

Core:
Purified micronized flavonoid fraction, substance - granules 613.00 mg
[The active substance of the substance - granules:
Purified micronized flavonoid fraction1 500.00 mg
Auxiliary substances of the substance - granules:
Microcrystalline cellulose 82.00 mg, povidone K-30 31.00 mg]
Excipients:
Sodium carboxymethyl starch 27.00 mg, talc 6.00 mg, Magnesium stearate 4.00 mg
Shell film:
Opadray orange 03Н325992 18.00 mg
1 Purified micronized flavonoid fraction contains 90% (450 mg) of diosmin and 10% (50 mg) of other flavonoids in terms of hesperidin.
2 Opadray orange 03Н32599 contains:
hypromellose 71.714%, titanium dioxide (E171) 15.936%, talc 6.972%, propylene glycol 4.980%, iron dye yellow oxide (E172) 0.332%, iron dye red oxide (E172) 0.066%
- feeling of heaviness in the legs;
- pain;
- "tired" legs.
Pregnancy
Animal experiments revealed no teratogenic effects.
To date, there have been no reports of any side effects when using the drug in pregnant women.
Breastfeeding period
Due to the lack of data on the removal of the drug in breast milk, women during breastfeeding is not recommended to take the drug.
Inside
The recommended dose for venous lymphatic insufficiency is 2 pills per day:
1 pill - in the middle of the day and 1 pill - in the evening, during the meal.
The duration of the course of treatment can be several months (up to 12 months). In the case of recurrence of symptoms, according to the recommendation of the doctor, the treatment can be repeated.
The recommended dose for acute hemorrhoids is 6 pills per day: 3 pills in the morning and
3 pills in the evening for 4 days, then 4 pills per day: 2 pills in the morning and 2 pills in the evening over the next 3 days.
The classification of the incidence of side effects recommended by the World Health Organization (WHO):
very often ≥ 1/10
often from ≥ 1/100 to <1/10
infrequently from ≥ 1/1000 to <1/100
rarely from ≥ 1/10000 to <1/1000
very rarely <1/10000
frequency unknown cannot be estimated based on available data.
From the side of the central nervous system:
seldom: dizziness, headache, general malaise.
Gastrointestinal:
often: diarrhea, dyspepsia, nausea, vomiting.
infrequently: colitis.
frequency unknown: abdominal pain.
From the skin:
rarely: skin rash, pruritus, urticaria.
frequency unknown: isolated swelling of the face, lips, eyelids. In exceptional cases, angioedema.
INFORM THE DOCTOR ABOUT THE APPEARANCE OF ANY ANYTHING IN YOU, NOT INCLUDED IN THIS INSTRUCTION, UNDESIRABLE REACTIONS AND SENSATIONS, AND ALTERING THE CHANGE OF LABORATORY INDICATORS IN THE SYSTEM
Cases of overdose are not described.
With an overdose of the drug Flebaven® seek medical attention immediately.
Not noted.
IT IS NECESSARY TO INFORM THE MEDICAL DOCTOR ABOUT ALL YOU TAKE MEDICAL PREPARATIONS.
Seek medical attention immediately if your condition worsens or there is no improvement in the treatment process.
Impact on the ability to perform potentially hazardous activities that require special attention and quick reactions (for example, driving, working with moving machinery)
Does not affect.
The combination of hesperidin + diosmin has venotonic and angioprotective properties. Reduces the elasticity of the veins and venous congestion, in microcirculation - reduces the permeability of capillaries and increases their resistance, improves venous hemodynamics. It affects the following venous plethysmographic parameters: venous capacity, venous distensibility, time of venous emptying. The optimal effect is achieved when taking 2 tablets.
The combination of hesperidin + diosmin increases venous tone by reducing the time of venous emptying. In patients with signs of pronounced impairment of microcirculation, there is an increase in capillary resistance.
The combination of hesperidin + diosmin is effective in the treatment of chronic diseases of the veins of the lower extremities, as well as in the treatment of hemorrhoids.
Drug Flebaven® mainly excreted through the intestines. The kidneys, on average, produce about 14% of the accepted dose of the drug.
The half-life is 11 hours.
The drug is subjected to active metabolism, as evidenced by the presence of phenolic acids in the urine.
Tablets, film coated, 500 mg.
On 16 pills in a blister strip packaging from a film of PVC and aluminum foil.
2, 4 or 6 blister packs together with instructions for use are placed in a pack of cardboard.
At a temperature not higher than 25 ° С, in the original package.
Keep out of the reach of children.
2 years.
Do not use the drug after the expiration date.
Let go without a prescription.