(Hymecromonum)
Cholestil contains the active substance hymecromon, which is a coumarin derivative. It acts as a spasmolytic on the smooth muscle of the bile ducts and the sphincter of Oddi, increases bile secretion, and accelerates its excretion through the bile ducts. This action reduces bile stasis and related symptoms, as well as prevents the formation of cholesterol deposits and gallstones.
Before taking Cholestil, discuss it with your doctor or pharmacist. If you experience symptoms of liver and/or kidney failure, stop taking the medicine. Consult your doctor, even if the above warnings refer to past situations.
Tell your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take.
Take the medicine half an hour before meals.
Do not use the medicine in patients with liver and/or kidney failure.
There is no need to change the dosage in elderly patients.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before taking this medicine. There is no data on the safety of using the medicine during pregnancy. It is not recommended to use Cholestil in pregnant women. There is no data on the safety of using the medicine during breastfeeding. It is not recommended to use the medicine during breastfeeding. Cholestil does not affect fertility.
Cholestil does not impair psychophysical abilities, the ability to drive vehicles, or operate machinery.
The medicine contains less than 1 mmol (23 mg) of sodium per maximum daily dose, which means the medicine is considered "sodium-free".
Always take this medicine exactly as your doctor has told you. If you are not sure, ask your doctor or pharmacist. Adults: 400 mg (1 tablet) half an hour before meals, three times a day, for two weeks. Do not divide the tablets.
There is no data on overdose. If you have taken more than the recommended dose, contact your doctor or pharmacist immediately.
Take the missed dose as soon as possible. Do not take a double dose to make up for the missed dose.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, Cholestil can cause side effects, although not everybody gets them. If you experience allergic reactions, including rash, face, lip, tongue, and/or throat swelling, which may cause difficulty breathing or swallowing, or other serious side effects, stop taking Cholestil and contact your doctor or the Emergency Department of the nearest hospital immediately.Cholestil is generally well-tolerated. Side effects are listed according to their frequency: Rare (may affect up to 1 in 10,000 people): diarrhea, feeling of fullness or pressure in the abdominal cavity, hypersensitivity reactions, rash, or other skin allergic reactions.
If you experience any side effects, including those not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: 22 49 21 301, fax: 22 49 21 309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children. There are no special precautions for storage. Do not use this medicine after the expiry date stated on the packaging. The expiry date (EXP) refers to the last day of the given month. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance is hymecromon. The other ingredients are potato starch, gelatin, sodium lauryl sulfate, magnesium stearate.
Cholestil is a white or almost white, oval, biconvex tablet without engraving.
Cholestil 400 mg tablets are packaged in PVC/Aluminum blisters, in a cardboard box. The pack contains 30 or 50 tablets. Not all pack sizes may be marketed.
Adamed Pharma S.A. Pieńków, ul. M. Adamkiewicza 6A 05-152 Czosnów
Adamed Pharma S.A. ul. Marszałka J. Piłsudskiego 5 95-200 Pabianice Date of last revision of the leaflet:
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