Venarus tab. p / o captivity. 500 mg # 30
Package quantity, pcs:
thirty
60
Dosage:
100mg + 900mg
50mg + 450mg
Category
Diseases of the veins
Scope of the drug
Heart, vessels, blood
Release form
Tablet
Manufacturer country
Russia
Package quantity, pcs
thirty
Amount in a package
thirty
Dosage form
pills
Manufacturer
Obolenskoe FP, Russia
Structure
Active ingredients: diosmina - 0.45 g, hesperidin - 0.05 g.
Excipients (core): gelatin, magnesium stearate, microcrystalline cellulose, starch, sodium glycolate, talc.
Excipients (shell): polyethylene glycol 6000, magnesium stearate, hydroxypropyl methylcellulose, sodium lauryl sulfate, titanium dioxide, iron oxide red, iron oxide yellow.
pharmachologic effect
Pharmacodynamics
It has an angioprotective and venotonic effect.
Reduces the elasticity of veins, increases their tone and reduces venous congestion
reduces the permeability, fragility of capillaries and increases their resistance
improves microcirculation and lymph drainage.
With systematic use, it reduces the severity of clinical manifestations of chronic venous insufficiency of the lower extremities of an organic and functional nature.
Pharmacokinetics
The main excretion of the drug occurs in the feces.
With urine, on average, about 14% of the taken amount of the drug is excreted.
The half-life is 11 hours.
The drug undergoes active metabolism, as evidenced by the presence of phenolic acids in the urine.
Indications
Venous insufficiency of the lower extremities of a functional and organic nature (feeling of heaviness in the legs, pain, convulsions, trophic disorders).
Acute and chronic hemorrhoids.
Application during pregnancy and lactation
Pregnancy
Animal experiments have not revealed teratogenic effects.
Until now, there have been no reports of any side effects when using the drug by pregnant women.
Breastfeeding period
Due to the lack of data on the excretion of the drug into breast milk, it is not recommended for lactating women to take the drug.
Contraindications
Hypersensitivity to active ingredients or excipients that make up the drug.
It is not recommended to take the drug for lactating women.
Side effects
The incidence of adverse reactions is presented as follows:
Very often (? 1/10 cases).
Often (? 1/100 and < 1/10 cases).
Uncommon (? 1/1000 and < 1/100 cases).
Rarely (? 1/10000 and < 1/1000 cases).
Very rare (< 1/10000 cases).
Adverse reactions, the frequency of which is not possible to estimate from the available data, have the designation frequency is unknown."
From the side of the central nervous system: rarely - dizziness, headache, general malaise
frequency unknown - convulsions.
From the gastrointestinal tract: often - diarrhea, dyspepsia, nausea, vomiting
infrequently - colitis
frequency unknown - abdominal pain.
From the respiratory system, chest and mediastinal organs: frequency unknown - sore throat, chest pain.
From the side of the skin: rarely - rash, itching, urticaria
frequency is unknown - allergic dermatitis, hyperemia, isolated edema of the face, lips, eyelids, in exceptional cases, angioedema.
If any of the adverse reactions indicated in the instructions are aggravated, or you notice other adverse reactions that are not indicated in the instructions, inform your doctor.
Interaction
Not noted.
The attending physician should be informed about all medications taken.
How to take, course of administration and dosage
30 pcs.
50 mg + 450 mg.
Overdose
Overdose cases have not been described.
In case of drug overdose, seek medical attention immediately.
Special instructions
In case of exacerbation of hemorrhoids, the appointment of this drug does not replace the specific treatment of other anal disorders.
The duration of treatment should not exceed the time specified in the section "Dosage and Administration".
In the event that the symptoms do not disappear after the recommended course of therapy, a proctological examination should be carried out and the therapy used should be reviewed.
In the presence of disorders of venous circulation, the maximum effect of treatment is provided by a combination of therapy with a healthy (balanced) lifestyle: it is advisable to avoid long exposure to the sun, prolonged stay on the legs, and also to reduce excess body weight.
Hiking and, in some cases, wearing special stockings can improve blood circulation.
Impact on the ability to drive vehicles and other mechanisms that require increased concentration
Does not affect.
Storage conditions
In a dry, dark place at a temperature not exceeding 25 ° C
Shelf life
2 years
Active substance
Hesperidin, Diosmin
Terms of dispensing from pharmacies
Without recipe
Name ENG
VENARUS
Clinical and pharmacological group
Venotonic drug.
ATX code
Diosmin in combination with other drugs
Dosage
50mg + 450mg
Structure
1 tablet contains: active ingredients: hesperidin (in terms of 100% substance) 100 mg, diosmin (in terms of 100% substance) 900 mg
excipients: microcrystalline cellulose 124 mg, sodium carboxymethyl starch (sodium starch glycolate) 54 mg, gelatin 62 mg, talc 12 mg, magnesium stearate 8 mg
excipients for the shell: hypromellose (hydroxypropyl methylcellulose 41.4 mg, macrogol 6000 (polyethylene glycol 6000) 6.76 mg, sodium lauryl sulfate 0.2 mg, magnesium stearate 2.48 mg, titanium dioxide 7.88 mg, iron oxide red 0, 6 mg, iron oxide yellow 0.68 mg.
Indications
Venarus is indicated for the treatment of symptoms of chronic venous disease (elimination and relief of symptoms).
Therapy for symptoms of venous lymphatic insufficiency:
- cramps of the lower extremities
- a feeling of heaviness and fullness in the legs
- pain
- "tiredness" of the legs.
Therapy of manifestations of venous-lymphatic insufficiency:
- edema of the lower extremities
- trophic changes in the skin and subcutaneous tissue
- venous trophic ulcers.
Symptomatic therapy of acute and chronic hemorrhoids.
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 4 years
INN / Active ingredient
hesperidin, diosmin
Contraindications
Hypersensitivity to active ingredients or excipients that make up the drug.
It is not recommended to take the drug for lactating women.
Specifications
Category
Diseases of the veins
Scope of the drug
Heart, vessels, blood
Release form
Tablet
Manufacturer country
Russia
Package quantity, pcs
thirty
Way of introduction
Through the mouth
Vacation conditions
Without recipe
Brand name
Obolenskoe FP
The amount of the dosage form in the primary package
15 pcs.
Primary packaging type
Blister
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Venotonic and venoprotective agent
Anatomical and therapeutic characteristics
C05CA53 Diosmin, in combination with other drugs
Dosage form
Film-coated tablets
Dosage (volume) of the substance in the preparation
450 mg + 50 mg
Expiration date in days
1460
Package weight, g
40
Mode of application
:
Inside. < br> < br> The recommended dose for venous-lymphatic insufficiency is 1 tablet per day, preferably in the morning, during meals. The risk on the tablet is intended solely for dividing in order to facilitate swallowing. < br> < br> The duration of the course of treatment can be several months (up to 12 months). In case of recurrence of symptoms, on the recommendation of a doctor, the course of treatment can be repeated. < br> < br> The recommended dose for acute hemorrhoids is 3 tablets per day (1 tablet in the morning, afternoon and evening) for 4 days, then 2 tablets per day (1 tablet in the morning and in the evening) for the next 3 days. < br> < br> The recommended dose for chronic hemorrhoids is 1 tablet per day.
Information on technical characteristics, delivery set, country of manufacture "