Anti-inflammatory
(2 Pages)
Algifor liquid caps 400 mg 10 pcs
AMZV What is Algifor Liquid caps 400 and when is it used? The soft gelatin capsule Algifor Liquid caps 400 contains the active ingredient ibuprofen. This has analgesic, antipyretic and anti-inflammatory properties.Algifor Liquid caps 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:pain in the area of joints and ligaments,back pain,headache,toothache,pain during the menstrual period,Pain after injury,Fever with a flu.When should Algifor Liquid caps 400 not be taken?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other painkillers or rheumatism drugs, so-called non-steroidal anti-inflammatory drugs.Im last trimester of pregnancy (see also chapter "Can Algifor Liquid caps 400 be taken during pregnancy or while breast-feeding?").If you have an active stomach and/or duodenal ulcer or stomach/intestinal bleeding that has occurred repeatedly in the past.If you have a history of bleeding or perforation (perforation) in the stomach or intestines in connection with previous therapy with so-called non-steroidal anti-inflammatory drugs.For chronic intestinal inflammation (Crohn's disease, ulcerative colitis).For severe impairment of liver or kidney function.For severe heart failure.For the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine).For varicella infection (chickenpox infection).In children under 12 years of age. Algifor Liquid caps 400 has not been tested for use in children under the age of 12.When should caution be taken when taking Algifor Liquid caps 400?During treatment with Algifor Liquid caps 400, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (gastrointestinal perforations) may occur. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine.Older people may be more sensitive to the medicine than younger adults. It is particularly important that older patients report any side effects to their doctor immediately.At the first sign of a sore throat, high fever, superficial mouth sores, flu-like symptoms, severe exhaustion, nose and skin bleeding, treatment with ibuprofen must be stopped immediately and the doctor consulted.In very rare cases, taking Algifor Liquid caps 400 can lead to severe headaches in connection with nausea and vomiting and neck stiffness. The treatment should then be stopped and a doctor consulted.You may only take Algifor Liquid caps 400 on prescription and under medical supervision in the following situations:if you are currently being treated by a doctor for a serious illness;if you have previously suffered from a stomach or duodenal ulcer;if you have already had a heart attack, stroke or vein thrombosis, or if you have risk factors (such as high blood pressure, diabetes (diabetes), high blood fat levels, smoking);For certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found at high doses and/or long-term treatment. It is unclear whether this increased risk also applies to Algifor Liquid caps 400not known;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; taking Algifor Liquid caps 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (edema);if you have liver disease;if you are being treated with anticoagulants (blood thinners, anticoagulants) or have a blood clotting disorder;if you suffer from asthma;if you are taking antirheumatic medicines or other painkillers (e.g. acetylsalicylic acid, aspirin);if you are taking medicines to treat diabetes (except insulin), medicines to increase urine output (diuretics), medicines to treat infections (quinolone antibiotics), medicines for AIDS (zidovudine), immunosuppressants (medicines used to treat transplant rejection (tacrolimus and cyclosporine), corticosteroids, antiplatelet medicines and selective S are taking erotonin reuptake inhibitors (SSRIs) or medicines containing any of the following: lithium, digoxin, methotrexate, baclofen, phenytoin, probenecid or sulfinpyrazone;if you have certain skin disorders (systemic lupus erythematosus (SLE) or mixed collagenosis). If you suffer from severe skin reactions such as exfoliative dermatitis, Stevens-Johnson syndrome or toxic epidermal necrolysis. The risk of such reactions appears to be highest at the start of therapy, since the majority of these reactions occurred within the first month of treatment. At the first sign of skin rashes, mucosal lesions or any other sign of hypersensitivity, Algifor Liquid caps 400 should be discontinued and your doctor consulted immediately;Acetylsalicylic acid or other painkillers should not be taken at the same time as ibuprofen, as the risk of side effects may increase.Inform your doctor if you have recently been treated for an abortion...
25.83 USD
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?< p>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. ..
37.47 USD
Ceres geranium robertianum mother tint bottle 20 ml
Ceres Geranium Robertianum Mother Tint Bottle 20ml Our Ceres Geranium Robertianum Mother Tint is a natural remedy made from the extracts of wild geranium plants, which are carefully selected according to our high standards. This beautiful plant, also known as stork's bill, has been used for centuries for its medicinal properties and is widely recognized as one of the most powerful anti-inflammatory and anti-bacterial agents in nature. The mother tint is made by steeping the geranium plant in a mixture of alcohol and water for an extended period. This process extracts the pure and potent essence of the plant, which is then highly concentrated and ready to use in a liquid form. Our mother tint is organic, vegan and gluten-free, making it safe for everyone to use. Benefits: Anti-inflammatory: Reduces swelling, pain, and inflammation. Anti-bacterial: Kills germs and bacteria, helps protect against infections. Regenerative: Supports the healing of damaged tissues and wounds, promotes cell rejuvenation. Purifying: Cleanses the body and helps eliminate toxins and waste. How to use: This mother tint can be diluted with water or enjoyed as is. Adults can take 5-10 drops orally, 3 times a day. It can also be added to your warm water for a relaxing bath or topical application. This product is suitable for external and internal use. Our Ceres Geranium Robertianum Mother Tint supports natural healing, promotes wellness, and enhances our body's ability to function optimally. Give it a try and experience the powerful benefits of this amazing plant! ..
43.12 USD
Dolo-spedifen forte filmtabl 400 mg 10 pcs
What is Dolo-Spedifen forte 400 and when is it used? Dolo-Spedifen forte 400 contains the active ingredient ibuprofen in the form of ibuprofen arginate. This has pain-relieving, anti-inflammatory and antipyretic properties. The effect occurs after about 30 minutes and lasts about 6 hours. Dolo-Spedifen forte 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of: Pain in the area of joints and ligaments; Back pain; Headache; Toothache; Pain during menstrual bleeding; Pain zen after injuries;Fever with flu-like illnesses.When should Dolo-Spedifen forte 400 not be taken?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other pain or rheumatism medicines, so-called non-steroidal anti-inflammatory drugs;if you are pregnant or breastfeeding (see also «Can Dolo-Spedifen forte 400 be taken during pregnancy or while breastfeeding?»);if you have active stomach and/or duodenal ulcers or gastrointestinal bleeding;if you have a history of gastrointestinal bleeding or perforation (perforation) in connection with previous therapy with so-called non-steroidal anti-inflammatory drugs;if you have chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in the case of cerebral hemorrhage;in the case of an increased tendency to bleed;in the case of severe impairment of liver or kidney function;in the case of severe heart failure;for the treatment of pain after a coronary bypass operation on the heart (or use of a heart-lung machine);in children under 12 years of age. Dolo-Spedifen forte 400 has not been tested for use in children under the age of 12. When is caution required when taking Dolo-Spedifen forte 400? During treatment with Dolo-Spedifen forte 400, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine.Older people may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.You may only take Dolo-Spedifen forte 400 with a prescription and under medical supervision in the following situations:if you are currently being treated by a doctor for a serious illness;if you have previously suffered from a stomach or duodenal ulcer;if you have already had a heart attack, stroke or a have had venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes, high levels of fat in your blood, smoking); for certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found at high doses and/or long-term treatment. It is not known whether this increased risk also applies to Dolo-Spedifen forte 400;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; theTaking Dolo-Spedife forte 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;if you are being treated with medicines that inhibit blood clotting (blood thinners, anticoagulants) or have a blood clotting disorder;if you suffer from asthma;if you are taking medicines for Treatment of diabetes, medicines to increase urine output (water tablets), medicines to treat infections (quinolone antibiotics), for AIDS (zidovudine), immunosuppressants (tacrolimus, cyclosporine), corticosteroids, antiplatelet medicines such as acetylsalicylic acid, selective serotonin reuptake inhibitors (SSRIs), antifungal medicines (voriconazole, fluconazole), or medicines containing any of the following: lithium, digoxin, are taking methotrexate, mifepristone, baclofen, phenytoin, probenecid or sulfinpyrazone;if you have certain skin diseases (systemic lupus erythematosus (SLE) or mixed collagenosis);if you have an infection. Dolo-Spedifen forte 400 can mask signs of infection such as fever and pain. It is therefore possible that Dolo-Spedifen forte 400 may delay adequate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Serious skin reactions such as acute generalized pustular exanthema, scaly skin inflammation or Stevens-Johnson syndrome have been reported in connection with treatment with medicines containing ibuprofen. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of allergy, you should stop taking Dolo-Spedifen forte 400 and seek immediate medical attention, as these may be the first signs of a very serious skin reaction (see «What side effects can Dolo-Spedifen forte 400 have?»).Acetylsalicylic acid, other painkillers or Cox-2 inhibitors should not be taken at the same time as ibuprofen as the risk of side effects may be increased.Patients who experience visual disturbances during Dolo-Spedifen forte 400 therapy should discontinue treatment and consult a doctor immediately.Excipients of particular interestDolo-Spedifen forte 400 film-coated tablets contain:Sucrose: Please take Do not use this medicine until you have consulted your doctor if you know that you have an intolerance to sugar.Sodium: 83 mg sodium (main component of cooking/table salt) per 400 mg film-coated tablet. This corresponds to 4% of the recommended maximum daily dietary intake of sodium for an adult.This medicine may impair your ability to react, drive and use tools or machines.Inform your doctor, pharmacist or druggist if you suffer from any other illnesses, have allergies or are taking or using other medicines (including those you have bought yourself)!May do Thurs lo-Spedifen forte 400 taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take Dolo-Spedifen forte 400 after consulting your doctor. In the last third of pregnancyDolo-Spedifen forte 400 must not be taken afterwards.BreastfeedingDolo-Spedifen forte 400 should not be taken while breastfeeding unless your doctor has expressly permitted it.How do you use Dolo-Spedifen forte 400?Adults and adolescents from the age of 12D olo-Spedifen forte 400: Take 1 film-coated tablet with plenty of liquid. Before taking the next dose, wait 4 to 6 hours. In the case of pain during menstrual bleeding, it is recommended to start treatment with 1 film-coated tablet of Dolo-Spedifen forte 400 at the first sign of symptoms.Maximum daily dose Do not take more than 3 film-coated tablets of Dolo- Spedifen forte 400 within 24 hours, unless prescribed by a doctor.Do not use Dolo-Spedifen forte 400 for more than 3 days and only to treat the symptoms listed above.The lowest effective dose should be used for the shortest time necessary to relieve symptoms.If the symptoms increase despite taking Dolo-Spedifen forte 400 or if the pain is painful en area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. If you have an infection, consult a doctor immediately if the symptoms (e.g. fever and pain) persist or worsen (see «When should you be careful when taking Dolo-Spedifen forte 400?»).If you have taken more Dolo-Spedifen forte 400 than you should, or if children have accidentally taken the medicine, always consult a doctor to get an assessment of the risk and advice on further treatment.Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.Children under the age of 12Dolo-Spedifen forte 400 must not be used in children under the age of 12. The use and safety of Dolo-Spedifen forte 400 in children under the age of 12 has not yet been systematically tested. Stick to the dosage given in the package insert or prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Dolo-Spedifen forte 400 have?The following side effects can occur when taking Dolo-Spedifen forte 400, which may require medical treatment.Please tell your doctor or your doctor immediately if you experience one or more of the following symptoms and stop taking Dolo-Spedifen forte 400:Very common side effects, which may occur in more than 1 in 10 casesStomach and intestine problems such as indigestion, diarrheaCommon side effects, which occur in more than 1 in 100 cases but less than 1 in 10 casesGastro-intestinal complaints such as nausea, feeling of fullness, heartburn, pain in the upper abdomen, anorexia, constipation, flatulence, vomiting, erosive inflammation of the gastric mucosa, blood stoolCentral nervous side effects wie Impaired reactions (especially when combined with alcohol), drowsiness, headache and dizzinessDepression, anxiety, confusionVisual disturbances (the visual disturbances are usually reversible if treatment is stopped)Ringing in the ears, hearing lossAcute skin rashOccasional side effects, occurring in more than 1 in 1,000 cases but less than 1 in 100 casesAllergic reactions, swelling of the faceAsthma, spasm of the muscles of the airways and shortness of breathStomach ulcer, gastrointestinal bleeding, tarry stools, gastritisRare side effects, occurring in more than 1 in 10,000 cases but less than 1 in 1,000 casesChanges in the blood countSymptoms of lupus erythematosus (butterfly plexus), aseptic meningitis (meningitis) in patients suffering from an autoimmune disease"Tingling" of the skinIrreversible visual disturbance or visual impairmentPatients with heart failure are at risk of acute pulmonary edema (water lung)Perforation in the stomach and intestines, vomiting blood, ulcers in the oral mucosa, worsening of colitis or Crohn's diseaseLiver failure, liver dysfunctionBlood in the urineVarious kidney diseases such as kidney toxicity, kidney dysfunction with fluid retention in the tissueVery rare side effects occurring in less than 1 in 10'00 0 casesPsychotic statesSevere allergic skin reactions with formation of blisters and/or extensive detachment of the skin, photosensitivity reactions, worsening of skin reactionsAcute kidney failureSide effects with unknown frequency:AnemiaAnaphyl acute shockHeart failureArterial thrombosis, blood pressure disordersThroat irritationHepatitis, jaundice, liver injuryGeneral swellingSevere skin reaction: Known as DRESS syndrome. Symptoms of DRESS include a rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell). Known as acute generalized pustular exanthema (AGEP); at the start of treatment there is a red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk and upper extremities. Discontinue use of Dolo-Spedifen forte 400 if you develop these symptoms and seek medical treatment immediately (see also «When should you be careful when taking Dolo-Spedifen forte 400?»).If you notice any side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What else needs to be taken into account?The medicine may only be used up to the date marked «EXP» on the container.Storage instructionsStore at room temperature (15–25 °C) and out of the reach of children.Further informationYour doctor or pharmacist can provide you with further information or druggist or your doctor, pharmacist or druggist. These people have the executiveHonest professional information. What does Dolo-Spedifen forte 400 contain? Active ingredients 1 film-coated tablet contains 400 mg ibuprofen as ibuprofen arginate. Excipients Arginine, sodium bicarbonate, crospovidone, magnesium stearate, film coating: hypromellose, sucrose, titanium dioxide (E1 71), Macrogol 4000.Authorization number56720 (Swissmedic).Where can you get Dolo-Spedifen forte 400? Which packs are available? in pharmacies and drugstores, without medical prescription. packs of 10 film -coated tablets for 400 mg. registration owner Zambon Switzerland AG 6814 Cadempino This package insert was last in August 2020 checked (Swissmedic). ..
20.29 USD
Ecofenac sandoz lipogel 1% tb 50g
Ecofenac Sandoz Lipogel 1% Tb 50 g Ecofenac Sandoz Lipogel 1% Tb 50 g is an effective topical pain relief medicine for the treatment of mild to moderate pain and inflammation. It is a non-steroidal anti-inflammatory drug (NSAID) and contains the active ingredient diclofenac diethylammonium. The gel is specially formulated in a lipophilic base that allows for easy and deep penetration into the skin, resulting in fast and long-lasting pain relief. It absorbs quickly into the skin without leaving any grease or residue, making it convenient for use during the day and at night. Ecofenac Sandoz Lipogel 1% Tb 50 g is suitable for the treatment of conditions such as arthritis, back pain, sprains, strains, and sports injuries. It provides targeted pain relief by reducing the production of prostaglandins, which are responsible for causing inflammation and pain in the affected area. The product comes in a convenient 50g tube, making it easy to carry and apply on-the-go. It is recommended to apply the gel to the affected area two to three times daily, gently massaging it into the skin until fully absorbed. Ecofenac Sandoz Lipogel 1% Tb 50 g is a safe and effective alternative to oral pain medications, as it works locally without affecting the rest of the body. However, it is still important to follow the recommended dosage and not exceed the maximum daily dose of 150 mg. If you are pregnant, breastfeeding, or have a history of stomach ulcers or hypersensitivity to NSAIDs, it is recommended to consult a healthcare provider before using this product. ..
11.61 USD
Hanseler yellowwood 5 x 10 g
Hänseler Gelbholz 5 x 10 g Hänseler Gelbholz is a natural remedy made from the inner bark of the Pterocarpus tree. The yellow wood contains a high amount of flavonoids and has anti-inflammatory, antiseptic, and antioxidant properties. It is traditionally used to treat a variety of ailments, including coughs, stomach problems, liver and kidney disorders, and skin conditions. This product comes in a pack of five 10-gram bags, perfect for those who prefer to consume Gelbholz in smaller portions or would like to have a supply at hand. Hänseler Gelbholz is easy to prepare by simply boiling a small amount in water and drinking the tea. It can also be added to soups, stews, or other dishes for an extra health boost. Hänseler is a trusted brand that has been producing natural remedies since All of their products are made from 100% natural ingredients and undergo strict quality controls to ensure their efficacy and safety. Hänseler Gelbholz 5 x 10 g is a convenient and effective way to incorporate this amazing natural remedy into your daily routine. ..
41.08 USD
Inflamac lotio emuls 1%tb 100g
Inflamac Lotio is an analgesic and anti-inflammatory preparation for external use. This cooling and non-greasy emulsion is easy to rub in and penetrates the skin to the site of inflammation. Inflamac Lotio is suitable for the local treatment of pain, inflammation and swelling such as after sprains, bruises and strains; as a supportive measure for the local treatment of rheumatic complaints of the musculoskeletal system. Swissmedic-approved patient information Inflamac® LotioSpirig HealthCare AGWhat is Inflamac Lotio and when is it used? Inflamac Lotio is an analgesic and anti-inflammatory preparation for external use. This cooling and non-greasy emulsion is easy to rub in and penetrates the skin to the site of inflammation. Inflamac Lotio is suitablefor the local treatment of pain, inflammation and swelling, e.g. after sprains, bruises and strains;as a supportive measure for the local treatment of rheumatic complaints of the musculoskeletal system.When should Inflamac Lotio not be used?Inflamac Lotio should not be used if you are hypersensitive to the active ingredient diclofenac or other pain-relieving and anti-inflammatory substances, especially acetylsalicylic acid /Aspirin, as well as hypersensitivity to one of the excipients. When is caution required when using Inflamac Lotio?Inflamac Lotio must not be applied to open skin wounds (e.g. abrasions, cuts) or to eczematous skin. Inflamac Lotio should not be used over large areas for long periods of time unless directed to do so by a doctor. Make sure that Inflamac Lotio does not come into contact with the eyes and mucous membranes. Inform your doctor, pharmacist or druggist if you have already used similar products (rheumatism ointments) and these have led to allergic reactions, if you suffer from other diseases, have allergies or other medicines ( also self-bought!) ingest or apply externally! Can Inflamac Lotio be used during pregnancy or while breastfeeding?Inflamac Lotio must not be used during pregnancy or while breastfeeding, unless specifically prescribed by a doctor. How do you use Inflamac Lotio?AdultsDepending on the size of the painful area or area to be treated, 3 – Apply an amount of 2 – 4 g Inflamac Lotio (the size of a hazelnut or walnut) 4 times a day, rub in lightly or massage in for muscle pain. Inform your doctor if the symptoms have not improved after 2 weeks or if they have even gotten worse. ChildrenThe use and safety of Inflamac Lotio in children has not been systematically 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 Inflamac Lotio have?The following side effects can occur when using Inflamac Lotio: Some rare or very rare side effects can be serious. If any of the following side effects occur, stop using Inflamac Lotio and tell your doctor immediately: severe rash with blisters, hiveswheezing, shortness of breath asthmaswelling of the face, lips, tongue and throat. These other side effects are usually mild and temporary: Common: skin rash, itching, redness, burning sensationIn very rare cases, increased sensitivity to sunlight may occur. Signs of this are sunburn with itching, swelling and blistering.Not known: burning sensation at the application site, dry skin.If you get any side effects, talk to your doctor Doctor, pharmacist or druggist 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 instructionsKeep out of the reach of children. Store at room temperature (15-25°C). Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Inflamac Lotio contain?Active ingredients10 mg Diclofenacum natricum ExcipientsPurified water, ethanol, triglycerides, polyacrylamide, isoparaffin, laureth-7, dimeticone, tocopherol. Approval number55375 (Swissmedic) Where can you get Inflamac Lotio? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Tubes of 50 and 100 g. Authorization holderSpirig HealthCare AG, 4622 EgerkingenThis leaflet was last checked by the Medicines Agency (Swissmedic) in June 2021. ..
15.72 USD
Irfen dolo forte lactab 400 mg 10 pcs
What is Irfen Dolo and when is it used? Irfen Dolo contains the active ingredient ibuprofen. This has analgesic, fever-reducing and anti-inflammatory properties.Irfen Dolo is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:pain in the area of joints and ligaments,back pain,headache,toothache,pain during the menstrual period, Pain after injuries,Fever with flu-like illnesses.When must Irfen Dolo not be used?Irfen Dolo must not be taken if you are allergic to any of the ingredients or after taking acetylsalicylic acid or other painkillers or anti-inflammatory drugs, so-called non-steroidal anti-inflammatory drugs, shortness of breath or allergy-like had skin reactions,if you are pregnant or breastfeeding (see also chapter "Can Irfen Dolo be taken during pregnancy or while breastfeeding?"),if you have active stomach and/or or duodenal ulcers or gastrointestinal bleeding,in chronic intestinal inflammation (Crohn's disease, ulcerative colitis),in severe impairment of liver or kidney function,for severe cardiac insufficiency,for the treatment of pain after coronary bypass surgery on the heart (or use of a heart-lung machine),For children under the age of 12: Irfen Dolo has not been tested for use in children under the age of 12.When is at caution when taking Irfen Dolo? During treatment with Irfen Dolo, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (stomach or intestinal perforations) may occur. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine.Older people may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.You may only take Irfen Dolo on prescription and under medical supervision in the following situations:If you are currently being treated by a doctor for a serious illness;If you have previously suffered from a stomach or duodenal ulcer;If you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes [diabetes], high blood fat levels [smoking]; high doses of certain similarly acting painkillers called COX-2 inhibitors have been used and/or long-term treatment has been found to be an increased risk of heart attack and stroke. It is not known whether this increased risk also applies to Irfen Dolo;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; taking Irfen Dolo can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;if you with anticoagulant medicineare being treated with medication (blood thinners, anticoagulants) or suffer from a blood clotting disorder;if you suffer from asthma;if you are taking rheumatism medicines or other painkillers (e.g. acetylsalicylic acid, aspirin); if you are taking medicines to treat diabetes (other than insulin), medicines to increase urine output (diuretics), medicines to treat infections (quinolone antibiotics) or medicines containing any of the following: lithium , digoxin, methotrexate, baclofen, phenytoin, probenecid or sulfinpyrazone.Serious skin reactions with reddening and blistering (exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis/Lyell's disease) have been reported with ibuprofen therapy. Syndrome).At the first sign of skin rashes, mucosal lesions or other signs of a hypersensitivity reaction, Irfen Dolo should be discontinued and your doctor, pharmacist or druggist should be consulted immediately.< li>Inform your doctor, pharmacist or druggist if you are being treated with medicines such as blood thinners, diuretics (water tablets), ACE inhibitors or β-blockers (preparations for high blood pressure and heart failure) , antibiotics, certain antifungal agents (e.g. Voriconazole or Fluconazole), immunosuppressants (preparations against transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, against AIDS, epilepsy and depression. Nonsteroidal anti-inflammatory drugs, such as ibuprofen, and the drugs listed above can interact.Side effects, particularly those affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Inform your doctor, pharmacist or druggist if yousuffer from other diseasesHave allergies ortake other medicines (including those you bought yourself!) or use them externally.Irfen Dolo can improve your ability to react, your ability to drive and your ability , use tools or machines! This applies in particular to taking it with alcohol.Can Ifen Dolo be taken while pregnant or breastfeeding?PregnancyShould you be pregnant or planning a pregnancy, you should only take Irfen Dolo after consulting your doctor. Irfen Dolo should not be taken during the last third of pregnancy.BreastfeedingIrfen Dolo should not be taken while breastfeeding unless your doctor has given you express permission to do so. How do you use Irfen Dolo?Adults and adolescents from 12 years of ageIrfen Dolo 200 mg1-2 Lactab Irfen Dolo Take 200 mg with plenty of liquid. Leave an interval of 4 to 6 hours before taking the next dose. Maximum daily dose: Do not take more than 6 Lactab Irfen Dolo 200 mg (1200 mg ibuprofen) in a 24-hour period, unless prescribed by a doctor .Irfen Dolo forte 400 mgTake 1 Lactab Irfen Dolo forte 400 mg with plenty of liquid. An interval of 4 to 6 hours should be observed before the next intake. Maximum daily dose: Do not take more than 3 Lactab Irfen Dolo forte 400 mg (1200 mg ibuprofen) within 24 hours, unless prescribed by a doctor Prescription.In the case of pain during the menstrual period, it is recommended to start treatment with 2 Lactab Irfen Dolo 200 mg or 1 Lactab Irfen Dolo forte 400 mg at the first sign of symptoms.&Do not use Irfen Dolo for more than 3 days and only to treat the symptoms listed above.If the symptoms increase despite taking Irfen Dolo or if the painful area is red or swollen is, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. Children under 12 Irfen Dolo must not be used in children under 12 years of age. The use and safety of Irfen Dolo in children under the age of 12 has not yet been tested.Elderly patientsElderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.Follow the dosage provided in the package leaflet or as prescribed by your doctor. If you have taken more Irfen Dolo than you should, or if children have accidentally taken the medicine, always contact a doctor for an assessment of the risk and advice on further treatment. These symptoms can include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.If you forget to take a dose, take it next dose, do not take more than the usual recommended amount.If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. Pharmacist.What side effects can Irfen Dolo have?The following side effects can occur when taking Irfen Dolo. They are listed according to their frequency:Common (affects 1 to 10 users in 100)Gastro-intestinal disorders such as indigestion, diarrhoea , nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizziness.Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.< /li>Hypersensitivity reactions.Insomnia, feeling anxious.Visual disturbances (the visual disturbances are usually reversible when treatment is stopped).Ringing in the ears, Hearing loss, dizziness.Asthma, spasm of the muscles of the airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung).Fatigue.Rare (affects 1 to 10 users in 10,000)Aseptic meningitis (inflammation of the brain).Angina, hoches Fever, swelling of the lymph nodes in the neck area.Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusional states."Tingling" of the Skin, drowsiness.Irreversible visual disturbance or poor eyesight.Inflammation of the gastric mucosa, stomach and intestinal ulcers, ulcers of the oral mucosa, stomach and intestinesbreakthroughs.Hepatitis, jaundice, liver dysfunction.Hives, itching, bleeding into the skin, swelling of the skin and mucous membranes, sensitivity to light.Various kidney diseases such as kidney dysfunction with accumulation of water in the tissue up to kidney failure.General swelling.Very rare (affects less than 1 in 10,000 users)< ul class="list-bullets">Psychotic conditions.Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Liver failure.Severe allergic skin reactions with formation of blisters and/or extensive detachment of the skin.Individual casesA severe skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include a rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).Aggravated colitis or Crohn's disease.A red, scaly , widespread rash with bumps under the skin and blisters located mainly in the skin folds, trunk and upper extremities, accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop taking Irfen Dolo if you experience these symptoms and see a doctor straight away.If you get any side effects, talk to your doctor or pharmacist or your doctor or pharmacist. This also applies in particular to side effects that are not listed in this leaflet.What else needs to be taken into account?The drug may only be used up to the end of the period marked "EXP" on the package Date are used.Storage instructionsDo not store above 30°C. Keep out of the reach of children.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Irfen Dolo contain?1 Lactab Irfen Dolo 200 mg contains: 200 mg ibuprofen as an active ingredient and excipients.< p>1 Lactab Irfen Dolo forte 400 mg contains: 400 mg ibuprofen as an active ingredient and excipients.Authorization number51547 (Swissmedic).Where can you get Irfen dolo? What packs are available? In pharmacies and drugstores without a doctor's prescription. Irfen Dolo 200 mg: packs of 20 Lactabs. Irfen Dolo forte 400 mg: Packs of 10 Lactab.Authorization holderMepha Pharma AG, Basel.This package leaflet was last checked by the drug authority (Swissmedic) in December 2020 .Internal version number: 9.2..
17.95 USD
Irfen dolo l forte lactab 400 mg 10 pcs
What is Irfen Dolo L forte 400 mg and when is it used? The Lactab Irfen Dolo L forte 400 mg contains the active ingredient ibuprofen as ibuprofen lysinate. It has pain-relieving, fever-reducing and anti-inflammatory properties. Ibuprofen lysinate shows the same properties as ibuprofen, but differs in its higher water solubility.Irfen Dolo L forte 400 mg is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of:Pain in the area of joints and ligaments,Back pain,Headache,Toothache,< li>Pain during menstrual bleeding,Pain after injury,Fever with flu-like illnesses.When should Irfen Dolo L forte 400 mg not be taken be used?If you are allergic to any of the ingredients or after taking acetylsalicylic acid or other pain or rheumatism medicines, so-called non-steroidal anti-inflammatory drugs, shortness of breath or had allergy-like skin reactions;if you are pregnant or breastfeeding (see also chapter "Can Irfen Dolo L forte 400 mg be taken during pregnancy or while breastfeeding?");if active gastric and/or duodenal ulcers or gastrointestinal bleeding;in chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in severe impairment of liver or kidney function;for severe heart failure;for the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine);in the case of a varicella infection (chickenpox infection);in children under the age of 12. Irfen Dolo L forte 400 mg has not been tested for use in children under the age of 12.When is caution required when taking Irfen Dolo L forte 400 mg?During treatment with Irfen Dolo L forte 400 mg, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) can occur in the upper gastrointestinal tract. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, your doctor will prescribe the smallest effective dose for the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under "Infections".Certain painkillers called COX-2 inhibitors have been shown to be associated with an increased risk of heart attack and stroke with long-term treatment. This risk can also be slightly increased with Irfen Dolo L forte 400 mg at a high dose (2400 mg/day). However, at the usual dosage (maximum 1200 mg/day), no increase in this risk was found. If you have already had a heart attack, stroke or venous thrombosis, the use of Irfen Dolo L forte 400 mg in high doses is no longer recommended. Do not exceed the recommended dose or duration of treatment and in any case tell your doctor if you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes (diabetes), high blood fat levels, smoking). Your doctor will decide whether you can still use Irfen Dolo L forte 400 mg and which dose is right for you. Taking Irfen Dolo L forte 400 mg can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor or nursedoctor if you have heart or kidney disease, if you are taking medicines to treat high blood pressure (e.g. diuretics, ACE inhibitors) or if you have increased fluid loss, e.g. through heavy sweating.This medicine can impair your ability to react, your ability to drive and ability to use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of stomach or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients and patients who suffer or have suffered from asthma, chronic inflammation of the nasal mucosa (chronic cold), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagenosis).In connection with treatment with Irfen Dolo L forte 400 mg, serious skin reactions have been reported. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of allergy, you should stop treatment with Irfen Dolo L forte 400 mg and seek medical attention immediately, as these can be the first signs of a very serious skin reaction. The risk of such reactions appears to be highest at the start of therapy, since the majority of these reactions occurred within the first month of treatment. At the first sign of skin rashes, mucosal lesions or other signs of a hypersensitivity reaction, Irfen Dolo L forte 400 mg should be discontinued and your doctor consulted immediately.Irfen Dolo L forte 400 mg should not be used if you have chickenpox.InfectionsIrfen Dolo L forte 400 mg may mask signs of infections such as fever and pain. It is therefore possible that Irfen Dolo L forte 400 mg may delay adequate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Tell your doctor if you have recently received treatment for an abortion.Maximum daily dose: do not take more than 3 Lactabs in 24 hours unless prescribed by a doctor.Do not use Irfen Dolo L forte 400 mg for longer than 3 days and only for Treatment of the symptoms listed above.If the symptoms increase despite taking Irfen Dolo L forte 400 mg or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified.Children under 12 years of age: Irfen Dolo L forte 400 mg must not be used in children under 12 years of age. The use and safety of Irfen Dolo L forte 400 mg in children under the age of 12 has not yet been tested. Stick to the dosage given in the package insert or prescribed by the doctor.< /p>If you have taken more Irfen Dolo L forte 400 mg than you should, or if children have accidentally taken the medicine, always contact a doctor for an assessment of the risk and Get advice on further treatment.Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.If you forget to take a dosenext dose, do not take more than the usual recommended amount.If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist Your doctor, pharmacist or druggist.What side effects can Irfen Dolo L forte 400 mg have?The following side effects can occur when taking Irfen Dolo L forte 400 mg.They are listed according to their frequency:Common (affects 1 to 10 users in 100)Stomach and intestine problems such as indigestion, diarrhea, nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction (especially in combination with alcohol), headache and dizziness .Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.Hypersensitivity reactions.Insomnia, feeling anxious.Visual disturbances (the visual disturbances are usually reversible when treatment is stopped). li>Ringing in the ears, hearing loss, dizziness.Asthma, spasm of the muscles of the airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung).Fatigue.Rare (affects 1 to 10 users in 10,000) Aseptic meningitis.Angina, high fever, swelling of the lymph nodes in the neck.Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusional states."Tingling" of the skin, drowsiness.Irreversible visual disturbance or poor eyesight.< li>Inflammation of the gastric mucosa, stomach and intestinal ulcers, mouth ulcers, gastric and intestinal perforations.Hepatitis, jaundice, liver dysfunction.Hives, itching, bleeding in the skin, swelling of the skin and mucous membranes, sensitivity to light.Various diseases of the kidneys such as kidney dysfunction with accumulation of water in the tissue and even kidney failure.General swelling. Very rare (affects less than 1 in 10,000 users)Psychotic states.Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Liver failure.Severe allergic reactions of the skin with formation of blisters and/or extensive detachment of the skin.< /ul>Frequency not known (cannot be estimated from the available data)A serious skin reaction known as DRESS syndrome can occur . Symptoms of DRESS include rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).Worsening of colitis or Crohn's diseaseAt the start of treatment, a red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk, and upper extremities (acute generalized pustular ex anthem). Discontinue use of Irfen Dolo L forte 400 mg if you develop these symptoms and seek medical attention immediately.If you notice any side effectsn, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What else should be observed?The medicinal product may only be used up to the end of the period marked "EXP" on the container Date are used.Storage instructionsStore in the original packaging and at room temperature (15-25°C).Keep out of the reach of children.Further information Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for professionals.What does Irfen Dolo L forte 400 mg contain?Active substances1 Lactab Irfen Dolo L forte 400 mg ( divisible) contains 400 mg ibuprofen as ibuprofen lysinate.ExcipientsMicrocrystalline cellulose, croscarmellose sodium, talc, colloidal silica, magnesium stearate, hypromellose, macrogol 6000, glycerol 85% (E422). Authorization number61210 (Swissmedic).Where can you get Irfen Dolo L forte 400 mg? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Irfen Dolo L forte 400 mg (divisible): pack of 10 Lactab. Authorization holderMepha Pharma AG, Basel.This package leaflet was last checked by the drug authority (Swissmedic) in December 2020. Internal version number: 7.2..
18.30 USD
Kamillosan liq 250 ml
Chamomile was already widely used in ancient times and was valued even then for its pain-relieving, antispasmodic, slightly disinfecting, wound-healing and wound-cleansing properties. Kamillosan Liquidum contains essential oil and flavones in quantified amounts as chamomile components that help determine its effectiveness. Kamillosan Liquidum is an anti-inflammatory, pain-relieving, itching-relieving, slightly disinfectant with calming and odor-eliminating properties. Kamillosan Liquidum can thus be used: For mouth rinsing and gargling: for inflammation of the oral cavity, pharynx, gums, bad breath. For inhalation and facial steam bath: for colds, inflammation of the paranasal sinuses, bronchitis. As a supportive measure for blemished skin, pustules, blackheads (acne vulgaris). For compresses, washing, partial and full baths: for itching, skin inflammation, for the after-treatment of open abscesses, boils, infected wounds, first burns Degrees. As a sitz bath: to relieve the symptoms of haemorrhoids, itching from eczema (also anal eczema) or inflammation in the area of the anus. As a children's bath: for inflammatory skin symptoms. For rinsing: for inflammatory diseases of the female genital organs. For brushing (undiluted): for inflammation of the oral mucosa, gums, paradontosis, bleeding gums. Swissmedic-approved patient information Kamillosan® LiquidumMEDA Pharma GmbHHerbal medicinal product AMZVWhat is Kamillosan Liquidum and when is it used?Camomile was already widely used in ancient times and was valued even then for its pain-relieving, antispasmodic, slightly disinfecting, wound-healing and wound-cleansing properties. Kamillosan Liquidum contains essential oil and flavones in quantified amounts as chamomile components that help determine its effectiveness. Kamillosan Liquidum is an anti-inflammatory, pain-relieving, itching-relieving, slightly disinfectant with calming and odor-eliminating properties. Kamillosan Liquidum can thus be used: For mouth rinsing and gargling: for inflammation of the oral cavity, pharynx, gums, bad breath.For inhalation and facial steam bath: for colds, inflammation of the paranasal sinuses, bronchitis. As a supportive measure for blemished skin, pustules, blackheads (acne vulgaris).For compresses, washing, partial and full baths: For itching, skin inflammation, for the after-treatment of open abscesses, boils, infected wounds, first burns Degrees.As a sitz bath: to relieve the symptoms of haemorrhoids, itching from eczema (also anal eczema) or inflammation in the area of the anus.As a children's bath: for inflammatory skin symptoms.For rinsing: for inflammatory diseases of the female genital organs.For brushing (undiluted): for inflammation of the oral mucosa, gums, paradontosis, bleeding gums.What should be considered?Kamillosan Liquidum is only suitable for external use. Don't ingest. Not for aerosol inhalation to avoid possible irritation. Before breastfeeding newborns, the mother must remove Kamillosan Liquidum from around her nipples. If local deterioration occurs or if healing does not occur within two to three weeks, a doctor should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. When should Kamillosan Liquidum not be used or only with caution?Kamillosan Liquidum should not be used if there is a known hypersensitivity to chamomile. Hypersensitivity to other daisy family (Asteraceae) such as Achillea millefolilum (sheep gift), Arnica montana (arnica), mugwort, Bellis perennis (daisy), Calendula officinalis (marigold), chrysanthemum, echinacea (coneflower) can lead to allergic cross-reactions (see under «What side effects can Kamillosan Liquidum have?») Especially if you suffer from asthma, you may only use Kamillosan Liquidum for inhalation after consulting your doctor. In addition, Kamillosan Liquidum must not be used for enemas (enema). Since Kamillosan Liquidum contains 43% alcohol by volume, it is important to dilute it correctly, especially for children. It must not be used in the area of the eyes. Inhalations and facial steam baths may not be carried out on small children. The inhalative application should only be carried out by means of water vapor inhalation. Kamillosan Liquidum should not be used in children under the age of 1 year. For further precautionary measures, see «What should be considered?». Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (including those you bought yourself) or using them externally! Can Kamillosan Liquidum be used during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child if used as directed. 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 Kamillosan Liquidum?Adults and children over 6 years:1 tablespoon (15 ml) Kamillosan Liquidum is diluted with 1 liter of warm water for: Facial steam baths (1-2 times a day),poultices,washes,partial baths,sitz baths, Rinses (once to several times a day).1 tablespoon in 1 liter of hot water: for one inhalation (1-3 times a day). Do not let children inhale unsupervised! ½ teaspoon in 1 glass of warm water: For mouth rinsing and gargling (3 or more times a day as needed). Children from 1 to 6 years:For baths: 1 tablespoon (15 ml) in 10 liters of water once a day.The unintentional oral administration of large amounts of Kamillosan Liquidum to children can lead to alcohol poisoning. Because of the danger to life of such poisoning, a doctor must be consulted immediately. 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 Kamillosan Liquidum have?Contact allergies (skin irritation) are observed with an unknown frequency. In patients with known sensitization to plants from the composite family (daisy family), e.g. yarrow, arnica, mugwort, daisy, marigold, coneflower, chrysanthemum, marguerite, a hypersensitivity reaction to chamomile can also occur due to a cross-reaction. There have been reports of skin reactions and of shortness of breath, swelling of the face and drop in blood pressure as well as anaphylactic shock after contact with the mucous membranes, especially in cases of improper use. In this case, the preparation should be discontinued and a doctor consulted if necessary. (see also «When should Kamillosan Liquidum not be used or only with caution?») If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Do not store above 30 °C. Use by period after opening: 12 months. Keep out of the reach of children. The medicinal product may only be used up to the date marked “EXP” on the package. Your doctor, pharmacist or druggist can provide you with further information. What does Kamillosan Liquidum contain?1 g of Kamillosan Liquidum contains 1 g of liquid extract from chamomile flowers (drug-extract ratio = DEV: 1:4.0-4 ,5), corresponding to 50-150 µg levomenol and 1.75-3.25 mg apigenin-7-glucoside. This preparation also contains auxiliary substances. Alcohol content 43% v/v. Approval number12537 (Swissmedic). Where can you get Kamillosan Liquidum? What packs are available? Kamillosan Liquidum is available in pharmacies and drugstores without a doctor's prescription. Packs of 100 ml, 250 ml and 500 ml are available. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen. This leaflet was last checked by the drug authority (Swissmedic) in September 2018. ..
40.28 USD
Kytta ointment tb 100 g
Kytta ointment contains an extract from the fresh roots of Symphytum officinale (commonwort) produced using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment does not smear or grease and is therefore easy to wash off. Kytta ointment is applied externally to support the treatment of degenerative rheumatoid diseases (e.g. knee osteoarthritis), muscle, joint and nerve pain, as well as blunt, bloodless injuries such as bruises, strains and sprains. Also for tendonitis and if the doctor recommends it, also for the aftercare of broken bones and dislocations. Swissmedic-approved patient informationKytta® ointmentProcter & Gamble International Operations SAHerbal medicinal product What is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (commonwort) using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment does not smear or grease and is therefore easy to wash off. Kytta ointment is applied externally to support the treatment of degenerative rheumatoid diseases (e.g. knee osteoarthritis), muscle, joint and nerve pain, as well as blunt, bloodless injuries such as bruises, strains and sprains. Also for tendonitis and if the doctor recommends it, also for the aftercare of broken bones and dislocations. When should Kytta ointment not be used or only with caution?Kytta ointment should not be used if there is a known hypersensitivity to one of the ingredients (see composition) or in small children under 3 years. 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 regions should be avoided from treatment with Kytta ointment. 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 Kytta ointment be used during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child if used as directed. 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 Kytta ointment?Unless otherwise prescribed by the doctor, apply a thin layer of Kytta ointment up to 5 times a day and massage in carefully. (Apply an ointment bandage in severe cases.) In children between the ages of 3 and 12, the treatment should not exceed one week. 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 Kytta ointment have?Rarely allergic local skin reactions (skin itching, skin redness, contact dermatitis, eczema, burning skin). Very rarely systemic hypersensitivity reactions e.g. generalized skin reactions. In such cases, the treatment should be interrupted and a doctor should be consulted. If you notice any side effects that are not described here, you should inform your doctor or pharmacist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. 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 can provide you with further information. What does Kytta ointment contain?1 g 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 auxiliary substances and flavorings, vanillin, lauryl sulfate, preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol. Approval number20713 (Swissmedic). Where can you get Kytta Ointment? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 50g, 100g and 150g. Marketing Authorization HolderProcter & Gamble International Operations SA, Lancy ManufacturerP&G Health Austria GmbH & Co. OG, Spittal, Austria. This leaflet was last checked by the drug authority (Swissmedic) in November 2014. ..
48.01 USD
Kytta ointment tb 50 g
Kytta ointment contains an extract from the fresh roots of Symphytum officinale (commonwort) produced using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment does not smear or grease and is therefore easy to wash off. Kytta ointment is applied externally to support the treatment of degenerative rheumatoid diseases (e.g. knee osteoarthritis), muscle, joint and nerve pain, as well as blunt, bloodless injuries such as bruises, strains and sprains. Also for tendonitis and if the doctor recommends it, also for the aftercare of broken bones and dislocations. Swissmedic-approved patient informationKytta® ointmentProcter & Gamble International Operations SAHerbal medicinal product What is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (commonwort) using a special process. Kytta ointment has a decongestant, pain-relieving and anti-inflammatory effect. Kytta ointment does not smear or grease and is therefore easy to wash off. Kytta ointment is applied externally to support the treatment of degenerative rheumatoid diseases (e.g. knee osteoarthritis), muscle, joint and nerve pain, as well as blunt, bloodless injuries such as bruises, strains and sprains. Also for tendonitis and if the doctor recommends it, also for the aftercare of broken bones and dislocations. When should Kytta ointment not be used or only with caution?Kytta ointment should not be used if there is a known hypersensitivity to one of the ingredients (see composition) or in small children under 3 years. 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 regions should be avoided from treatment with Kytta ointment. 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 Kytta ointment be used during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child if used as directed. 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 Kytta ointment?Unless otherwise prescribed by the doctor, apply a thin layer of Kytta ointment up to 5 times a day and massage in carefully. (Apply an ointment bandage in severe cases.) In children between the ages of 3 and 12, the treatment should not exceed one week. 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 Kytta ointment have?Rarely allergic local skin reactions (skin itching, skin redness, contact dermatitis, eczema, burning skin). Very rarely systemic hypersensitivity reactions e.g. generalized skin reactions. In such cases, the treatment should be interrupted and a doctor should be consulted. If you notice any side effects that are not described here, you should inform your doctor or pharmacist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. 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 can provide you with further information. What does Kytta ointment contain?1 g 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 auxiliary substances and flavorings, vanillin, lauryl sulfate, preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol. Approval number20713 (Swissmedic). Where can you get Kytta Ointment? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 50g, 100g and 150g. Marketing Authorization HolderProcter & Gamble International Operations SA, Lancy ManufacturerP&G Health Austria GmbH & Co. OG, Spittal, Austria. This leaflet was last checked by the drug authority (Swissmedic) in November 2014. ..
28.78 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. ..
20.83 USD
Nutergia vectiséryl gélules (sera) 60 pcs
Nutergia Vectiséryl Gélules (sera) 60 pcs The Nutergia Vectiséryl Gélules (sera) is a dietary supplement in capsule form that helps maintain joint health and reduce joint pain. It is specially formulated with natural ingredients that provide excellent anti-inflammatory and antioxidant properties to improve the overall health and mobility of the joints. This supplement contains Boswellia, Turmeric root, Devil's Claw root, and Grape seed extracts, which are well-known for their therapeutic benefits on joints and bones. Boswellia and Turmeric root extracts have excellent anti-inflammatory properties that can help reduce joint pain, stiffness, and swelling. Devil's claw root also has anti-inflammatory properties that can help ease various types of joint pain, while Grape seed extracts contain antioxidants that help protect the joints from oxidative stress and damage. The Nutergia Vectiséryl Gélules (sera) is free from chemical preservatives, gluten, and lactose, making it safe and suitable for people with dietary restrictions. This product is recommended for people who suffer from joint pain, arthritis, and other related conditions. It is also suitable for those who want to maintain healthy joint function and prevent joint problems in the future. Each bottle contains 60 capsules that are easy to take, making it convenient for daily use. It is recommended to take two capsules daily, preferably with meals. However, it is important to note that this supplement should not be used as a substitute for a varied and balanced diet and a healthy lifestyle. Key Features: Dietary supplement in capsule form Contains Boswellia, Turmeric root, Devil's Claw root, and Grape seed extracts Has excellent anti-inflammatory and antioxidant properties Helps reduce joint pain, stiffness, and swelling Free from chemical preservatives, gluten, and lactose Recommended for people with joint pain, arthritis, and related conditions Suitable for maintaining healthy joint function and preventing joint problems 60 capsules per bottle Recommended daily dose is two capsules The Nutergia Vectiséryl Gélules (sera) is an excellent dietary supplement that can help improve joint health and reduce joint pain. It is formulated with natural ingredients that provide anti-inflammatory and antioxidant properties to support joint function and mobility. Order yours today and experience the benefits of healthy and pain-free joints...
47.88 USD
Phytopharma aloe vera spray 50 ml
Phytopharma Aloe Vera Spray 50ml If you are looking for an all-natural and effective solution to soothe and moisturize your skin, Phytopharma's Aloe Vera Spray is the perfect product for you. Made with 100% pure and organic Aloe Vera, this spray provides multiple benefits, including anti-inflammatory, anti-itch, anti-bacterial, and anti-fungal properties. Key Features: 100% pure and organic Aloe Vera Soothes and moisturizes skin Anti-inflammatory and anti-itch properties Anti-bacterial and anti-fungal properties Easy to apply – comes in a convenient spray bottle Phytopharma's Aloe Vera Spray is perfect for those with sensitive or irritated skin, sunburns, insect bites, rashes, or allergies. This gentle formula hydrates and nourishes your skin, leaving it feeling soft and smooth. The spray bottle makes it easy to apply, and it gets absorbed quickly, leaving no sticky residue. Directions for use: Shake well before use Hold the bottle 5-10 cm away from the affected area Spray evenly and gently Allow it to absorb and dry Use as needed With this 50ml Aloe Vera Spray, you can take care of your skin anytime, anywhere. Keep it in your bag or purse and use it whenever your skin needs a quick boost of hydration and soothing. Order now and experience the wonders of Phytopharma's Aloe Vera Spray! ..
26.98 USD
Phytopharma msm kaps 1000 mg ds 90 pcs
The capsules contain 1000mg of distilled methylsulfonylmethane (MSM) per capsule. They can have anti-inflammatory and antioxidant effects.Composition1000 mg Distilled Methylsulfonylmethane 88.9 %, Per capsule.PropertiesVegan, lactose-free, gluten-free. Capsule shell made of hydroxypropylmethylcellulose.ApplicationTake 1 capsule daily with liquid...
65.68 USD
Pyralvex solvent with brush 10 ml
For the local treatment of acute and inflammatory diseases in the mouth and throat. Due to its anti-inflammatory and analgesic effect, Pyralvex is also prescribed by a doctor for the treatment of acute and chronic inflammation of the oral mucosa and gums, aphthae, discharge of pus from tooth cavities and eruption of teeth. Pyralvex should only be used in adolescents with fever associated with a viral disease if prescribed by a doctor and only as a second-line treatment (see "When should you be careful with the use of Pyralvex?"). Swissmedic-approved patient informationPyralvex® solutionMEDA Pharma GmbHWhat is Pyralvex and when is it used?For the local treatment of acute and inflammatory diseases in the mouth and throat. Due to its anti-inflammatory and analgesic effect, Pyralvex is also prescribed by a doctor for the treatment of acute and chronic inflammation of the oral mucosa and gums, aphthae, discharge of pus from tooth cavities and eruption of teeth. Pyralvex should only be used in adolescents with fever associated with a viral disease if prescribed by a doctor and only as a second-line treatment (see "When should you be careful with the use of Pyralvex?"). What should be considered?If Pyralvex comes into contact with the oral mucosa, but also with the skin, a temporary brown discoloration occurs. When not to use Pyralvex?If you are allergic to salicylic acid or any of the other ingredients, you should not use Pyralvex. Do not use in children under 12 years of age as internally acting salicylates are associated with Reye's syndrome in children. Reye's Syndrome is a very rare disease that damages the brain and liver and can be fatal. No confirmed cases of Reye's syndrome have been reported with Pyralvex. Due to the alcohol content, Pyralvex is not suitable for use in alcohol dependence. When should caution be taken when using Pyralvex?Adolescents with a fever associated with influenza, chickenpox or other viral diseases should only use Pyralvex on the advice of their doctor or nurse. the doctor and only use it as a second choice. If these diseases lead to disorders of consciousness with vomiting or after they have disappeared, the doctor should be consulted immediately. Do not exceed the recommended frequency of application of 3 to 4 brush strokes per day. Salicylates can be harmful if the frequency of use above is exceeded. Temporary discoloration of teeth, dentures and dentures may occur. Pyralvex contains 59.5% v/v alcohol. Do not swallow. 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 Pyralvex be used during pregnancy or while breastfeeding?Pyralvex should not be used during pregnancy or while breastfeeding unless advised by a doctor for necessary. How do you use Pyralvex?Adults and adolescents over 12 years: 1 brush stroke of Pyralvex 3 to 4 times a day (after removing from dentures) to the inflamed areas. The mouth should not be rinsed immediately afterwards. Do not eat or drink immediately after application. Each brush stroke contains approximately 0.02-0.03ml of solution. This corresponds to approximately 1-1.5 mg dry extract of rhubarb root and approximately 0.2-0.3 mg salicylic acid. Salicylates can have a damaging effect on one brush stroke if the specified application frequency of 3 to 4 times a day is exceeded. Pyralvex may only be used in adolescents with fever associated with a viral disease if prescribed by a doctor and only as a second-line drug (see “When should you be careful when using Pyralvex?”). Pyralvex should not be used in children under 12 years of age. 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 Pyralvex have?Very common (affects more than 1 user in 10)Transient local Burning at the application site. Common (affects 1 to 10 users in 100)Temporary discoloration of the teeth and oral mucosa (predominantly brown). Note: If Pyralvex comes into contact with the oral mucosa and skin, it will turn brown temporarily. Temporary discoloration of teeth, dentures and dentures can also occur. Rare (affects 1 to 10 users in 10,000)Allergic reactions. Frequency not known (cannot be estimated from the available data)Rash and hives. Reye's syndrome, which can cause life-threatening damage to the brain and liver. So far, this side effect has only occurred in children after internally administered salicylic acid or acetylsalicylic acid. No confirmed cases of Reye's syndrome have been reported with Pyralvex (see «When should you use Pyralvex with caution?» and «When should Pyralvex not be used?») 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 instructionsKeep medicines out of the reach of children. Store at room temperature (15-25°C). Close the bottle well after use. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Pyralvex contain?Active ingredients1 ml Pyralvex contains the following active ingredients: 50 mg ethanolic rhubarb root dry extract ( DER 6-8:1) containing 5 mg anthraquinone glycoside and 10 mg salicylic acid. Excipients1 ml of Pyralvex contains ethanol 96% and purified water as excipients. Alcohol content 59.5% by volume. Authorization number10700 (Swissmedic) Where can you get Pyralvex? What packs are available?In pharmacies and drugstores, without a doctor's prescription. 10 ml bottles with brush. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen. This leaflet was last checked by the Medicines Agency (Swissmedic) in November 2021. [Version 201 D] ..
30.11 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?< p>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] ..
25.95 USD
Saridon neo filmtablet 400 mg 10 pcs
What is Saridon neo 400 and when is it used? Saridon neo 400 contains the active ingredient ibuprofen. This has pain-relieving, fever-reducing and anti-inflammatory properties.Saridon neo 400 is suitable for short-term treatment, i.e. for a maximum of 3 days treatment of: Pain in the joints and ligaments;Back pain;Headache;Toothache;Pain during the menstrual period;Pain after injury;Fever with a flu.When should Saridon neo 400 not be used?Saridon neo 400 must not be takenif you are allergic to any of the ingredients or have shortness of breath after taking acetylsalicylic acid or other painkillers or anti-inflammatory drugs, so-called non-steroidal anti-inflammatory drugs , or had allergic-like skin reactions,If you are pregnant or breastfeeding (see also the chapter "Can Saridon neo 400 be taken during pregnancy or while breastfeeding?").If you a stomach and/or duodenal ulcer or gastrointestinal bleeding,in chronic intestinal inflammation (Crohn's disease, ulcerative colitis),in severe impairment of liver or kidney function,< /li>for severe heart failure,for the treatment of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine)In children under 12 years of age. Saridon neo 400 has not been tested for use in children under the age of 12.When is caution required when taking Saridon neo 400?During treatment with Saridon neo 400, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (perforation in the stomach or intestines) can occur in the upper gastrointestinal tract. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under "Infection".Certain painkillers called COX-2 inhibitors have been shown to be associated with an increased risk of heart attack and stroke at high doses and/or long-term treatment. This risk can also be slightly increased with Saridon neo 400 at a high dose (2400 mg/day). However, at the usual dosage (maximum 1200 mg/day), no increase in this risk was found. If you have already had a heart attack, stroke or venous thrombosis, the use of Saridon neo 400 in high doses is no longer recommended. Do not exceed the recommended dose or duration of treatment and in any case tell your doctor if you have already had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes (diabetes), high blood fat levels, smoking). Your doctor will decide whether you can still use Saridon neo 400 and which dose is right for you.Taking Saridon neo 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid accumulation (oedema). Tell your doctor if you have heart or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or if you lose more fluids, e.g. through heavy sweating.This medicine can the reactionimpair your ability to drive and use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of stomach or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients and patients who suffer or have suffered from asthma, chronic inflammation of the nasal mucosa (chronic cold), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases).In connection with the ibuprofen-containing medicines serious skin reactions reported. You should stop taking Saridon neo 400 and see a doctor straight away if you develop a skin rash, mucosal lesions, blisters or other signs of allergy, as these can be the first signs of a very serious skin reaction.The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of an allergy, you should stop taking Saridon neo 400 and seek medical treatment immediately, as these can be the first signs of a very serious skin reaction (see the section «What side effects can Saridon neo 400 have?»).Saridon neo 400 should not be used if you have chickenpox.InfectionsSaridon neo 400 can cause signs of infections such as cover up fever and pain. It is therefore possible that Saridon neo 400 may delay appropriate treatment of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Tell your doctor, pharmacist or druggist if you have recently been treated for an abortion.Tell your doctor, pharmacist or druggist if you are being treated with medicines such as blood thinners (e.g. low dose acetylsalicylic acid), diuretics (water tablets), ACE inhibitors or β-blockers (medicines for high blood pressure and heart failure), antibiotics, certain medicines for fungal infections (e.g. voriconazole or fluconazole), immunosuppressants (medicines for transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, anti-AIDS, epilepsy and depression. Non-steroidal anti-inflammatory drugs such as ibuprofen and the drugs listed above can interact. In particular, long-term treatment with Saridon neo 400 may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other painkillers should not be taken at the same time as ibuprofen, as the risk of side effects can increase. Concomitant consumption of alcohol can cause side effects, particularly those affecting the gastrointestinal tract or the central nervous system , be intensified.Long-term use of painkillers can cause headaches. Do not treat them with an increased dose of the drug, but inform your doctor.Elderly patientsElderly patients are more likely to experience side effects after using non-steroidal anti-inflammatory drugs, in particular bleeding and perforation in the stomach and intestines. Therefore, particularly careful medical supervision is required in elderly patients.Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!) or using them externally!Can Saridon neo 400 be taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take Saridon neo 400 after consulting your doctor or your doctor. Saridon neo 400 must not be taken during the last third of pregnancy.BreastfeedingSaridon neo 400 should not be taken while breastfeeding unless your doctor has expressly instructed you to do so permitted. How do you use Saridon neo 400? Adults and adolescents over the age of 12 Take 1 film-coated tablet of Saridon neo 400 with plenty of liquid. A gap of 6 hours must be observed before the next dose.Maximum daily dose: Do not take more than 3 film-coated tablets of Saridon neo 400 within 24 hours, unless prescribed by a doctor. In the case of pain during the menstrual period, it is recommended to start treatment at the first sign of the symptoms. Do not use Saridon neo 400 for longer than 3 days and only to treat the symptoms listed above.If the symptoms increase despite taking Saridon neo 400 or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. Children under the age of 12 Saridon neo 400 must not be used in children under the age of 12. The use and safety of Saridon neo 400 in children under the age of 12 have not yet been systematically tested.Elderly patientsElderly patients can react more sensitively to the drug than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.If you have taken more Saridon neo 400 than you should, always consult a doctor for an assessment of the risk and advice on further treatment.Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported. If you forget to take a dose, do not take more than the usual recommended amount for the next dose. Follow the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Saridon neo 400 have?The following side effects can occur when taking Saridon neo 400. They are listed according to their frequency:Common (affects 1 to 10 users in 100)Gastro-intestinal disorders such as indigestion, diarrhoea , nausea, vomiting, constipation, pain in the upper abdomen, flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizziness.Acute skin rash.Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.Hypersensitivity reactions.Insomnia, feeling anxious.Visual disturbances (the visual disturbances are usually reversible if treatment is stopped), ringing in the ears, hearing loss, dizziness.< li>Asthma, spasm of the muscles of the airways and shortness of breath, There is a risk of acute pulmonary edema (water lung) in patients with heart failure.Fatigue.Rare (affects 1 up to 10 out of 10,000 users)Aseptic meningitis (inflammation of the meninges).Angina, high fever, swelling of the lymph nodes in the neck area.< /li>Allergic reactions, symptoms of lupus erythematosus (butterfly plexus), anemia.Depression, confusion."Tingling" of the skin, drowsiness.< li>Irreversible visual impairment or poor eyesight.Inflammation of the gastric mucosa, gastric and intestinal ulcers, ulcers of the oral mucosa, gastric and intestinal perforations.Hepatitis, jaundice, liver dysfunction.< li>Hives, itching, bleeding into the skin, swelling of the skin and mucous membranes, sensitivity to light.Various kidney diseases such as kidney dysfunction with water accumulation in the tissue and even kidney failure.General swelling .Very rare (affects less than 1 in 10,000 users)Psychotic states.< li>Heart failure, heart attack.High blood pressure.Inflammation of the pancreas.Aggravation of colitis or Crohn's disease.Liver failure.Severe allergic skin reactions with formation of blisters and/or extensive detachment of the skin.Individual cases A severe skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).worsening of colitis or Crohn's disease.A red, scaly, widespread rash with bumps under the skin and blisters, mostly located in the skin folds on the trunk and upper extremities (acute generalized exanthematous pustulosis). Stop taking Saridon neo 400 if you experience these symptoms and see a doctor straight away.Frequency unknown..
21.56 USD
Shaolin muscle fluid spray 100 ml
Shaolin Muskel Fluid Spray 100 ml: A soothing recovery aid for athletes Shaolin Muskel Fluid Spray is a specialized recovery aid designed for athletes, especially those who participate in high-intensity sports. Suitable for both novice and professional athletes, this spray is designed to help soothe tired muscles and reduce inflammation resulting from intense physical activity. It provides quick relief from muscle soreness that can slow one down and prevent optimal performance. What is Shaolin Muskel Fluid Spray? Shaolin Muskel Fluid Spray is a highly effective blend of traditional Chinese herbal extracts, combined with modern scientific knowledge to provide a deep penetrating and soothing effect on sore muscles. The spray contains vital components, such as camphor, peppermint oil, and menthol, which are known for their anti-inflammatory and analgesic properties. How to use Shaolin Muskel Fluid Spray? To use Shaolin Muskel Fluid Spray, simply apply a small amount to the affected area, and massage gently for a few minutes. The non-greasy formula allows for quick absorption and delivers fast relief to the sore areas. For best results, use daily or as required to keep the muscles supple and conditioned. Benefits of using Shaolin Muskel Fluid Spray Reduces inflammation and swelling in muscles and joints Soothes muscle soreness and stiffness Improves mobility and flexibility Helps to prevent injuries and improve recovery time Non-greasy formula that is easy to apply Shaolin Muskel Fluid Spray is a must-have for every athlete looking to improve their performance and maintain optimal health. Order yours today and experience the benefits of traditional Chinese herbal medicine, combined with modern scientific methods for total muscle recovery and conditioning. ..
42.64 USD
Sportusal emgel tb 50 g
Sportusal Emgel and Gel contain a combination of analgesic, anti-inflammatory and decongestant active ingredients. Hydroxyethyl salicylate fights pain and inflammation. Heparin counteracts blood clotting and improves the reduction of bruising and swelling. DMSO promotes the absorption of these active ingredients through the skin into the organism. Sportusal Emgel and Gel are suitable for external use for the following complaints: Sports and accident injuries such as bruises, strains, contusions, sprains with bruising and swelling; Inflammation of muscles and ligaments; Venous leg disorders with symptoms such as pain, Heaviness, swollen legs (stasis oedema). With a doctor's prescription, Sportusal Emgel/Gel can also be used to treat superficial phlebitis. Sportusal Emgel and Gel have a cooling effect and not greasy. Swissmedic-approved patient informationSportusal® Emgel/GelPermamed AGWhat is Sportusal Emgel/Gel and when is it used? Sportusal Emgel and Gel contain a combination of analgesic, anti-inflammatory and decongestant active ingredients. Hydroxyethyl salicylate fights pain and inflammation. Heparin counteracts blood clotting and improves the reduction of bruising and swelling. DMSO promotes the absorption of these active ingredients through the skin into the organism. Sportusal Emgel and Gel are suitable for external use for the following complaints: Sports and accident injuries such as bruises, strains, contusions, sprains with bruising and swelling;Inflammation of muscles and ligaments;Venous leg disorders with symptoms such as pain, Heaviness, swollen legs (stasis edema).With a doctor's prescription, Sportusal Emgel/Gel can also be used to treat superficial phlebitis.Sportusal Emgel and Gel have a cooling effect and not greasy. What should be considered?Follow the advice of your doctor that goes beyond the actual dosage recommendations, such as doing gymnastics or support stockings for vein diseases to wear. When must Sportusal Emgel/Gel not be used?Sportusal Emgel and Gel must not be applied to open wounds or damaged skin or brought into the eyes or on mucous membranes, and they may be used in the case of known hypersensitivity or intolerance to one of the ingredients, severe liver and kidney dysfunction, bleeding tendency, blood clotting disorders, known heparin-induced/associated thrombocytopenia (HIT, heparin-induced lack of blood platelets), circulatory disorders, bronchial asthma and in children children under the age of five should not be used. When is caution required when using Sportusal Emgel/Gel?In children and patients with kidney problems, Sportusal Emgel and Gel should only be used on small areas of skin and not used for more than a few days. If you have experienced hypersensitivity reactions to previous treatments with certain anti-inflammatory medicines, you should talk to your doctor before using Sportusal Emgel und Gel. Body parts treated with Sportusal Emgel and Gel should not be covered with airtight bandages. In the case of venous diseases that are due to the presence of a blood clot (so-called thrombosis), massage must not be performed. If symptoms worsen, see a doctor. This medicine contains coumarin as a fragrance and may cause allergic reactions. Sportusal Gel contains 70 mg/g propylene glycol as an excipient which may cause skin irritation. Sportusal Gel contains 200 mg/g alcohol (ethanol). It can cause a burning sensation on damaged skin. Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (including those you bought yourself) or using them externally. Can Sportusal Emgel/Gel be used during pregnancy or while breastfeeding?Sportusal Emgel and Gel must not be used during pregnancy or while breastfeeding, unless unless expressly prescribed by a doctor. How do you use Sportusal Emgel/Gel?AdultsUnless otherwise prescribed by the doctor , Sportusal Emgel or Gel several times a day on the affected areas and spread lightly. Do not apply Sportusal Emgel and Gel to open wounds or damaged skin. If bandages are necessary for therapeutic reasons, they should be permeable to air and should be put on no earlier than 5 minutes after Sportusal Emgel/Gel has been applied. Vein patients who wear compression stockings or bandages during the day should only use Sportusal Emgel and Gel in the evening. The use and safety of Sportusal Emgel/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 Sportusal Emgel/Gel have?The following side effects can occur when using Sportusal Emgel and Gel: In rare cases, allergic skin reactions may occur. If such reactions occur, the drug should be discontinued immediately and, if necessary, the doctor informed. Occasional skin redness, itching and burning are caused by the vasodilating effect of Sportusal Emgel/Gel and generally disappear during further treatment. The use of Sportusal Emgel and Gel can temporarily result in a garlic-like odor on the breath. In rare cases, nausea and headaches may occur. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Do not take Sportusal Emgel/Gel and keep out of the reach of children. Store at room temperature (15-25 °C) and protect from direct sunlight and frost. 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 Sportusal Emgel/Gel contain?Active ingredients1 g Sportusal Emgel contains as active ingredients: 500 IU heparin sodium, 100 mg hydroxyethyl salicylate, 50 mg dimethyl sulfoxide (DMSO), 25 mg macrogol 9 lauryl ether (Polidocanol 600). 1 g Sportusal Gel contains as active ingredients: 500 IU heparin sodium, 100 mg hydroxyethyl salicylate, 50 mg dimethyl sulfoxide (DMSO), 20 mg macrogol 9 lauryl ether (Polidocanol 600). Excipients1 g Sportusal Emgel contains as auxiliaries: glycerol monostearate, macrogol 100 stearate, macrogol 2 stearate, dexpanthenol, dimethicone , Carbomer 974P, Levomenthol, Rosemary Oil, Coumarin, Lavandin Oil, Polyquaternium 11, Pentadecalactone, Sodium Hydroxide, Purified Water. 1 g Sportusal Gel contains as auxiliary substances: dexpanthenol, carbomer 980, ethanol 96%, propylene glycol (E 1520), glycerin 85%, isopropanol, levomenthol, rosemary oil, coumarin, lavandin oil, pentadecalactone, sodium hydroxide , purified water. Approval number47077, 47078 (Swissmedic). Where can you get Sportusal Emgel/Gel? What packs are available?In pharmacies and drugstores without a doctor's prescription. Packs of 50g and 100g. Authorization holderPermamed AG, Dornach. This leaflet was last checked by the Medicines Agency (Swissmedic) in February 2022. ..
25.48 USD
Tonopan forte drag 25 mg 10 pcs
What is Tonopan forte 25 mg coated tablets and when is it used? Tonopan forte 25 mg coated tablets contain the active ingredient diclofenac potassium. This belongs to the group of non-steroidal anti-inflammatory drugs (prostaglandin synthesis inhibitors) and has an analgesic, fever-reducing and anti-inflammatory effect. The effect occurs within 30-60 minutes and lasts about 4-6 hours. Tonopan forte 25 mg coated tablets are suitable for short-term treatment, i.e. for a maximum of 3 days of treatment of: headache, toothache, menstrual pain , pain in the area of joints and ligaments, back pain, pain from injuries and to reduce fever with flu-like illnesses.When should Tonopan forte 25 mg dragées not be taken?If you are allergic to diclofenac or any of the excipients, or have had shortness of breath or allergy-like skin reactions, e.g. swelling of the face, lips, tongue, throat and /or on the extremities (signs of angioedema),if you are pregnant or breastfeeding (see also the chapter "Can Tonopan forte 25 mg coated tablets be taken during pregnancy or while breastfeeding?"),if you have an active stomach and/or duodenal ulcer or gastrointestinal bleeding or perforation (this may manifest itself as blackening of the stool, blood in the stool or vomiting of coffee grounds-like material),for chronic intestinal inflammation (Crohn's disease or ulcerative colitis),for severe impairment of liver or kidney function,for severe heart failure,for the treatment of pain after a coronary bypass operation on the heart (or Use of a heart-lung machine),in children and adolescents under the age of 14. Tonopan forte 25 mg coated tablets have not been tested for use in children and adolescents under 14 years of age. For this reason, Tonopan forte 25 mg dragees must not be used in children and adolescents under the age of 14.When is caution required when taking Tonopan forte 25 mg dragees?< p>During treatment with Tonopan forte 25 mg coated tablets, ulcers in the mucous membranes of the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. These complications can occur at any time during treatment, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine.Older people may be more sensitive to the medicine than younger adults. It is particularly important that older patients report any side effects to their doctor immediately.In the following situations, you may only take Tonopan forte 25 mg coated tablets if prescribed by a doctor and under medical supervision: if you are currently being treated by a doctor for a serious illness;if you have previously suffered from a stomach or duodenal ulcer;if you have a heart or blood vessel disease (known as cardiovascular disease, including uncontrolled high blood pressure, heart failure, existing ischemic heart disease or peripheral arterial disease), have ever had a heart attack, stroke or venous thrombosis, or if you have risk factors (such as high blood pressure, Diabetes [diabetes], high levels of fats in the blood [cholesterol, triglycerides], smoking). tonopan forte 25 mg dragées is usually not recommended in these situations. For certain painkillers with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found with high doses and/or long-term treatment. It is not known whether this increased risk also applies to Tonopan forte 25 mg coated tablets. It is important that you use the lowest effective dose to relieve your pain and that you take Tonopan forte 25 mg coated tablets for the shortest time necessary to reduce the risks to keep cardiovascular side effects as low as possible.if you have kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating or during Diarrhea; taking Tonopan forte 25 mg coated tablets can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;< li>if you are being treated with anticoagulants (blood thinners, anticoagulants) or have a blood clotting disorder or any other blood disorder, including the rare disease hepatic porphyria;if you have asthma;if you are taking anti-rheumatic drugs or other painkillers (e.g. acetylsalicylic acid, aspirin, ibuprofen) or other anti-inflammatory drugs (corticosteroids);if you are taking the following medicines: lithium or specific serotonin reuptake inhibitors (SSRI's, medicines to treat depression), digoxin (medicine for heart problems), diuretics (medicines to increase urine output), medicines (e.g. metformin) to treat diabetes/diabetes with the exception of insulin, methotrexate (used to treat arthritis and cancer), ciclosporin or Tacrolimus (for organ transplants), trimethoprim (for urinary tract infections), quinolone antibiotics (to treat infections), voriconazole (to treat fungal infections), phenytoin (to treat epileptic seizures), or sulfinpyrazone (gout medicine).If you notice signs or symptoms while taking Tonopan forte 25 mg coated tablets that indicate problems with the heart or blood vessels, such as chest pain, shortness of breath, weakness or slurred speech, contact your doctor immediately.In very rare cases, anti-inflammatory drugs (including Tonopan forte 25 mg coated tablets) can cause serious skin reactions (e.g. skin rash). At the first sign of a skin reaction, treatment with Tonopan forte 25 mg coated tablets should be discontinued and medical attention sought immediately. Tonopan forte 25 mg coated tablets can reduce the symptoms of an infection (e.g. high fever) and thus the diagnosis of the Complicate infection.Information on the excipientsSucrose:Tonopan forte 25 mg coated tablets contain sucrose (45,416 mg per coated tablet). Please only take Tonopan forte 25 mg dragées after consulting your doctor if you know that you suffer from sugar intolerance. This medicine contains less than 1 mmol sodium (23 mg ) per dragee, i.e. it is almost "sodium-free".This medicine may impair your ability to react, the ability to drive and the ability to use tools or machines. In particular, if you experience dizziness or visual disturbances, you should refrain from driving or using machines.Inform your doctor, pharmacist or druggist if yousuffer from other diseases,Have allergies oruse other medicines (including those you bought yourself!)!Can Tonopan forte 25 mg coated tablets be taken during pregnancy or while breastfeeding?< /h3>PregnancyIf you are pregnant or planning a pregnancy, you should only take Tonopan forte 25 mg coated tablets after consulting your doctor. Tonopan forte 25 mg dragees should not be taken during the last third of pregnancy.BreastfeedingTonopan forte 25 mg dragees should not be taken while breastfeeding, unless your doctor has told you expressly allowed you to do so.Like other anti-inflammatory drugs, Tonopan forte 25 mg coated tablets can make it more difficult to become pregnant. After stopping the drug, this effect ends. If you are planning to become pregnant or are having difficulties conceiving, talk to your doctor.How do you use Tonopan forte 25 mg coated tablets?How many Tonopan forte 25 mg dragées should be taken?The recommended dosage must not be exceeded.The lowest effective dose should always be taken for the shortest possible time. Adults and adolescents from the age of 14: Swallow 1 dragée Tonopan forte 25 mg up to 3 times a day with plenty of water, preferably with or after eating. Before the next dose an interval of at least 4 to 6 hours must be observed. Maximum daily dose: Do not take more than 3 tablets Tonopan forte 25 mg within 24 hours, unless prescribed by a doctor. How long should Tonopan forte 25 mg dragees be taken?Do not take Tonopan forte 25 mg dragees for longer than 3 days and only to treat the symptoms listed above.If the symptoms persist or worsen, consult your doctor so that the reason can be clarified. A serious illness can be the cause.If you have taken more Tonopan forte 25 mg coated tablets than you should?If you have accidentally taken more coated tablets, contact your doctor immediately Doctor, to your doctor. Children and adolescents under the age of 14: Tonopan forte 25 mg coated tablets should not be used in children and adolescents under the age of 14. The use and safety of Tonopan forte 25 mg dragées in children and adolescents under the age of 14 has not yet been tested.Elderly patients:Elderly patients can react more sensitively to the drug than younger ones Adult. It is particularly important that elderly patients report any side effects to their doctor immediately.Follow the dosage provided in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Tonopan forte 25 mg coated tablets have? The following side effects may occur after taking Tonopan forte 25 mg coated tablets: Common side effects (in 1 to 10 out of 100 patients): Abdominal pain, stomach pain, diarrhea, nausea, vomiting, gas, indigestion, decreased appetite;Headache, lightheadedness;Rash;Dizziness;Increased liver enzyme levels.Uncommon side effects (affects 1 to 10 patients in 1000):palpitations, sudden and oppressive chest pain (signs of heart attack and heart attack)*;shortness of breath, difficulty breathing when lying down, swelling of the feet or legs (signs of heart failure)*.Rare side effects (affects 1 to 10 patients in 10,000):Unusual tiredness; Itchy rash;Upper gastrointestinal tract, blood in stools or blackening of stools, vomiting blood, bloody diarrhea;Allergic reaction including Difficulty breathing or swallowing, swelling of the face, mouth, tongue or throat often with a rash, collapse;Wheezing or shortness of breath, feeling choked (signs of asthma);Swelling of the arms, legs and feet (oedema);Yellow skin or eyes (signs of liver inflammation or liver failure).Very rare side effects (less than 1 in 10,000 patients):Bleeding or unusual bruising;Low white blood cells (causing a high fever or persistent sore throat, frequent infections), low red blood cells;Constipation, sore mouth, sore and red tongue, taste disturbance, upper abdominal cramps;Itching and reddening of the skin, hair loss;Tingling or rigidity of the hands or feet, tremors;blurred vision, ringing in the ears, hearing problems;Mood swings, trouble sleeping, confusion;If you notice any side effects, talk to your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.* This frequency can occur when taking a high daily dose (150 mg) over a longer period of time.What is other things to note?Shelf lifeThe medicinal product may only be used up to the date marked «EXP» on the container.Storage instructions Store at 15-30°C. Keep out of the reach of children. Further information Your doctor, pharmacist or druggist can provide you with further information Your doctor, pharmacist or druggist. These people have the detailed technical information.What does Tonopan forte 25 mg dragee contain?Active substance1 Tonopan forte 25 mg dragee contains 25 mg diclofenac Potassium.ExcipientsSucrose, tricalcium phosphate, corn starch, sodium starch glycolate (type A), colloidal anhydrous silicon dioxide, povidone, magnesium stearate, talc, macrogol 8000, microcrystalline cellulose, iron oxide (E 172 ), titanium dioxide (E 171).Approval number66826 (Swissmedic).Where can you get Tonopan forte 25 mg coated tablets? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Packs of 10 dragées Tonopan forte 25 mg. Approval inhaberinGSK Consumer Healthcare Schweiz AG, Risch.This leaflet was last checked by the drug authority (Swissmedic) in June 2020...
28.51 USD
Traumalix forte emgel tb 40 g
h1,h2,h3,h4{font-size: 14px !important;font-family: Verdana, Geneva, Tahoma, sans-serif;font-weight: bold !important ;} p,li,ul{font-size: 14px !important;font-family: Verdana,sans-serif;} div#desc h3 {font-size: 14px !important;}#777{font-family: Verdana; font-size: 14px;} What is Traumalix forte EmGel and when is it used ? Traumalix forte EmGel is used externally and has anti-inflammatory and analgesic properties. The active ingredient etofenamate penetrates the skin and reaches the diseased tissue areas. Traumalix forte EmGel does not grease or smear. Traumalix forte EmGel is used to treat pain, inflammation and swelling in sprains, bruises and strains (e.g. after sports injuries). When should Traumalix forte EmGel not be used? On injured or eczematous skin and if you are hypersensitive to the active ingredient etofenamate , Flufenamic acid and other non-steroidal anti-inflammatory drugs (anti-rheumatic drugs) and the excipient propylene glycol. Do not use on babies and toddlers! When should you be careful when using Traumalix forte EmGel? Traumalix forte EmGel should not be used over a long period of time, unless a doctor prescribes it. The eyes and mucous membranes should not come into contact with the gel. Inform your doctor, pharmacist or chemist if you have already used similar products (rheumatoid ointments) and are allergic to them Reactions resulted if you suffer from other diseases, have allergies or other medicines (including those you bought yourself! ) or apply externally. May Traumalix forte EmGel be used during pregnancy or while breastfeeding ? Traumalix forte EmGel must not be used during pregnancy and breastfeeding unless expressly prescribed by a doctor. As a precaution, you should use during pregnancy and breastfeeding as much as possible Refrain from medication or ask your doctor, pharmacist or druggist for advice . How do you use Traumalix forte EmGel? Adults: Traumalix forte EmGel several times a day - depending on the size of the painful areas - apply a 5-10 cm long strand and rub it into the skin. Inform your doctor if the symptoms worsen or have not improved after 2 weeks. Children The application and safety of Traumalix forte EmGel in children and adolescents has not yet been tested. Adhere to the dosage given in the package insert or prescribed by your doctor. If you think that the medicine is too weak or too strong, talk to your doctor, pharmacist or chemist. What side effects can Traumalix forte EmGel have? The following side effects can occur when using Traumalix forte EmGel: In rare cases In some cases, local allergic reactions such as reddening, skin rashes can occur, which usually resolve quickly after discontinuation of the preparation. Otherwise, contact your doctor. 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 should you watch out for? The drug may only be used up to the date marked «EXP» on the container. Store out of the reach of children at room temperature (15 - 25 ° C). Your doctor, pharmacist or druggist can provide you with further information. These persons have the detailed technical information. What does Traumalix forte EmGel contain? 1 g Traumalix forte EmGel 10% contains: Active ingredient: 100 mg Etofenamate Excipients: Propylene glycol, Aromatica, other excipients Authorization number 66403 (Swissmedic). Where can you get Traumalix forte EmGel? Which packs are available? In pharmacies and drugstores without a doctor's prescription Traumalix forte EmGel Tb 100 gTraumalix forte EmGel Tb 40 g Authorization holder Drossapharm AG, Basel. ..
21.18 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. ..
54.68 USD
Weleda berberis fructus unguentum 10% 25 g
Weleda Berberis Fructus Unguentum 10% 25 g Product Description The Weleda Berberis Fructus Unguentum 10% 25 g is a unique, natural ointment that offers a wide range of benefits for the skin. This product is made with berberis fructus extract, which is known to have strong anti-inflammatory and antiseptic properties that make it ideal for soothing and treating a variety of skin conditions. The Weleda Berberis Fructus Unguentum 10% 25 g is specially formulated for individuals who have dry, irritated or sensitive skin. This product helps to soothe and heal the skin, while protecting it from further damage caused by environmental factors. It also helps to reduce redness, itching and inflammation, providing relief from a range of skin irritations. Whether you suffer from eczema, rosacea, psoriasis, or other skin conditions, the Weleda Berberis Fructus Unguentum 10% 25 g can provide the relief that you need. It is also great for general skin care and can be used to treat minor cuts, burns, and bruises. This product is gentle and safe for all skin types, and is free from synthetic fragrances, colorants or preservatives. When using the Weleda Berberis Fructus Unguentum 10% 25 g, it is recommended to apply a small amount to the affected area of the skin and gently massage it in. This ointment can be used as often as needed, and is best applied before going to bed to allow the skin to heal overnight. Overall, the Weleda Berberis Fructus Unguentum 10% 25 g is an excellent product for those who want to keep their skin healthy and happy, and is a must-have addition to any skincare routine...
32.04 USD
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