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TROXEVASIN 300mg.CPS N50

Attention: Information on this site is provided for informational purposes and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for treating a health problem or disease, or prescribing any medication. iDrugs24.com is not responsible for any damage to your health as the result of self treatment.

# On 2024-Mar-28
TROXEVASIN-drug/medicine -capsules -tablets aproximate price on "TROXEVASIN 300mg.CPS N50" in Riga city, Latvia is:
  • 10.94€  11.83$  9.38£  1263Rub  125.9SEK  47PLN  43.3₪ 

TROXEVASIN, 300 mg, kietosios kapsulės, N50


Maximum allowed state defined price ( from ZVA webpage) Euro:State defined maximum allowed price indicated on the picture on drug/medicine -capsules -tablets  TROXEVASIN 300mg.CPS N50     Recheck

Reģ. Nr.: 99-0186

ATC codeC05CA04 

Active substances: Troxerutinum

 


Vendor, principal: Balkanpharma-Troyapharm
No prescription needed/Patient care products, dressings, gloves, medical devices,...

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TROXEVASIN 300 mg kapsulas, 50 gab.

 .

TROXEVASIN 300MG N50

Package leaflet: Information for the user Troxevasin, 300 mg hard capsules

Troxerutin

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you.
-   Keep this leaflet. You may need to read it again.
-   Ask your pharmacist if you need more information or advice.
-   If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet

1.   What Troxevasin is and what it is used for
2.   What you need to know before you take Troxevasin
3.   How to take Troxevasin
4.   Possible side effects
5.   How to store Troxevasin
6.   Contents of the pack and other information

1.   What Troxevasin is and what it is used for

Troxevasin reduces the permeability of small blood vessels, or capillaries, preventing the damage of the basal membrane of endothelial cells by various factors (capillary protection effect).
The effect of the medicine is associated with its anti-oxidising action. The main effect of Troxevasin is improving venous and capillary tone. Furthermore, its effects include stabilisation of membranes, retardation of bleeding, as well as anti-inflammatory, liver protection, radiation protection, detoxifying and anti-allergenic actions. Troxevasin inhibits aggregation of thrombocytes and promotes improvement of various trophic disorders in case of varicose syndrome.
Most of absorbed tri-, di- and mono hydroxyethylrutosides are excreted in bile and a significantly smaller part through renal route. Tetra(hydroxyethyl)rutoside is absorbed to a small extent from the gastrointestinal tract and excreted mainly in urine. 11% of an orally administered dose is excreted in urine and bile. Maximum plasma concentration is reached, on average, in 4 hours after oral administration and 15% of the administered dose is excreted through kidneys in the first 24 hours.
Indications. Supplementary medicine for swelling caused by chronic venous insufficiency on feet.

2.   What you need to know before you take Troxevasin Do not take Troxevasin

-   if you are allergic to active substance(s) or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor or pharmacist before taking Troxevasin.
Do not use this medicine in children.

Other medicines and Troxevasin

Tell your doctor or pharmacist if you are using or have recently used or might use any other medicines.
No adverse interactions with other medicines or substances have been reported.

Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Only use this medicine during pregnancy if this is indicated and prescribed for you by your doctor. While passing into breast milk is minimal, it is advisable to discontinue breast-feeding during treatment.

Driving and using machines

No effects on the ability drive and use machines have been reported.

Troxevasin contains lactose and Sunset Yellow dye

This medicine contains lactose. If you have been told by your doctor that you have intolerance to some sugars, consult your doctor before taking this medicine.
This medicine contains lactose and colourant E110 (Sunset Yellow dye). Use of this medicine can cause allergic reactions, incl. asthma. The risk of allergy is higher in patients who are allergic to aspirin.

3. How to use Troxevasin

Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
Take Troxevasin orally with meals.
Take Troxevasin in the evening before bed and in the morning after waking up, as well as in the case you experience symptoms of sensitivity disorders - numbness of feet and tonic spasms.
Initial dose - 1 capsule twice a day (600 mg).
Maintenance treatment - 1 capsule per day (300 mg) for 2-4 weeks.
Use in children
Do not use this medicine in children.
Success of treatment with Troxevasin largely depends on regular use of sufficient quantities over an extended period of time. Clinical experiences show that doses exceeding 600 mg per day may sometimes be need to achieve the desired effect.
If you have the impression that the effect of Troxevasin is too strong or too weak, talk to your doctor or pharmacist.

If you take more Troxevasin than you should

No cases of overdose have been reported.

If you forget to take Troxevasin

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.

4. Possible side effects

Like all medicines, Troxevasin can cause side effects, although not everybody gets them. Possibility of allergic reactions: itching, rash, urticaria.
Stomach and gastrointestinal problems, such as nausea, vomiting, diarrhoea, have been observed in very rare cases and they subside after treatment is discontinued.
There have been very rare reports of headache and sleep problems.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via www.ravimiamet.ee. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Troxevasin

Do not store above 25°. Store in the original packaging away from light and humidity.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information What Troxevasin contains

-   The active substance is troxerutin. One hard capsule contains 300 mg of troxerutin.
-   The excipients are: magnesium stearate, lactose monohydrate. Capsule hull: gelatine and colourants (quinoline yellow (E104), Sunset Yellow (E110) titanium dioxide (E171)).

What Troxevasin looks like and contents of the pack

Opaque yellow gelatine capsule containing a yellow or yellowish-brown powder. PVC/aluminium or PVC/PVdC/aluminium blisters, 50 or 100 hard capsules per pack.
Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder
Actavis Group PTC ehf Reykjavikurvegi 76-78 220 Hafnarfjördur Iceland
Manufacturer
Balkanpharma-Razgard AD,
68 Aprilsko vastanie Blvd,
7200 Razgrad,
Bulgaria
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
Teva Eesti esindus
UAB Sicor Biotech Eesti filiaal
Hallivanamehe 4
11317 Tallinn
Tel: +372 6610 801

This leaflet was last revised in May 2018.

3





  Instruction, annotation source for medicine: State Agency of Medicines, Estonia





• Medicaments images are for illustrative purposes only and may differ from the actual product.


[*1]

Information source DDD German Institute of Medical Documentation and Information - DIMDI [23.11.2011]


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