Vinpocetine
Cavinton Forte contains the active substance vinpocetine.
Vinpocetine is a compound used to treat diseases or alleviate symptoms associated with
blood circulation disorders in the brain.
Indications for use of Cavinton Forte:
Before starting treatment with Cavinton Forte, you should discuss it with your doctor or pharmacist.
If the patient has certain heart diseases, the doctor will recommend performing control ECG tests
(electrocardiologic examination - examination of heart function). This is especially important for patients who have been diagnosed with QT interval prolongation or patients who are taking medications that cause QT interval prolongation.
The use of this medicine is contraindicated in children and adolescents due to the lack of sufficient clinical trial data in this age group.
You should tell your doctor or pharmacist about all the medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Cavinton Forte may interfere with the action of other medicines or other medicines may affect its action.
You should tell your doctor, especially if you are taking the following medicines:
Cavinton Forte should be taken after meals.
If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, you should consult your doctor or pharmacist before using this medicine.
If you are of childbearing age, you must use an effective contraceptive method during treatment with Cavinton Forte. Otherwise, the administration of vinpocetine is contraindicated.
Cavinton Forte is contraindicated during pregnancy and breastfeeding.
There is no data on the effect of vinpocetine on the ability to drive and use machines.
If you have been diagnosed with an intolerance to some sugars, you should contact your doctor before taking the medicine.
This medicine should always be used as directed by your doctor. If you are unsure, you should consult your doctor or pharmacist.
The usual dose of Cavinton Forte is 1 tablet (10 mg) three times a day (30 mg).
Tablets should be taken after meals.
The dividing line on the tablet is not intended for breaking the tablet.
There is no need to change the dosage if the patient has kidney or liver function disorders.
There is no need to change the dosage if the patient is over 65 years old.
If you have taken a higher dose of Cavinton Forte than recommended, you should immediately consult your doctor or go to the nearest hospital.
You should not take a double dose to make up for a missed dose. The next dose should be taken at the usual time.
If you have any further doubts about using this medicine, you should consult your doctor or pharmacist .
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The side effects listed below are grouped by frequency of occurrence.
Uncommon side effects(may affect up to 1 in 100 people):
Rare side effects(may affect up to 1 in 1,000 people):
If you experience any side effects, including any side effects not listed in this leaflet, you should 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.
By reporting side effects, you can help provide more information on the safety of this medicine.
The medicine should be stored out of sight and reach of children.
The blister pack should be stored in the outer packaging to protect it from light.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
White or almost white tablets, flat in the shape of a disc, with beveled edges, approximately 8 mm in diameter, with the inscription "10 mg" on one side and a dividing line on the other side.
The medicine is packaged in PVC/Aluminum blisters.
The carton packaging contains 30 or 90 tablets.
To obtain more detailed information, you should contact the marketing authorization holder or the parallel importer.
Gedeon Richter Plc.
Gyömrői út 19-21.
1103 Budapest, Hungary
Gedeon Richter Plc.
Gyömrői út 19-21.
1103 Budapest, Hungary
InPharm Sp. z o.o.
ul. Strumykowa 28/11, 03-138 Warsaw
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249, 04-458 Warsaw
Marketing authorization number in Bulgaria, the country of export:20010989
Parallel import authorization number:154/20
[Information about the trademark]
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