Trimebutine maleate
Trikolon Forte contains trimebutine maleate as the active substance. Trimebutine acts on the smooth muscles of the gastrointestinal tract, regulating its function (peristalsis). The action of the medicine depends on the functional state of the gastrointestinal tract, and the regulation of peristalsis covers the entire gastrointestinal tract. Trimebutine does not affect the central nervous system. Trikolon Forte is used for symptomatic treatment of:
Before taking Trikolon Forte, discuss it with your doctor, pharmacist, or nurse.
It is not recommended to use in children under 12 years of age.
Tell your doctor or pharmacist about all medicines you are taking, or have recently taken, and any you plan to take. In particular, inform your doctor if you are taking zotepine (an antipsychotic medicine).
See section 3.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. Pregnancy There are no sufficient studies to confirm the safety of trimebutine during pregnancy. Therefore, trimebutine is not recommended during the first trimester of pregnancy. It is not expected to have a harmful effect on the mother or the child, however, the use of trimebutine during the second or third trimester should be considered only if necessary. Breastfeeding The safety of trimebutine in breastfeeding women has not been established. Fertility There are no data on the effect of trimebutine on fertility.
Trikolon Forte has no or negligible influence on the ability to drive and use machines.
If you have been told you have an intolerance to some sugars, contact your doctor before taking the medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially sodium-free.
Always take this medicine exactly as your doctor has told you. If you are not sure, check with your doctor or pharmacist. The medicine should be taken orally. The recommended dose is 100 mg (half a tablet), 3 times a day, before meals. In justified cases, the dose can be increased to 600 mg per day in divided doses. Swallow the tablet whole with a glass of water. The dividing line on the tablet allows you to divide the medicine into equal doses.
The medicine can be used in adolescents over 12 years of age in a dose not exceeding 6 mg/kg body weight per day.
In case of overdose, contact your doctor, who will recommend appropriate symptomatic treatment.
Do not take a double dose to make up for a forgotten dose. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. 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.: +48 22 49 21 301, Fax: +48 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. Store in a temperature below 25°C. Store in the original package to protect from light and moisture. Do not use this medicine after the expiry date stated on the package. The expiry date refers to the last day of the month stated. 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.
Trikolon Forte is a white, oval, biconvex coated tablet with a size of 14x8 mm, with a dividing line on both sides. One pack contains 30 or 60 coated tablets in PVC/PVDC/Aluminum blisters in a cardboard box.
"PRZEDSIĘBIORSTWO PRODUKCJI FARMACEUTYCZNEJ HASCO-LEK" S.A., 51-131 Wrocław, ul. Żmigrodzka 242 E
tel.: 22 742 00 22, e-mail: informacjaoleku@hasco-lek.pl
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