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antihistamine

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Antihistamines are medications designed to relieve or prevent the symptoms of allergic reactions, such as sneezing, itching, and runny nose, by blocking the action of histamine, a substance in the body that causes allergic symptoms. Our range of Swiss-manufactured antihistamines includes products for systemic use and nasal applications, offering effective relief for conditions like hay fever, urticaria, and allergic rhinitis. Shop our selection for safe and reliable health and beauty solutions tailored to manage allergies and enhance your well-being.
Arbid n drops fl 30ml

Arbid n drops fl 30ml

 
Product code: 4868528

What is Arbid N, oral drops and when is it used? Arbid N contains an antihistamine, chlorphenamine maleate. It is used in inflammatory and allergic diseases of the upper respiratory tract such as colds, hay fever, chronic runny nose, vasomotor or allergic rhinitis, rhinopharyngitis, allergic sinusitis and as an adjuvant in influenza and colds. For the symptomatic treatment of allergic conditions such as urticaria (nettle rash), conjunctivitis (conjunctivitis). When should Arbid N, drops to be used not be used? If you are sensitive to any component of the drug, at risk of narrow-angle glaucoma (increased pressure in the eye) or have difficulty urinating, or during concomitant treatment and for up to 2 weeks after stopping treatment with certain drugs for depression (especially MAO-He always). In addition, Arbid N must not be used during the last trimester of pregnancy or while breastfeeding (see «Can Arbid N be taken during pregnancy and while breastfeeding?»).Arbid N must not be used in children under the age of 3 years.When should caution be taken when taking/using Arbid N, oral drops?Arbid N must not be used for a long time or in higher than recommended doses without medical advice.Stepping Allergic reactions to or narrowing of the bronchi with breathing difficulties, so-called bronchospasm (see under «What side effects can Arbid N have?»), the treatment must be stopped immediately and the doctor informed.This medicine can impair the ability to react, the ability to drive and the ability to use tools or machines.Arbid N contains sucrose. Therefore, if you know that you have an intolerance to certain sugars, please consult your doctor before taking Arbid N before taking Arbid N.Arbid N contains sodium methyl parahydroxybenzoate (E219) and sodium propyl parahydroxybenzoate (E217), which may cause allergic reactions (possibly delayed).This medicinal product contains less than 1 mmol sodium (23 mg) per gram (20 drops), i.e. it is almost «sodium-free». Inform your doctor, pharmacist or pharmacist or your doctor, pharmacist or pharmacist if you suffer from other illnesses, have allergies or are taking other medicines (including those you bought yourself!) or using them externally.May Arbid N, swallow drops be taken/used during pregnancy or while breastfeeding?If you foresee becoming pregnant, if you If you are pregnant or breastfeeding, you should avoid taking medicines. It is known that taking Arbid N during the last trimester can adversely affect the health of the fetus. For this reason, Arbid N must not be taken during the last trimester. Arbid N can be taken during the first and second trimester if there is a strong indication and if the doctor prescribes it.Arbid N must not be taken during breast-feeding. However, if you absolutely have to take Arbid N when prescribed by a doctor, you must refrain from breastfeeding.How do you use Arbid N, drops to swallow?Unless otherwise prescribed by the doctor, the usual dosage for children aged 3-5 years is: 10 drops 4-6 times a day; for children aged 6-12 years: 20 drops 4-6 times a day, for adults: 40 drops 4-6 times a day. Preferably take between meals. Observe the dosage given in the package leaflet or described by your doctor. WhomIf you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Arbid N, swallow drops have?The following side effects can occur when taking Arbid N:Sensitive people can have allergic reactions (rash, itching, increased heart rate, breathing disorders, loss of consciousness). In this case, you should stop taking the medicine and talk to your doctor as soon as possible.If you take an overdose of the active ingredient chlorphenamine, you may experience cramps, difficulty breathing, even acute shortness of breath and coma. Children, especially small children, react with particular sensitivity if the dosage is too high.Common (affects 1 to 10 users in 100)Drowsiness and reduced responsiveness (see «When should caution be taken when taking/using Arbid N, drops to swallow?»).Uncommon (affects 1 to 10 users in 1000)Stomach and intestinal disorders such as constipation; dry mouth; trouble urinating; visual disturbances (accommodation disorders); increase in intraocular pressure; restlessness (especially in children); Nervousness; Sleep disturbances.OccasionallySkin rash and bone marrow depression.If you nevertheless observe side effects, inform 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 Arbid N at room temperature (15-25 °C) in the original packaging out of the reach of children. Close the opened container carefully after taking a dose.Further informationThe Arbid N bottles have a child-resistant closure. To open, the cap must be pressed down and turned at the same time. The childproof lock is only effective if the cap is firmly screwed on as far as it will go after use. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information. What does Arbid N, drops to swallow contain? 1 g (approx. 20 drops) drops to swallow contains: Active ingredients 2 mg chlorphenamine maleate. Excipients Sucrose, citric acid monohydrate, sodium methyl(4-hydroxybenzoate) (E 219), sodium propyl(4-hydroxy benzoate) (E 217), orange aroma, purified water.Authorization number58373 (Swissmedic).Where can you get Arbid N, drops to swallow? Which packs are available? In pharmacies and drugstores, without a doctor's prescription, in 30 ml dropper bottles. Authorization holder VERFORA SA, 1752 Villars-sur-Glâne. This leaflet was last checked by the medicinal products authority (Swissmedic) in December 2020...

28.64 USD

Ceteco sandoz filmtablet 10 mg 10 pcs

Ceteco sandoz filmtablet 10 mg 10 pcs

 
Product code: 4962983

What Ceteco Sandoz is and what it is used forCeteco Sandoz is effective in the basic treatment of allergic diseases. It blocks the action of histamine, which is released in the body during allergic reactions. Ceteco Sandoz is used in adults and children from 6 years of age to treat allergic diseases such as hay fever, allergic rhinitis and allergic conjunctivitis and chronic hives (which are often associated with itching). The treatment duration for children with allergic rhinitis must not exceed 4 weeks. Ceteco Sandoz is available in the form of film-coated tablets or drops.When should Ceteco Sandoz not be taken?Patients who are hypersensitive to the active substance, other related substances or any other component of Ceteco Sandoz should not use the preparation.Women who are breastfeeding should not use Ceteco Sandoz. Pregnant women should only take Ceteco Sandoz if prescribed by a doctor.Since Ceteco Sandoz film-coated tablets contain lactose, patients with rare hereditary disorders such as galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption syndrome should not take the film-coated tablets.Patients with end-stage kidney disease (with a glomerular filtration rate (GFR) below 15 ml/min) should not take Ceteco Sandoz.When is caution required when taking Ceteco Sandoz?Children under 6 years of age should not be treated with Ceteco Sandoz. You should only take Ceteco Sandoz film-coated tablets and theophylline (an active substance used to treat shortness of breath) after consulting your doctor. Ceteco Sandoz and preparations containing glipizide (a drug used to treat diabetes) should not be taken together. It is recommended to take the Glipizide medication in the morning and Ceteco Sandoz in the evening.Ceteco Sandoz should be used with caution in epileptics as it could potentially trigger seizures.Caution should be exercised when using Ceteco Sandoz at the same time as sedatives or painkillers.Caution should be exercised when driving a motor vehicle or using machines as taking Ceteco Sandoz may make you drowsy.It is advisable not to drink alcohol during treatment with Ceteco Sandoz.If you are going to have an allergy test, ask your doctor if you should stop taking Ceteco Sandoz for a few days before the test, as this medicine could affect the result of an allergy test.Ceteco Sandoz can increase the risk of urinary retention in patients with a tendency to urinary retention (such as spinal cord injury, prostate enlargement).Tell your doctor, pharmacist or druggist if yousuffer from other diseaseshave allergies orare taking other medicines (including those you bought yourself!).Can Ceteco Sandoz be taken during pregnancy or while breastfeeding?No undesirable effects have been found in animal experiments. However, like other medicines, Ceteco Sandoz should not be taken during pregnancy. If you accidentally take Ceteco Sandoz during pregnancy, no harmful effects on the unborn child are to be expected, but the treatment should be stopped immediately. Talk to your doctor if you are pregnant or planning to become pregnant. Ceteco Sandoz should not be taken during breast-feeding as the active ingredient passes into breast milk.How do you use Ceteco Sandoz?For adults and children over 6 years: The usual dose is one Ceteco Sandoz film-coated tablet once a day. For children from 6 to 12 years of age, the dosage can be divided into two intakes (half a film-coated tablet in the morning and half in the evening). If slight side effects (tiredness, headaches, gastrointestinal disorders) occur that do not resolve on their own, it is also advisable for adults to take half a film-coated tablet in the morning and half in the evening.Patients with moderate to severe renal impairmentPatients with impaired kidney function (kidney failure) may receive a lower dose, which depends on the severity of the kidney disease and is determined by the doctor treating you. The Ceteco Sandoz film-coated tablets should be swallowed whole with a glass of liquid.Ceteco Sandoz can be taken with or without food. The duration of treatment depends on the type, duration and course of the symptoms and is determined by the doctor. If you forget to take a dose of Ceteco Sandoz, simply continue the treatment. Please do not take a double dose to make up for a missed dose. In the event of an overdose, you should contact your doctor immediately.Follow the dosage given in the package leaflet or prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Ceteco Sandoz have?The following side effects can occur when taking Ceteco Sandoz:Common (affects 1 to 10 users in 100)Mild tiredness, mild headache, drowsiness, dizziness, dry mouth, nausea have been reported.Uncommon (affects 1 to 10 users in 1000)Gastrointestinal disorders (e.g. diarrhea, abdominal pain), feeling unwell, itching, rash, agitation, abnormal sensations on the skin, runny nose, sore throat, feeling weak.Rare (affects 1 to 10 users in 10,000)Hypersensitivity reactions, seizures, circulatory failure, liver damage, urticaria (nettle rash), tachycardia, edema (swelling), weight gain, confusion, hallucinations, insomnia, aggression, extreme tiredness, depression.Very rare (affects less than 1 in 10,000 people)Movement disorders, tremors, nervous twitches (tics), photosensitivity reactions, allergic shock, urination disorders (abnormal urination), visual disturbances and uncontrollable circling movements of the eyes, thrombocytopenia (low blood platelet count), dysgeusia (altered sense of taste), syncope (fainting).Frequency not known (cannot be estimated from the available data)Loss of memory (amnesia), memory problems, difficulty concentrating, dizziness (sensation of spinning or moving), urinary retention, increased appetite, suicidal thoughts, nightmares, joint pain, muscle pain, acute skin rash over the whole body with pustules and liver inflammation, vasculitis, hearing loss.Pruritus and/or urticaria have been reported following discontinuation of cetirizine.If you experience any of these side effects, stop taking Ceteco Sandoz and tell your doctor.If you notice side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What should also be noted?DurabilityThe medicinal product may only be used up to the date marked “EXP” on the package.Storage NoticeStore in the original packaging, at room temperature (15-25°C) and out of the reach of children.More informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists.What does Ceteco Sandoz contain?1 film- coated tablet (divisible) contains 10 mg cetirizine dihydrochloride as an active ingredient and excipients.Registration Number57360 (Swissmedic)Where can you get Ceteco Sandoz? What packs are available?You can get Ceteco Sandoz in packs of 10 film-coated tablets in pharmacies and drugstores without a doctor's prescription.Marketing Authorization HolderSandoz Pharmaceuticals AG, Risch; Domicile: Red Cross..

20.37 USD

Claritine pollen tabl 10 mg 10 pcs

Claritine pollen tabl 10 mg 10 pcs

 
Product code: 2930306

Claritine pollen is a preparation used to treat allergic diseases. It has a long-lasting, blocking effect on histamine, which is released in the body during allergic reactions. The long duration of action means that it can be taken once a day. In the usual dosage, Claritine pollen does not usually impair performance or concentration and does not usually make you sleepy. Claritine pollen is used in adults and adolescents from the age of 12 for the preventive and symptomatic treatment of hay fever and for the treatment of allergic conjunctivitis caused by pollen allergy. The tablet must not be divided at the decorative groove. Swissmedic-approved patient informationClaritine-Pollen®Bayer (Schweiz) AGWhat is Claritine-Pollen and when is it used?Claritine pollen is a preparation used to treat allergic diseases. It has a long-lasting, blocking effect on histamine, which is released in the body during allergic reactions. The long duration of action means that it can be taken once a day. In the usual dosage, Claritine pollen does not usually impair performance or concentration and does not usually make you sleepy. Claritine pollen is used in adults and adolescents from the age of 12 for the preventive and symptomatic treatment of hay fever and for the treatment of allergic conjunctivitis caused by pollen allergy. The tablet must not be divided at the decorative groove. What should be considered?This medicine contains 89.3 mg of usable carbohydrates per single dose. When should Claritine-Pollen not be taken?In case of known hypersensitivity to the active substance of Claritine-Pollen or one of the ingredients. When is caution required when taking Claritine pollen?Taking higher doses can lead to sedation (tiredness, sleepiness). When driving a motor vehicle or using machines, the recommended dosage should not be exceeded. Claritine pollen does not increase the depressant effect of alcohol or diazepam. If you suffer from liver dysfunction, the doctor will usually reduce the dose, i.e. you only take Claritine pollen every other day. If you know that you suffer from a sugar intolerance, please consult your doctor before taking Claritine pollen. 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 Claritine pollen be taken while pregnant or breastfeeding?It is not recommended to take Claritine pollen if you are pregnant or breastfeeding. Ask your doctor, pharmacist or druggist for advice before taking any medicines while you are pregnant or breastfeeding. How do you use Claritine pollen?Adolescents from the age of 12 and adults1 tablet once a day Claritine pollen. Correct way of takingYou can take it regardless of the time of day. In order to achieve the fastest possible onset of action, you should take Claritine pollen on an empty stomach. If you prefer to take Claritine pollen with a meal, the onset of action may be delayed. Claritine pollen tablets are swallowed whole with some liquid. 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 Claritine pollen have?The following side effects can occur when taking Claritine pollen: Very common:Headache. Common:Dizziness, lightheadedness, nausea, cough, nosebleeds, runny nose, upper respiratory tract infection, diarrhea, dry mouth, indigestion, increased appetite, sore throat, tiredness . Uncommon:agitation, anxiety, confusion, depression, migraine, nervousness, sweating, thirst, vomiting, pins and needles, conjunctivitis, eye pain, ear pain, tinnitus, chest pain , high blood pressure, palpitations, bronchitis, asthma, dry/blocked nose, shortness of breath, inflammation of the paranasal sinuses, sneezing, disturbances in voice production, change in sense of taste, wind (flatulence), inflammation of the stomach, constipation, toothache, itching, skin rashes, feeling hot, Hives, joint pain, general weakness, back pain, urinating more or less often, painful periods, fever, feeling unwell. Rare:Allergic reactions, worsening of allergy, memory loss, loss of appetite, difficulty concentrating, restlessness, tactile sensitivity, tremor, blurred vision, change in tear flow, coughing up blood, lower Blood pressure, swelling, momentary unconsciousness, palpitations, laryngitis, sore mouth, bleeding in the skin, dry hair, dry skin, sensitivity to light, leg cramps, swelling of the extremities, swelling of the face and around the eyes, swelling of the lips, tongue and larynx, impotence, loss of libido, increased menstrual bleeding, flushing. Very rare:Weight loss, hallucinations, seizure, spasm of the eyelids, changes in salivation, abnormal liver function (hepatitis), liver necrosis, jaundice, hair loss, flushing, muscle pain, discolouration of the urine, vaginal inflammation, breast enlargement in men (gynaecomastia), chills. If you notice dark urine, light-colored stools and possibly yellowing of the skin, you should stop taking Claritine pollen immediately and consult a 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 needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Storage InstructionsStore at room temperature (15 – 25°C). Keep out of reach of CHILDREN. Further information:If an allergy test is carried out, the Claritine pollen therapy should be interrupted 48 hours before the test is carried out, since the administration of antihistamines prevent or mitigate positive reactions. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What is in Claritine pollen?1 tablet contains: Active ingredientsLoratidine 10 mg ExcipientsLactose, corn starch and magnesium stearate. Approval number56919 (Swissmedic). Where can you get Claritine pollen? What packs are available? Claritine pollen is available in pharmacies and drugstores without a doctor's prescription. There are packs of 10 tablets with a decorative groove. Authorization holderBayer (Switzerland) AG, Zurich. This leaflet was last checked by the medicines authority (Swissmedic) in October 2021. ..

21.33 USD

Feniallerg drops 1 mg/ml bottle 20 ml

Feniallerg drops 1 mg/ml bottle 20 ml

 
Product code: 4047725

Feniallerg blocks the action of histamine, one of the substances released during allergic reactions. Feniallerg relieves itching and skin irritation caused by allergic reactions, reduces edema (abnormal accumulation of fluid in the skin or mucous membranes) and relieves the symptoms of allergic rhinitis such as runny nose, tearing and sneezing. Feniallerg is used in the following cases: for allergic skin conditions: itching of various origins (except itching associated with jaundice), eczema and other itchy skin diseases, nettle fever, itching associated with diseases with skin rashes such as chickenpox; for insect bites; for allergic diseases of the upper respiratory tract:hay fever and other forms of allergic rhinitis; for the treatment of symptoms caused by food or drug allergies. Swissmedic-approved patient information Feniallerg GSK Consumer Healthcare Schweiz AG What is Feniallerg and when is it used? Feniallerg inhibits the effects of histamine, a of the substances released in allergic reactions. Feniallerg relieves itching and skin irritation caused by allergic reactions, reduces edema (abnormal accumulation of fluid in the skin or mucous membranes) and relieves the symptoms of allergic rhinitis such as runny nose, tearing and sneezing. Feniallerg is used in the following cases: for allergic skin diseases: itching of various origins (except itching associated with jaundice), eczema and other itchy skin diseases, nettle fever, itching associated with diseases with skin rashes such as chickenpox; for insect bites;for allergic diseases of the upper respiratory tract:hay fever and other forms of allergic rhinitis;for the treatment of symptoms caused by food or drug allergies.When should Feniallerg not be used?You must not use Feniallerg if you are allergic (hypersensitive) to the active substance dimetinden maleate or any of the excipients . Feniallerg should not be used in newborn babies less than 1 month old, especially premature babies. Talk to your doctor or pharmacist if the above applies, because then Feniallerg is not suitable for you. When is caution required when using Feniallerg?Inform your doctor or pharmacist before taking Feniallerg drops if you glaucoma,urinary retention (e.g. due to an enlarged prostate),epilepsy, suffer from chronic obstructive pulmonary disease or other diseases.Elderly patients should consult their doctor before taking this medicine, as side effects such as agitation and tiredness may occur. If you are taking any of the following medicines, you should only take Feniallerg after consulting your doctor: Medicines for depression (MAOIs or tricyclic antidepressants),Anticholinergics such as bronchodilators (medicines used to treat asthma or bronchospasm), gastrointestinal antispasmodics (medicines used to treat stomach intestinal spasms), mydriatics (medicines to dilate the pupil), urological antispasmodics (medicines to treat the symptoms of urinary incontinence or an overactive bladder),medicines that depress the central nervous system (such as sedatives or sleeping pills), Medicines for epilepsy,Opioid painkillers (strong painkillers),Antihistamines (medicines used for coughs, colds or allergies),Antiemetics (medicines against vomiting),Procarbazine (medicine to treat certain types of cancer),Scopolamine (medicine to prevent motion sickness),if alcohol is taken at the same time.This medicine can impair your ability to react, the ability to drive and the ability to use tools or machines! Like other antihistamines, Feniallerg can increase the effects of alcohol. In small children from 1 month to 1 year, Feniallerg may only be used on medical recommendation. The recommended dosage must not be exceeded. The depressant effect may be accompanied by pauses in breathing during sleep. Antihistamines can trigger states of excitement, especially in children and elderly patients. This medicinal product contains propylene glycol 100 mg/ml (or per 20 drops). This medicinal product contains benzoic acid 1 mg/ml (or per 20 drops). This medicinal product contains less than 1 mmol (=23 mg) sodium per 1 ml (or per 20 drops), i.e. essentially 'sodium-free'. it is almost «sodium-free». Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies oruse other medicines (including those you bought yourself!)! Can Feniallerg be used while pregnant or breastfeeding?If you are pregnant, you should not take Feniallerg unless your doctor has told you to. Taking Feniallerg while breastfeeding is not recommended. If you are pregnant or breast-feeding, think you may be pregnant or planning to become pregnant, consult your doctor before taking this medicine. How do you use Feniallerg?Adults and adolescents over 12 yearsRecommended daily dose:drops 1 mg/ml: 20-40 drops, 3 times a day. ChildrenIn small children from 1 month to 1 year, Feniallerg drops may only be used as recommended by a doctor. The recommended daily dose is:2 drops per kg of body weight per day, divided into 3 intakes. Age/WeightDose in drops 1 month - 1 year / 4.5 - 15 kg 3-10 drops, 3 times a day 1-3 years / 15-22.5 kg 10-15 drops, 3 times a day 3-12 Years / 22.5-30kg 15-20 drops, 3 times a day The optimal dose will be determined by your doctor. The Feniallerg drops are sensitive to heat. Therefore, add the drops to the lukewarm baby bottle at the last moment. If the child can already eat with a spoon, give him the pleasant-tasting drops undiluted with a teaspoon. Feniallerg, drops should not be taken for more than 14 days without medical advice. If you have taken too much Feniallerg: Talk to your doctor or pharmacist immediately. If you miss a dose: Take Feniallerg as soon as you remember, unless it is less than 2 hours until the scheduled dose. In this case you should not take the missed dose but take the next dose at the usual time according to the dosing schedule. Do not take a double dose to make up for the missed dose. 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 Feniallerg have?Like all medicines, Feniallerg can cause side effects, although not everyone gets them. Stop taking Feniallerg and tell your doctor straight away if you get any of the following symptoms, which may be signs of an allergic reaction: difficulty breathing or swallowing,swelling of the face, lips, tongue or throat,severe itching of the skin with a red rash or blisters, muscle spasms .These side effects are very rare (affects less than 1 in 10,000 people). Other side effects are usually mild and temporary. They occur mainly at the beginning of treatment. Very common (affects more than 1 in 10 people)Fatigue Common (affects 1 to 10 users in 100)Drowsiness, nervousnessRare (affects 1 to 10 users in 10,000)Excitement, headache, dizziness, gastrointestinal disorders such as vomiting, dry mouth or throat. 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› are used. Storage instructionsProtect from light and store at room temperature (15-25°C). 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 Feniallerg contain?1 ml of Feniallerg oral drops, solution contains Active ingredient1 mg dimetindene maleate. ExcipientsBenzoic acid (E 210), propylene glycol (E 1520), disodium phosphate dodecahydrate (E 339), citric acid monohydrate (E 330), sodium edetate, saccharin Sodium (E 954), purified water. Approval number27528 (Swissmedic) Where can you get Feniallerg? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 20 and 50 ml. Authorization holderGSK Consumer Healthcare Schweiz AG, Risch. This leaflet was last checked by the Medicines Agency (Swissmedic) in June 2021. ..

15.34 USD

Fexo allerg spirig hc filmtabl 120 mg

Fexo allerg spirig hc filmtabl 120 mg

 
Product code: 1045304

Inhaltsverzeichnis Was ist Fexo Allerg Spirig HC 120 und wann wird es angewendet? Wann darf Fexo Allerg Spirig HC 120 nicht eingenommen werden? Wann ist bei der Einnahme von Fexo Allerg Spirig HC 120 Vorsicht geboten? Darf Fexo Allerg Spirig HC 120 während einer Schwangerschaft oder in der Stillzeit eingenommen werden? Wie verwenden Sie Fexo Allerg Spirig HC 120? Welche Nebenwirkungen kann Fexo Allerg Spirig HC 120 haben? Was ist ferner zu beachten? Was ist in Fexo Allerg Spirig HC 120 enthalten? Zulassungsnummer Wo erhalten Sie Fexo Allerg Spirig HC 120? Welche Packungen sind erhältlich? Zulassungsinhaberin COMPENDIUM Swissmedic-genehmigte Patienteninformation Fexo Allerg® Spirig HC 120, Filmtabletten Spirig HealthCare AG Was ist Fexo Allerg Spirig HC 120 und wann wird es angewendet? Fexo Allerg Spirig HC 120 ist ein Antihistaminikum. Es dient zur Behandlung von Heuschnupfen und wirkt gegen dessen Krankheitszeichen wie Niesen, brennende, wässrige oder gerötete Augen, gereizte Nasen- oder Rachenschleimhaut, verstopfte Nase. Wann darf Fexo Allerg Spirig HC 120 nicht eingenommen werden? Personen mit einer bekannten Überempfindlichkeit auf einen der Bestandteile der Fexo Allerg Spirig HC 120 Filmtabletten dürfen Fexo Allerg Spirig HC 120 nicht einnehmen.Kinder unter 12 Jahren dürfen Fexo Allerg Spirig HC 120 nicht einnehmen. Wann ist bei der Einnahme von Fexo Allerg Spirig HC 120 Vorsicht geboten? Es wird empfohlen, magensäurehemmende Präparate mit Aluminium- und Magnesiumhydroxid zwei Stunden getrennt von Fexo Allerg Spirig HC 120 einzunehmen.Spezielle Untersuchungen (z.B. Fahrtest) haben gezeigt, dass Fexo Allerg Spirig HC 120 die Leistungs- und Konzentrationsfähigkeit in der Regel ebenso wenig beeinträchtigt und ebenso wenig müde oder schläfrig macht wie Placebo (Tabletten ohne Wirkstoff). Bei besonders empfindlichen Personen ist jedoch vorher die individuelle Reaktion auf Fexo Allerg Spirig HC 120 zu überprüfen.Dieses Arzneimittel enthält mg weniger als 1 mmol (23 mg) Natrium pro Filmtablette, d.h. es ist nahezu «natriumfrei».Informieren Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin, wenn Siean anderen Krankheiten leiden,Allergien haben oderandere Arzneimittel (auch selbst gekaufte!) einnehmen oder äusserlich anwenden. Darf Fexo Allerg Spirig HC 120 während einer Schwangerschaft oder in der Stillzeit eingenommen werden? Aufgrund der bisherigen Erfahrungen ist bei bestimmungsgemässer Anwendung kein Risiko für das Kind bekannt. Systematische wissenschaftliche Untersuchungen wurden aber nicht durchgeführt. Vorsichtshalber sollten Sie während der Schwangerschaft und Stillzeit möglichst auf die Einnahme von Arzneimitteln verzichten oder den Arzt, Apotheker oder Drogisten bzw. die Ärztin, Apothekerin oder Drogistin um Rat fragen. Wie verwenden Sie Fexo Allerg Spirig HC 120? Erwachsene und Jugendliche ab 12 Jahren:Fexo Allerg Spirig HC 120: 1 x täglich 1 Filmtablette (120 mg) einnehmen (vorzugsweise morgens).Ändern Sie nicht von sich aus die verschriebene Dosierung.Halten Sie sich an die in der Packungsbeilage angegebene oder vom Arzt oder der Ärztin verschriebene Dosierung.Wenn Sie glauben, das Arzneimittel wirke zu schwach oder zu stark, so sprechen Sie mit Ihrem Arzt, Apotheker oder Drogisten bzw. mit Ihrer Ärztin, Apothekerin oder Drogistin. Welche Nebenwirkungen kann Fexo Allerg Spirig HC 120 haben? Folgende Nebenwirkungen können bei der Einnahme oder Anwendung von Fexo Allerg Spirig HC 120 auftreten:Häufig (betrifft 1 bis 10 von 100 Behandelten)Kopfschmerzen, Schläfrigkeit, Schwindel, Übelkeit.Die Häufigkeit dieser mit Fexo Allerg Spirig HC 120 beobachteten Nebenwirkungen entspricht derjenigen, die unter einer Behandlung mit Placebo (Tabletten ohne Wirkstoff) beobachtet wird.Gelegentlich (betrifft 1 bis 10 von 1000 Behandelten)Durchfall, Mundtrockenheit, Tachykardie und Herzklopfen.Selten (betrifft 1 bis 10 von 10'000 Behandelten)Müdigkeit, Schlaflosigkeit, Nervosität, Schlafstörungen oder Alpträume, Hautausschläge, Nesselsucht und Juckreiz.In Einzelfällen wurde über Überempfindlichkeitsreaktionen berichtet, die sich durch Ödeme (Wasseransammlung im Gewebe), Atemnot, Brustenge oder Hautrötung mit Hitzegefühl manifestieren.Wenn Sie Nebenwirkungen bemerken, wenden Sie sich an Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin. Dies gilt insbesondere auch für Nebenwirkungen, die nicht in dieser Packungsbeilage angegeben sind. Was ist ferner zu beachten? HaltbarkeitDas Arzneimittel darf nur bis zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.LagerungshinweisNicht über 30°C in der Originalverpackung lagern und ausser Reichweite von Kindern aufbewahren.Weitere HinweiseWeitere Auskünfte erteilt Ihnen Ihr Arzt, Apotheker oder Drogist bzw. Ihre Ärztin, Apothekerin oder Drogistin. Diese Personen verfügen über die ausführliche Fachinformation. Was ist in Fexo Allerg Spirig HC 120 enthalten? Eine Filmtablette Fexo Allerg Spirig HC 120 enthält:Wirkstoffe120 mg Fexofenadini hydrochloridum.HilfsstoffeMikrokristalline Cellulose, Croscarmellose-Natrium, Maisstärke, Povidon K-30, Magnesiumstearat.Filmüberzug: Hypromellose (E464), Titandioxid (E171), Macrogol 400, Macrogol 4000, gelbes Eisenoxid (E172), rotes Eisenoxid (E172). Zulassungsnummer 68854 (Swissmedic) Wo erhalten Sie Fexo Allerg Spirig HC 120? Welche Packungen sind erhältlich? In Apotheken und Drogerien, ohne ärztliche Verschreibung.Erhältlich in Packungen zu 10 und 30 Filmtabletten. Zulassungsinhaberin Spirig HealthCare AG, 4622 Egerkingen Diese Packungsbeilage wurde im November 2023 letztmals durch die Arzneimittelbehörde (Swissmedic) geprüft. 31083 / 16.07.2024 ..

26.27 USD

Lorado pollen sandoz tabl 10 mg 10 pcs

Lorado pollen sandoz tabl 10 mg 10 pcs

 
Product code: 4963008

What Lorado Pollen Sandoz is and what it is used forLorado Pollen Sandoz is a preparation used to treat allergic diseases. It has a long-lasting, blocking effect on histamine, which is released in the body during allergic reactions. The long duration of action means that it can be taken once a day. In the usual dosage, Lorado Pollen Sandoz does not usually impair the ability to perform or concentrate and also does not usually make you drowsy.Lorado Pollen Sandoz is used in adults and adolescents from the age of 12 for the preventive and symptomatic treatment of hay fever and for the treatment of allergic conjunctivitis caused by pollen allergy.When should Lorado Pollen Sandoz not be taken?Known hypersensitivity to the active ingredient in Lorado Pollen Sandoz or to one of the ingredients.When should I be careful when taking Lorado Pollen Sandoz?Taking higher doses can lead to sedation (tiredness, sleepiness).When driving a motor vehicle or using machines, the recommended dosage should not be exceeded.The depressant effect of alcohol or diazepam is not increased by Lorado Pollen Sandoz.If you suffer from liver dysfunction, the doctor will usually reduce the dose, ie you only take Lorado Pollen Sandoz every other day.Please only take this medicine after consulting your doctor if you know that you suffer from an intolerance to sugar.Tell your doctor, pharmacist or druggist if yousuffer from other diseaseshave allergies ortake other medicines (including those you bought yourself!) or use them externally.Can Lorado Pollen Sandoz be taken during pregnancy or while breastfeeding?If you are pregnant or breastfeeding, taking Lorado Pollen Sandoz is not recommended. Ask your doctor, pharmacist or druggist for advice before taking any medicines while you are pregnant or breastfeeding.How do you use Lorado Pollen Sandoz?Adolescents from 12 years and adults1 tablet of Lorado Pollen Sandoz once a day.Correct way of takingIt can be taken regardless of the time of day. In order to achieve the fastest possible onset of action, you should take Lorado Pollen Sandoz on an empty stomach. If you prefer to take Lorado Pollen Sandoz with a meal, the onset of action may be delayed.Lorado Pollen Sandoz, tablets are swallowed whole with some liquid.Follow the dosage given in the package leaflet or prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Lorado Pollen Sandoz have?The following side effects can occur when taking Lorado Pollen Sandoz:Very often:Headache.Frequently:Dizziness, lightheadedness, nausea, cough, nosebleeds, runny nose, upper respiratory tract infection, diarrhoea, dry mouth, indigestion, increased appetite, sore throat, tiredness.Occasionally:Agitation, anxiety, confusion, depression, migraine, nervousness, sweating, thirst, vomiting, pins and needles, conjunctivitis, eye pain, ear pain, tinnitus, chest pain, high blood pressure, palpitations, bronchitis, asthma, dry/blocked nose, shortness of breath, inflammation of the Paranasal sinuses, sneezing, voice disorders, change in sense of taste, gas (flatulence), stomach inflammation, constipation, toothache, itching, skin rashes, feeling hot, hives, joint pain, general feeling of weakness, back pain, more or less frequent urination, painful menstrual bleeding, fever, Malaise.Rarely:Allergic reactions, worsening of allergy, memory loss, loss of appetite, difficulty concentrating, restlessness, tactile sensitivity, tremor, blurred vision, changes in the flow of tears, coughing up blood, low blood pressure, swelling, temporary loss of consciousness, palpitations, laryngitis, sore mouth, bleeding in the skin , dry hair, dry skin, sensitivity to light, leg cramps, swelling of extremities, swelling of the face and around the eyes, swelling of the lips, tongue and larynx, impotence, loss of libido, increased menstrual bleeding, flushing.Very rare:Weight loss, hallucinations, seizures, eyelid spasms, changes in salivation, abnormal liver function (hepatitis), liver necrosis, jaundice, hair loss, skin redness, muscle pain, discolored urine, vaginal inflammation, enlarged breasts in men (gynecomastia), chills.If you observe dark urine, light-colored stools and possibly yellowing of the skin, you should stop taking Lorado Pollen Sandoz immediately and consult a doctor.If you notice side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed in this leaflet.What should also be noted?DurabilityThe medicinal product may only be used up to the date marked “EXP” on the package.Storage NoticeStore in the original packaging, at room temperature (15-25°C) and out of the reach of children.More informationIf an allergy test is carried out, the Lorado Pollen Sandoz therapy should be stopped 48 hours before the test is carried out, as the administration of antihistamines can prevent or weaken the positive reactions.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists.What does Lorado Pollen Sandoz contain?1 tablet containsActive Ingredients10 mg loratadine.ExcipientsLactose monohydrate, corn starch, colloidal anhydrous silicon dioxide, magnesium stearate.Registration Number57517 (Swissmedic)Where can you get Lorado Pollen Sandoz? What packs are available?Lorado Pollen Sandoz is available in pharmacies and drugstores without a doctor's prescription.There are packs of 10 tablets.Marketing Authorization HolderSandoz Pharmaceuticals AG, Risch; Domicile: Red Cross..

18.94 USD

Otriduo cold dosing spray 15 ml

Otriduo cold dosing spray 15 ml

 
Product code: 4173358

What is Otriduo cold and when is it used? Otriduo cold contains a mild decongestant and an antihistamine. Otriduo cold brings rapid and lasting relief from swollen nasal mucosa (blocked nose) and runny nose. Otriduo cold is suitable for the short-term symptomatic treatment of blocked nose and itching such as colds, sinusitis (inflammation of the sinuses), hay fever, allergic non-seasonal rhinitis (inflammation of the nasal mucosa, e.g. triggered by house dust, animal hair, mould).Otriduo Cold can also be used before or after an operation and as a supportive medicine in the treatment of acute middle ear infections if prescribed by a doctor.When should Otriduo Cold not be used? Otriduo cold should not be used in the following cases:if you are hypersensitive to one of the active ingredients (dimetindene maleate, phenylephrine) or one of the excipients according to the composition,if you suffer from chronic rhinitis that has led to a thinning of the nasal mucosa,if you are currently taking monoamine oxidase inhibitors (MAO inhibitors, medicines for depression en) are taking or have taken within the last 14 days,if you suffer from glaucoma (i.e. an eye disease with increased intraocular pressure),after transnasal surgery (surgical interventions in the nose area where the epidermis has been exposed).When should caution be exercised when using Otriduo cold? Talk to your doctor before use if you havehigh blood pressure, cardiovascular disease,overactive thyroid gland,suffer from diabetes (diabetes) orepilepsy,difficulty urinating (e.g. prostatic hypertrophy),blood are taking pressure-lowering medicines (e.g. beta blockers), mood-enhancing medicines (MAO inhibitors, tri- or tetracyclic antidepressants) or anti-Parkinson medicines (see also «When should Otriduo cold not be used?»).Otriduo cold should not be used for more than 3 days uninterrupted. If there is no improvement after 3 days or if the symptoms worsen, you should seek medical advice. Long-term or excessive use can cause chronic inflammation of the nasal mucosa (rhinitis medicamentosa).Otriduo cold can cause sleep disorders, drowsiness and tremors in sensitive people.Otriduo cold is not intended for use in the mouth or in the eyes.The prescribed dose must not be exceeded, especially in small children and elderly people.Otriduo cold Dosing spray is not recommended for children under 6 years of age. Otriduo Schnupfen should be used in children from 6 to 12 years of age under adult supervision. Information on the excipients Benzalkonium chloride can cause irritation or swelling of the nasal mucosa, especially with prolonged use. Inform your doctor, pharmacist or druggist or your doctor, pharmacist or druggist if yousuffer from other illnesses,have allergies oruse other medicines (including those you bought yourself!)!Can Otriduo cold be used during pregnancy or while breastfeeding? Systematic scientific research has never been conducted. Phenylephrine and dimetindene maleate may be excreted in breast milk. Otriduo SchnuTo be on the safe side, pf should not be used during pregnancy and breastfeeding.How do you use Otriduo Schnupfen dosing spray?Do not exceed the stated dosage and frequency of use.The lowest effective dosage should always be used for the shortest possible duration of therapy.Adults and children over 6 years of age (under adult supervision):1-2 sprays into each nostril 3 to 4 times a day give.Children under the age of 6Otriduo nasal dosing spray is not recommended for children under the age of 6.Use of the dosing sprayClean your nose thoroughly before use (e.g. blow your nose).Be careful not to get the spray mist in your eyes.Remove the protective cap. Before the very first use, press the pump 5 times to start the spraying process. The dosing spray is now ready for any further application. If the product has not been used for a long time, the pump must be operated 5 times again before use.Insert the spray head into one nostril, spray 1 time (press firmly) and inhale through your nose at the same time. Repeat the process for the other nostril.Wipe and dry the spray head before replacing the protective cap.A bottle of Otriduo nasal dosing spray should only be used by one person to avoid the possible spread of infection.Do not use continuously for more than 3 days. If there is no improvement after 3 days or if the symptoms worsen, you should seek medical advice.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 Otriduo cold have? The following side effects may occur when using Otriduo cold: In rare cases (affects 1 to 10 in 10,000 people treated), local and temporary burning or dryness of the nose and nosebleeds may occur. 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 should I be aware of? Shelf life The medicinal product may only be used up to the date marked «EXP» on the container. Storage instructions Keep out of the reach of children. Otriduo cold dosing spray: Protect from light and store at 15-30°C. Further information Your doctor, pharmacist or druggist can provide you with further information or your doctor, pharmacist or druggist. These people have the detailed information for professionals.What does Otriduo nasal dosing spray contain? Active ingredients 1 ml Otriduo nasal dosing spray contains 0.25 mg dimetindene maleate and 2.5 mg phenylephrine. 1 spray (=0.14 ml) contains: 0.035 mg dimetindene maleate and 0.35 mg phenylephrine. Excipients Sorbitol, sodium monohydrogen phosphate, citro renic acid monohydrate, lavandin oil, benzalkonium chloride, purified water.Authorization number60125 (Swissmedic).Where can you get the Otriduo Cold Dosing Spray? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Otriduo nasal dosing spray (microdoseur): PaPack of 15 ml.Authorization holderGSK Consumer Healthcare Schweiz AG, Risch.This package leaflet was last checked by the drug authority (Swissmedic) in January 2021...

37.39 USD

Stilex gel tb 45 g

Stilex gel tb 45 g

 
Product code: 6865623

What is Stilex Gel and when is it used? Experience has shown that Stilex is used for the symptomatic treatment of allergic, itchy and inflammatory skin diseases, e.g. small areas of light sunburn, insect bites, small areas of allergic skin diseases, minor burns (first degree). When shouldn't Stilex Gel be used? Stilex should not be used: If you are known to be hypersensitive to one of the active ingredients or excipients,in the case of acute moist skin diseases and on broken skin or infected wounds.When should caution be exercised when using Stilex Gel?This medicinal product contains 0.25 mg benzalkonium chloride per dose, equivalent to 0.25 mg per 1 g. Benzalkonium chloride may cause skin irritation.This medicinal product contains a perfume composed of coumarin, α-amylcinnamaldehyde, citronellol, geraniol, hexylcinnamaldehyde, hydroxycitronellal, isoeugenol and linalool. These allergens can trigger allergic reactions. Avoid contact with the eyes and mucous membranes. Do not use Stilex on large areas or for a long time. If there is no improvement after 7 days, seek professional advice.Stilex should only be used on children under the age of 2 after medical advice.The occurrence of a new type of skin reaction requires discontinuation of treatment.Inform your doctor, pharmacist or druggist:if you suffer from other diseases Have allergies ortake other medicines (including those you bought yourself) or use them externally!Can Stilex Gel be used during pregnancy or while breastfeeding?Based on previous experience, there is no known risk for the child if used as intended. However, systematic scientific investigations have never been carried out. Therefore, Stilex should not be used during pregnancy unless absolutely necessary.Lidocaine is excreted in human milk, so Stilex should not be used during breast-feeding. This medicine contains benzalkonium chloride. If you are breastfeeding, you must not apply this medicine to the breast, as your baby could ingest it with the milk.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 Stilex Gel?Apply a thin layer to the affected areas of the skin several times a day.Hold up to the dosage stated in the leaflet 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 Stilex Gel have?The following side effects can occur when using Stilex:Skin reactions and skin sensitization cannot be ruled out in certain people. In this case, the treatment must be interrupted.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 instructionsStilex can be stored at room temperature (15-25 °C) and out of temperaturekeep out of the reach of children.Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Stilex Gel contain?1 g gel contains:Active ingredients15 mg mepyramine maleate, 15 mg lidocaine hydrochloride monohydrate, 50 mg dexpanthenol.ExcipientsCarbomers, polysorbate 80, sodium hydroxide, perfume (contains coumarin, α -amylcinnamaldehyde, citronellol, geraniol, hexylcinnamaldehyde, hydroxycitronellal, isoeugenol, linalool), disodium edetate, benzalkonium chloride, purified water.Authorization number41312 (Swissmedic).Where can you get Stilex Gel? Which packs are available? In pharmacies and drugstores without a doctor's prescription. Tubes of 20 g and 45 g. Authorization holder VERFORA SA, 1752 Villars-sur-Glâne This leaflet was last checked by the medicinal products authority (Swissmedic) in July 2020....

35.39 USD

Tavegyl tabl 1 mg 20 pcs

Tavegyl tabl 1 mg 20 pcs

 
Product code: 388056

Tavegyl Tabl 1 mg 20 pcs Tavegyl Tabl 1 mg 20 pcs is a medication used to treat various allergic conditions such as hay fever, hives, and itching. This medication contains the active ingredient clemastine, which works by blocking the effect of histamine in our body. Ingredients Clemastine - 1mg Lactose monohydrate Microcrystalline cellulose Magnesium stearate Usage Tavegyl Tabl 1 mg 20 pcs should be taken orally with or without food as directed by the doctor. The usual recommended dose for adults and children above 12 years is 1 tablet every 12 hours. For children aged between 6-12 years, the dose should be 0.5 tablets every 12 hours. Precautions Avoid alcohol intake while on this medication as it may increase the risk of drowsiness and dizziness. Do not drive or operate heavy machinery after taking Tavegyl Tabl 1 mg 20 pcs as it may cause drowsiness and impair your ability to concentrate Consult your doctor before taking this medication if you are pregnant or breastfeeding. Do not exceed the recommended dose as it may cause adverse effects on your health. Side Effects Tavegyl Tabl 1 mg 20 pcs may cause the following side effects: Dizziness Drowsiness Headache Dry mouth Upset stomach Difficulty urinating If you experience any of the above side effects, contact your doctor immediately. Overall, Tavegyl Tabl 1 mg 20 pcs is an effective medication for treating various allergies, but it is essential to follow the recommended dose and precautions to avoid any adverse effects...

45.81 USD

Triofan rhinitis retard caps 10 pcs

Triofan rhinitis retard caps 10 pcs

 
Product code: 7000078

What is Triofan Rhinitis Retard, capsules and when is it used?Triofan Rhinitis Retard capsules contain:an antihistamine, chlorphenamine maleate. It relieves the symptoms of nasal inflammation (runny nose) such as runny nose, sneezing, tingling and tearing;a vasoconstrictor, phenylephrine hydrochloride, which has a decongestant effect on the inflamed nasal mucosa, unblocking the nasal passages and thereby facilitating breathing.The 10-12 hour long-term effect of Triofan Rhinitis Retard is based on dialysis of the active ingredients (D iffucap®), which are contained in the hundreds of microgranules in each capsule.Triofan Rhinitis Retard is used in inflammatory and allergic diseases of the upper respiratory tract such as colds, hay fever, chronic runny nose, vasomotor or allergic rhinitis, and as an adjuvant in influenza and colds. When must Triofan Rhinitis Retard, capsules not be used?Triofan Rhinitis Retard must not be taken together with monoamine oxidase inhibitors (MAO inhibitors). In the case of severe coronary artery disease, hypersensitivity to one of the ingredients and severely elevated blood pressure, Triofan Rhinitis Retard may only be used after consulting your doctor.Must not be used in children under the age of 12.In the last trimester of pregnancy and while breastfeeding.When should Triofan be taken Rhinitis Retard, capsules Caution required?Caution required for: angle-closure glaucoma, diabetes, prostate hypertrophy, overactive thyroid gland, bronchial asthma (attacks of shortness of breath with difficult exhalation). Triofan Rhinitis Retard should not be used too frequently or over a long period of time. If the symptoms last longer than normal or keep coming back, you should see a doctor.This medicine can affect your ability to react, drive and use tools or machines!If you know that you have an intolerance to sugars, please consult your doctor before taking this medicine.Tell your doctor, pharmacist or druggist, or your doctor, Pharmacist or druggist if you suffer from other illnesses, have allergies or take other medicines (including those you bought yourself!) or use them externally.Can Triofan Rhinitis Retard capsules be taken during pregnancy or breastfeeding?Systematic scientific studies have never been carried out with Triofan Rhinitis Retard. As a precaution, you should avoid taking medicines if possible during pregnancy and breast-feeding, or ask your doctor, pharmacist or druggist for advice.In the last trimester of pregnancy and while breast-feeding, this medicine carries a risk of serious adverse effects.How do you use Triofan Rhinitis Retard, capsules?Unless otherwise prescribed by your doctor:Adults and children over 12 years of age:If symptoms occur, take 1 capsule every 12 hours, i.e. 1 capsule in the morning and 1 capsule in the evening.Observe the dosage indicated 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 Triofan Rhinitis Retard, capsules have?The following side effects can occur when taking Triofan Rhinitis Retard:Common (affects 1 to 10 users in 100)Transient drowsiness or decreased alertness.Uncommon (affects 1 to 10 users in1000 users)Blurred vision or dry mouth.Very rare (affects less than 1 in 10,000 users)Blood count changes.Isolated casesSkin rash, bone marrow depression.If you notice 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 instructionsTriofan Rhinitis Retard out of reach for children, store dry, at room temperature (15–25 °C) and protected from light.Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for professionals.What does Triofan Rhinitis Retard, capsules contain?1 capsule contains:Active ingredients4 mg chlorphenamine maleate; 20 mg phenylephrine hydrochloride.ExcipientsSugar pellets (contain sucrose and corn starch), talc, shellac, gelatin, erythrosine, indigotine.Approval number3344 5 (Swissmedic).Where can you get Triofan Rhinitis Retard, capsules? What packs are available?In pharmacies and drugstores, without a doctor's prescription.Pack of 10 capsules.Authorization holderVERFORA SA, Villars-sur-Glâne. This leaflet was last checked by the medicines authority (Swissmedic) in August 2020.Show technical information about the medicine..

31.36 USD

Vibrocil microdos 15ml

Vibrocil microdos 15ml

 
Product code: 877536

Vibrocil contains a mild decongestant and an antihistamine. Vibrocil provides rapid and lasting relief from nasal congestion (blocked nose) and runny nose. Vibrocil is suitable for the short-term symptomatic treatment of blocked nose and itching such as colds, sinusitis (inflammation of the paranasal sinuses), hay fever, allergic non-seasonal rhinitis (inflammation of the nasal mucosa, e.g. triggered by house dust, animal hair, mould). With a doctor's prescription, Vibrocil can also be used before or after surgery and as an adjuvant drug in the treatment of acute middle ear infections. Swissmedic-approved patient informationVibrocil, dosing sprayGSK Consumer Healthcare Schweiz AGWhat is Vibrocil, dosing spray and when is it used?Vibrocil contains a mild decongestant and an antihistamine. Vibrocil provides rapid and lasting relief from nasal congestion (blocked nose) and runny nose. Vibrocil is suitable for the short-term symptomatic treatment of blocked nose and itching such as colds, sinusitis (inflammation of the paranasal sinuses), hay fever, allergic non-seasonal rhinitis (inflammation of the nasal mucosa, e.g. triggered by house dust, animal hair, mould). With a doctor's prescription, Vibrocil can also be used before or after surgery and as an adjuvant drug in the treatment of acute middle ear infections. When must Vibrocil, dosing spray not be used?Vibrocil must not be used in the following cases: if you are hypersensitive to one of the active ingredients (dimethine maleate, phenylephrine) or to one of the excipients according to the composition,if you suffer from chronic rhinitis that has led to thinning of the nasal mucosa,if you are currently taking or have taken within the last 14 days monoamine oxidase inhibitors (MAOIs, medicines for depression),if you have glaucoma (i.e. an eye disease with increased pressure in the eye) ,after transnasal surgery (surgical interventions in the nose area where the inner skin was exposed).When should you use Vibrocil, dosing spray Caution required? Talk to your doctor before use if you have high blood pressure, cardiovascular disease,overactive thyroid,diabetes orepilepsy are suffering,have difficulty urinating (e.g. prostatic hypertrophy),are taking medicines to lower blood pressure (e.g. beta-blockers), mood-enhancing medicines (MAOIs, tri- or tetracyclic antidepressants) or anti-Parkinson medicines ( See also «When should Vibrocil not be used?»).Vibrocil should not be used continuously for more than 3 days. If there is no improvement after 3 days or if the symptoms worsen, you should seek medical advice. Long-term or excessive use can cause chronic inflammation of the nasal mucosa (rhinitis medicamentosa). Vibrocil can cause insomnia, drowsiness and tremors in sensitive individuals. Vibrocil is not intended for use in the mouth or in the eyes. The prescribed dose must not be exceeded, especially for small children and the elderly. Vibrocil dosing spray is not recommended for children under 6 years of age. The nose drops should be used for children between the ages of 2 and 6 years. Vibrocil should be used in children from 2 to 12 years of age under adult supervision. Information on the excipientsBenzalkonium chloride can cause irritation or swelling of the nasal mucosa, especially with prolonged use. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies oruse other medicines (including those you bought yourself!)! Can Vibrocil, dosing spray be used during pregnancy or breastfeeding?Systematic scientific studies have never been carried out. Phenylephrine and dimetindene maleate may be excreted in breast milk. As a precaution, Vibrocil should therefore not be used during pregnancy and breastfeeding. How do you use Vibrocil, dosing spray?Do not exceed the indicated dosage and application frequency. The lowest effective dose should always be used over the shortest possible duration of therapy. Adults and children over 6 years of age (with adult supervision):Apply 1-2 mists into each nostril 3 to 4 times daily. Children under 6 years of ageVibrocil dosing spray is not recommended for children under 6 years of age. Application of the dosing sprayClean your nose thoroughly before use (e.g. blow your nose).Be careful not to let the spray mist into the eyes.Remove protective cap. Before the very first use, press the pump 5 times to start the spraying process. The dosing spray is now ready for any further application. If the product has not been used for a long time, the pump must be operated 5 times again before use.Insert the spray head into one nostril, spray 1 time (press firmly) and inhale through your nose at the same time . Repeat the process for the other nostril.Wipe and dry the spray head before replacing the protective cap.A bottle of Vibrocil dosing spray should only be used by one person to avoid possible spread of infection. Do not use continuously for more than 3 days. If there is no improvement after 3 days or if the symptoms worsen, you should seek medical advice. 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 Vibrocil, dosing spray have?The following side effects can occur when using Vibrocil:In In rare cases (affects 1 to 10 users in 10,000), local and temporary burning or dryness of the nose and nosebleeds may occur. 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 out of the reach of children. Vibrocil dosing spray: Protect from light and store at 15-30°C. Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Vibrocil dosing spray contain?Active substances1 ml Vibrocil dosing spray contains: 0.25 mg dimetindene maleate and 2.5 mg phenylephrine. 1 spray (=0.14 ml) contains: 0.035 mg dimetindene maleate and 0.35 mg phenylephrine. ExcipientsSorbitol, sodium monohydrogen phosphate, citric acid monohydrate, lavandin oil, benzalkonium chloride, purified water. Approval number50421 (Swissmedic). Where can you get Vibrocil, dosing spray? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Vibrocil dosing spray (microdoseur): pack of 15 ml. Authorization holderGSK Consumer Healthcare Schweiz AG, Risch. This package leaflet was last checked by the Medicines Agency (Swissmedic) in January 2021. ..

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