Swissmedic-approved
(1 Pages)
Elotrans plv 20 bags 6.03 g
Diarrheal diseases are often accompanied by a massive loss of water and mineral salts. Elotrans is a mixture of mineral salts which, from infancy, balances out salt and water loss in diarrheal diseases. Swissmedic-approved patient informationElotrans®Helvepharm AGAMZVWhat is Elotrans and when is it used?Diarrheal diseases are often accompanied by a massive loss of water and mineral salts. Elotrans is a mixture of mineral salts which, from infancy, balances out salt and water loss in diarrheal diseases. What should be considered?In addition to treatment with Elotrans, care must be taken to ensure a sufficient supply of water and/or low-salt solutions. A bag of 6.03 g contains 1⁄3 bread unit (BE), corresponding to 0.4 BW (bread value). When not to use Elotrans?In the event of renal dysfunction, metabolic alkalosis, sugar absorption disorders, unconsciousness, shock, persistent vomiting and if you are hypersensitive to any of the ingredients in Elotrans (react allergic. When is caution required when taking Elotrans?For use in children under 3 years of age with diarrhea, a doctor must be consulted. Patients with heart disease and high blood pressure should only take Elotrans after consulting their doctor. Due to the high sugar content (glucose), diabetics should only use Elotrans after consulting their doctor. If the diarrhea is accompanied by fever and if blood is found in the stool, a doctor should be consulted. Elotrans should also only be used in the following cases after consulting a doctor: If you have recurrent or persistent diarrheaIf you have liver or kidney diseaseIf you are on a low-potassium or low-sodium diet li>If your blood has low levels of potassium or sodiumElotrans should only be prepared with the specified amount of water. If more water than recommended is used, the salts will not be at an optimal concentration and if less water than recommended is used, this can lead to an increase in the imbalance of mineral salts in the blood. If the diarrhea lasts longer than 24 to 36 hours, you should see a doctor. If the diarrhea is associated with nausea or vomiting, begin by taking small but frequent sips. 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 Elotrans be taken during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child when used as directed. Elotrans can be taken during pregnancy or while breastfeeding. However, medical supervision is recommended. How do you use Elotrans?Oral use after dissolving in drinking water or in boiled, cooled water or unsweetened tea. Elotrans should not be administered with fruit juice, milk or other liquids containing mineral salts. The content of one sachet is dissolved in 200 ml of liquid. Unless otherwise prescribed, children under one year take a maximum of 600 to 1000 ml (3-5 sachets), children up to 4 years of age a maximum of 1000 to 2000 ml Elotrans solution (5-10 sachets) spread over the day. In older children and adults, the Elotrans intake can be increased accordingly up to 20 sachets (4 l Elotrans solution). Up to 1 year: maximum 600-1000 ml per day. Up to 4 years: maximum 1000-2000 ml per day. From 4 years: up to 4000 ml depending on fluid loss per day. Elotrans treatment for infants usually lasts 6 to 12 hours, up to a maximum of 24 hours. Small children, school children and adults take Elotrans as instructed by the doctor until the diarrhea has subsided. If you have taken too much Elotrans, contact your doctor. Follow the dosage given in this leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Elotrans have?The following side effects can occur when taking Elotrans: In individual cases, there may be a change in the amount of sodium chloride in the body. It is therefore important to ensure an adequate supply of water and low-salt solutions. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?When traveling to warm or tropical countries, care must be taken to ensure that medicines are always carefully protected from heat and moisture. Elotrans bags should be stored at room temperature (15-25°C) and out of the reach of children. The medicinal product may only be used up to the date marked «EXP» on the container. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Elotrans contain?1 sachet of Elotrans contains: glucose, anhydrous 4.0 g, sodium chloride 0.7 g, sodium citrate × 2 H2O 0.59 g, potassium chloride 0.30 g. Excipients: saccharin, aroma (contains bergamot oil, among other things), coloring agent: caramel (E150). Total osmolarity of the ready-to-use solution: 311 mosm/l. Electrolyte content of the ready-to-use solutionNa+ 90 mmol/l = 90 mval/l. K+ 20 mmol/l = 20 meq/l. Cl– 80 mmol/l = 80 meq/l. Citrate3– 10 mmol/l = 30 meq/l. Approval number44644 (Swissmedic). Where can you get Elotrans? What packs are available?In pharmacies and drugstores without a doctor's prescription. Packs of 20 sachets. Authorization holderHelvepharm AG, Frauenfeld. This package leaflet was last checked by the medicines authority (Swissmedic) in June 2018. ..
20.25 USD
Infludoron glob fl 10g
Swissmedic-approved patient information Infludoron® globules Weleda AG Anthroposophic medicinal products AMZV When is Infludoron used? According to anthroposophical knowledge of man and nature, Infludoron can be used to treat influenza , flu infections and feverish colds. Infludoron is a combination of potentised substances of plant and mineral origin. It is suitable for use at the first signs as well as when the disease has already fully broken out. Symptoms such as fever, runny nose, shivering, drowsiness, muscle and joint pain, heavy sweating or signs of exhaustion are alleviated and healing is promoted. Infludoron is well tolerated and is therefore particularly suitable for use in children and infants. What do you need to know about this? If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether you are taking Infludoron at the same time may be taken. When should Infludoron not be taken or only with caution? Infludoron should not be used if you are hypersensitive to one of the ingredients. Tell your doctor, pharmacist or druggist if you suffer from other diseases, have allergies or take other medicines (including those you bought yourself!). Can Infludoron be taken during pregnancy or while breastfeeding? Based on previous experience, there is no known risk for the child when 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 Infludoron? Unless otherwise prescribed by your doctor, take Infludoron at the first sign of a cold such as shivering, feeling of pressure in the head, body aches. Swallow the pellets whole or let them melt in your mouth. Adults and children (from 6 years): 10-15 pellets 3-6 times a day; in the acute stage 10-15 globules every 1-2 hours; if the fever is gone, reduce the dosage to 10-15 pellets 3 times a day. Infants (2-6 years): 5 globules 3-6 times a day. Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Infludoron have? No side effects have been observed for Infludoron when used as directed. If you do notice any side effects, tell your doctor, pharmacist or druggist. What else needs to be considered? If the symptoms worsen or if there is no improvement, discontinue Infludoron and inform your doctor, pharmacist or druggist or druggist. Keep the medicine out of the reach of children. Store at room temperature (15-25°C) and away from moisture. 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. What does Infludoron contain? 1 g of globules contains: monkshood D4 10 mg / iron phosphate D6 10 mg / bryony D1 6 mg / eucalyptus D1 5 mg / water hazel D1 4 mg / Sabadill D1 1 mg. Excipient: sugar. Approval number 46444 (Swissmedic). Where can you get Infludorone? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Glass container of 10 g. Authorization holder Weleda AG, Arlesheim, Switzerland. This leaflet was last checked by the drug authority (Swissmedic) in June 2005. 37470380 / Index 7 Swissmedic-approved patient information Infludoron® globulesWeleda AGAnthroposophic medicinal products AMZVWhen is Infludoron used?According to anthroposophical knowledge of man and nature, Infludoron can be used to treat influenza , flu infections and feverish colds. Infludoron is a combination of potentised substances of plant and mineral origin. It is suitable for use at the first signs as well as when the disease has already fully broken out. Symptoms such as fever, runny nose, shivering, drowsiness, muscle and joint pain, heavy sweating or signs of exhaustion are alleviated and healing is promoted. Infludoron is well tolerated and is therefore particularly suitable for use in children and infants. What do you need to know about this?If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether you are taking Infludoron at the same time may be taken. When should Infludoron not be taken or only with caution?Infludoron should not be used if you are hypersensitive to one of the ingredients. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!).Can Infludoron be taken during pregnancy or while breastfeeding?Based on previous experience, there is no known risk for the child when 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 Infludoron?Unless otherwise prescribed by your doctor, take Infludoron at the first sign of a cold such as shivering, feeling of pressure in the head, body aches. Swallow the pellets whole or let them melt in your mouth. Adults and children (from 6 years): 10-15 pellets 3-6 times a day; in the acute stage 10-15 globules every 1-2 hours; if the fever is gone, reduce the dosage to 10-15 pellets 3 times a day. Infants (2-6 years): 5 globules 3-6 times a day. Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Infludoron have?No side effects have been observed for Infludoron when used as directed. If you do notice any side effects, tell your doctor, pharmacist or druggist. What else needs to be considered?If the symptoms worsen or if there is no improvement, discontinue Infludoron and inform your doctor, pharmacist or druggist or druggist. Keep the medicine out of the reach of children. Store at room temperature (15-25°C) and away from moisture. 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. What does Infludoron contain?1 g of globules contains: monkshood D4 10 mg / iron phosphate D6 10 mg / bryony D1 6 mg / eucalyptus D1 5 mg / water hazelnut D1 4 mg / Sabadill D1 1 mg. Excipient: sugar. Approval number46444 (Swissmedic). Where can you get Infludorone? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Glass container of 10 g. Authorization holderWeleda AG, Arlesheim, Switzerland. This leaflet was last checked by the drug authority (Swissmedic) in June 2005. 37470380 / Index 7 ..
43.94 USD
Luffa compositum heel nasal spray 20 ml
LUFFA COMPOSITUM Heel Nasal SpraySwissmedic-approved patient informationLuffa comp.- Heel, nasal sprayebi-pharm agHomeopathic medicineWhen will Luffa comp.-Heel nasal spray used?According to the homeopathic drug picture, Luffa comp.-Heel nasal spray can be used for hay fever.What should be considered?If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether Luffa comp.-Heel nasal spray can be used at the same time.When should Luffa comp.-Heel nasal spray not be used or only with caution?Luffa comp.-Heel nasal spray should not be used if you have a known allergy to benzalkonium chloride. Tell your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies orother medicines (including self-bought) or use externally.May Luffa comp.-Heel nasal spray be used during pregnancy or breastfeeding?Due to the Based on previous experience, there is no known risk for the child when used as intended. However, systematic scientific investigations have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding or ask your doctor, pharmacist or druggist for advice.How do you use Luffa comp .-Heel Nasal Spray? Unless otherwise prescribed by the doctor, spray 1-2 sprays into each nostril 3 - 5 times a day; in children aged 2-6 years 1 spray 3-4 times a day. Follow the dosage given in the package leaflet or prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child / child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.Side effects Luffa comp.-Heel nasal spray? When using Luffa comp.-Heel nasal spray, irritation of the nasal mucosa with burning, increased nasal secretion (and nosebleeds) can occur in rare cases. In these cases, the drug should be discontinued. In very rare cases, bronchospasm may occur due to benzalkonium chloride in predisposed asthmatic patients. When using homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, stop using the Luffa comp.-Heel nasal spray and tell your doctor, pharmacist or druggist.What else should you watch out for? The medicinal product may only be used up to the date marked "Use by" on the container. Store drug out of reach of children. Store at room temperature (15-25°C). Your doctor, pharmacist or druggist can provide you with further information.What does Luffa comp.-Heel Nasal Spray contain?1 ml solution contains: Histaminum D12 50 mg, Histaminum D30 50 mg, Histaminum D200 50 mg, Luffa operculata D4 100 mg, Luffa operculata D12 100 mg, Luffa operculata D30 100 mg, Sulfur D12 50 mg, Sulfur D30 50 mg, Sulfur Thryallis glauca D4 100 mg, Thryallis glauca D12 100 mg, Thryallis glauca D30 100 mg. This preparation also contains auxiliary substances and benzalkonium chloride as a preservative.Authorization number52492 (Swissmedic) Where can you get Luffa comp.-Heel nasal spray? What packs are available?In pharmacies and drugstores without a doctor's prescription. 20 ml dosing spray.Authorization holderebi-pharm ag, Lindachstr. 8c, 3038 KirchlindachThis leaflet was last checked by the drug authority (Swissmedic) in June 2013...
42.53 USD
Maltofer drops bottle 30 ml
Maltofer drops are an iron preparation used to treat iron deficiency without anemia and iron deficiency anemia. Iron is an indispensable component of the red blood pigment, the red muscle pigment and the iron-containing enzymes. Iron deficiency can lead to the following general symptoms: increased tiredness, reduced mental performance, irritability, restlessness, headaches, loss of appetite, weakened immune system, noticeable paleness, cracked corners of the mouth, dry skin, brittle hair and nails. Swissmedic-approved patient informationMaltofer® oral dropsVifor (International) Inc.What are Maltofer drops and when are they used?Maltofer drops are an iron preparation used to treat iron deficiency without anemia and iron deficiency anemia. Iron is an indispensable component of the red blood pigment, the red muscle pigment and the iron-containing enzymes. Iron deficiency can lead to the following general symptoms: increased tiredness, reduced mental performance, irritability, restlessness, headaches, loss of appetite, weakened immune system, noticeable paleness, cracked corners of the mouth, dry skin, brittle hair and nails. What should be considered?Before you start taking Maltofer drops, the iron and blood pigment (haemoglobin) content of the blood should be checked by a doctor have been clarified by appropriate investigations. If the symptoms are not due to iron deficiency, Maltofer drops will not be effective. Your doctor would like to see the progress of your treatment through regular check-ups and may also want to carry out blood tests. This is normal and should not concern you. If your symptoms do not improve within 3 weeks, consult your doctor. During treatment with Maltofer, the stool may turn dark, but this is harmless. When should Maltofer drops not be taken/used?If you have a known hypersensitivity (allergy) or intolerance to the active ingredient iron( III)-hydroxide polymaltose complex or one of the excipients (see «What does Maltofer Drops contain?»)In the case of excess iron in the body (e.g. due to rare iron storage diseases which lead to iron deposits in the tissues)In the case of so-called iron utilization disorders (if the anemia is due, for example, to insufficient iron utilization)In the case of anemia that is not due to an iron deficiency (e.g. due to increased hemoglobin degradation or a lack of vitamin B12. When is caution required when taking / using Maltofer drops?Inform before taking Maltofer your doctor, pharmacist or druggist if you have an infection or a tumor. Tell your doctor, pharmacist or druggist if you have recently been treated or may be treated with injectable iron preparations. Such iron preparations should not be used at the same time as Maltofer. Tell your doctor, pharmacist or druggist if you have received blood transfusions as there is a risk of iron overload with supplemental iron. This medicinal product contains 5 mg sodium (main component of cooking/table salt) per ml. This is equivalent to 0.25% of the recommended maximum daily dietary intake of sodium for an adult. Maltofer drops contain sodium methyl parahydroxybenzoate (E219) and sodium propyl parahydroxybenzoate (E217). These can cause allergic reactions, including delayed reactions. Maltofer drops contain sucrose. Please only take Maltofer drops after consulting your doctor if you know that you suffer from sugar intolerance. Sucrose can be harmful to teeth. No relevant studies have been conducted. However, Maltofer is unlikely to have any effect on the ability to drive and use machines. Tell your doctor, pharmacist or druggist if you: Suffer from other diseasesHave allergiesTake other medicines (including those you bought yourself!). May Maltofer drops be taken / used during pregnancy or breastfeeding? If you are pregnant, want to become pregnant or are breastfeeding, you may only use Maltofer after consulting your doctor or apply to your doctor. How do you use Maltofer drops?1 drop corresponds to 0.050 ml corresp. 2.5 mg iron. 1 ml corresponds to 20 drops corresp. 50 mg iron. Maltofer drops should be taken during or immediately after eating. They can be mixed with fruit or vegetable juices or with bottle feeding. The slight coloring affects neither the effect nor the taste. The daily dose can be taken all at once or divided into several individual doses. Hold the bottle upside down and upright. A drop will form immediately at the end of the dropper bottle. If not, tap bottle gently until a drop forms. Don't shake the bottle. Iron deficiency anemiaPremature babies: 1-2 drops/kg body weight daily for 3-5 months. Infants up to 1 year: 10-20 drops daily. Children (1-12 years): 20-40 drops daily. Adolescents from 12 years and adults: 40-120 drops daily. Iron deficiency without anemiaInfants up to 1 year: 6-10 drops daily. Children (1-12 years): 10-20 drops daily. Adolescents from 12 years and adults: 20-40 drops daily. The dosage and duration of treatment depends on the extent of the iron deficiency. For iron deficiency anemia, treatment takes an average of 3-5 months for blood test results to return to normal. The treatment is then continued for several weeks with the dosage as described for iron deficiency without anemia in order to replenish iron stores. For iron deficiency without anemia, treatment lasts about 1-2 months. The doctor decides on the exact duration of treatment in each individual case. If you have taken more Maltofer than you should, talk to your doctor, pharmacist or druggist. If you forget to take Maltofer, just take the next dose at the usual time. Do not take a double dose to make up for the missed dose. Follow the dosage given in this leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can Maltofer drops have?The following side effects can occur when taking Maltofer drops: Very common (affects more than 1 user in 10): A very common side effect is discolored stool due to iron excretion, but this is harmless. Common (affects 1 to 10 users in 100): Commonly observed side effects are nausea, constipation, diarrhea and abdominal pain. Uncommon (affects 1 to 10 users in 1000): uncommon: vomiting, discoloration of the teeth, inflammation of the stomach (gastritis), itching, rash, hives, reddening of the skin (erythema) and headaches come. Rare (affects 1 to 10 users in 10,000): in rare cases, patients experience muscle spasms and muscle pain (myalgia). These side effects are usually temporary. 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 packaging. Storage instructionsStore at room temperature (15-25°C). Keep out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Maltofer Drops contain?Active ingredients1 ml Maltofer Drops (= 20 drops) contains 50 mg iron in the form of ferric hydroxide polymaltose complex. ExcipientsSucrose, sodium methyl parahydroxybenzoate (E219), sodium propyl parahydroxybenzoate (E217), cream flavoring (contains propylene glycol), sodium hydroxide, purified water. Approval number38593 (Swissmedic) Where can you get Maltofer drops? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Maltofer drops are available in packs of 30 ml. Authorization holderVifor (International) AG 9001 St GallenThis package leaflet was last checked by the Medicines Agency (Swissmedic) in August 2021. ..
22.05 USD
Midro tea 15 bags 1.5 g
Midro Tea is a herbal laxative for the treatment of occasional constipation (e.g. when changing diet, changing location or bed rest). Swissmedic-approved patient informationMidro® teaMidro AGHerbal medicinal product AMZVWhat is Midro Tea and when is it used?Midro Tea is a herbal laxative treatment of occasional constipation (e.g. when changing diet, changing location or bed rest). What should be considered?In order to educate your intestines to function normally, the following tips can be helpful: Eat right: Eat a low-calorie, high-fiber mixed diet (e.g. vegetables, salads, wholemeal bread, etc.) with regular meals with sufficient fluid intake.As much exercise as possible (especially when working sedentarily).No suppression of the urge to defecate.When should Midro Tea not be used or only with caution?For everyone Disorders of the gastrointestinal tract (e.g. inflammation, bleeding, constrictions in the gastrointestinal system, intestinal obstruction, suspected appendicitis) or hypersensitivity to the active ingredient or the excipients, Midro Tee must not be taken. Laxatives should only be taken occasionally and for no longer than 1-2 weeks because of possible habituation. Chronic use/abuse or use of higher than recommended doses can result in diarrhea with dehydration and salt imbalance (especially potassium depletion). Special caution is therefore required in patients who are also taking certain water-propagating medicines (diuretics), medicines containing liquorice root, corticosteroids, certain antihistamines (such as terfenadine), medicines for heart muscle weakness (cardiac glycosides such as digoxin) and certain medicines for heart rhythm disorders (antiarrhythmics). Inform your doctor, pharmacist or druggist if you suffer from illnesses, have allergies or are taking other medicines (even those you bought yourself!). Long-term treatments belong under medical supervision. Can Midro Tea be taken during pregnancy or while breastfeeding?During pregnancy and while breastfeeding, Midro Tea may only be taken after consulting a doctor. How do you use Midro Tea?Adults and adolescents from the age of 12:Unless otherwise prescribed by a doctor, Chew ½ to a maximum of 1½ level measuring spoons or ¼ to 1 sachet (max. 1.5 g) preferably before going to bed and swallow with water (onset of effect after approx. 8 hours). Start with ½ scoop or ¼ sachet of Midro Tea. Reduce or increase the dosage as individually as you need it for defecation. The maximum daily intake must not be more than 30 mg hydroxyanthracene derivatives (calculated as sennoside B). This corresponds to approx. 1½ measuring spoons or 1 bag content. Stick to the dosage provided in the package insert or prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. The use and safety of Midro Tee in children under 12 years of age has not been systematically tested. For children under 12 only on medical prescription. What side effects can Midro Tea have?The following side effects can occur when taking or using Midro Tea: In rare cases, Midro Tea can cause flatulence or abdominal cramps. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Medicines should be kept out of the reach of children. Protect from heat and moisture and store at room temperature (15-25°C). 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 Midro Tea contain?Sennae folium 75% corresp. hydroxyanthracenae 2.7%, malvae flos 1%, calcatrippae flos 1%, menthae piperitae 7%, carvi fructus 10%, liquiritae radix 6%. Approval number10567 (Swissmedic). Where can you get Midro Tea? What packs are available? In pharmacies and drugstores without a doctor's prescription: 15× 1.5g. In pharmacies only against a doctor's prescription: 80g packs. Hospital pack of 1,000 g. Authorization holderMidro AG, 4125 Riehen. This leaflet was last checked by the drug authority (Swissmedic) in May 2006. ..
16.06 USD
Minorga lös 2% bottle 60 ml
Inhaltsverzeichnis Was ist Minorga 2% Lösung und wann wird es angewendet? Was sollte dazu beachtet werden? Wann darf Minorga 2% Lösung nicht angewendet werden? Wann ist bei der Anwendung von Minorga 2% Lösung Vorsicht geboten? Darf Minorga 2% Lösung während einer Schwangerschaft oder in der Stillzeit angewendet werden? Wie verwenden Sie Minorga 2% Lösung? Welche Nebenwirkungen kann Minorga 2% Lösung haben? Was ist ferner zu beachten? Was ist in Minorga 2% Lösung enthalten? Zulassungsnummer Wo erhalten Sie Minorga 2% Lösung? Welche Packungen sind erhältlich? Zulassungsinhaberin COMPENDIUM Swissmedic-genehmigte Patienteninformation Minorga 2% Bailleul (Suisse) SA Was ist Minorga 2% Lösung und wann wird es angewendet? Minorga 2% Lösung ist ein nur äusserlich anzuwendendes Haarwuchsmittel, das den Wirkstoff Minoxidil enthält.Minorga 2% Lösung wird zur Behandlung von übermässigem, erblich hormonell bedingtem Haarausfall und beginnender Glatzenbildung (androgenetische Alopezie) bei Erwachsenen im Alter von 18 bis 65 Jahren verwendet. Es kann weiteren Haarausfall verhindern und das Wachstum neuer Haare fördern. Die Wirkungsweise ist nicht vollständig geklärt. Was sollte dazu beachtet werden? Typisch für Männer und Frauen mit erblichem Haarausfall ist eine Verdünnung des Haarwuchses bzw. Glatzenbildung oberhalb der Schläfen und in der Scheitelregion (siehe Abbildung).Das Nachwachsen der neuen Haare benötigt mindestens 2-4 Monate. Ein kosmetisch befriedigendes Nachwachsen der neuen Haare wird normalerweise nach ca. einem Jahr Behandlung beobachtet. Der Wirkungseintritt und Grad der Verdichtung des Kopfhaares sind jedoch je nach Person verschieden.Wenn Sie auf die Behandlung ansprechen, ist Ihr neues Haar wahrscheinlich weich und flaumig (Vellushaar) und zunächst kaum sichtbar.Bei Fortführung der Behandlung wird der neue Haarwuchs dicker und dunkler, bis er in Farbe und Struktur dem vorhandenen Kopfhaar gleicht.Fortgeschrittene Fälle von Glatzenbildung und seit mehr als zehn Jahren bestehende Glatzen sprechen selten bzw. nicht auf die Behandlung an. Wann darf Minorga 2% Lösung nicht angewendet werden? Wenn Sie allergisch auf Minoxidil, Propylenglykol oder Alkohol sind, dürfen Sie Minorga 2% Lösung nicht benutzen. Ebenso bei nicht erblich bedingtem plötzlichem und/oder kreisrundem Haarausfall, bei Haarausfall, der im Zusammenhang mit einer Schwangerschaft oder Geburt auftritt, bei Haarausfall unbekannter Ursache, bei Haarausfall, der mit einer Entzündung der Kopfhaut einhergeht, oder falls in Ihrer Familie keine Fälle von frühzeitigem Haarausfall vorkommen.Minorga 2% Lösung ist auch nicht geeignet zur Behandlung bei vollständiger Kahlheit oder bei totalem Verlust der Körperbehaarung.Wenn Sie unsicher sind, wodurch Ihr Haarausfall verursacht wird, suchen Sie Ihren Arzt bzw. Ihre Ärztin auf. Bei Patienten über 65 Jahren sowie bei Patienten unter 18 Jahren soll Minorga 2% Lösung nicht angewendet werden.In der Schwangerschaft und Stillzeit darf das Präparat nicht angewendet werden (siehe «Darf Minorga 2% Lösung während einer Schwangerschaft oder in der Stillzeit angewendet werden?») Wann ist bei der Anwendung von Minorga 2% Lösung Vorsicht geboten? Wird Minorga 2% Lösung eingenommen, kann dies zu schwerwiegenden Blutdruck- und Herz-Kreislaufproblemen führen. Daher muss das Produkt für Kinder unzugänglich aufbewahrt und darf nur äusserlich angewendet werden.Kontaktieren Sie im Falle des versehentlichen Verschluckens sofort einen Arzt bzw. eine Ärztin.Das Einatmen der Spraydämpfe ist zu vermeiden.Minorga 2% Lösung darf nur auf die gesunde Kopfhaut aufgetragen werden.Wenn Ihre Kopfhaut gerötet, entzündet, gereizt, infiziert oder schmerzhaft ist wie z.B. nach Sonnenbrand oder bei Dermatitis, sollte Minorga 2% Lösung nicht angewendet werden. Zusammen mit anderen örtlich anzuwendenden Arzneimitteln (Salben, Cremes, Lotionen etc.) darf Minorga 2% Lösung nicht aufgetragen werden.Sollten Sie unter Herz-Kreislauferkrankungen leiden (z.B. Herzrhythmusstörungen, Angina pectoris oder Brustschmerzen, Bluthochdruck und/oder Kreislaufstörungen) ist vor der ersten Anwendung von Minorga 2% Lösung ein Arzt bzw. eine Ärztin zu befragen.Sie sollten Minorga 2% Lösung absetzen und Ihren Arzt/Ihre Ärztin aufsuchen,•wenn eine Erniedrigung des Blutdrucks festgestellt wird, oder•wenn eine oder mehrere der folgenden Erscheinungen auftreten oder diese sich verschlimmern: Brustschmerzen, beschleunigter Herzschlag, Schwächegefühl oder Schwindel, plötzliche und unerklärliche Gewichtszunahme, geschwollene Hände oder Füsse, anhaltende Rötung oder Reizung der Kopfhaut.Bei diesem Arzneimittel kann niedriger Blutdruck und/oder Schwindel auftreten und dadurch die Reaktionsfähigkeit, die Fahrtüchtigkeit und die Fähigkeit, Werkzeuge oder Maschinen zu bedienen, beeinträchtigen! Führen Sie bei Auftreten niedrigen Blutdrucks und/oder Schwindels kein Fahrzeug und bedienen Sie keine Maschinen.Minorga 2% Lösung enthält Alkohol und kann Brennen und Reizung in den Augen verursachen. Wenn Sie aus Versehen Minorga 2% Lösung in Ihre Augen, den Mund oder auf eine Wunde bringen, spülen Sie die betroffene Hautstelle gründlich mit reichlich kaltem Wasser ab.Informieren Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin, wenn Sie an anderen Krankheiten leiden, Allergien haben oder andere Arzneimittel (auch selbstgekaufte!) einnehmen oder äusserlich anwenden. Darf Minorga 2% Lösung während einer Schwangerschaft oder in der Stillzeit angewendet werden? Wenn Sie schwanger werden möchten oder schwanger sind oder wenn Sie stillen, dürfen Sie Minorga 2% Lösung nicht anwenden. Wie verwenden Sie Minorga 2% Lösung? Haare und die Kopfhaut müssen vollkommen trocken sein, bevor Sie Minorga 2% Lösung anwenden können. Minorga 2% Lösung ist ausschliesslich für die äusserliche Anwendung auf der Kopfhaut bestimmt.Erwachsene im Alter von 18 bis 65 JahrenTragen Sie 2x täglich je 1 ml Lösung (morgens und abends) direkt auf die vom Haarausfall betroffene Kopfhaut auf.Überschreiten Sie nicht die Dosis von 1 ml Minorga 2% Lösung pro Anwendung und wenden Sie Minorga 2% Lösung nicht mehr als 2x pro Tag an (Eine häufigere Anwendung oder die Verwendung grösserer Mengen bringt keine verbesserten Ergebnisse). Verteilen Sie Minorga 2% Lösung sanft mit dem Applikator oder den Fingerspitzen auf der Kopfhaut (nicht einmassieren!), wobei Sie mit der Behandlung in der Mitte der betroffenen Stellen beginnen.Waschen Sie sich nach jeder Anwendung gründlich die Hände, damit Minorga 2% Lösung nicht ungewollt durch Ihre Hände an andere Körperstellen gerät. Falls Sie die Lösung aus Versehen an einer anderen Körperstelle als der Kopfhaut aufgetragen haben, spülen Sie diese Stelle gründlich mit viel Wasser, um mögliche Nebenwirkungen auf der Haut zu vermeiden.Um das neue Haarwachstum zu fördern und zu erhalten, ist eine regelmässige Anwendung (2x täglich) erforderlich. Anderenfalls wird der Haarausfall wieder einsetzen.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.Es gibt zwei verschiedene Sprühgeräte zum Auftragen des Arzneimittels: Pumpsprayapplikator (indiziert, wenn die zu behandelnden Bereiche gross sind), Pumpsprayapplikator mit Applikator (indiziert, wenn die zu behandelnden Bereiche klein sind oder mit Haaren bedeckt sind).Art der AnwendungDie Art der Anwendung hängt von dem verwendeten Pumpsprayapplikator ab.PumpsprayapplikatorDieser Applikator ist indiziert, wenn die zu behandelnden Bereiche gross sind.1Kappe von Flasche entfernen.2Pumpe auf die zu behandelnde Fläche richten; 1 x aufsprühen und das Produkt mit den Fingerspitzen verteilen, um den zu behandelnden Bereich vollständig zu bedecken. Wiederholen Sie diesen Vorgang 6 x, um eine 1 ml-Dosis zu verabreichen.7 Sprühstösse ergeben die Dosis von 1 ml. Spraydämpfe nicht einatmen.3Spülen Sie den Pumpsprayapplikator und/oder den Applikator und setzen Sie die Kappe nach Gebrauch wieder auf.Pumpsprayapplikator mit ApplikatorDieser Applikator ist indiziert, wenn die zu behandelnden Bereiche klein sind oder mit Haaren bedeckt sind.1Kappe von Flasche entfernen.2Entfernen Sie die Oberseite der Pumpe. Befestigen Sie den Applikator und drücken Sie fest.3Fahren Sie dann wie für den Pumpsprayapplikator beschrieben fort.Morgens und abends eine Dosis von 1 ml anwenden. 7 Sprühstösse ergeben die Dosis von 1 ml. Dosis und Häufigkeit der Anwendung nicht erhöhen. Welche Nebenwirkungen kann Minorga 2% Lösung haben? Folgende Nebenwirkungen können bei der Anwendung von Minorga 2% Lösung auftreten:In den ersten 2-6 Wochen der Anwendung kann es vorübergehend zu verstärktem Haarausfall kommen, da die alten Haare von neuen nachwachsenden Haaren verdrängt werden («Shedding»). Dieser temporär verstärkte Haarausfall tritt in der Regel 2-6 Wochen nach Therapiebeginn auf und klingt nach ein paar Wochen ab (erstes Zeichen der Minoxidil-Wirkung). Falls der vermehrte Haarausfall länger anhält, sollten Sie die Behandlung mit Minorga beenden und ärztlichen Rat einholen.Sehr häufig können Kopfschmerzen auftreten.Häufig können Atemnot, Dermatitis, Akne ähnliche Dermatitis, Hautreaktionen wie Ausschlag, lokale Hautreizungen und -rötungen, Juckreiz, trockene, schuppende Haut oder Ekzeme, Haarausfall, unerwünschter Haarwuchs ausserhalb der Kopfhaut (einschliesslich Wachstum von Gesichtshaaren bei Frauen), geschwollene Hände oder Beine sowie Gewichtszunahme auftreten.Gelegentlich können allergische Reaktionen, Nesselsucht, allergischer Schnupfen, allgemeine Wassereinlagerung (Schwellung) oder Schwellung (Ödem) des Gesichts, Schwindel und Übelkeit auftreten.Selten können niedriger Blutdruck, Veränderungen der Haarfarbe und Haarstruktur (dies ist insbesondere bei grauem Haar, beim Schwimmen in chemisch aufbereitetem Wasser (Schwimmbecken), oder falls Minorga 2% Lösung sich verfärbt hat möglich) auftreten.Sehr selten wurde auch von folgenden Nebenwirkungen berichtet:Schwere Überempfindlichkeitsreaktionen und Angioödem, die sich mit Schwellung von Gesicht, Lippen, Mund, Zunge und/oder Rachen sowie allgemeinem Juckreiz, allgemeinen Hautauschlag und Engegefühl im Hals äussern. Bei Auftreten dieser Anzeichen brechen Sie die Behandlung ab und suchen sofort ärztliche Hilfe. Es kann eine allergische Kontaktdermatitis auftreten. Auch an der Applikationsstelle (und an in der Nähe liegenden Körperteilen, wie Ohren und Gesicht) kann es zu Reaktionen kommen. Typischerweise bestehen diese aus Hautreizungen, Schmerzen, Schwellungen (Ödemen) und Rötungen. Mit Hautabschuppung, Blasenbildung, Blutungen und Geschwürbildung können diese Reaktionen auch schwerwiegender ausfallen. Zudem wurde von depressiver Verstimmung, Erbrechen, Augenirritationen sowie Brustschmerzen, Herzrasen (Tachykardie) oder bewusster Wahrnehmung des Herzschlags (Palpitationen), Sehstörungen inkl. Verminderung der Sehschärfe und sexuellen Funktionsstörungen berichtet.Wenn Sie unter der Behandlung mit Minorga 2% Lösung plötzlich Brustschmerzen, Herzklopfen oder einen niedrigen Blutdruck bekommen, dürfen Sie sich nicht mehr mit Minorga 2% Lösung behandeln und sollten einen Arzt bzw. eine Ärztin aufsuchen. Das gleiche gilt für auftretenden Ohnmachtsanfall und/oder Schwindel, plötzliche unerklärliche Gewichtszunahme, geschwollene Hände oder Füsse, anhaltende Rötung oder Reizung der behandelten Kopfhaut oder andere unerwartete Symptome.Wenn Sie Nebenwirkungen bemerken, die hier nicht beschrieben sind, sollten Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin informieren.Dies gilt insbesondere für Nebenwirkungen, die in dieser Packungsbeilage nicht erwähnt werden. Was ist ferner zu beachten? Da Minorga 2% Alkohol enthält, ist es leicht entzündbar. Daher während der Anwendung von Minorga 2% Lösung nicht rauchen und nicht in die Nähe von offenem Feuer oder anderen Hitzequellen geraten. Den Spray vorsichtig benutzen.In der Originalverpackung aufbewahren. Bei Raumtemperatur (15 – 25 °C) lagern. Ausser Reichweite von Kindern aufbewahren.Das Arzneimittel darf nur bis zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.Weitere Auskünfte erteilt Ihnen Ihr Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin. Diese Personen verfügen über die ausführliche Fachinformation. Was ist in Minorga 2% Lösung enthalten? 1 ml Minorga 2% Lösung enthält 20 mg Minoxidil als Wirkstoff und die Hilfsstoffe Ethanol, Propylenglycol und gereinigtes Wasser. Zulassungsnummer 66655 (Swissmedic). Wo erhalten Sie Minorga 2% Lösung? Welche Packungen sind erhältlich? In Apotheken und in Drogerien ohne ärztliche Verschreibung.1 Flasche zu 60 ml (jede Packung enthält 1 Applikator).3 Flaschen zu 60 ml (jede Packung enthält 2 identische Applikatoren). Zulassungsinhaberin Bailleul (Suisse) SA, 1203 Genève Diese Packungsbeilage wurde im Februar 2018 letztmals durch die Arzneimittelbehörde (Swissmedic) geprüft. 29071 / 05.04.2022 ..
79.60 USD
Pulmex ointment tb 40 g
The active ingredients in Pulmex make breathing easier, have a mild disinfecting effect and promote coughing. Experience has shown that Pulmex alleviates the symptoms of a cold with a runny nose or cough.Swissmedic-approved patient informationPulmex ® OintmentSpirig HealthCare AGWhat is Pulmex and when is it used?The active ingredients of Pulmex work easier to breathe and slightly disinfectant and promote coughing. Experience has shown that Pulmex reduces the symptoms of a cold with a runny nose or cough.What should be considered?If you have a cough that lasts longer than 7 days, you must consult your doctor, pharmacist or druggist.When should Pulmex not be used?In the event of hypersensitivity to a of the ingredients and if you have a history of seizures, Pulmex must not be used.The use of Pulmex is not recommended in children.When is the application from Pulmex Caution required? Do not use Pulmex ointment on mucous membranes (especially not in the nose or mouth), on burns or on injured skin. In case of contact with the eyes or mucous membranes rinse immediately with cold water. Do not swallow, do not suck. In patients with kidney dysfunction, Pulmex ointment may only be used for a short time and not over large areas. If the If symptoms persist or worsen, seek medical advice.Tell your doctor, pharmacist or druggist if youhave any other illness sufferhave allergies ortake other medicines (including those you bought yourself!) or use them externally. Can Pulmex be used during pregnancy or breastfeeding?Pulmex should not be used during pregnancy and breastfeeding.How do you use Pulmex?Adults:Pulmex ointment lightly rub into the chest and back 2 to 3 times a day. To do this, apply an approx. 10 cm long strand of ointment (corresponds to approx. 5 g of ointment) along the center line of the upper chest and back area. Rub in the ointment lightly, then cover with a dry and warm woolen or fabric towel. Wash hands well after use. The use of Pulmex in children is not recommended due to the lack of systematic data on efficacy and safety. Follow the guidelines in the Dosage indicated 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.Side effects Have Pulmex?In rare cases, allergic reactions with a rash and skin irritation can occur. In this case, stop the treatment and talk to your doctor, pharmacist or druggist. If you notice any side effects that are not described here, you should tell your doctor, Inform your pharmacist or druggist.What else needs to be considered?The medicinal product may only be used up to the point on the container date marked «EXP».Keep out of the reach of children. Store in the original packaging.Store at room temperature (15-25 °C).Your doctor, pharmacist or druggist can provide you with further information.What does Pulmex contain?1 g Pulmex ointment contains 60 mg artificial balsam of Peru (with vanilla flavor), 125 mg racemic camphor, 50 mg essential eucalyptus oil, 50 mg rosemary essential oil. This preparation also contains auxiliary substances.Approval number14991 (Swissmedic).Where can you obtain it Pulmex? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Pulmex ointment: packs of 40 and 80 g.Authorization holder Spirig HealthCare AG, 4622 Egerkingen This leaflet was last checked by the drug authority (Swissmedic) in June 2016...
31.72 USD
Sédatif pc tabl 40 pcs
Swissmedic-approved patient information SEDATIF PC®, tablets Boiron SA Homeopathic medicinal product When is SEDATIF PC used? According to homeopathic medicinal products, SEDATIF PC can be used to treat anxiety and tension, as well as mild sleep disorders. What should be considered? If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether SEDATIF PC may be taken at the same time. When should SEDATIF PC not be used or only with caution? If the symptoms persist for more than a month, contact your doctor. To date, no application restrictions are known. When used as intended, no special precautionary measures are necessary. Tell 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 SEDATIF PC be taken during pregnancy or breastfeeding? Based on previous experience, there is no known risk for the child when 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 SEDATIF PC? Unless otherwise prescribed by the doctor: suck 2 tablets every 2 hours. The slightly sweet tablets can be sucked or crushed in a little water. Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can SEDATIF PC have? If you notice any side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed on this leaflet. When taking homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, discontinue SEDATIF PC and inform your doctor, pharmacist or druggist. Up to now, no side effects have been observed for SEDATIF PC when used as intended. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. What else needs to be considered? The medicinal product may only be used up to the date marked "EXP" on the container. Storage Instructions Store at room temperature (15-25°C). Keep out of the reach of children. What does SEDATIF PC contain? Active ingredients Abrus precatorius 6 CH Aconite napellus 6 CH Atropa belladonna 6 CH Calendula officinalis 6 CHChelidonium majus 6 CH Viburnum opulus 6 CHEqual parts. Excipients Sucrose, lactose and magnesium stearate. Approval number 51020 (Swissmedic). Where can you get SEDATIF PC? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Pack of 40 or 90 tablets. Authorization holder BOIRON AG – CH-3007 Bern. Manufacturer BOIRON AG – France. This leaflet was last checked by the drug authority (Swissmedic) in December 2019. Swissmedic-approved patient information SEDATIF PC®, tabletsBoiron SAHomeopathic medicinal product When is SEDATIF PC used?According to homeopathic medicinal products, SEDATIF PC can be used to treat anxiety and tension, as well as mild sleep disorders. What should be considered?If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether SEDATIF PC may be taken at the same time. When should SEDATIF PC not be used or only with caution? If the symptoms persist for more than a month, contact your doctor. To date, no application restrictions are known. When used as intended, no special precautionary measures are necessary. Tell your doctor, pharmacist or druggist if you suffer from other diseaseshave allergies ortake other medicines (including those you bought yourself!) or use them externally!Can SEDATIF PC be taken during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child when 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 SEDATIF PC?Unless otherwise prescribed by the doctor: suck 2 tablets every 2 hours. The slightly sweet tablets can be sucked or crushed in a little water. Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can SEDATIF PC have?If you notice any side effects, contact your doctor, pharmacist or druggist. This also applies in particular to side effects that are not listed on this leaflet. When taking homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, discontinue SEDATIF PC and inform your doctor, pharmacist or druggist. Up to now, no side effects have been observed for SEDATIF PC when used as intended. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Storage InstructionsStore at room temperature (15-25°C). Keep out of the reach of children. What does SEDATIF PC contain?Active substancesAbrus precatorius 6 CH Aconite napellus 6 CH Atropa belladonna 6 CH Calendula officinalis 6 CHChelidonium majus 6 CH Viburnum opulus 6 CHEqual parts. ExcipientsSucrose, lactose and magnesium stearate. Approval number51020 (Swissmedic). Where can you get SEDATIF PC? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Pack of 40 or 90 tablets. Authorization holderBOIRON AG – CH-3007 Bern. ManufacturerBOIRON AG – France. This leaflet was last checked by the drug authority (Swissmedic) in December 2019. ..
36.69 USD
Sidroga lime blossoms 20 bags 1.8 g
Sidroga lime blossom tea is used for feverish colds. Swissmedic-approved patient information Sidroga® Linden blossom tea Sidroga AGHerbal medicinal product What is Sidroga linden blossom tea and when is it used? Sidroga linden blossom tea contains dried linden blossoms and finely chopped quality (tested according to the pharmacopoeia). Sweat-inducing properties are traditionally attributed to lime blossoms.Sidroga lime blossom tea is used for feverish colds. What should be considered? In the case of persistent or recurring feverish colds, it is advisable to consult a doctor and have the causes clarified. When shouldn't Sidroga lime blossom tea be used or only with Be used with caution? Sidroga lime blossom tea must not be used if there is a known hypersensitivity to lime. The use of this medicine is not recommended for small children under the age of 1 year. Inform your doctor, pharmacist or druggist if you suffer from other diseaseshave allergies orTake other medicines (including those you bought yourself!). Can Sidroga lime blossom tea be taken during pregnancy or while breastfeeding? Based on previous experience, there is no known risk for the child when used as intended. However, systematic scientific investigations have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding or ask your doctor, pharmacist or druggist for advice. How do you use Sidroga lime blossom Tea? Adults, school children and small children from the age of 1 take 1 cup 2 to 3 times a day before, during or after meals.Preparation: Pour boiling water over one tea bag per cup and let the bag steep in it for 5 to 10 minutes. Then take out the tea bag and squeeze it out lightly over the cup. Only use one tea bag per cup of tea and only sweeten your tea after removing the tea bag from the cup. You can use both natural and artificial sugar for sweetening. Sidroga lime blossom tea should be drunk as hot as possible and distributed throughout the day. Make sure you drink plenty of fluids.The use and safety of Sidroga lime blossom tea in small children under the age of 1 year has not yet been tested.Observe the instructions given in the leaflet or dosage prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. Side effects Have Sidroga lime blossom tea? No side effects have been observed for Sidroga lime blossom tea when used as directed. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. What else should be observed? Sidroga lime blossom tea should be stored at room temperature (15?25 °C) and out of the reach of children. The double chamber bags in aroma protection packaging may only be used up to the date marked «EXP» on the container.Your doctor, pharmacist or druggist can provide you with further information. What does Sidroga lime blossom tea contain? 1 double chamber bag contains 1.8 g dried and finely chopped linden blossoms. Approval number 41674 (Swissmedic) p> Where can you get Sidroga lime blossom tea? Which packs are available? This is an over-the-counter medicinal product. Boxes with 20 double-chamber sachets in aroma-protection packaging. Authorization holderSidroga AG, 4310 RheinfeldenThis leaflet was last checked by the drug authority (Swissmedic) in September 2010. ..
7.51 USD
Sidroga verbena 20 bags 1 g
Sidroga verbena tea is used both for states of tension and for nervous indigestion. Swissmedic-approved patient information Sidroga® verbena, tea Sidroga AGHerbal medicinal product AMZVWhat is Sidroga Verbena Tea and when is it used? Sidroga Verbena Tea contains lemon leaves (Verveine ) in dried form and finely chopped quality. Calming properties are traditionally attributed to the leaves of the lemon tree. Sidroga verbena tea is used both for states of tension and for nervous indigestion. What should be considered? In the case of persistent or recurring states of tension and nervous digestive problems, it is advisable to consult a doctor and have the causes clarified . Stomach pain that manifests itself as pain or pressure pain in a specific area or is associated with a general feeling of illness requires a medical evaluation. Remember that certain stimulants such as coffee, alcohol, nicotine, as well as certain medications such as painkillers and rheumatism drugs can cause stomach problems. When should Sidroga verbena tea not be used or only with caution? Sidroga verbena tea should not be used if there is a known hypersensitivity to verbena, especially its essential oil. The use of this medicine is not recommended in children under 6 years of age. Tell your doctor, pharmacist or druggist if you suffer from other diseaseshave allergies ortake other medicines (including those you bought yourself!). Can Sidroga verbena tea be taken during pregnancy or while breastfeeding? Based on previous experience, there is no known risk for the child when 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 Sidroga Verbena Tea? Adults and school children from the age of 6 take 1 cup up to 5 times a day during or as needed after meals; to promote sleep, 1 to 2 cups should be taken half an hour before bedtime. Preparation: Pour boiling water over one tea bag per cup and let the bag steep in it for 5 to 10 minutes. Then take out the tea bag and squeeze it out lightly over the cup. Only use one tea bag per cup of tea and only sweeten your tea after removing the tea bag from the cup. You can use both natural and artificial sugar for sweetening. The use and safety of Sidroga Verveine Tea in children under the age of 6 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 Sidroga Verbena Tea have? No side effects have been observed for Sidroga Verbena Tea when used as intended. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. What else needs to be considered? Sidroga Verveine Tea should be kept at room temperature (15-25°C) and out of the reach of children. The double-chamber bags in aroma protection packaging may only be used up to the end marked on the container with «Exp.» designated date are used. Your doctor, pharmacist or druggist can provide you with further information. What does Sidroga Verbena tea contain? 1 double chamber bag contains 1.0 g of dried and finely chopped lemon bush leaves (verbena). Approval number 41687 (Swissmedic). Where can you get Sidroga Verbena Tea? What packs are available? In pharmacies and drugstores, without a doctor's prescription. Boxes of 20 double chamber bags in aroma protection packaging. Authorization holder Sidroga AG, 4310 Rheinfelden. This leaflet was last checked by the drug authority (Swissmedic) in April 2010. ..
10.42 USD
Venucreme cream tb 100 g
Venucreme and Venugel 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. Venucreme and Venugel are suitable for external use with 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). Venucreme/Venugel can also be used to treat superficial phlebitis if prescribed by a doctor. Venucreme and Venugel have a cooling effect and are greasy not. Swissmedic-approved patient informationVenucreme®/Venugel®Permamed AGWhat is Venucreme/Venugel and when will it be applied? Venucreme and Venugel 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. Venucreme and Venugel are suitable for external use with 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).Venucreme/Venugel can also be used to treat superficial phlebitis if prescribed by a doctor.Venucreme and Venugel have a cooling effect and are greasy not. 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 should Venucreme/Venugel not be used?Venucreme and Venugel 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 under five years are not applicable. When is caution required when using Venucreme/Venugel?In children and patients with kidney disease, Venucreme and Venugel should only be applied to small areas of skin and not longer than be used for 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 Venucreme and Venugel. Body parts treated with Venucreme and Venugel should not be covered with airtight bandages. In the case of venous disorders that can be traced back to the presence of a blood clot (so-called thrombosis), not the massage. If symptoms worsen, see a doctor. This medicine contains coumarin as a fragrance and may cause allergic reactions. Venucreme contains 70 mg/g propylene glycol as an excipient which may cause skin irritation. 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 Venucreme/Venugel be taken/used during pregnancy or while breastfeeding?Venucreme and Venugel must not be used during pregnancy or while breastfeeding, unless unless expressly prescribed by a doctor. How do you use Venucreme/Venugel?AdultsUnless otherwise prescribed by the doctor, Apply Venucreme or Venugel to the affected areas several times a day and distribute. Do not apply Venucreme and Venugel to open wounds or damaged skin. If bandages are necessary for therapeutic reasons, they should be permeable to air and applied at the earliest 5 minutes after applying Venucreme/Venugel. Vein patients who wear compression stockings or bandages during the day should only use Venucreme and Venugel in the evening. The use and safety of Venucreme/Venugel 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 Venucreme/Venugel have?The following side effects can occur when using Venucreme and Venugel: 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 Venucreme/Venugel and generally disappear during further treatment. The use of Venucreme and Venugel can cause a temporary 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 Venucreme/Venugel 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 Venucreme/Venugel contain?Active ingredients1 g Venucreme 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 Venugel 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) and 10 mg dexpanthenol Auxiliary substances1 g Venucreme contains as auxiliary substances: glycerol monostearate, macrogol 100 stearate, macrogol 2 stearate, dexpanthenol, dimethicone, Carbomer 974P, Levomenthol, Rosemary Oil, Coumarin (2mg), Lavandin Oil, Polyquaternium 11, Pentadecalactone, Sodium Hydroxide, Purified Water. 1 g Venugel contains as excipients: carbomer 980, ethanol 96%, propylene glycol (E 1520), glycerin 85%, isopropanol, levomenthol, rosemary oil, coumarin (2 mg), lavandin oil, pentadecalactone, Sodium Hydroxide, Purified Water. Approval number54254, 54255 (Swissmedic). Where can you get Venucreme/Venugel? What packs are available?In pharmacies and drugstores without a doctor's prescription. Packs of 50g and 100g. Authorization holderPermamed AG, DornachThis leaflet was last checked by the Medicines Agency (Swissmedic) in October 2020. ..
56.29 USD
Vertigoheel tabl ds 250 pcs
Vertigoheel TablSwissmedic-approved patient informationVertigoheel, homeopathic tabletsebi-pharm agHomeopathic medicinal productAMZVWhen is Vertigoheel, tablets used?According to homeopathic medicinal products, Vertigoheel, tablets can be used for dizziness of various causes (especially arteriosclerotic) and motion sickness. What should be considered?If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether Vertigoheel, tablets at the same time may be taken. Medical advice should be obtained in the event of recurring symptoms.When should Vertigoheel tablets not be taken or should only be taken with caution?To date, no application restrictions are known. When used as intended, no special precautionary measures are necessary. Tell your doctor 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 Vertigoheel , tablets are taken/used during pregnancy or while breastfeeding? Based on previous experience, there is no known risk for the child when 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 or pharmacist for advice.How do you use Vertigoheel, tablets? Unless otherwise prescribed by the doctor, let 1 tablet dissolve under the tongue 3 times a day. In the case of acute symptoms, initially 1 tablet every 15 minutes (up to a maximum of 3 tablets). Follow the dosage that is on the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor or pharmacist.What side effects can Vertigoheel, tablets have?For Vertigoheel, tablets, no side effects have been observed when used as directed. If you do notice any side effects, tell your doctor or pharmacist. When taking homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, stop taking Vertigoheel tablets and tell your doctor or pharmacist.What else should you watch out for? The medicinal product may only be used up to the date marked “Use by” on the container. Store drug out of reach of children. Store at room temperature (15-25°C). Your doctor or pharmacist can provide you with further information.What does Vertigoheel, tablets contain?1 tablet contains: Ambergris grisea D6 30 mg, Anamirta cocculus D4 210 mg, Conium maculatum D3 30 mg, Petroleum D8 30 mg. This preparation also contains auxiliary substances.Approval number41460 (Swissmedic)Where can you get Vertigoheel , tablets? What packs are available?In pharmacies without a doctor's prescription. Packs of 50 and 250 tablets.Authorization holderebi-pharm ag, Lindachstr. 8c, 3038 KirchlindachThis leaflet was last checked by the drug authority (Swissmedic) in July 2010...
97.33 USD
Wala pulmonium cough syrup bottle 90 ml
Swissmedic-approved patient information Wala Pulmonium cough syrup WALA Schweiz AG Medicines based on anthroposophic knowledge When should WALA Pulmonium Hustensaft be used? According to anthroposophical knowledge of man and nature, WALA Pulmonium Hustensaft can be used for diseases of the respiratory tract and to promote expectoration in coughs and bronchial coughs . What should be considered? If the cough lasts longer than seven days, a doctor or pharmacist must be consulted. If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether WALA Pulmonium Hustensaft can be taken at the same time. Note: 1 tablespoon (15 ml) of syrup contains 7.1 g of sucrose (sugar). 1 teaspoon (5 ml) of syrup contains 2.4 g of sucrose (sugar). When should Wala Pulmonium Hustensaft not be taken or only with caution? WALA Pulmonium Hustensaft may only be used on children under two years of age if prescribed by a doctor. Tell your doctor, pharmacist or druggist if you −suffer from other diseases, −have allergies or −Take other medicines (including those you bought yourself!) or use them externally! Can WALA Pulmonium Hustensaft be taken during pregnancy or breastfeeding? Based on previous experience, there is no known risk to 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 WALA Pulmonium Hustensaft? Unless otherwise prescribed by the doctor, adults and children over 6 years 1 tablespoon 3 times a day, in acute In cases, take 1 teaspoon of syrup in warm water every 2 hours. Toddlers take 1 teaspoon of syrup in warm water 3-4 times a day. Shake before use! Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can WALA Pulmonium Hustensaft have? The following side effects can occur when taking WALA Pulmonium Hustensaft: In rare cases, allergic reactions such as itching, skin rash, hives (urticaria ), skin/mucous membrane swelling (oedema), in very rare cases also skin reddening, blistering, cracked lips, itchy eyes and fever. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered? The medicinal product may only be used up to the date marked "EXP" on the container. Do not store above 30 °C and out of reach of children. After opening, it can be kept for 12 weeks in a refrigerator (2 – 8 °C). Your doctor, pharmacist or druggist can provide you with further information. What does WALA Pulmonium cough syrup contain? 10 ml of syrup contains: 0.12 g fermented butterbur roots (Petasites hybridus e radice ferm 33c) D3 (HAB), 1.77 g aqueous Extract with sugar from 0.07 g spruce tips (Picea abies, Summitates), 4.13 g aqueous extract with sugar from 0.83 g buckhorn leaf (Plantago lanceolata, Folium rec.). Excipients: purified water, sugar. Approval number 39460 (Swissmedic) Where can you get WALA Pulmonium cough syrup? What packs are available? In pharmacies and drugstores, without a doctor's prescription. WALA Pulmonium cough syrup is available in 90 ml bottles. Approval holder WALA Schweiz AG, 3011 Bern Manufacturer WALA Heilmittel GmbH, D-73085 Bad Boll/Eckwälden This leaflet was last checked by the drug authority (Swissmedic) in June 2012. Swissmedic-approved patient information Wala Pulmonium cough syrup WALA Schweiz AG Medicines based on anthroposophic knowledgeWhen should WALA Pulmonium Hustensaft be used?According to anthroposophical knowledge of man and nature, WALA Pulmonium Hustensaft can be used for diseases of the respiratory tract and to promote expectoration in coughs and bronchial coughs . What should be considered?If the cough lasts longer than seven days, a doctor or pharmacist must be consulted. If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether WALA Pulmonium Hustensaft can be taken at the same time. Note: 1 tablespoon (15 ml) of syrup contains 7.1 g of sucrose (sugar). 1 teaspoon (5 ml) of syrup contains 2.4 g of sucrose (sugar). When should Wala Pulmonium Hustensaft not be taken or only with caution?WALA Pulmonium Hustensaft may only be used on children under two years of age if prescribed by a doctor. Tell your doctor, pharmacist or druggist if you −suffer from other diseases, −have allergies or −Take other medicines (including those you bought yourself!) or use them externally! Can WALA Pulmonium Hustensaft be taken during pregnancy or while 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 WALA Pulmonium Hustensaft?Unless otherwise prescribed by the doctor, adults and children over 6 years of age 1 tablespoon 3 times a day, in acute In cases, take 1 teaspoon of syrup in warm water every 2 hours. Toddlers take 1 teaspoon of syrup in warm water 3-4 times a day. Shake before use! Follow the dosage given in the package leaflet or as prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. What side effects can WALA Pulmonium Hustensaft have?The following side effects can occur when taking WALA Pulmonium Hustensaft: In rare cases, allergic reactions such as itching, skin rash, hives (urticaria ), skin/mucous membrane swelling (oedema), in very rare cases also skin reddening, blistering, cracked lips, itchy eyes and fever. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Do not store above 30 °C and out of reach of children. After opening, it can be kept for 12 weeks in a refrigerator (2 – 8 °C). Your doctor, pharmacist or druggist can provide you with further information. What does WALA Pulmonium cough syrup contain?10 ml syrup contains: 0.12 g fermented butterbur roots (Petasites hybridus e radice ferm 33c) D3 (HAB), 1.77 g aqueous Extract with sugar from 0.07 g spruce tips (Picea abies, Summitates), 4.13 g aqueous extract with sugar from 0.83 g buckhorn leaf (Plantago lanceolata, Folium rec.). Excipients: purified water, sugar. Approval number39460 (Swissmedic) Where can you get WALA Pulmonium cough syrup? What packs are available?In pharmacies and drugstores, without a doctor's prescription. WALA Pulmonium cough syrup is available in 90 ml bottles. Authorization holderWALA Schweiz AG, 3011 BernManufacturerWALA Heilmittel GmbH, D-73085 Bad Boll/Eckwälden This leaflet was last checked by the drug authority (Swissmedic) in June 2012. ..
37.16 USD
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