Venolife (Gel) Instructions for Use
Marketing Authorization Holder
Akrikhin Chemical and Pharmaceutical Plant, JSC (Russia)
Contact Information
AKRIKHIN JSC (Russia)
ATC Code
C05BA53 (Heparin in combination with other drugs)
Active Substances
Dexpanthenol (Rec.INN registered by WHO)
Heparin sodium (Rec.INN registered by WHO)
Troxerutin (Rec.INN registered by WHO)
Dosage Form
| Venolife | Gel for external use 0.25 g+5 g+2 g/100 g: tubes 40 g or 100 g |
Dosage Form, Packaging, and Composition
Gel for external use transparent or almost transparent, light yellow in color, with a specific odor.
| 100 g | |
| Heparin sodium calculated on dry substance | 0.25 g (30000 IU) |
| Dexpanthenol calculated on 100% substance | 5 g |
| Troxerutin calculated on 100% substance | 2 g |
Excipients: phenylethanol, propylene glycol, carbomer 940 or 980, trometamol, purified water.
40 g – aluminum tubes (1) – cardboard packs.
100 g – aluminum tubes (1) – cardboard packs.
Clinical-Pharmacological Group
A drug with antithrombotic, angioprotective, venotonic, and tissue regeneration-improving action for topical use
Pharmacotherapeutic Group
Direct-acting anticoagulant for topical use + other drugs
Pharmacological Action
A combined drug for external use, the pharmacological properties of which are determined by the action of its constituent substances.
Heparin is a direct-acting anticoagulant, a natural anticoagulant factor of the body. It has an anti-inflammatory effect, promotes the regeneration of connective tissue by inhibiting the activity of hyaluronidase; prevents thrombus formation, activates the fibrinolytic properties of blood, and improves local blood flow.
Dexpanthenol is a provitamin B5 that is converted in the skin into pantothenic acid, which is part of coenzyme A, which plays an important role in acetylation and oxidation processes. By improving metabolic processes, dexpanthenol promotes the regeneration of damaged tissues; improves the absorption of heparin.
Troxerutin is an angioprotective agent. It has P-vitamin activity, in particular, it reduces vascular-tissue permeability and capillary fragility, promotes the normalization of microcirculation and tissue trophism, reduces congestion in the veins and paravenous tissues, and has an anti-exudative and anti-inflammatory effect.
Pharmacokinetics
With topical application, the active substances are quickly absorbed through the skin. Heparin accumulates in the upper layers and actively binds to skin proteins, dexpanthenol penetrates all layers of the skin and is converted into pantothenic acid, troxerutin is detected in the dermis after 30 minutes, and after 2-5 hours – in the subcutaneous adipose tissue.
Indications
- Edema-pain syndrome and microcirculatory-trophic disorders caused by venous insufficiency of the lower extremities (varicose veins, acute and chronic thrombophlebitis, post-thrombophlebitic syndrome, chronic lymphostasis);
- Soft tissue injuries (hematomas, dislocations, sprains);
- To accelerate granulation and epithelialization of trophic ulcers in the regeneration phase (in the absence of pronounced exudation).
ICD codes
| ICD-10 code | Indication |
| I80 | Phlebitis and thrombophlebitis |
| I83 | Varicose veins of lower extremities |
| I83.2 | Varicose veins of lower extremities with ulcer and inflammation |
| I87.0 | Postthrombotic syndrome |
| I87.2 | Venous insufficiency (chronic) (peripheral) |
| I89 | Other noninfective disorders of lymphatic vessels and lymph nodes |
| L89 | Decubitus ulcer and pressure area |
| L98.4 | Chronic skin ulcer, not elsewhere classified |
| T14.0 | Superficial injury of unspecified body region (including abrasion, bruise, contusion, hematoma, bite of nonvenomous insect) |
| T14.3 | Dislocation, sprain and strain of joint and ligament of unspecified body region |
| ICD-11 code | Indication |
| BD70.0 | Superficial thrombophlebitis of lower extremities |
| BD70.Z | Superficial thrombophlebitis, unspecified |
| BD71.4 | Deep vein thrombosis of lower extremity |
| BD74.1Z | Varicose veins of lower extremities, unspecified |
| BD74.Z | Chronic venous insufficiency of lower extremities, unspecified |
| BD7Z | Diseases of veins, unspecified |
| BD9Z | Disease of lymphatic vessels or lymph nodes, unspecified |
| EA40 | Tropical phagedenic ulcer |
| EF60 | Ischemic ulceration of the skin |
| EH90.Z | Pressure ulcer of unspecified degree |
| EH92 | Dermatoses provoked by friction or mechanical impact |
| EH92.1 | Blister due to friction |
| EM0Z | Unspecified skin disorder |
| ME60.2 | Ulcerative skin lesion of unspecified nature |
| ND56.0 | Superficial injury of unspecified body region |
| ND56.3 | Dislocation, sprain or strain of unspecified body region |
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. |
Externally. Apply a thin layer to the affected area 2-3 times/day, evenly distributing over the skin surface with light rubbing movements until completely absorbed. The course of treatment is 2-3 weeks.
For trophic ulcers with weak exudation, before using the drug, the wound surface should be cleaned of exudate and necrotic tissues, if necessary, rinsed with a 3% hydrogen peroxide solution, 1:5000 nitrofural solution, or 0.05% chlorhexidine digluconate solution and dried. The gel is applied in a uniform thin layer so that the entire affected surface is covered with the drug, and a sterile gauze bandage is applied. Dressings are changed once a day. With the open method of treatment, the drug is applied 1-2 times/day. The duration of treatment is determined by the dynamics of epithelialization.
Adverse Reactions
Possible local manifestations of allergic reactions (skin rash, itching).
Contraindications
- Open infected wounds or wounds with abundant exudation at the site of application;
- Children under 1 year of age;
- Hypersensitivity to the components of the drug.
Use in Pregnancy and Lactation
Venolife can be used during pregnancy and lactation (breastfeeding).
Pediatric Use
Contraindicated for use in children under 1 year of age.
Special Precautions
Venolife is not intended for use in ophthalmology, for intravaginal and rectal administration.
Overdose
Overdose is unlikely due to the low systemic absorption of the gel components.
Drug Interactions
No interactions of Venolife with other medicinal products have been identified.
Storage Conditions
The drug should be stored out of the reach of children at a temperature from 15°C (59°F) to 25°C (77°F).
Shelf Life
Shelf life – 2 years. Do not use after the expiration date.
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 Disclaimer