of children. Store at room temperature (15-25 °C) and dry. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Ichtholan 10%, 20%, 50% Zugsalve contain?Active ingredients10% and 20%: 1 g ointment contains: Ichthammolum (ammonium bituminosulfonate) 100 mg/200 mg. 50%: 1 g of ointment contains: Ichthammolum (ammonium bituminosulfonate) 500 mg. Excipients10%: wool wax, butylated hydroxytoluene (E321), yellow vaseline, purified water. 20%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, purified water. 50%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, microcrystalline wax, purified water. Approval number10751 (Swissmedic) Where can you get Ichtholan 10%, 20%, 50% Zugsalve? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Tubes of 40g ointment. Authorization holderMerz Pharma (Switzerland) AG, 4123 Allschwil ManufacturerIchthyol-Gesellschaft Cordes, Hermanni & Co. (GmbH & Co.) KG, Hamburg, Germany This leaflet was last checked by the drug authority (Swissmedic) in April 2019. ..
54.68 USD
Ichtholan ointment 20% tb 40 g
Ichtholan Zugsalbe contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, anti-inflammatory and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseases ICHTHOLAN 20% ointment for deeper inflammatory skin diseases, such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands. ICHTHOLAN 50% Ointment for the maturation of boils Swissmedic-approved patient information ICHTHOLAN® 10%, 20%, 50% traction ointmentMerz Pharma (Switzerland) AGWhat is Ichtholan 10%, 20%, 50% traction ointment and when is it used? Ichtholan traction ointment contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, anti-inflammatory and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseasesICHTHOLAN 20% ointment for deeper inflammatory skin diseases such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands.ICHTHOLAN 50% Pulling ointment for the maturation of boilsWhen may Ichtholan 10 %, 20%, 50% traction ointment not to be used? Known hypersensitivity to Ichthammolum (ammonium bituminosulfonate), or one of the excipients according to the composition. The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. When is caution required when using Ichtholan 10%, 20%, 50% traction ointment?In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation is passed on by smear infection and eventually a hard-to-control furunculosis (the recurrence of boils) develops. Careful bandaging technique is therefore necessary (see «How do you use Ichtholan Zugsalbe?»). If a local deterioration occurs or if there is no healing within 2-3 weeks, a doctor or pharmacist should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. During treatment with Ichtholan traction ointment in the genital and anal area, the fats and emulsifiers contained as auxiliary substances and the simultaneous use of latex condoms can lead to a reduction in the tear strength and thus to an impairment of the safety of the condoms. The use of other ointments or creams can impair the effect of Ichtholan Zugsalbe. Ichtholan can increase the solubility of other active ingredients and thus enhance their absorption into the skin. Ichtholan contains butylated hydroxytoluene and wool wax, which can cause localized skin reactions (e.g. contact dermatitis). Butylated hydroxytoluene can also cause irritation to the eyes and mucous membranes. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Ichtholan 10%, 20%, 50% traction ointment be used during pregnancy or breastfeeding?PregnancyThere are insufficient data for the use of Ichtholan Zugsalbe during pregnancy. If you are pregnant or would like to become pregnant, only use Ichtholan Zugsalbe on the prescription of your doctor. A large area application during pregnancy will Generally discouraged. BreastfeedingIt is not known whether the active ingredient in Ichtholan is excreted in human milk. Breastfeeding women should only use Ichtholan Zugsalbe if prescribed by their doctor. Ichtholan traction ointment should not be used on the breasts while breastfeeding. How do you use Ichtholan 10%, 20%, 50% Draw Balm?Ichtholan 10% Draw BalmIf unless otherwise prescribed by the doctor, Ichtholan 10% Zugsalbe is applied thinly to the inflamed skin regions once a day and distributed well. The treatment can be carried out until the inflammation of the skin has subsided. Ichtholan 20% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 20% traction ointment is applied thickly to the skin regions to be treated and covered over a large area with a bandage . For this purpose, a cotton swab can be placed on the applied ointment, for example, and this can be covered over a large area with a plaster. The dressing is changed daily. Every time the bandage is changed, the ointment residues on the skin must be washed off with warm water and soap before you start treating again with Ichtholan 20% Zugointment. The duration of treatment depends on the response. ICHTHOLAN 50% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 50% traction ointment is applied to the skin region to be treated as thick as a knife back and covered over a large area with a bandage . The bandage should be changed after 3 days at the latest. The duration of use depends on the success of the treatment. Whenever the bandage is changed, the ointment residue should be washed off with lukewarm water and soap before treating again with 50% Zugointment. In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation will be passed on by smear infection and furunculosis (the repeated occurrence of boils) may develop that is difficult to influence. Therefore, a careful bandaging technique is necessary: Meticulous cleanliness, cleaning and disinfection of the surrounding healthy skinPut on a well-covering, non-slipping and non-abrasive bandagePossibly bathing with disinfectant additives.The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. 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 Ichtholan 10%, 20%, 50% Zugointment have?The following side effects can occur when using Ichtholan Zugointment: Rarely (affects 1 to 10 users in 10,000)Intolerance reactions of the skin that manifest themselves as itching, burning or reddening of the skin; allergic skin reactions (contact dermatitis). Very rare (affects less than 1 in 10,000 people)severe skin reactions, e.g. blistering (under an airtight bandage). If these symptoms occur, a doctor should be consulted. If you get any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Tubes should be closed well after opening. Any ointment stains can be easily removed from the laundry by first using an organic solvent (e.g. petrol) and then washing with a detergent. Storage instructionsMedicines should be kept out of the reach of children. Store at room temperature (15-25 °C) and dry. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Ichtholan 10%, 20%, 50% Zugsalve contain?Active ingredients10% and 20%: 1 g ointment contains: Ichthammolum (ammonium bituminosulfonate) 100 mg/200 mg. 50%: 1 g of ointment contains: Ichthammolum (ammonium bituminosulfonate) 500 mg. Excipients10%: wool wax, butylated hydroxytoluene (E321), yellow vaseline, purified water. 20%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, purified water. 50%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, microcrystalline wax, purified water. Approval number10751 (Swissmedic) Where can you get Ichtholan 10%, 20%, 50% Zugsalve? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Tubes of 40g ointment. Authorization holderMerz Pharma (Switzerland) AG, 4123 Allschwil ManufacturerIchthyol-Gesellschaft Cordes, Hermanni & Co. (GmbH & Co.) KG, Hamburg, Germany This leaflet was last checked by the drug authority (Swissmedic) in April 2019. ..
58.75 USD
Kytta ointment 100 g
Herbal medicineWhat is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (common comfrey) using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment is non-greasy and non-lubricating and is therefore easy to wash off. Kytta ointment is used externally to support the treatment of degenerative-rheumatoid diseases (e.g. knee arthritis), muscle, joint and nerve pain, and blunt, bloodless injuries such as bruises, strains and sprains. It is also used for tendonitis and, if the doctor recommends it, for the aftercare of bone fractures and dislocations.When should Kytta ointment not be used or should it only be used with caution?Kytta ointment must not be used in case of known hypersensitivity to any of the ingredients (see composition) or in children under 3 years of age.Do not use if you are prone to allergies. Kytta ointment must not be used on open wounds or mucous membranes. The eye, nose and mouth areas should be excluded from treatment with Kytta ointment.Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking or using other medicines externally (including those you have bought yourself)!Can Kytta ointment be used during pregnancy or while breastfeeding?Based on experience to date, there is no known risk to the child when used as directed. However, systematic scientific studies have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, pharmacist or druggist for advice.How do you use Kytta ointment?Unless otherwise prescribed by the doctor, apply Kytta ointment thinly up to 5 times a day and massage in carefully. (In severe cases, apply an ointment dressing.) In children between 3 and 12 years of age, the treatment period should not exceed one week.Follow the dosage instructions 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 Kytta ointment have?Rarely, allergic local skin reactions (itching of the skin, reddening of the skin, contact dermatitis, eczema, burning of the skin). Very rarely, systemic hypersensitivity reactions, e.g. generalized skin reactions.In such cases, treatment should be stopped and a doctor should be consulted.If you notice any side effects not listed here, you should inform your doctor or pharmacist.What should also be noted?This medicine should only be used until the date stated on the container with “EXP”.Keep Kytta ointment out of the reach of children. Store at room temperature (15–25 °C). Shelf life after opening: 12 months.Your doctor, pharmacist or druggist will be able to provide you with further information.What is contained in Kytta ointment?1 g of ointment contains: 350 mg liquid comfrey extract from fresh roots, drug-extract ratio 1:2, extraction agent: ethanol 52% (m/m). This preparation also contains excipients and flavourings, vanillin, lauryl sulphate, the preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol.Registration number20713 (Swissmedic).Where can you get Kytta ointment? What packages are available?In pharmacies and drugstores, without medical prescription.Packs of 50 g, 100 g and 150 g.Marketing Authorisation HolderProcter & Gamble International Operations SA, Lancy.Domicile: 1213 Petit-LancyManufacturerP&G Health Austria GmbH & Co. OG, Spittal, Austria. ..
68.09 USD
Kytta ointment 50 g
Herbal medicineWhat is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (common comfrey) using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment is non-greasy and non-lubricating and is therefore easy to wash off. Kytta ointment is used externally to support the treatment of degenerative-rheumatoid diseases (e.g. knee arthritis), muscle, joint and nerve pain, and blunt, bloodless injuries such as bruises, strains and sprains. It is also used for tendonitis and, if the doctor recommends it, for the aftercare of bone fractures and dislocations.When should Kytta ointment not be used or should it only be used with caution?Kytta ointment must not be used in case of known hypersensitivity to any of the ingredients (see composition) or in children under 3 years of age.Do not use if you are prone to allergies. Kytta ointment must not be used on open wounds or mucous membranes. The eye, nose and mouth areas should be excluded from treatment with Kytta ointment.Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking or using other medicines externally (including those you have bought yourself)!Can Kytta ointment be used during pregnancy or while breastfeeding?Based on experience to date, there is no known risk to the child when used as directed. However, systematic scientific studies have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, pharmacist or druggist for advice.How do you use Kytta ointment?Unless otherwise prescribed by the doctor, apply Kytta ointment thinly up to 5 times a day and massage in carefully. (In severe cases, apply an ointment dressing.) In children between 3 and 12 years of age, the treatment period should not exceed one week.Follow the dosage instructions 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 Kytta ointment have?Rarely, allergic local skin reactions (itching of the skin, reddening of the skin, contact dermatitis, eczema, burning of the skin). Very rarely, systemic hypersensitivity reactions, e.g. generalized skin reactions.In such cases, treatment should be stopped and a doctor should be consulted.If you notice any side effects not listed here, you should inform your doctor or pharmacist.What should also be noted?This medicine should only be used until the date stated on the container with “EXP”.Keep Kytta ointment out of the reach of children. Store at room temperature (15–25 °C). Shelf life after opening: 12 months.Your doctor, pharmacist or druggist will be able to provide you with further information.What is contained in Kytta ointment?1 g of ointment contains: 350 mg liquid comfrey extract from fresh roots, drug-extract ratio 1:2, extraction agent: ethanol 52% (m/m). This preparation also contains excipients and flavourings, vanillin, lauryl sulphate, the preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol.Registration number20713 (Swissmedic).Where can you get Kytta ointment? What packages are available?In pharmacies and drugstores, without medical prescription.Packs of 50 g, 100 g and 150 g.Marketing Authorisation HolderProcter & Gamble International Operations SA, Lancy.Domicile: 1213 Petit-LancyManufacturerP&G Health Austria GmbH & Co. OG, Spittal, Austria. ..
42.77 USD
Naturkraftwerke aloe vera tube gel 120 ml
Naturkraftwerke Aloe Vera Gel 99% 120 ml Naturkraftwerke Aloe Vera Gel is a natural and pure product that is perfect for all skin types. Made with 99% pure Aloe Vera extract, this gel moisturizes and nourishes the skin from within, leaving it soft, supple, and healthy-looking. The Aloe Vera plant is known for its healing properties and has been used for centuries to treat various skin issues such as burns, scars, and dryness. This non-greasy formula gets easily absorbed into the skin and provides instant relief from itching and redness. It soothes and calms irritated skin with its anti-inflammatory and antibacterial properties. Naturkraftwerke Aloe Vera Gel restores the skin's natural balance and helps in reducing fine lines, wrinkles, and pigmentation. This gel is also suitable for sensitive skin types and can be used as a daily moisturizer. Key Features: 99% pure Aloe Vera gel Non-greasy formula Moisturizes and nourishes the skin Relieves itching and redness Restores the skin's natural balance Directions for Use: Apply Naturkraftwerke Aloe Vera Gel onto clean skin and massage gently until it gets absorbed. Use it as a daily moisturizer or whenever required. Store the gel in a cool and dry place, away from direct sunlight. ..
27.94 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
Repair gel 100g
Reparil N Gel is an alcoholic drug with a decongestant, anti-inflammatory and analgesic effect. The active ingredient aescin reduces accumulations of water in the tissue and causes the tissue to decongest. The salicylic acid compound has analgesic and anti-inflammatory effects. Reparil N Gel is suitable for the local treatment of inflammation, pain, bruising and swelling, e.g. as a result of sprains, bruises and strains. Swissmedic-approved patient informationReparil® N GelMEDA Pharma GmbHWhat is Reparil N Gel and when is it used?Reparil N Gel is an alcohol-based drug with a decongestant, anti-inflammatory and analgesic effect. The active ingredient aescin reduces accumulations of water in the tissue and causes the tissue to decongest. The salicylic acid compound has analgesic and anti-inflammatory effects. Reparil N Gel is suitable for the local treatment of inflammation, pain, bruising and swelling, e.g. as a result of sprains, bruises and strains. When must Reparil N Gel not be used?Reparil N Gel must not be used In the event of hypersensitivity to one of the active ingredients or excipients or in the event of hypersensitivity to other pain-relieving and anti-inflammatory substances, in particular acetylsalicylic acid/aspirin,open injuries, inflammation or infections of the skin and eczema or on mucous membranes and on radiation-treated skin areas,in infants and small children under the age of 2 years.When is Reparil N Gel used Caution required?Reparil N Gel should not be applied to open areas of skin. Avoid contact with eyes. Before applying a bandage, Reparil N Gel should dry on the skin for a few minutes. The use of an occlusive dressing is not recommended. Special care is required when using Reparil N Gelif you suffer from asthma, hay fever, swelling of the nasal mucosa (so-called nasal polyps) or chronic obstructive pulmonary diseases or chronic respiratory infections (especially combined with hay fever-like symptoms)if you are hypersensitive (allergic) to pain and and rheumatism drugs of all kinds, you are more at risk of asthma attacks (analgesic intolerance/analgesic asthma), local swelling of the skin and mucous membranes (Quincke's edema) or urticaria than other patients;if you are taking other substances hypersensitive (allergic) reactions, e.g. with skin reactions, itching or hives;in acute conditions that are accompanied by severe redness, swelling or overheating of the joints, in the case of persistent or worsening symptoms. In this case, you should consult a doctor.Veneitis caused by a blood clot (thrombosis) should not be massaged. Reparil N Gel should not be used on large areas over a long period of time, unless prescribed by a doctor. Since the salicylic acid compound contained in the drug penetrates the skin to a considerable extent and can lead to undesirable effects, caution is advised in patients with kidney dysfunction and in children. Long-term treatment over large areas should be avoided in such patients. Furthermore, it cannot be ruled out that if the gel is applied to large areas and if blood-thinning medication or medication to treat high blood sugar is taken at the same time, their effect will be increased. The undesirable effects of methotrexate can be increased. Inform your doctor, pharmacist or druggist if you have used similar products in the past and these led to allergic reactions and if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Reparil N Gel be used during pregnancy or breastfeeding?Reparil N Gel must not be used during pregnancy and breastfeeding unless expressly prescribed by a doctor. Then it should only be used for a short time and not over a large area, and it should not be used in the breast area during breastfeeding. How do you use Reparil N Gel?AdultsUnless otherwise directed, once or several times a day apply and spread over the skin over the diseased area. It is not necessary to massage in the gel, but it is possible if desired. Wash hands after use. Tell your doctor if the symptoms worsen or if the symptoms have not improved after 2 weeks. Children and adolescentsThe use and safety of Reparil N Gel in children and adolescents has not yet been tested. 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 Reparil N Gel have?The following side effects can occur when using Reparil N Gel: Frequency not known (cannot be estimated from the available data)allergic skin reactions (e.g. dry skin, skin redness, dermatitis, itching, hives, exfoliation of the skin) ; Hypersensitivity reactions (e.g. non-specific allergic reactions up to anaphylactic reactions; reactions of the respiratory tract, such as bronchospasm or shortness of breath; hypersensitivity reactions of the skin). If such symptoms occur, treatment should be discontinued. If you get any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Storage instructionsKeep out of the reach of children. Store at room temperature (15-25°C). Keep container tightly closed. Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Reparil N Gel contain?100 g of gel contain:Active ingredientsAescin 1.0 g Diethylamine Salicylate 5.0 g Excipientspurified water, sodium edetate, carbomers, macrogol-6-glycerol-caprylocaprate, trometamol, 2-propanol, lavender oil, bitter orange blossom oil. Approval number51830 (Swissmedic) Where can you get Reparil N Gel? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 40g and 100g gel. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen This leaflet was last checked by the Medicines Agency (Swissmedic) in July 2021. [REPA_nG_201D] ..
31.24 USD
Sidroga chamomile blossoms 20 bags 1.5 g
Sidroga chamomile flowers: For gastrointestinal complaints and for the local treatment of inflammation. Swissmedic-approved patient information Sidroga® chamomile blossom tea Sidroga AGHerbal medicinal product What is Sidroga chamomile blossom tea and when is it used? Sidroga chamomile blossom tea contains dried chamomile blossoms and finely chopped quality (tested according to the pharmacopoeia). Anti-inflammatory and antispasmodic properties are traditionally attributed to chamomile flowers. Sidroga chamomile blossom tea is used for gastrointestinal complaints, indigestion such as flatulence, acid reflux and a feeling of fullness, but can also be used for the local treatment of inflammation and abrasions as a bath, gargle and rinsing solution. What should be considered? In the case of persistent severe gastrointestinal complaints and inflammation or abrasions that do not heal, it is advisable to consult a doctor and have the to clarify the reasons for this. Stomach pain that manifests itself as pain or pressure pain in a specific area or is associated with a general feeling of illness requires a medical evaluation. Remember that certain stimulants such as coffee, alcohol, nicotine as well as certain medications such as painkillers and rheumatism drugs can cause stomach problems. When should Sidroga chamomile blossom tea not be taken/used or only with caution? Sidroga chamomile blossom tea should not be taken/used if there is a known hypersensitivity to plants of the daisy family (Composites). Tell your doctor, pharmacist or druggist if you have suffer from other illnesseshave allergies ortake other medicines (including those you bought yourself!) or use them externally. Can Sidroga chamomile blossom tea be taken/used during pregnancy or while breastfeeding? Based on previous experience, there is no known risk for the child when used as intended. However, systematic scientific investigations have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding or ask your doctor, pharmacist or druggist for advice. How do you use Sidroga Chamomile Blossom Tea? For digestive problems take adults, school children and small children from 6 months 1 cup 3 to 4 times a day between meals. In case of inflammation of the mucous membrane (mouth/throat), gargle or rinse with the freshly prepared tea several times a day. In the case of skin irritation (grazes, small wounds), bathe or dab the affected parts of the body with the freshly prepared tea several times a day. Preparation: Pour boiling water over one or two tea bags per cup and let the bags steep for 5 to 10 minutes. Then take out the tea bags and squeeze them out lightly over the cup. 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 Sidroga chamomile blossom tea have? The following side effects can occur when taking or using Sidroga chamomile blossom tea: rarely allergic skin reactions (skin itching, reddening of the skin, rash). If these symptoms occur, a doctor should be consulted if necessary. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered? Sidroga chamomile blossom tea is to be stored at room temperature (15-25 °C), protected from light, in a dry place and out of the reach of to keep for children. The double-chamber bags in aroma protection packaging may only be used up to the date marked «EXP» on the container. Your doctor, pharmacist or druggist can provide you with further information. What does Sidroga chamomile blossom tea contain? 1 double chamber bag contains 1.5 g of dried and finely chopped chamomile blossoms. Approval number 41673 (Swissmedic) Where can you get Sidroga chamomile blossom tea? What packs are available? This is an over-the-counter medicine. Boxes of 20 double chamber bags in aroma protection packaging. Authorization holder Sidroga AG, 4310 Rheinfelden This leaflet was last checked by the drug authority (Swissmedic) in September 2010. ..
9.26 USD
Traumeel ointment tb 50 g
TRAUMEEL ointment Tb 50 g - Product Description TRAUMEEL ointment Tb 50 g Looking for an effective ointment to alleviate pain and inflammation? TRAUMEEL ointment is here! Made with natural ingredients, this ointment is a reliable remedy for all kinds of pain, injuries, and swelling. It is a homeopathic medicine that is safe and gentle on the skin yet highly potent in providing quick relief. TRUAMEEL ointment is a must-have in everyone's medicine kit! Features: Contains natural ingredients, no synthetic compounds Used for treating a wide range of conditions Safe and suitable for adults and children Relieves pain, inflammation, and swelling effectively Non-greasy and easily absorbable Benefits: Quick and effective relief from pain and inflammation Promotes natural healing without harmful side-effects Soothes sore muscles and joints, reduces swelling and stiffness Can be used for sports injuries, sprains, bruises, strains, and many other conditions Provides a cooling sensation and an overall sense of relaxation Directions for Use: Apply a small amount of TRAUMEEL ointment to the affected area and gently massage until absorbed. Repeat 3 to 4 times daily or as directed by a healthcare professional. For external use only, avoid contact with eyes and open wounds. Precautions: Keep away from children Store in a cool and dry place Do not use if you are allergic to any of the ingredients Consult a healthcare professional if symptoms persist or worsen Ingredients: TRAUMEEL ointment contains a unique blend of natural compounds known for their anti-inflammatory, analgesic, and healing properties. The active ingredients include: Arnica montana, Calendula officinalis, Bellis perennis, and many others. For a full list, please refer to the package insert. Package: TRAUMEEL ointment is available in 50g tubes and comes in a convenient and hygienic packaging. ..
35.29 USD
Voltaren dolo emulgel tb 180g
Voltaren Dolo Emulgel contains the active substance diclofenac, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (medicines used to relieve pain and inflammation). Voltaren Dolo Emulgel has analgesic and anti-inflammatory properties and, thanks to the water-alcoholic base, has a soothing, cooling effect. Voltaren Dolo Emulgel is used for the local treatment of pain, inflammation and swelling in sports and accident injuries such as sprains, bruises and strains as well as back pain caused by sports and accidents. Voltaren Dolo Emulgel can also be used for the short-term local treatment of acute pain in osteoarthritis of small and medium-sized joints that are close to the skin, such as finger joints or knees. Voltaren Dolo Emulgel is intended for use in adults and adolescents from 12 years of age. Swissmedic-approved patient informationVoltaren Dolo, Emulgel GSK Consumer Healthcare Schweiz AGWhat is Voltaren Dolo Emulgel and when is it used? Voltaren Dolo Emulgel contains the active substance diclofenac, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (medicines that relieve pain and inflammation). Voltaren Dolo Emulgel has analgesic and anti-inflammatory properties and, thanks to the water-alcoholic base, has a soothing, cooling effect. Voltaren Dolo Emulgel is used for the local treatment of pain, inflammation and swelling in sports and accident injuries such as sprains, bruises and strains as well as back pain caused by sports and accidents. Voltaren Dolo Emulgel can also be used for the short-term local treatment of acute pain in osteoarthritis of small and medium-sized joints that are close to the skin, such as finger joints or knees. Voltaren Dolo Emulgel is intended for use in adults and adolescents from 12 years of age. When should Voltaren Dolo Emulgel not be used?Voltaren Dolo Emulgel should not be used if there is a known hypersensitivity to the active ingredient diclofenac or other pain-relieving, anti-inflammatory and antipyretic substances ( especially acetylsalicylic acid/aspirin and ibuprofen) and hypersensitivity to one of the excipients (e.g. propylene glycol, isopropyl alcohol; for a full list of excipients see the section “What does Voltaren Dolo Emulgel contain?”). Such hypersensitivity is manifested, for example, by wheezing or shortness of breath (asthma), breathing difficulties, skin rash with blistering, hives, swelling of the face and tongue, runny nose. Voltaren Dolo Emulgel must not be used during the last 3 months of pregnancy (see also «Can Voltaren Dolo Emulgel be used during pregnancy or while breastfeeding?»). When is caution required when using Voltaren Dolo Emulgel?Voltaren Dolo Emulgel must not be applied to open skin wounds (e.g. after abrasions, cuts) or to damaged skin skin (e.g. eczema, skin rashes).Stop treatment immediately if a skin rash occurs after using the product.Voltaren Dolo Emulgel should not be applied to large areas over a long period of time unless prescribed by a doctor.Eyes and mucous membranes should not come into contact with the preparation. If this does happen, rinse your eyes thoroughly with tap water and inform your doctor if the symptoms persist. Do not take the medicine. Wash hands after use, except when treating the finger joints (see also «How do you use Voltaren Dolo Emulgel?»).Voltaren Dolo Emulgel must not be used with an airtight bandage (occlusive bandage).Information on the excipientsVoltaren Dolo Emulgel contains propylene glycol (E 1520) and benzyl benzoate: Propylene Glycol may cause skin irritation. Benzyl benzoate may cause local irritation. Voltaren Dolo Emulgel contains thick paraffin. Materials (clothing, bedding, bandages, etc.) that have come into contact with the preparation are more flammable and pose a fire hazard with the risk of severe burns. Do not smoke or go near open flames during use become. Even washing clothes and bedding does not completely remove paraffin. This medicine contains a fragrance with linalool, benzyl alcohol, geraniol, citronellol, benzyl benzoate, coumarin, citral, eugenol. These ingredients can cause allergic reactions. Inform your doctor, pharmacist or druggist if you have previously had allergic symptoms after using similar preparations ("rheumatism ointments") if you suffer from other diseases,have allergies oruse other medicines (including those you bought yourself!). Can Voltaren Dolo Emulgel be used during pregnancy or while breastfeeding?Voltaren Dolo Emulgel must not be used during the 1st and 2nd trimester of pregnancy or while breastfeeding, es unless expressly prescribed by a doctor. Voltaren Dolo Emulgel must not be used during the last 3 months of pregnancy as it may harm the unborn baby or cause problems during delivery. If you are planning to become pregnant, you should ask your doctor, pharmacist or druggist for advice before use. How do you use Voltaren Dolo Emulgel?The preparation is for external use only. Adults and adolescents from the age of 12Depending on the size of the painful or swollen areas or areas to be treated, an amount of 2-4 g Voltaren Dolo Emulgel (amount the size of a cherry to a walnut) applied, rubbed in lightly or massaged in for muscle pain. After use:Wipe hands with a dry paper towel, then wash hands well, except when treating fingers. Dispose of the paper towel with the household waste.Before showering or bathing, you should wait until the emulgel has dried on the skin.You should consider a treatment with Voltaren Dolo If you forget to use Emulgel, make up for it as soon as possible. Do not apply double the amount to make up for the forgotten treatment. Tell your doctor if your symptoms get worse or if your symptoms have not improved after a week. Voltaren Dolo Emulgel should not be used for longer than 2 weeks without a doctor's prescription. Use the preparation for the shortest time necessary, applying no more than necessary. Instructions for use of Voltaren Dolo Emulgel with applicator: see at the end of the patient information. Children under the age of 12The use and safety of Voltaren Dolo Emulgel in children under the age of 12 has not yet been systematically tested. Its use is therefore not recommended. If you or your child swallow Voltaren Dolo Emulgel (accidentally), contact your doctor immediately. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Voltaren Dolo Emulgel have?The following side effects can occur when using Voltaren Dolo Emulgel: Some rare or very rare side effects can be serious. If any of the following side effects occur, stop treatment with Voltaren Dolo Emulgel and tell your doctor immediately: rash with blisters, hives;wheezing, shortness of breath, or a tightness in the chest (asthma);swelling of the face, lips, tongue and throat.These other side effects are usually mild and temporary: Common (affects 1 to 10 users in 100): Rash, itching, redness, burning sensation of the skin.Very rare (affects less than 1 in 10,000 people treated): Rash with pustules, increased sensitivity to sunlight. Signs of this are sunburn with itching, swelling and blistering.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 considered?Shelf lifeThe medicinal product may only be used up to the date marked on the container with « EXP» can be used. Storage instructionsStore at room temperature (15-25°C). Keep out of the reach of children. Further informationVoltaren Dolo Emulgel should not be used near open flames or heat. Do not throw away any medicines via wastewater (e.g. not down the toilet or sink). This helps protect the environment. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Voltaren Dolo Emulgel contain?Active substance100 g Voltaren Dolo Emulgel contain: 1.16 g diclofenac diethylamine, equivalent to 1 g diclofenac sodium. ExcipientsCarbomers, cocoyl caprylocaprate, diethylamine, isopropyl alcohol, macrogolcetostearyl ether, viscous paraffin, propylene glycol (E 1520), fragrance (contains linalool, benzyl alcohol, geraniol, citronellol, benzyl benzoate, coumarin, citral, eugenol), purified water. Approval number55846 (Swissmedic). Where can you get Voltaren Dolo Emulgel? What packs are available?In pharmacies and drugstores, without a doctor's prescription. 60g, 120g and 180g tubes. 75 g tubes with applicator. Authorization holderGSK Consumer Healthcare Schweiz AG, Risch. This leaflet was last checked by the drug authority (Swissmedic) in December 2022. Application note for Voltaren Dolo Emulgel with applicator:1. Remove transparent protective cap. 2. Unscrew applicator. 3. Remove the tube seal using the key on the side of the applicator. 4. Screw the applicator back onto the tube. 5. To open, pull the white part of the applicator upwards. 6. Squeeze the tube gently until the emulsule comes out. 7. Apply Voltaren Dolo Emulgel to the affected area; the applicator closes automatically due to the light pressure when applying. 8. After use, clean the applicator with a cotton cloth or paper towel. After cleaning, screw the transparent protective cap back on. Do not immerse in water or rinse. Do not clean the surface of the applicator with solvents or detergents. ..
88.58 USD
Voltaren dolo forte liquid caps 25 mg 10 pcs
What is Voltaren Dolo forte 25 mg Liquid Caps and when is it used? Voltaren Dolo forte 25 mg Liquid Caps contain the active ingredient diclofenac potassium. This belongs to the group of non-steroidal anti-inflammatory drugs (prostaglandin synthesis inhibitors) and has an analgesic, antipyretic and anti-inflammatory effect. Voltaren Dolo forte 25 mg Liquid Caps are suitable exclusively for short-term treatment, i.e. for a maximum of 3 days treatment of: Headaches, toothaches, menstrual pains, pain in the area of joints and ligaments, back pain, pain in the event of injuries and to reduce fever in the event of grip Palen diseases.When should Voltaren Dolo forte 25 mg Liquid Caps not be taken?If you are allergic to diclofenac or one of the excipients, or have had shortness of breath or allergy-like skin reactions, e.g. swelling of the face, lips, tongue, throat and /or on the extremities (signs of angioedema);if you are pregnant or breastfeeding (see also chapter "Can Voltaren Dolo forte 25 mg Liquid Caps be taken during pregnancy or while breastfeeding?");if you have active stomach and/or duodenal ulcers or gastrointestinal bleeding or perforation (this can be manifested by blackening of the stool, blood in the stool or vomiting of material similar to coffee grounds express);in chronic intestinal inflammation (Crohn's disease or ulcerative colitis);in severe impairment of liver or kidney function;in severe cardiac output weakness;for the treatment of pain after coronary bypass surgery on the heart (or use of a heart-lung machine);in children and adolescents under the age of 14. Voltaren Dolo forte 25 mg liquid caps have not been tested for use in children and adolescents under 14 years of age. For this reason, Voltaren Dolo forte 25 mg Liquid Caps must not be used in children and adolescents under the age of 14.When is caution required when taking Voltaren Dolo forte 25 mg Liquid Caps?During treatment with Voltaren Dolo forte 25 mg Liquid Caps, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (gastrointestinal, breakthroughs) 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 Voltaren Dolo forte 25 mg Liquid Caps 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 suffer from heart or blood vessel disease (so-called cardiovascular diseases, including uncontrolled high blood pressure, heart failure, existing ischemic heart disease or peripheral arterial disease), have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes [diabetes], high levels of fat [cholesterol, triglycerides] in the blood, smoking). Voltaren Dolo forte 25mg Liquid Caps is not usually recommended in these situations. For certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found with high doses and/or long-term treatment. It is not known whether this increased risk also applies to Voltaren Dolo forte 25 mg Liquid Caps. It is important that you use the lowest effective dose to relieve your pain and that you take Voltaren Dolo Liquid Caps for the shortest time necessary to minimize the risk of cardiovascular side effects.if you have kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or if you are experiencing increased fluid loss, e.g. due to heavy sweating or diarrhea; Taking Voltaren Dolo forte 25 mg Liquid Caps can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have a liver problem;if you are being treated with medicines that inhibit blood clotting (blood thinners, anticoagulants) or have a blood clotting disorder or any other blood disease, including the rare disease called hepatic pores phyria;if you suffer from asthma;if you take rheumatism medicines or other painkillers (e.g. acetylsalicylic acid, aspirin, ibuprofen) or other anti-inflammatory drugs (corticosteroids);if you take the following medicines: lithium or specific serotonin reuptake inhibitors (SSRI's, medicines used to treat depression), digoxin (medicines for heart problems), diuretics (Ar medicines to increase urine output), medicines (e.g. metformin) to treat diabetes with the exception of insulin, methotrexate (used to treat arthritis and cancer), ciclosporin or tacrolimus (for organ transplantation), trimethoprim (for urinary tract infections), quinolone antibiotics (used to treat infections), voriconazole (used to treat fungal infections), phenytoin (used to treat epileptic seizures) or sulfinpyrazone (G medication).If you notice signs or symptoms while taking Voltaren Dolo forte 25 mg Liquid Caps that indicate problems with the heart or blood vessels, such as chest pain, shortness of breath, weakness or slurred speech, contact your doctor immediately.In very rare cases, anti-inflammatory drugs (including Voltaren Dolo) can cause serious skin reactions (e.g. skin rash). At the first sign of a skin reaction, treatment with Voltaren Dolo should be discontinued and medical attention sought immediately. Voltaren Dolo forte 25 mg Liquid Caps can reduce the symptoms of an infection (e.g. high fever) and thus make it more difficult to diagnose the infection. This medicine contains 19 mg sorbitol per liquid cap. This medicine may impair your ability to react, drive and use tools or machines. In particular, if you experience dizziness or visual disturbances, you should refrain from driving or using machines.Inform your doctor, pharmacist or druggist if yousuffer from other illnesses,have allergies oruse other medicines (even those you bought yourself!)!May Voltaren Dolo forte 25 mg Liquid Caps should be taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take diclofenac after consulting your doctor. In the last third of pregnancy, Voltaren Dolo forte 25 mg Liquid Caps should not be taken.BreastfeedingVoltaren Dolo forte 25 mg Liquid Caps should not be taken while breastfeeding unless your doctor has expressly permitted you to do so.Like other anti-inflammatory drugs, Voltaren Dolo forte 25 mg Liquid Caps can make it more difficult to become pregnant. After stopping the drug, this effect ends. If you are planning a pregnancy or are having difficulties conceiving, talk to your doctor.How do you use Voltaren Dolo forte 25 mg Liquid Caps?The recommended dosage must not be exceeded.The lowest effective dose should always be taken for the shortest possible time.Adults and adolescents from 14 years of age:1 Voltaren Dolo forte 25 mg Swallow the Liquid Cap up to 3 times a day with plenty of water, preferably with or after a meal. Before taking the next dose, leave an interval of at least 4 to 6 hours. Maximum daily dose: Do not take more than 3 Voltaren Dolo forte 25 mg Liquid Caps within 24 hours, unless prescribed by a doctor. Should you accidentally take more Voltaren Dolo forte 2 5 mg Liquid Caps, contact your doctor immediately. Do not take Voltaren Dolo forte 25 mg Liquid Caps for longer than 3 days and only to treat the symptoms listed above. If the symptoms persist or worsen, consult your doctor so that the reason can be clarified. A serious illness can be the cause.Children and adolescents under the age of 14: Voltaren Dolo forte 25 mg Liquid Caps must not be used in children and adolescents under the age of 14. The use and safety of Voltaren Dolo forte 25 mg Liquid Caps in children and adolescents under the age of 14 has not yet been tested. Elderly patients: Elderly patients may react more sensitively to the drug than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.Follow the dosage provided in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Voltaren Dolo forte 25 mg Liquid Caps have?After taking Voltaren Dolo forte 25 mg Liquid Caps, the following side effects can occur:Common (affects 1 to 10 out of 10 0 users):Abdominal pain, stomach pain, diarrhea, nausea, vomiting, flatulence, indigestion, decreased appetite;Headache, drowsiness;Rash;Dizziness;Increased liver enzymes.Uncommon (affects 1 to 10 users in 1000):..
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