Venarus® (Tablets) Instructions for Use
ATC Code
C05CA53 (Diosmin in combination with other drugs)
Active Substances
Diosmin (Rec.INN)
Hesperidin (Grouping Name)
Clinical-Pharmacological Group
Venotonic drug
Pharmacotherapeutic Group
Venotonic and venoprotective agent
Pharmacological Action
Venarus® exerts an angioprotective and venotonic action.
It reduces venous distensibility, increases venous tone, and reduces venous stasis; it decreases capillary permeability and fragility and increases capillary resistance; it improves microcirculation and lymphatic drainage.
With systematic use, it reduces the severity of clinical manifestations of chronic venous insufficiency of the lower limbs of organic and functional nature.
The optimal dose-effect ratio is observed at a dose of 1000 mg/day.
Pharmacokinetics
The main route of excretion of the drug is through the intestine.
On average, about 14% of the administered dose is excreted via the kidneys.
The T1/2 is 11 hours.
The drug Venarus® undergoes active metabolism, which is confirmed by the presence of phenolic acids in the urine.
Indications
Venarus® is indicated for the therapy of symptoms of chronic diseases (elimination and relief of symptoms).
Therapy of symptoms of venolymphatic insufficiency
- Cramps in the lower limbs;
- Sensation of heaviness and distension in the legs;
- Pain;
- “tired” legs.
Therapy of manifestations of venolymphatic insufficiency
- Edema of the lower limbs;
- Trophic changes of the skin and subcutaneous tissue;
- Venous trophic ulcers.
Symptomatic therapy of acute and chronic hemorrhoids.
ICD codes
| ICD-10 code | Indication |
| I83.2 | Varicose veins of lower extremities with ulcer and inflammation |
| I87.2 | Venous insufficiency (chronic) (peripheral) |
| I89.0 | Lymphedema, not elsewhere classified |
| K64 | Hemorrhoids and perianal venous thrombosis |
| R60 | Edema, not elsewhere classified |
| ICD-11 code | Indication |
| BD74.Z | Chronic venous insufficiency of lower extremities, unspecified |
| BD93.Z | Lymphedema, unspecified |
| DB6Z | Hemorrhoids or perianal venous diseases, unspecified |
| MG29.Z | Edema, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Tablets
Orally.
The recommended dose for venolymphatic insufficiency is 1 tablet/day, preferably in the morning, with meals.
The score on the tablet is intended solely for dividing to facilitate swallowing.
The duration of the treatment course can be several months (up to 12 months).
In case of recurrence of symptoms, on the doctor’s recommendation, the treatment course can be repeated.
The recommended dose for acute hemorrhoids is 3 tablets/day (1 tablet in the morning, afternoon, and evening) for 4 days, then 2 tablets/day (1 tablet in the morning and evening) for the next 3 days.
The recommended dose for chronic hemorrhoids is 1 tablet/day.
Adverse Reactions
The frequency of adverse reactions is presented as follows: very common (≥1/10), common (≥1/100 and <1/10), uncommon (≥1/1000 and <1/100), rare (≥1/10,000 and <1/1000), and very rare (<1/10,000).
Adverse reactions, the frequency of which cannot be estimated from the available data, are designated as “frequency unknown”.
Nervous system disorders rare – dizziness, headache, general malaise.
Gastrointestinal disorders common – diarrhea, dyspepsia, nausea, vomiting; uncommon – colitis; frequency unknown – abdominal pain.
Skin and subcutaneous tissue disorders rare – rash, pruritus, urticaria; frequency unknown – isolated edema of the face, lips, eyelids, in exceptional cases angioedema.
If any of the adverse reactions listed in the instructions worsen, or the patient notices any other adverse reactions not listed in the instructions, they should inform their doctor.
Contraindications
- Hypersensitivity to the active substances or to any of the excipients included in the drug;
- Use of the drug is not recommended for women during breastfeeding.
Use in Pregnancy and Lactation
Pregnancy
Experiments on animals have not revealed teratogenic effects.
To date, there have been no reports of any adverse effects when the drug was used by pregnant women.
Breastfeeding period
Due to the lack of data regarding the excretion of the drug in breast milk, the use of the drug is not recommended for women during breastfeeding.
Effect on the reproductive system
Reproductive toxicity studies did not show any effect on reproductive function in rats of both sexes.
Special Precautions
Before starting to take Venarus®, it is recommended to consult a doctor.
In case of exacerbation of hemorrhoids, the prescription of Venarus® does not replace specific treatment for other anal disorders.
The duration of treatment should not exceed the terms specified in the “Dosage Regimen” section.
If the symptoms do not disappear after the recommended course of therapy, a proctologist should be consulted to select further therapy.
In the presence of venous circulation disorders, the maximum therapeutic effect is achieved by combining therapy with a healthy (balanced) lifestyle: it is advisable to avoid prolonged exposure to the sun, prolonged standing, and weight reduction is recommended in case of excess body weight.
Walking and, in some cases, wearing special stockings, promotes better blood circulation.
The patient should immediately consult a doctor if their condition worsens or does not improve during treatment.
Effect on ability to drive vehicles and operate machinery
No effect.
Overdose
No cases of overdose have been reported.
In case of drug overdose, the patient should immediately seek medical help.
Drug Interactions
None noted.
The treating physician should be informed about all medications being taken.
Storage Conditions
The drug should be stored at a temperature not exceeding 25°C (77°F).
Shelf Life
The shelf life is 3 years. Do not use after the expiration date printed on the package.
Dispensing Status
The drug is available without a prescription.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Film-coated tablets, 900 mg+100 mg: from 9 to 135 pcs.
Marketing Authorization Holder
Aliym, JSC (Russia)
Contact Information
ALIUM JSC (Russia)
Dosage Form
| Venarus® | Film-coated tablets, 900 mg+100 mg: from 9 to 135 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets orange-pink in color, biconvex, oblong in shape with rounded ends, with a score; the core on the cross-section is from grayish-yellow to brownish-gray in color.
| 1 tab. | |
| Diosmin | 900 mg |
| Hesperidin | 100 mg |
Excipients: microcrystalline cellulose, sodium carboxymethyl starch (sodium starch glycolate), gelatin, talc, magnesium stearate.
Shell composition: hypromellose (hydroxypropyl methylcellulose), macrogol 6000 (polyethylene glycol 6000), sodium lauryl sulfate, magnesium stearate, titanium dioxide, iron oxide red dye, iron oxide yellow dye.
From 9 to 15 pcs. – blister packs (from 1 to 9 pcs.) – cardboard packs.
Set – blister packs (3 pcs.) – cardboard packs, in a set: blister pack (tablets 15 pcs.) – 2 pcs. and blister pack (tablets 15 pcs.) – 1 pcs.
Set – blister packs (4 pcs.) – cardboard packs, in a set: blister pack (tablets 10 pcs.) – 3 pcs. and blister pack (tablets 15 pcs.) – 1 pcs.
Film-coated tablets, 450 mg+50 mg: 20, 30, 40, 45, 60, 70, 80, 90, 105, 120, or 135 pcs.
Marketing Authorization Holder
Aliym, JSC (Russia)
Contact Information
ALIUM JSC (Russia)
Dosage Form
| Venarus® | Film-coated tablets, 450 mg+50 mg: 20, 30, 40, 45, 60, 70, 80, 90, 105, 120, or 135 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets orange-pink in color, biconvex, oblong in shape with rounded ends, with a score; the core on the cross-section is from grayish-yellow to brownish-gray in color.
| 1 tab. | |
| Diosmin | 450 mg |
| Hesperidin | 50 mg |
Excipients: microcrystalline cellulose, sodium carboxymethyl starch (sodium starch glycolate), gelatin, talc, magnesium stearate.
Shell excipients: hypromellose (hydroxypropyl methylcellulose), macrogol 6000 (polyethylene glycol 6000), sodium lauryl sulfate, magnesium stearate, titanium dioxide, iron oxide red dye, iron oxide yellow dye.
10 pcs. – blister packs (2) – cardboard packs.
10 pcs. – blister packs (3) – cardboard packs.
10 pcs. – blister packs (4) – cardboard packs.
10 pcs. – blister packs (6) – cardboard packs.
10 pcs. – blister packs (7) – cardboard packs.
10 pcs. – blister packs (8) – cardboard packs.
10 pcs. – blister packs (9) – cardboard packs.
15 pcs. – blister packs (2) – cardboard packs.
15 pcs. – blister packs (3) – cardboard packs.
15 pcs. – blister packs (4) – cardboard packs.
15 pcs. – blister packs (6) – cardboard packs.
15 pcs. – blister packs (7) – cardboard packs.
15 pcs. – blister packs (8) – cardboard packs.
15 pcs. – blister packs (9) – cardboard packs.
