Constipation relief
(1 Pages)
Agiolax with senna gran (d) ds 150 g
Agiolax with senna is a herbal laxative based on psyllium and senna for short-term use in occasional constipation. The components psyllium and psyllium husk (Plantago ovata) increase the volume of the stool in the intestine. These ingredients in the granules swell to a multiple of their volume when they absorb water. This stimulates intestinal activity and creates a smooth, soft intestinal contents. The senna contained in the granulate has a laxative effect. Swissmedic-approved patient informationAgiolax® with senna, granules 150 gMEDA Pharma GmbHHerbal medicinal product What is Agiolax with Senna and when is it used?Agiolax with Senna is a herbal laxative based on psyllium and senna, for short-term use in occasional constipation. The components psyllium and psyllium husk (Plantago ovata) increase the volume of the stool in the intestine. These ingredients in the granules swell to a multiple of their volume when they absorb water. This stimulates intestinal activity and creates a smooth, soft intestinal contents. The senna contained in the granulate has a laxative effect. What should be considered?Make sure you drink enough fluids! Delayed absorption may occur when other drugs are administered at the same time. Therefore, before using Agiolax with Senna, a gap of half an hour to one hour should be observed after taking other medicines. If you suffer from constipation, you should eat fiber-rich food (vegetables, fruit, wholemeal bread),take plenty of fluids regularly andensure physical activity (sport)!In the case of chronic constipation, it is advisable to see a doctor who may be able to treat the cause. When should Agiolax with Senna not be taken or only with caution? Agiolax with senna must not be taken in the case of all diseases of the gastrointestinal tract, especially pathological constrictions in the oesophagus, gastrointestinal tract, large diaphragmatic hernia, acute inflammatory diseases of the intestine (e.g. Crohn's disease, Ulcerative colitis, appendicitis), abdominal pain of unknown cause, nausea, vomiting, constipation, difficulty swallowing (risk of shortness of breath), severe dehydration with loss of fluids and salts/minerals and in the case of difficult-to-control diabetes (diabetes mellitus), pregnancy or breastfeeding and hypersensitivity to one of the active ingredients or excipients (see «What does Agiolax with Senna contain?»). Children under the age of 12 should not take Agiolax with Senna. Agiolax with Senna should not be taken if you are suffering from acute or persistent gastrointestinal symptoms, nausea or vomiting, as these symptoms may indicate a possible intestinal obstruction. For this reason, Agiolax with Senna should only be taken under medical supervision at the same time as medication that inhibits intestinal activity (e.g. opioid-type painkillers) (risk of intestinal obstruction). Laxatives should only be taken occasionally and for no longer than a week because of possible habituation. Long-term treatments should be under medical supervision. With chronic use/abuse or use in excess of recommended doses, diarrhea with dehydration and salt/mineral imbalance (especially potassium depletion) may occur. Particular care is therefore required in patients who are simultaneously taking certain water-repellent medicines (diuretics), medicines or foods containing liquorice root (e.g. liquorice), medicines containing cortisol, certain anti-allergic medicines, medicines for heart muscle weakness (cardiac glycosides such as digoxin) and certain medicines for heart rhythm disorders (antiarrhythmics) or are taking thyroid hormone preparations (levothyroxine). Caution is also advised if you suffer from kidney disease. In these cases, consult your doctor before taking Agiolax with Senna. Please only take Agiolax with Senna after consulting your doctor if you know that you suffer from a sugar intolerance. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!). Can Agiolax with Senna be taken during pregnancy or while breastfeeding?Agiolax with Senna must not be used during pregnancy or while breastfeeding. How do you use Agiolax with Senna?Swallow Agiolax with Senna whole with at least ¼ l of liquid (water, tea, milk, fruit juice) and then drink plenty of liquid again . The granules can also be taken mixed with yoghurt. In addition, plenty of fluids should be drunk. Adults and adolescents over 12 years: Take 1-2 measuring spoons of Agiolax with Senna in the evening after a meal or in the morning before breakfast; maximum 2 scoops (10 g) / day. The individually correct dosage is the lowest required to obtain a soft-formed stool. Agiolax with Senna should not be taken immediately before bedtime and in an upright position. If the symptoms decrease, the intake can be reduced to every 2nd or 3rd day. Use no longer than 1 week. The use and safety of Agiolax with Senna in children under 12 years of age has not 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 Agiolax with Senna have?The following side effects can occur when taking or using Agiolax with Senna: When taking Agiolax with Senna, gas may occur and there is a risk of blockage of the esophagus or intestines, especially if not drinking enough fluids. Hypersensitivity reactions (reddening of the skin, itching, eczema) may occur after ingestion or contact with the skin. The frequency is not known. In this case, a doctor must be consulted immediately. Abdominal pain, abdominal cramps and diarrhea can also occur, especially in patients with irritable bowel syndrome. These symptoms can also be the result of an individual overdose. In such cases, a reduction in dosage is necessary. Nausea and vomiting may occur. The frequency is not known. Very rarely (affects less than 1 user in 10,000) anaphylactic reactions may occur. An overdose leads to increased side effects, it can lead to heart problems and muscle weakness, in the long term the liver can be damaged. Furthermore, the intestinal mucosa and the urine can turn yellow-reddish-brown, which usually disappears after the drug is stopped. 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. Use by after openingShelf life 6 months after opening. Storage InstructionsStore at room temperature (15-25 °C). Keep out of 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 Agiolax with Senna contain?5 g granules (= 1 measuring spoon) contain: Active ingredientsIndian psyllium (Plantago ovata Forssk., semen) 2.6 g, Indian psyllium husks (Plantago ovata em> Forssk., semenis tegumentum) 0.11 g, senna fruits (Senna alexandrina Mill., fructus) 0.34-0.66 g, corresponding to 15 mg sennosides (calculated as sennoside B). ExcipientsThis medicine also contains: Sucrose, Talc, Gum Arabic, Black Iron Oxide (E172), Yellow Iron Oxide (E172), Red Iron Oxide (E172), Titanium Dioxide (E171), Liquid Paraffin, Hard Paraffin, Sage Oil, Peppermint Oil, Caraway Oil. 1 scoop contains 0.9 to 1.2 g of sucrose. Approval number26821 (Swissmedic) Where can you get Agiolax with Senna? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 150 g granules. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen. This leaflet was last checked by the medicines authority (Swissmedic) in October 2022. [Version 203 D] ..
35.52 USD
Aptamil confort 2 eazypack 800 g
Description: The Aptamil Confort 2 EaZypack 800 g is a specially formulated infant milk suitable for babies aged 6-12 months who have developed colic, constipation, or other digestive discomforts. This product is designed with a unique blend of ingredients that can help soothe and relieve digestive issues within 24 hours. Features: Easy to digest formula that is gentle on babies' tummies Contains partially hydrolysed protein that reduces the amount of lactose in the milk Enriched with prebiotics that promote the growth of beneficial bacteria in the gut Has a blend of essential vitamins and minerals that support the overall development of your baby EaZypack packaging makes it convenient to use and store Benefits: Can relieve colic, constipation, and other digestive discomforts within 24 hours Suitable for babies who have difficulty digesting regular milk Can help prevent future digestive issues Supports your baby's growth and development EaZypack makes it easy to take on-the-go Directions for use: Wash your hands before preparing the milk. Use the feeding guide on the pack to measure out the required amount of formula. Add the formula to previously boiled and cooled water (40°C). Close the bottle and shake well until the powder is fully dissolved. Test the temperature before giving it to your baby. Use within two hours of preparation. Ingredients: Skimmed milk, lactose (from milk), vegetable oils, partially hydrolysed whey protein concentrate (from milk), lactulose, emulsifier (citric acid ester of mono- and diglycerides), potassium dihydrogen phosphate, fish oil, calcium chloride, sodium chloride, choline chloride, vitamin C, taurine, ferrous sulphate, inositol, zinc sulphate, vitamin E, L-carnitine, niacin, pantothenic acid, folic acid, copper sulphate, vitamin A, biotin, vitamin B1, vitamin B12, vitamin D3, vitamin B6, manganese sulphate, potassium iodide, vitamin K1, sodium selenite. ..
60.70 USD
Bekunis dragées 5 mg bisacodyl ds 30 pcs
What are Bekunis Dragées Bisacodyl and when are they used? Bekunis Dragées Bisacodyl is a laxative that acts on the colon. It triggers the stool-promoting movement of the large intestine. Bekunis Dragées Bisacodyl can also be administered when pressure has to be avoided, e.g. in the case of haemorrhoids and anal cracks. Bekunis Dragées Bisacodyl are used in the short term for constipation, constipation due to bed rest, unfamiliar food or when travelling. Before X-rays in the gastrointestinal area and before operations, Bekunis Dragées Bisacodyl help to empty the bowel.What should be considered? Medical advice is required for children and patients with serious illnesses. In the case of chronic constipation, its origin must be determined by the doctor. Long-term treatment must be under medical supervision.General informationIf you are constipated, you should, if possible, eat fiber-rich food (vegetables, fruit, wholemeal bread) and drink plenty of fluids regularly and pay attention to physical activity (sport).When should Bekunis Dragées Bisacodyl not be used? Bekunis Dragées Bisacodyl must not be used if there is a known hypersensitivity to the active ingredient or one of the ingredients (galactose and fructose intolerance: see "When should caution be exercised when taking/using Bekunis Dragées Bisacodyl"), in the case of intestinal constriction, intestinal obstruction (ileus), acute diseases in the abdominal cavity such as acute appendicitis and acute intestinal inflammation as well as severe abdominal pain in combination with nausea and vomiting, which indicate a serious illness interpret. Bekunis Dragées Bisacodyl must not be used in the case of severe fluid and potassium deficiency.When is caution required when taking Bekunis Dragées Bisacodyl? Bekunis Dragées Bisacodyl should only be given to children under the age of 12 if recommended by a doctor. As with all laxatives, continuous daily use over a period of more than 1-2 weeks is not indicated for Bekunis Dragées Bisacodyl. If laxatives are used daily, the cause of the constipation should be investigated. Long-term treatments belong under medical supervision. With long-term or high-dose use, water and mineral losses (potassium) can occur and lead to disorders of the heart muscle function and muscle weakness as well as an increase in constipation. Patients who take diuretic drugs, oral corticosteroids or digitalis preparations should only take Bekunis Dragées Bisacodyl after consulting their doctor. In very rare cases, patients who have taken Bekunis Dragées Bisacodyl have experienced dizziness or short-term unconsciousness (syncope). According to the corresponding case reports, this is probably due to syncope, which is either due to the purging process itself, to straining or to vascular reactions mediated via the nervous system due to abdominal pain caused by constipation, but not necessarily to the use of Bekunis Dragées Bisacodyl itself. One Bekunis Dragée Bisacodyl contains 226 mg lactose and 88.34 mg sucrose. When treating constipation in adults and children over 12 years of age, this equates to up to 452 mg lactose and 176.68 mg sucrose daily. Patients with a rare hereditary galactose intolerance, e.g. galactosemia or a rare hereditary fructose intolerance should not take the dragées. Inform your doctor, pharmacist or druggist if you suffer from other diseases, have allergies or otherTake other medicines (including those you bought yourself!) or use them externally!Can Bekunis Dragées Bisacodyl be taken during pregnancy or while breastfeeding? As a precaution, you should avoid taking medicines during pregnancy and breastfeeding. Only your doctor can decide whether Bekunis Dragées Bisacodyl can be used during pregnancy or breastfeeding.How do you use Bekunis Dragées Bisacodyl? Unless otherwise prescribed by the doctor: Adults and children over 12 years of age: average single dose: 1 - 2 tablets. Children from 4 - 12 years of age: as prescribed by the doctor. The dragées should be taken in the evening before going to bed so that the bowel movements can take place the next morning. If taken in the evening, after about 10 hours, i.e. without disturbing the night’s sleep, there will be one or two emptyings the next morning. Bekunis Dragées Bisacodyl are swallowed whole with sufficient liquid (no milk). Milk and medicines against gastric hyperacidity should not be taken at the same time as Bekunis Dragées Bisacodyl, otherwise the dragées will dissolve more quickly than desired. If you need an antacid (medicine against acidification of the stomach), take it half an hour after Bekunis Dragées Bisacodyl. Observe the dose 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 Bekunis Dragées Bisacodyl have? After taking Bekunis Dragées Bisacodyl, you may experience unpleasant sensations such as flatulence and abdominal pain (possibly with nausea and/or vomiting) or diarrhea and inflammation of the colon. Hypersensitivity reactions have also been reported, which in very rare cases can lead to allergic skin reactions and shock (angioneurotic edema, anaphylactic reactions). The occurrence of diarrhea is a sign that the dosage is too high and is only desirable before an X-ray or before an operation.If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What else should you watch out for? The medicinal product may only be used up to the end of the period marked "Exp." on the container. designated date. Store 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 technical information.What does Bekunis Dragées Bisacodyl contain? 1 enteric-coated dragee contains the active substance: 5 mg bisacodyl and excipients. Approval number 55278 (Swissmedic) Where can you get Bekunis Dragées Bisacodyl? What packs are available? In pharmacies and drugstores without a doctor's prescription: Packs of 30 dragees Authorization holder Tentan AG, CH-4452 Itingen Manufacturer roha Arzneimittel GmbH, D-28333 Bremen This package leaflet was last published in March 2022 by the drug authority (p wissmedic).PI038040/05.22..
31.24 USD
Laxipeg plv flavor-free can 200 g
What is Laxipeg/- aromafrei and when is it used? Laxipeg/- aromafrei is an osmotically active laxative made from macrogol, which enables stool regulation in the event of constipation. Macrogol is an indigestible substance that binds water. This stimulates intestinal activity, making the stool softer and more slippery. This makes bowel movements easier.Laxipeg/- aromafrei is used in adults and children to regulate bowel movements in the case of sluggish bowels and constipation of various origins (constipation).What should be considered? Laxipeg/- flavor free contains neither sugar nor polyols and can therefore also be taken by diabetics or patients who follow a galactose-free diet. If you suffer from constipation, you should You eat fiber-rich food (vegetables, fruit, wholemeal bread) and drink plenty of fluids regularly and pay attention to physical activity (sport).When should Laxipeg/- aromafrei not be taken? Laxipeg/- aromafrei should not be taken if you are known to be hypersensitive to one of the ingredients, if you have severe inflammatory bowel and colon diseases (e.g. ulcerative colitis, Crohn's disease), a disruption in the intestinal passage as a result of intestinal paralysis or an intestinal obstruction (ileus), an intestinal perforation (perforation), or the risk of intestinal perforation, with abdominal pain of undetermined origin.When should caution be taken when taking Laxipeg/- aromafrei?In children over the age of 6 Months to 2 years and with a body weight of at least 6 kg, the drug may only be used after consultation with the doctor. Laxipeg/- aromafrei should not be used on younger or lighter children. If the symptoms of constipation persist after 2 weeks, you should see your doctor. Elderly patients, patients with impaired liver or kidney function, and patients taking diuretics should contact a doctor if diarrhea occurs to consider checking electrolytes.If you need to thicken fluids to To be able to swallow them safely, Laxipeg/- aromafrei can counteract the effect of the thickening agent.Tell your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally.Can Laxipeg/- aromafrei 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 or ask your doctor, pharmacist or druggist for advice.The active ingredient is not absorbed by the digestive tract and therefore does not enter the bloodstream or via breast milk.Laxipeg/- aromafrei can be taken while breastfeeding.How do you use Laxipeg/- aromafrei?General informationChildren should not take Laxipeg/- aromafrei for longer than 3 months.The dose can be adjusted depending on the effect achieved.The daily dose can be taken in one dose or in two Doses should be taken on an empty stomach.The entire amount should be drunk quickly (within a few minutes) and not in small sips over a long period of time.A fluid-rich diet favors the effect of the drug. Unless otherwise prescribed by the doctor: Bags: Adults and children over 8 years of age and weighing more than 20 kg 1-2 sachets daily. Do not exceed the maximum dose of 20 g powder per day. The indicated dose must be adjusted to individual response. Put the contents of one sachet into at least 1 Dissolve 25 mL (1 glass) of water. You can also choose another drink with Laxipeg aromafrei.Do not add any other ingredients.Can:Adults and children over 8 years and weighing more than 20 kg4-8 full measuring spoons a day (one level measuring spoon contains 2.5 g powder).Do not exceed the maximum daily dose of 20 g powder.Children under 8 years of age or with a weight under 20 kg The usual starting dose is 0.7 g/kg per day. In children aged 6 months to 2 years and with a body weight of at least 6 kg, the drug may only be used after consulting a doctor. Laxipeg/- aromafrei should not be used on younger or lighter children.Table for calculating the Laxipeg/- aromafrei dose for children up to 20 kg:Body weight (kg)Daily doseNumber of measuring spoons 10 g 4>16-2012.5 g5The specified dose must be adjusted to individual response. It may be recommended to increase or decrease the dose indicated in the table by 1 measuring spoon.The content of the measuring spoon (2.5 g) is dissolved in at least half a glass of water (approx. 60 ml). Another drink can also be chosen for Laxipeg unflavoured. Do not add any other ingredients. Observe the dosage given in the package insert or prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Laxipeg/- aromafrei have?The following side effects can occur when taking Laxipeg/- aromafrei: diarrhoea, abdominal pain, flatulence, nausea and/or vomiting. There have been isolated reports of hypersensitivity reactions, which very rarely can lead to allergic skin reactions and shock (angioneurotic oedema).The occurrence of diarrhea and the urge to defecate and faecal incontinence that usually follows are signs of too high a dosage. These side effects usually subside when the dose is reduced or treatment is temporarily stopped. Diarrhea can cause soreness in the anus.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 information leaflet.What else should be observed?Shelf lifeThe medicinal product may only be used up to the date marked «EXP» on the containerbe used.Use-by period after openingThe drug in the jar can be used for 90 days after opening.Storage instructionsIn the Keep the original packaging at room temperature (15–25 °C) and out of the reach of children.Further informationYour doctor, pharmacist or druggist can provide you with further information druggist. These people have the detailed specialist information.What does Laxipeg/- aromafrei contain?Active ingredientsLaxipeg:1 sachet with powder for oral use as a solution contains 9.736 g Macrogolum 4000.1 can with powder for oral use as a solution contains 194.72 g Macrogolum 4000.Laxipeg flavor-free:1 sachet of oral powder as a solution contains 10.00 g Macrogolum 4000.1 jar of oral powder as a solution contains 200.00 g Macrogolum 4000.ExcipientsLaxipeg:1 sachet of oral powder solution contains sweetener: acesulfamum potassium (E950), Aromatica: banana aroma.1 jar of oral powder as a solution contains sweetener: acesulfamum potassium (E950), Aromatica: banana aroma.Laxipeg unflavoured:1 sachet of powder for oral use as a solution contains no excipients.1 can of powder for oral use as a solution contains no excipients.Authorization number62765 (Swissmedic).Where can you get Laxipeg/- aromafrei? What packs are available? In pharmacies and drugstores, without a doctor's prescription. The following packs are available: Laxipeg: 20 and 100 sachets of powder for oral solution of 10 g.1 can of powder for oral solution of 200 g and a measuring spoon.Laxipeg unflavoured: 20 and 100 sachets of oral powder solution of 10 g.1 jar of oral powder solution of 200 g and a measuring spoon.Marketing Authorization HolderZambon Schweiz AG, 6814 CadempinoThis leaflet was last checked by the drug authority (Swissmedic) in August 2021...
28.40 USD
Laxiplant soft gran ds 400 g
Laxiplant soft consists of the seed shells of Indian psyllium and is used for gentle stool regulation and facilitation of defecation for hemorrhoids for anal disorders such as painful tears in the anal mucosa for constipation when bedridden after operations during pregnancy or breastfeeding The intestinal activity is influenced with Laxiplant soft as follows: seed shells of psyllium swell with water until they are 40 years old -fold in volume, causing the colon to fill and stretch. Plant slime also forms a natural lubricant. Swissmedic-approved patient informationLaxiplant® softSchwabe Pharma AGHerbal medicinal product What is Laxiplant soft and when is it used?Laxiplant soft consists of the seed shells of Indian psyllium and is used for gentle stool regulation and facilitation of defecationfor hemorrhoidsfor anal disorders such as painful tears in the anal mucosafor constipation when bedriddenafter operationsduring pregnancy or breastfeedingLaxiplant soft influences the intestinal activity as follows: seed shells of psyllium swell with water until they are 40 years old -fold in volume, causing the colon to fill and stretch. Plant slime also forms a natural lubricant. What should be considered?If you suffer from constipation, you should food rich in fiber (vegetables, fruit, wholemeal bread) andtake plenty of fluids regularly andmake sure you are physically active (sport)!5 g Laxiplant soft (= 1 teaspoon) contains 1.5 g sugar (sucrose) corresponds to 26.2 kJ (6.2 kcal). When should Laxiplant soft not be taken or should it only be taken with caution?Laxiplant soft should not be used if there is an imminent or complete obstruction of the bowel or if there is a problem with the esophagus. Tell your doctor, pharmacist or druggist if you suffer from other diseaseshave allergies oruse other medicines (including those you bought yourself!)!..
54.68 USD
Metamucil n mite plv 5.8 g orange 30 bags 5.8 g
Metamucil N Mite is a herbal stool regulator made from Plantaginis ovatae seed coats. Metamucil N Mite swells when it absorbs water and thus increases the volume of the stool in the intestine. This stimulates the intestinal activity in a natural way. In addition, Metamucil N Mite gives the intestinal contents a soft and supple texture. This also promotes and facilitates elimination. Metamucil N Mite is suitable for regulating stool in the event of constipation, with a tendency to constipation, to facilitate bowel movements in the case of haemorrhoids and after surgical interventions, during pregnancy and childbirth, when confined to bed and during convalescence. If Metamucil N Mite is taken half an hour before meals, the appetite will be reduced. Swissmedic-approved patient informationMetamucil® N Mite OrangeProcter & Gamble International Operations SAHerbal medicinal product What is Metamucil N Mite and when is it used?Metamucil N Mite is a herbal stool regulator made from Plantaginis ovatae seed coats. Metamucil N Mite swells when it absorbs water and thus increases the volume of the stool in the intestine. This stimulates the intestinal activity in a natural way. In addition, Metamucil N Mite gives the intestinal contents a soft and supple texture. This also promotes and facilitates elimination. Metamucil N Mite is suitable for regulating stool in the event of constipation, with a tendency to constipation, to facilitate bowel movements in the case of haemorrhoids and after surgical interventions, during pregnancy and childbirth, when confined to bed and during convalescence. If Metamucil N Mite is taken half an hour before meals, the appetite will be reduced. What should be considered?If you suffer from constipation, you should eat fiber-rich food (vegetables, fruit, wholemeal bread) and drink plenty of fluids regularly physical activity (sport). When should Metamucil N Mite not be used or only with caution?Metamucil N Mite should not be used if you are hypersensitive to psyllium husk or psyllium husk powder or to other ingredients (see also «What is in Metamucil N Mite?» and «How do you use Metamucil N Mite?»). Metamucil N Mite should not be used by children under 6 years of age. Metamucil N Mite must not be taken if you have a diaphragmatic hernia (hiatus hernia), narrowing of the esophagus, changed bowel habits that last longer than 2 weeks, intestinal obstruction (ileus), intestinal narrowing (stenosis), intestinal paralysis (paralysis), excessive hardening of the stool (faecal stones) and abdominal pain unknown cause. Metamucil N Mite must not be taken in the event of unexplained bleeding from the intestines or if no laxative effect has repeatedly occurred after ingestion. In the case of chronic constipation, it is advisable to see a doctor. If the powder is inhaled repeatedly, Metamucil N Mite can, in rare cases, cause allergic reactions, including those of the respiratory tract, in people who are sensitive to it. Medical or nursing staff who have been preparing products containing psyllium husk powder for patients to ingest over a long period of time may have become and may become sensitized to these products due to prolonged inhalation of powder, particularly if they are allergic react allergic. If allergic symptoms occur (listed under «What side effects can Metamucil N Mite have?»), the product must no longer be used or prepared with immediate effect. Patients who are hypersensitive to azo dyes, acetylsalicylic acid and rheumatism and painkillers (prostaglandin synthesis inhibitors) should not use Metamucil N Mite. Metamucil N Mite should only be taken by diabetics under medical supervision because the blood sugar levels may change (see also "What does Metamucil N Mite contain?"). Patients with simultaneous thyroid hormone therapy should only take Metamucil N Mite under medical supervision. The absorption of medicines taken at the same time, e.g. digitalis preparations, preparations for blood thinning, those for seizure disorders or depression as well as minerals or vitamins can be impaired by taking them at the same time as Metamucil N Mite, which is why an interval of at least 1 hour is required when taking them. Tell your doctor, pharmacist or druggist if you: suffer from other illnesseshave allergies ortake other medicines (including those you bought yourself!) or use them externally.Can Metamucil N Mite be taken during pregnancy or while breastfeeding?If necessary, Metamucil N Mite can also be taken during pregnancy and while breastfeeding if a change in diet is not possible was successful. 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 Metamucil N Mite?Adults: 1 heaped teaspoon (approx. 5.8 g) (children from 6 years: 1⁄2 teaspoon), or 1 sachet of 5.8 g (children over 6 years: 1/2 sachet), take 1-3 times a day before or after meals and with plenty of liquid. For each dose, fill a large glass with cold water, add powder, stir and drink immediately. It is possible to use fruit juices, other table drinks or milk. Whenever possible, a second glass of liquid should be drunk. 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. When preparing the product for ingestion, it is important to avoid inhaling the powder to minimize the risk of developing an allergy to the ingredients. What side effects can Metamucil N Mite have?The following side effects can occur when taking Metamucil N Mite: Occasional bloating (flatulence) and a feeling of fullness, especially at the beginning of the treatment. The swelling can cause abdominal distension and narrowing of the esophagus or stool retention, especially if the fluid intake is too low. Other symptoms such as nausea, diarrhea and abdominal discomfort or pain have been reported in isolated cases. Psyllium husks contain allergenic substances. Allergic reactions may occur when ingesting the product, coming into contact with the skin or inhaling the powder. Allergic reactions include a runny nose, reddening of the conjunctiva, difficulty breathing (bronchospasm), skin reactions, itching, and sometimes anaphylaxis (a sudden, generalized allergic reaction that which can lead to life-threatening shock). People who routinely prepare powder formulations (e.g. as carers) have an increased risk of these reactions due to frequent contact with the powder (see also «When should Metamucil N Mite not be used or should only be used with caution?»). If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Delayed absorption can occur if other medicines are administered at the same time. Therefore, before using Metamucil N Mite, a gap of half an hour to one hour should be observed after taking other medicines. It is extremely important to drink enough fluids to bring the hardened stool mass to a normal moisture level. If you have difficulty swallowing, the preparation should only be used after consultation with your doctor. It is not advisable to take it just before bedtime. This product contains aspartame. Persons with phenylketonuria should take this into account. If your symptoms persist, talk to your doctor or pharmacist. The medicinal product may only be used up to the date marked «EXP» on the container. Store at room temperature (15-25°C) and dry; Keep out of reach of children. Your doctor, pharmacist or druggist can provide you with further information. What does Metamucil N Mite contain?1 g of Metamucil N Mite contains 0.56 g of Plantaginis ovatae seed coat powder. 1 sachet of 5.8 g Metamucil N Mite contains 3.26 g powder from Plantaginis ovatae seed coats. This preparation also contains maltodextrin, the sweetener aspartame, the coloring agent yellow orange (E 110) as well as flavorings and other additives. For diabetics: 1 heaped teaspoon of Metamucil N Mite contains 1.9 g of usable carbohydrates. 1 sachet of Metamucil N Mite contains 1.9 g of usable carbohydrates. Approval number55'112 (Swissmedic). Where can you get Metamucil N Mite? What packs are available?In pharmacies and drugstores without a doctor's prescription. Metamucil N Mite powder: 283 g doses. Metamucil N Mite, sachets (5.8 g each): 30 sachets. Authorization holderProcter & Gamble International Operations SA, Lancy. Domicile: 1213 Petit-Lancy. This leaflet was last checked by the drug authority (Swissmedic) in January 2015. ..
46.83 USD
Metamucil n mite powder orange 283 g
Herbal medicineWhat is Metamucil N Mite and when is it used?Metamucil N Mite is a herbal stool regulator made from Plantaginis ovatae seed husks. Metamucil N Mite swells when it absorbs water and thus increases the volume of stool in the intestine. This naturally stimulates intestinal activity. Metamucil N Mite also gives the intestinal contents a soft and supple texture. This also promotes and facilitates excretion. Metamucil N Mite is suitable for stool regulation in cases of constipation, in cases of a tendency to constipation, to facilitate bowel movements in cases of hemorrhoids and after surgical interventions, during pregnancy and the postpartum period, in cases of bedridden patients and during convalescence.If Metamucil N Mite is taken half an hour before meals, appetite will be reduced.What precautions should be taken?If you suffer from constipation, you should eat foods rich in fiber (vegetables, fruit, whole grain bread), drink plenty of fluids regularly, and exercise.When should Metamucil N Mite not be used or should it be used with caution?Metamucil N Mite must not be used in case of hypersensitivity to Indian psyllium husks or psyllium husk powder or to other ingredients (see also “What does Metamucil N Mite contain?” and “How do you use Metamucil N Mite?”).Metamucil N Mite must not be used by children under 6 years of age. Metamucil N Mite must not be taken in the case of a hiatal hernia, narrowing of the esophagus, changes in bowel habits lasting longer than 2 weeks, intestinal obstruction (ileus), intestinal narrowing (stenosis), intestinal paralysis (paralysis), excessive stool hardening (fecal stones) and abdominal pain of unknown cause.Metamucil N Mite must not be taken in case of unexplained bleeding from the intestines or if no laxative effect has occurred repeatedly after taking the medication.In case of chronic constipation, it is advisable to consult a doctor. If the powder is inhaled repeatedly, Metamucil N Mite can, in rare cases, cause allergic reactions, including respiratory reactions, in sensitive people.Medical staff or nursing staff who have prepared products containing psyllium husk powder for patients to take over a long period of time may have become sensitized to these products - especially if they are allergic - due to the prolonged inhalation of powder and may react allergically in the future. If allergic symptoms occur (listed under "What side effects can Metamucil N Mite have?"), the product must not be used or prepared any further with immediate effect.Patients who are hypersensitive to azo dyes, acetylsalicylic acid, rheumatism medication and painkillers (prostaglandin synthesis inhibitors) should not use Metamucil N Mite.Metamucil N Mite should only be taken by diabetics under medical supervision, as blood sugar levels may change (see also “What does Metamucil N Mite contain?”). Patients who are also receiving thyroid hormone therapy should only take Metamucil N Mite under medical supervision.The absorption of medicines taken at the same time, e.g. digitalis preparations, blood thinning preparations, those for seizure disorders or depression as well as minerals or vitamins can be impaired by simultaneous intake with Metamucil N Mite, which is why an interval of at least 1 hour between intake is required.Tell your doctor, pharmacist or druggist if you:•suffer from other diseases•Have allergies or•take other medicines (including those you bought yourself!) or apply them externally.Can Metamucil N Mite be taken during pregnancy or while breastfeeding?If necessary, Metamucil N Mite may also be taken during pregnancy and while breastfeeding if a change in diet has not been successful.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 Metamucil N Mite?Adults: 1 heaped teaspoon (approx. 5.8 g) (children over 6 years: 1/2 teaspoon), or 1 sachet of 5.8 g (children over 6 years: 1/2 sachet), 1-3 times daily before or after meals and with plenty of liquid. For each dose, fill a large glass with cold water, add the powder, stir and drink immediately. It is possible to use fruit juice, other table drinks or milk. Whenever possible, a second glass of liquid should be drunk afterward.Follow the dosage instructions provided in the package leaflet or as prescribed by your doctor.If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.When preparing the product for ingestion, it is important to avoid inhaling the powder to minimize the risk of developing an allergy to the ingredients.What side effects can Metamucil N Mite have?The following side effects may occur when taking Metamucil N Mite:Occasional flatulence and a feeling of fullness, particularly at the beginning of treatment. The swelling can cause the abdomen to swell and the esophagus to narrow or cause constipation, particularly if the fluid intake is too low.In isolated cases, the occurrence of other symptoms such as nausea, diarrhea and abdominal discomfort or pain has been reported.Psyllium husks contain allergenic substances. Allergic reactions can occur when the product is ingested, when it comes into contact with the skin or when the powder is inhaled.The allergic reaction manifests itself, for example, in a runny nose, reddening of the conjunctiva, difficulty breathing (bronchospasm), skin reactions, itching and in some cases in the form of anaphylaxis (a sudden, generalized allergic reaction that can lead to life-threatening shock). People who routinely prepare powder formulations (e.g. as caregivers) are at increased risk of these reactions due to frequent contact with the powder (see also "When should Metamucil N Mite not be used or should it only be used with caution?" ).If you notice any side effects not listed here, you should inform your doctor, pharmacist or druggist.What should also be noted?If other medicines are administered at the same time, absorption may be delayed. Therefore, an interval of half an hour to one hour should be observed before using Metamucil N Mite after taking other medicines.It is extremely important to drink enough fluids to restore the hardened stool to a normal level of moisture.If you have difficulty swallowing, the product should only be used after consulting your doctor.Taking it shortly before going to bed is not advisable.This product contains aspartame. People with phenylketonuria should take this into consideration.If your symptoms persist, talk to your doctor or pharmacist.This medicine should only be used until the date stated on the container with "EXP". Store at room temperature (15-25°C) in a dry place; keep out of the reach of children.Your doctor, pharmacist or druggist will be able to provide you with further information.What is contained in Metamucil N Mite?1 g of Metamucil N Mite contains 0.56 g of Plantaginis ovatae seed husk powder.1 sachet of 5.8 g Metamucil N Mite contains 3.26 g of Plantaginis ovatae seed husk powder.This preparation also contains maltodextrin, the sweetener aspartame, the colorant sunset yellow (E 110) as well as flavorings and other excipients.For diabetics: 1 heaped teaspoon of Metamucil N Mite contains 1.9 g of usable carbohydrates.1 sachet of Metamucil N Mite contains 1.9 g of usable carbohydrates.Registration number55'112 (Swissmedic).Where can you get Metamucil N Mite? What packs are available?In pharmacies and drugstores, without medical prescription.Metamucil N Mite, powder: 283 g cans.Metamucil N Mite, sachets (5.8 g each): 30 sachets.Marketing Authorisation HolderProcter & Gamble International Holdings S.A., Lancy.Domicile: 1213 Petit-Lancy...
64.22 USD
Metamucil regular plv ds 336g
What is Metamucil Regular Powder and when is it used?Metamucil Regular Powder is a herbal stool regulator made from Plantaginis ovatae seed coats. Metamucil Regular Powder swells when it absorbs water and thus increases the volume of the stool in the intestine. This stimulates the intestinal activity in a natural way. In addition, Metamucil Regular Powder gives the intestinal contents a soft and supple texture. This also promotes and facilitates elimination.Metamucil Regular Powder is suitable for regulating stool in the event of constipation, with a tendency to constipation, to facilitate bowel movements in the case of haemorrhoids and after surgical interventions, during pregnancy and childbirth, when confined to bed and during convalescence.If Metamucil Regular Powder is taken half an hour before meals, a reduction in appetite occurs.What precautions should be taken?If you suffer from constipation, you should eat fiber-rich food (vegetables, fruit, wholemeal bread) and drink plenty of fluids regularly and pay attention to physical activity (sport).When should Metamucil Regular Powder not be used or only with caution?Metamucil Regular Powder should not be used if you are hypersensitive to psyllium husk or psyllium husk powder or to other ingredients (see also "What does Metamucil Regular Powder contain?" and "How do you use Metamucil Regular?").Metamucil Regular Powder should not be used by children under 6 years of age. Metamucil Regular must not be taken if you have a diaphragmatic hernia (hiatus hernia), narrowing of the esophagus, changed bowel habits that last longer than 2 weeks, intestinal obstruction (ileus), intestinal narrowing (stenosis), intestinal paralysis (paralysis), excessive hardening of the stool (faecal stones) and abdominal pain of unknown origin Cause. Metamucil Regular Powder must not be taken in the event of unexplained bleeding from the intestine or if no laxative effect has repeatedly occurred after ingestion.In the case of chronic constipation, it is advisable to see a doctor.If the powder is inhaled repeatedly, Metamucil Regular Powder can, in rare cases, cause allergic reactions, including those of the respiratory tract, in people who are sensitive to it.Members of the medical staff or nursing staff who have prepared products with psyllium husk powder for patients to take over a longer period of time may have become sensitized to these products - especially if they are allergic - due to the prolonged inhalation of powder and may react allergically in the future. If allergic symptoms occur (listed under "What side effects can Metamucil Regular have ? " ), the product must not be used or prepared any further with immediate effect.Metamucil Regular Powder should only be taken by diabetics under medical supervision because the blood sugar levels may change (see also " What does Metamucil Regular contain?" ).Patients with simultaneous thyroid hormone therapy should only take Metamucil Regular under medical supervision.The absorption of medicines taken at the same time, e.g. digitalis preparations, preparations for blood thinning, those for seizure disorders or depression as well as minerals or vitamins can be impaired by taking them at the same time as Metamucil Regular, which is why an interval of at least 1 hour is required when taking them. 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 Metamucil Regular be taken during pregnancy or while breastfeeding?If necessary, Metamucil Regular Powder may also be taken during pregnancy and breastfeeding if a change in diet was unsuccessful.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 Metamucil Regular Powder ?Adults: 1 heaped teaspoon (approx. 7g) (children over 6 years: ½ teaspoon), take 1-3 times a day before or after meals and with plenty of liquid. For each dose, fill a large glass with cold water, add powder, stir and drink immediately. It is possible to use fruit juices, other table drinks or milk. Whenever possible, a second glass of liquid should be drunk.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.When preparing the product for ingestion it is important to avoid inhaling the powder to minimize the risk of developing an allergy to the ingredients.What side effects can Metamucil Regular Powder have?The following side effects can occur when taking Metamucil Regular Powder:Occasional wind (flatulence) and feeling of fullness, especially at the beginning of treatment. The swelling can cause abdominal distension and narrowing of the esophagus or stool retention, especially if the fluid intake is too low.There have been isolated reports of other symptoms such as nausea, diarrhea and abdominal discomfort or pain.Flea seed shells contain allergenic substances. Allergic reactions may occur when ingesting the product, coming into contact with the skin or inhaling the powder.Examples of allergic reactions include a runny nose, reddening of the conjunctiva, difficulty breathing (bronchospasm), skin reactions, itching, and sometimes anaphylaxis (a sudden, generalized allergic reaction that can become life-threatening). shock). People who routinely prepare powder formulations (e.g. as caregivers) have an increased risk of these reactions due to frequent contact with the powder (see also "When should Metamucil Regular not be used or should only be used with caution ?").If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What should also be noted?Delayed absorption may occur if other drugs are administered at the same time. Therefore, before using Metamucil Regular Powder , a gap of half an hour to one hour should be observed after taking other medicines.Drinking enough fluids is extremely important to bring the hardened stool mass to a normal moisture level.If there are difficulties in swallowing, the preparation should only be used after consultation with the doctor.It is not advisable to take it just before bedtime.If your symptoms persist, talk to your doctor or pharmacist.The medicinal product may only be used up to the date marked “EXP” on the container. Store at room temperature (15-25°C) and dry; Keep out of reach of children.Your doctor, pharmacist or druggist can provide you with further information.What does Metamucil Regular Powder contain?1 g of Metamucil Regular contains 0.49 g powder from Plantaginis ovatae seed coats.This preparation also contains 0.51 g sucrose.For diabetics: 1 heaped teaspoon of Metamucil Regular contains 3.6 g usable carbohydrates.Registration Number17,387 (Swissmedic).Where can you get Metamucil Regular Powder? What packs are available?In pharmacies and drugstores, without medical prescription.Metamucil Regular, powder: 336 g cansMarketing Authorization HolderProcter & Gamble International Operations, Lancy..
22.83 USD
Microlax klist 4 tb 5ml
What is Microlax and when is it used? Microlax is a product for rectal use. The active components of Microlax together lead to a softening of the stool and the bowels are gently emptied within 5 - 20 minutes.Microlax is used for short-term use in cases of hardened stool and the resulting constipation of the lower sections of the intestine, to facilitate stool movement in case of stool thickening, before and after operations and as a stool aid during pregnancy, before birth, in childbirth and while breastfeeding.When should Microlax not be used ? Microlax must not be used in case of hypersensitivity to one of the ingredients. When is caution required when using Microlax? Long-term or high-dose use can result in loss of water and minerals (potassium) and damage to the intestinal mucosa with increased intestinal sluggishness. Contains sorbic acid (E 200): Can cause localized skin irritation (e.g. contact dermatitis). .Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!See a doctor if symptoms persist or become worse and do not use Microlax for a long time clean up.Can Microlax be used 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 Microlax?Break off the tip.Adults and children over 3 years of age: In adults and children over 3 years of age, the cannula is fully inserted.Children under 3 years of age: In children under 3 years of age, the cannula is only inserted up to half of its length. Please pay attention to the marking ring on the cannula. A drop of the contents of the tube, applied to the cannula, is sufficient as a lubricant. In stubborn cases, 2 tubes may be needed. The effect usually occurs after 5-20 minutes.Stick to 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 Microlax have?The following side effects have been reported with the use of Microlax, although the frequency of the side effects is unknown: Hypersensitivity reactions (e.g. itching, reddening of the skin, swelling in the ear, hives), pain and discomfort in the Abdomen, discomfort in the area of the anus, loose stools.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 drug may only be used up to the date marked "EXP" on the package.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, Apotheker or druggist. These people have the detailed technical information. What does Microlax contain? Active substances Sodium citrate dihydrate 90 mg, sodium dodecylsulfoacetate 9 mg, sorbitol 625 mg per 1 ml solution. Excipients Sorbic acid (E 200), glycerol, purified water. Approval number29869 (Swissmedic).Where can you get Microlax? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Disposable enema with 5 ml solution: packs of 4, 12 and 50 tubes. Authorization holder Janssen-Cilag AG, Zug, ZG This package leaflet was last checked by the drug authority (Swissmedic) in August 2021 ...
18.34 USD
Microlax klist 50 tb 5ml
Microlax is a product for rectal use. The active components of Microlax together lead to a softening of the stool and the bowels are gently emptied within 5 - 20 minutes. Microlax is used for short-term use in case of hardened stool and the resulting constipation of the lower sections of the intestine, to facilitate stool movement in case of stool thickening, before and after operations and as a stool aid during pregnancy, before childbirth, during childbirth and while breastfeeding. Swissmedic-approved patient informationMicrolax®Janssen-Cilag AGWhat is Microlax and when is it used?Microlax is a product for rectal use. The active components of Microlax together lead to a softening of the stool and the bowels are gently emptied within 5 - 20 minutes. Microlax is used for short-term use in case of hardened stool and the resulting constipation of the lower sections of the intestine, to facilitate stool movement in case of stool thickening, before and after operations and as a stool aid during pregnancy, before childbirth, during childbirth and while breastfeeding. When must Microlax not be used?Microlax must not be used if you are hypersensitive to any of the ingredients. When is caution required when using Microlax?Long-term or high-dose use can result in loss of water and minerals (potassium) as well as damage to the intestinal mucosa with increased intestinal sluggishness . Contains sorbic acid (E 200): May cause localized skin irritation (e.g. contact dermatitis). Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!See a doctor if symptoms persist or worsen and do not use Microlax for long periods of time. Can Microlax be used 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 Microlax?Break off the tip. Adults and children over 3 years old: For adults and children over 3 years old, the cannula is fully inserted. Children under 3 years of age: For children under 3 years of age, the cannula is inserted only half way. Please note the marking ring on the cannula. A drop of the contents of the tube applied to the cannula is sufficient as a lubricant. In stubborn cases, 2 tubes may be needed. The effect usually occurs after 5-20 minutes. 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 Microlax have?The following side effects have been reported when using Microlax, although the frequency of the side effects is unknown: Hypersensitivity reactions (e.g. itching, reddening of the skin, swelling ear, hives), abdominal pain and discomfort, anus discomfort, loose stools. 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 reach of CHILDREN. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Microlax contain?Active ingredientsSodium citrate dihydrate 90 mg, sodium dodecylsulfoacetate 9 mg, sorbitol 625 mg per 1 ml of solution. ExcipientsSorbic acid (E 200), glycerol, purified water. Approval number29869 (Swissmedic). Where can you get Microlax? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Disposable enema with 5 ml solution: packs of 4, 12 and 50 tubes. Authorization holderJanssen-Cilag AG, Zug, ZG This package leaflet was last checked by the Medicines Agency (Swissmedic) in August 2021. ..
180.83 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
Milupa aptamil comfort 1 800g
Aptamil Confort 1 has been specially developed for babies from birth with colic and constipation.The unique formulation of this infant formula contains less lactose, the GOS/FOS dietary fiber blend of Aptamil and ? palmitate, which is a special fat structure. In addition, partially hydrolyzed protein, also called partially split protein, is included in the formula. Application Weight approx. Measuring spoon per bottleWater (ml) per bottleReady to drink (ml) per bottleBottle per day3.5 kg390100 63.9 kg41201305 4.7 kg51501705< p>5.4 kg61802004-56.2 kg210230< p>4 Note According to the WHO, breastfeeding is the best nutrition for babies, so it is recommended to breastfeed for the first 6 months. After that, continued breastfeeding, but together with a balanced diet appropriate to the baby's age. If supplementary feeding is required or the baby is no longer being breastfed, information should be obtained from care professionals (paediatrician, maternal adviser, midwife). Composition Hydrolysed whey protein (from milk), vegetable oils (palm oil, rape oil, sunflower oil, coconut oil), glucose syrup, galacto- oligosaccharides (from milk), maltodextrin, starch, maize starch, lactose (from milk), fructo-oligosaccharides, fish oil, potassium salts of orthophosphoric acid, calcium orthophosphate, calcium chloride, choline chloride, oil from Mortierella alpina, magnesium orthophosphate, potassium chloride, sodium chloride, vitamin C, inositol, taurine, ferrous sulphate, L-carnitine, zinc sulphate, nucleotides (cytidine, uridine, adenosine, inosine, guanosine 5'-monophosphate), vitamin E, pantothenic acid, niacin, copper sulphate, riboflavin (vitamin B?) emulsifier (soy lecithin), vitamin A, thiamine (vitamin B?), vitamin B?, potassium iodide, folate, antioxidant (L-ascorbyl palmitate), manganese sulphate, sodium selenite, vitamin K, vitamin D, biotin, vitamin B??..
58.49 USD
Optifibre plv 16 stick 5g
OptiFibre Plv 16 Stick 5g 100% PLANT SOLUBLE DIETARY FIBER (PHGG) TO SUPPORT THE INTESTINAL ACTIVITY IndicationsFor diet management with impaired intestinal activity such as ? Constipation ? Diarrhea ? Irritable bowel syndrome Product properties ? Dietary fibers: partially hydrolyzed guar gum ? Tasteless and odorless ? No change in consistency ? Not swelling? easy to use? no additional fluid intake Age/pregnancy/breastfeeding? Suitable from 3 years? Suitable for pregnant and breastfeeding women StorageStore in a cool and dry place. After opening, use the contents of the can within 8 weeks. Consume prepared food and drinks immediately or cover and cool them within 24 hours. ..
23.37 USD
Paragol n emuls bottle 1000ml
Paragol N with the active ingredient paraffin oil is a laxative that softens the stool, makes it slippery and stimulates intestinal movement. All of this leads to improved and normal bowel movements. It is absolutely essential that you drink plenty of fluids when using Paragol N. Paragol N is used to treat occasional constipation. Under no circumstances should a treatment last more than 10 days and should only be carried out after a change in diet to predominantly fiber-containing food components (vegetables, fruits) has failed. It can also be used in the short term for diseases that require easier bowel movements (e.g. haemorrhoids, intestinal diseases). Swissmedic-approved patient informationParagol® N Streuli Pharma AGWhat is Paragol N and when is it used? Paragol N with the active ingredient paraffin oil is a laxative that softens the stool, makes it slippery and stimulates intestinal movement. All of this leads to improved and normal bowel movements. It is absolutely essential that you drink plenty of fluids when using Paragol N. Paragol N is used to treat occasional constipation. Under no circumstances should a treatment last more than 10 days and should only be carried out after a change in diet to predominantly fiber-containing food components (vegetables, fruits) has failed. It can also be used in the short term for diseases that require easier bowel movements (e.g. haemorrhoids, intestinal diseases). When must Paragol N not be taken/used?Paragol N must under no circumstances be taken in the case of severe abdominal diseases (appendicitis, intestinal cramps and severe abdominal pain). Paragol N should not be taken even if there is a known hypersensitivity to the active ingredient or one of the excipients. When is caution required when taking/using Paragol N?Paragol N may only be taken occasionally and for no longer than 10 days . Long-term treatments belong under medical supervision. Propylene glycol alginateThis medicinal product contains 12,306 mg propylene glycol alginate per measuring spoon (5 ml) equivalent to 2.46 mg propylene glycol alginate per ml. Methyl parahydroxybenzoate (E 218)This medicinal product contains methyl parahydroxybenzoate (E 218). Methyl 4-hydroxybenzoate can cause allergic reactions, including delayed reactions. SucroseIf you know that you suffer from a sugar intolerance, please only take Paragon N after consulting your doctor. EthanolThis medicine contains small amounts of ethanol (alcohol). The small amount of alcohol in this medicine has no noticeable effects. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Paragol N be taken/used during pregnancy or breastfeeding?As a precautionary measure, you should avoid taking medicines during pregnancy and breastfeeding if possible . If you are pregnant or want to become pregnant, you should only take Paragol N after consulting your doctor. During breast-feeding, the drug should be discontinued or breast-feeding discontinued. How do you use Paragol N?Unless otherwise prescribed by the doctor: Adults and adolescents over 12 years3-9 measuring spoons (= 15-45 ml) before going to bed, if necessary the same dose in the morning on an empty stomach. Children under the age of 12Use only on medical prescription. Children from 2 years1-3 measuring spoons (= 5-15 ml) - depending on age - before going to bed. Children under the age of 2The application and safety in children under the age of 2 have not yet been tested. This medicine should therefore not be used in this age group. Paragol N should be shaken well before use. Phase separation of the emulsion may occur during storage. The product can be homogenized again by shaking. It may only be taken in an upright posture. Paragol N can be taken undiluted, but also with water, fruit juices or other drinks. Do not increase the dose if the medicine does not work immediately after taking it. The effect usually sets in 6-8 hours later, i.e. not until the next morning. 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 Paragol N have?The following side effects can occur when taking Paragol N: Long-term and high-dose use can lead to a lack of fat-soluble vitamins and loss of fluid and salt. With high dosages, paraffin oil can often seep out of the anus and itching in the anal area is rare. 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. Keep at room temperature (15-25°C) and out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Paragol N contain?Active ingredients5 ml emulsion for Ingestion contains: Viscous paraffin 1.9 g ExcipientsDried gum arabic (E 414), citric acid monohydrate (E 330), propylene glycol alginate (E 405), tragacanth (E 413), vanillin, saccharin ( E 954), bergamot flavor/pear flavor (contains small amounts of ethanol and bergamot oil), sucrose, methyl parahydroxybenzoate (E 218), purified water. Approval number55041 (Swissmedic). Where can you get Paragol N? What packs are available?In pharmacies and drugstores without a doctor's prescription. Packs of 200 ml, 500 ml and 1000 ml. Authorization holderStreuli Pharma AG, 8730 Uznach. This leaflet was last checked by the drug authority (Swissmedic) in March 2022. ..
81.59 USD
Paragol n emuls bottle 500ml
Paragol N with the active ingredient paraffin oil is a laxative that softens the stool, makes it slippery and stimulates intestinal movement. All of this leads to improved and normal bowel movements. It is absolutely essential that you drink plenty of fluids when using Paragol N. Paragol N is used to treat occasional constipation. Treatment should under no circumstances last more than 10 days and should only be carried out after a change in diet to predominantly fiber-containing food components (vegetables, fruits) has failed. It can also be used in the short term for diseases that require easier bowel movements (e.g. haemorrhoids, intestinal diseases). Swissmedic-approved patient informationParagol® N Streuli Pharma AGWhat is Paragol N and when is it used? Paragol N with the active ingredient paraffin oil is a laxative that softens the stool, makes it slippery and stimulates intestinal movement. All of this leads to improved and normal bowel movements. It is absolutely essential that you drink plenty of fluids when using Paragol N. Paragol N is used to treat occasional constipation. Treatment should under no circumstances last more than 10 days and should only be carried out after a change in diet to predominantly fiber-containing food components (vegetables, fruits) has failed. It can also be used in the short term for diseases that require easier bowel movements (e.g. haemorrhoids, intestinal diseases). When must Paragol N not be taken/used?Paragol N must under no circumstances be taken in the case of severe abdominal diseases (appendicitis, intestinal cramps and severe abdominal pain). Paragol N should not be taken even if there is a known hypersensitivity to the active ingredient or one of the excipients. When is caution required when taking/using Paragol N?Paragol N may only be taken occasionally and for no longer than 10 days . Long-term treatments belong under medical supervision. Propylene glycol alginateThis medicinal product contains 12,306 mg propylene glycol alginate per measuring spoon (5 ml) equivalent to 2.46 mg propylene glycol alginate per ml. Methyl parahydroxybenzoate (E 218)This medicinal product contains methyl parahydroxybenzoate (E 218). Methyl 4-hydroxybenzoate can cause allergic reactions, including delayed reactions. SucroseIf you know that you suffer from a sugar intolerance, please only take Paragon N after consulting your doctor. EthanolThis medicine contains small amounts of ethanol (alcohol). The small amount of alcohol in this medicine has no noticeable effects. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Paragol N be taken/used during pregnancy or breastfeeding?As a precautionary measure, you should avoid taking medicines during pregnancy and breastfeeding if possible . If you are pregnant or want to become pregnant, you should only take Paragol N after consulting your doctor. During breast-feeding, the drug should be discontinued or breast-feeding discontinued. How do you use Paragol N?Unless otherwise prescribed by the doctor: Adults and adolescents over 12 years3-9 measuring spoons (= 15-45 ml) before going to bed, if necessary the same dose in the morning on an empty stomach. Children under the age of 12Use only on medical prescription. Children from 2 years1-3 measuring spoons (= 5-15 ml) - depending on age - before going to bed. Children under the age of 2The application and safety in children under the age of 2 have not yet been tested. This medicine should therefore not be used in this age group. Paragol N should be shaken well before use. Phase separation of the emulsion may occur during storage. The product can be homogenized again by shaking. It may only be taken in an upright posture. Paragol N can be taken undiluted, but also with water, fruit juices or other drinks. Do not increase the dose if the medicine does not work immediately after taking it. The effect usually sets in 6-8 hours later, i.e. not until the next morning. 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 Paragol N have?The following side effects can occur when taking Paragol N: Long-term and high-dose use can lead to a lack of fat-soluble vitamins and loss of fluid and salt. With high dosages, paraffin oil can often seep out of the anus and itching in the anal area is rare. 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. Keep at room temperature (15-25°C) and out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Paragol N contain?Active ingredients5 ml emulsion for Ingestion contains: Viscous paraffin 1.9 g ExcipientsDried gum arabic (E 414), citric acid monohydrate (E 330), propylene glycol alginate (E 405), tragacanth (E 413), vanillin, saccharin ( E 954), bergamot flavor/pear flavor (contains small amounts of ethanol and bergamot oil), sucrose, methyl parahydroxybenzoate (E 218), purified water. Approval number55041 (Swissmedic). Where can you get Paragol N? What packs are available?In pharmacies and drugstores without a doctor's prescription. Packs of 200 ml, 500 ml and 1000 ml. Authorization holderStreuli Pharma AG, 8730 Uznach. This leaflet was last checked by the drug authority (Swissmedic) in March 2022. ..
45.57 USD
Prontolax supp 10 mg 10 pcs
Prontolax is a laxative that acts on the colon. It triggers the stool-promoting movement of the large intestine. Prontolax is used for short-term use in the event of sluggish bowel movements (constipation), constipation as a result of bed rest, unfamiliar food or when travelling. The following uses are under medical supervision: Prontolax can also be used when it is necessary to avoid pressure such as hemorrhoids and anal fissures, before gastrointestinal X-rays and before surgery to aid in defecation. Swissmedic-approved patient informationProntolax®, suppositoriesStreuli Pharma AGWhat is Prontolax and when is it used? Prontolax is a laxative that acts on the colon. It triggers the stool-promoting movement of the large intestine. Prontolax is used for short-term use in the event of sluggish bowel movements (constipation), constipation as a result of bed rest, unfamiliar food or when travelling. The following uses are under medical supervision: Prontolax can also be used when it is necessary to avoid pressure such as hemorrhoids and anal fissures, before gastrointestinal X-rays and before surgery to aid in defecation. What should be considered?Children and patients with serious illnesses require medical advice. In the case of chronic constipation, its origin must be determined by the doctor. Long-term treatment should be under medical supervision. General informationIf you are constipated, you should, if possible, eat high-fiber food (vegetables, fruit, wholemeal bread) and drink plenty of fluids regularly and pay attention to physical activity (sport). . When should Prontolax not be used?Prontolax should not be used if there is a known hypersensitivity to the active ingredient or one of the ingredients, if there is a narrowing of the intestines, Intestinal obstruction (ileus), acute diseases in the abdominal cavity such as acute appendicitis and acute intestinal inflammation as well as severe abdominal pain in combination with nausea and vomiting, which indicate a serious illness. Prontolax must not be used in the case of severe fluid and potassium deficiency. When should you be careful when using Prontolax?Children under the age of 12 should only be given Prontolax on the advice of a doctor. As with all laxatives, continuous daily use for longer than 1-2 weeks is not indicated for Prontolax. If laxatives are used daily, the cause of the constipation should be investigated. Long-term treatments belong under medical supervision. Long-term or high-dose use can result in loss of water and minerals (potassium) and lead to muscle weakness and increased constipation. Loss of fluid in the intestines can promote fluid loss in the body, which can cause thirst and reduced urination. In patients where this could be detrimental, such as renal insufficiency and the elderly, Prontolax should be discontinued and only resumed under medical supervision. A generally mild, self-limiting bloody stool may occur. Patients who take diuretic drugs, oral corticosteroids or digitalis preparations should only take Prontolax after consulting their doctor. In very rare cases, patients who have taken Prontolax have experienced dizziness or short-term unconsciousness (syncope). According to the corresponding case reports, these are probably syncopes, which are either due to the purging process itself, to straining or to vascular reactions mediated via the nervous system due to abdominal pain caused by constipation, but not necessarily to the use of Prontolax itself. If abdominal cramps occur, potentially hazardous activities such as driving or operating machinery should be avoided. Prontolax works in the large intestine. It is not effective in influencing nutrient absorption and thus calorie intake, since nutrient absorption mainly takes place in the small intestine. Stimulant laxatives, including Prontolax, therefore do not contribute to weight loss. Concomitant use of other laxatives may increase the side effects of Prontolax in the gastrointestinal tract. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Prontolax be used during pregnancy or breastfeeding?As a precautionary measure, you should avoid taking medicines during pregnancy if possible. Only your doctor can decide whether Prontolax can be used during pregnancy. Prontolax can be used while breastfeeding. How do you use Prontolax?Unless otherwise prescribed by the doctor: Adults and children over 12 yearsAverage single dose: 1 suppository per day, which is removed from the foil cover and inserted into the rectum with the pointed end. The triggering of one to two symptom-free emptyings within 20 minutes (in the range of 10-30 minutes) is characteristic of the effect. Children from 4 to 12 yearsAs prescribed by the doctor: ½ suppository per day. Suppositories can cause pain and local irritation, especially in patients with anal fissures and acute rectal inflammation. 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 Prontolax have?After taking Prontolax, you may experience unpleasant sensations in the abdominal area:Abdominal cramps, abdominal pain, or diarrhea often occur; occasionally there is vomiting, dizziness, bloody stools and discomfort in the abdominal and/or anal area. Rarely, syncope (short-lasting unconsciousness), dehydration, inflammation of the colon (including symptoms such as intestinal cramps, pain in the stomach area, diarrhea and bloody stools) and hypersensitivity reactions occur, which can go as far as allergic skin and shock symptoms (angioedema, anaphylactic reactions ) being able to lead. The occurrence of diarrhea is a sign of too high a dose and is only desirable before an X-ray or before an operation. 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 pack with « EXP» can be used. Storage instructionsStore at room temperature (15-25°C) and out of the reach of children. Further informationYour doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does Prontolax contain?Active ingredientsBisacodyl 10 mg per suppository . ExcipientsHard fat. Approval number38077 (Swissmedic) Where can you get Prontolax? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 10 suppositories. In pharmacies only with a doctor's prescription. Packs of 50 suppositories. Authorization holderStreuli Pharma AG, 8730 UznachThis leaflet was last checked by the drug authority (Swissmedic) in April 2018. ..
14.38 USD
Valverde constipation film tablets 20 pcs
Valverde Constipation contains the standardized extracts of senna and butterbur and dried figs. By standardizing the active ingredients, a consistent quality of this herbal medicinal product for constipation is achieved. In the recommended dosage, the extract of senna produces a soft, slippery stool. This effect is supported by the mucilage, fructose and fruit acid of the dried figs. The butterbur extract supports this effect thanks to its antispasmodic properties. Valverde Constipation is therefore indicated for short-term use in the following conditions: occasional constipation of a general nature, constipation caused by a change in eating habits (e.g. when travelling) or bed rest. Swissmedic-approved patient informationValverde® constipation, film-coated tabletsSidroga AGHerbal medicinal product What is Valverde Constipation and when is it used?Valverde Constipation contains the standardized extracts of senna and butterbur and dried figs. By standardizing the active ingredients, a consistent quality of this herbal medicinal product for constipation is achieved. In the recommended dosage, the extract of senna produces a soft, slippery stool. This effect is supported by the mucilage, fructose and fruit acid of the dried figs. The butterbur extract supports this effect thanks to its antispasmodic properties. Valverde Constipation is therefore indicated for short-term use in the following conditions: occasional constipation of a general nature, constipation caused by a change in eating habits (e.g. when travelling) or bed rest. What should be considered?If you suffer from constipation, you should food rich in fiber (vegetables, fruit, wholemeal bread) andtake plenty of fluids regularly andmake sure you are physically active (sport)!This medicinal product contains approx. 185 mg of usable carbohydrates per single dose (1 film-coated tablet). When should Valverde constipation not be taken or only with caution?In small children, with diseases of the gastrointestinal tract, e.g. with existing, inflammatory bowel diseases, with intestinal obstruction Valverde constipation must not be used. Laxatives should only be taken occasionally and for no longer than one to two weeks because of possible habituation. With long-term use, higher than the recommended doses, diarrhea with loss of water and disturbances in the salt balance can occur, as well as damage to the intestinal mucosa. Long-term treatments belong under medical supervision. Children from 6-12 years of age may only take the preparation if prescribed by a doctor. Very rare but sometimes serious liver damage has been observed in connection with a preparation containing a certain butterbur extract (CO2 extract). However, a liver-damaging effect cannot be ruled out for the alcoholic butterbur extract used in Valverde constipation. In the case of existing liver damage, it is therefore generally not recommended to take medicines containing butterbur. Unusual tiredness, weakness or loss of appetite and unintentional weight loss, yellowing of the conjunctivae of the eyes or skin, dark urine or discolored stools may indicate liver damage. Should such symptoms occur, Valverde constipation must be discontinued immediately and a doctor consulted immediately. Tell your doctor, pharmacist or druggist if you: suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!)!Can Valverde constipation 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 Valverde constipation?Adults and adolescents from 12 years take 1-2 film-coated tablets for constipation, children from 6 up to 12 years (unless otherwise prescribed by the doctor) 1 film-coated tablet in the evening before going to bed. The preparation must be taken with enough liquid (at least 1 glass of water). The onset of action occurs after approx. 8 hours. 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 Valverde constipation have?The following side effects may occur when taking Valverde constipation: On rare occasions, the supplement may cause bloating or abdominal cramps. If there is a liquid stool, the amount taken should be reduced. Very rare but sometimes serious liver damage has been observed in connection with a preparation containing a certain butterbur extract (CO2 extract). However, a liver-damaging effect cannot be ruled out for the alcoholic extract used in Valverde constipation either. See “When should Valverde constipation not be used or used with caution?”. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Store at room temperature (15-25°C) in the original packaging. Keep the medicine 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 Valverde constipation contain?1 film-coated tablet contains 370 mg of dried fig fruit powder (Ficus carica ), 60 mg of a standardized dry extract from senna fruits (Cassia senna) corresponding to 12 mg hydroxyanthracene glycosides, calculated as sennoside B (DEV 7-12:1, extractant ethanol 60% v/v), 40 mg a dry extract of butterbur roots (Petasites hybridus rhizoma) (DEV 7-14:1, extractant ethanol 90% m/m). This preparation contains additional excipients. Approval number47620 (Swissmedic) Where do you get Valverde constipation? What packs are available? In pharmacies and drugstores, without a doctor's prescription, in blister packs of 20 film-coated tablets. Authorization holderSidroga AG, 4310 Rheinfelden This leaflet was last checked by the drug authority (Swissmedic) in February 2009. ..
26.27 USD
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