Veinofytil is a herbal medicinal product containing dry extract of horse chestnut seeds.
Veinofytil is used to treat chronic venous insufficiency, which is characterized by swelling of the legs, varicose veins, feeling of heaviness in the legs, painful symptoms, fatigue, itching, tension, and cramps in the calves.
Before starting to use Veinofytil, the doctor or pharmacist should be consulted.
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LEAFLET
Taking Veinofytil does not replace other preventive measures, such as taking cold showers or wearing compression stockings, if prescribed by the doctor.
If the treatment of chronic venous disease requires the use of Veinofytil for more than 8 weeks, the doctor should be consulted.
There are no indications for the use of Veinofytil in children under 12 years of age.
The use of Veinofytil is not recommended in adolescents under 18 years of age due to the lack of data on safety and efficacy.
There are no reports. No drug interaction studies have been conducted.
The doctor or pharmacist should be informed about all medicines currently or recently taken by the patient, as well as any medicines planned to be taken.
Not applicable.
If the patient is pregnant or breastfeeding, thinks she may be pregnant, or plans to have a child, she should consult her doctor or pharmacist before using this medicine.
Due to the lack of sufficient data on the use of Veinofytil during pregnancy and breastfeeding, the use of this medicine is not recommended during this time. There are no data on the effect of the medicine on fertility.
There are no data on dosing in patients with hepatic and/or renal impairment.
No studies have been conducted on the effect of the medicine on the ability to drive and use machines.
This medicine contains the colorant Allura Red AC, aluminum lake (E 129), which may cause allergic reactions.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means the medicine is considered "sodium-free".
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LEAFLET
This medicine should always be taken exactly as described in the patient leaflet or
according to the doctor's or pharmacist's instructions. In case of doubts, the doctor or pharmacist should be consulted.
Adults
The recommended dose of Veinofytil for adults is 1 tablet twice a day.
The tablets should be swallowed with a full glass of water.
The first signs of the beneficial effect of the medicine may only be visible after 4 weeks of use.
If symptoms worsen or do not improve after 8 weeks, the doctor should be consulted.
In case of long-term use, the treatment should be periodically evaluated by the doctor.
The doctor or pharmacist should be contacted immediately, or the Poison Control Center.
A double dose should not be taken to make up for a missed tablet.
Any further questions about the use of this medicine should be directed to the doctor or pharmacist.
Like all medicines, Veinofytil can cause side effects, although not everybody gets them.
There are reports of gastrointestinal disorders, headaches, dizziness, itching (pruritus), and allergic reactions.
The frequency of occurrence is not known.
If any side effects occur, including any side effects not listed in this leaflet, the doctor or pharmacist should be informed. Side effects can be reported directly to the Department of Post-Marketing Surveillance of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181 C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
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LEAFLET
Side effects can also be reported to the marketing authorization holder or its representative.
Reporting side effects will help gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
The medicine should not be used after the expiration date (EXP) stated on the blister pack and carton. The expiration date refers to the last day of the specified month.
Store in the original packaging.
This medicinal product does not require special storage temperature recommendations.
Medicines should not be disposed of via wastewater or household waste containers.
The pharmacist should be asked how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substance is dry extract of horse chestnut seeds, which corresponds to 21 mg of triterpenoid glycosides calculated as protoescigenin.
One tablet contains 192-258 mg of extract (as dry extract) from Aesculus hippocastanumL., semen(horse chestnut seeds) (DER 5-8:1), which corresponds to 21 mg of triterpenoid glycosides calculated as protoescigenin.
Extraction solvent: ethanol 50% V/V.
Other ingredients:
Core:maltodextrin, microcrystalline cellulose, calcium hydrogen phosphate, pregelatinized starch, talc, colloidal anhydrous silica, magnesium stearate.
Coating:methacrylic acid and ethyl acrylate copolymer (1:1), talc, titanium dioxide (E 171), Allura Red AC, aluminum lake (E 129), colloidal anhydrous silica, sodium bicarbonate, sodium lauryl sulfate, triethyl citrate. Auxiliary substances used in the extract: maltodextrin, colloidal anhydrous silica.
Veinofytil is a red, oblong, biconvex tablet with dimensions of 18 × 8 mm.
The medicine is available in blisters, in cardboard boxes of 42 tablets or 98 tablets, or in single-dose blisters in cardboard boxes of 100 × 1 tablet.
Not all pack sizes may be marketed.
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LEAFLET
Tilman S.A.
Zone d'Activités Sud 15
5377 Somme-Leuze
Belgium
+32 (0) 84 320 360
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