Venolife gel d / nar. approx. 0.25% + 5% + 2% tube 100g
Dosage:
0.25% + 5% + 2% x 100g
0.25% + 5% + 2% x 40g
Scope of the drug
Heart, vessels, blood
Release form
Gel
Manufacturer country
Russia
Package quantity, pcs
one
Way of introduction
On the skin
Amount in a package
100 g
Dosage form
gel for external use
Manufacturer
Akrikhin, Russia
Structure
Active ingredients: troxerutin 2g
dexpanthenol 5 g
sodium heparin 0.25 g (30,000 IU)
Excipients: phenylethyl alcohol, propylene glycol, carbomer 940 or 980, trometamol, purified water.
pharmachologic effect
Venolife is a combined preparation for external use.
Dexpanthenol, a provitamin B5, is converted in the skin into pantothenic acid, which is a part of coenzyme A, which plays an important role in the processes of acetylation and oxidation.
Improving metabolic processes, dexpanthenol promotes the regeneration of damaged tissues
improves the absorption of heparin.
Heparin is a direct anticoagulant, a natural anticoagulant factor in 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, improves local blood flow.
Troxerutin is an angioprotective agent.
It has P-vitamin activity, in particular, it reduces vascular tissue permeability and capillary fragility, contributes to the normalization of microcirculation and tissue trophism, reduces congestion in veins and paravenous tissues, and has anti-edema and anti-inflammatory effects.
In addition, due to the presence of an antiseptic preservative, phenylethyl alcohol, the drug has a bactericidal and fungicidal effect, helping to prevent infection of the wound surface.
The composition of the gel base provides the drug with moderate hyperosmolar properties.
Indications
Soft tissue injuries (hematomas, dislocations, sprains)
edematous 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)
to accelerate the granulation and epithelization of trophic ulcers in the regeneration phase (in the absence of pronounced exudation).
Application during pregnancy and lactation
Venolife® is not contraindicated during pregnancy and lactation.
Contraindications
Hypersensitivity, open, infected wounds or wounds with profuse exudation.
Side effects
Local manifestations of allergic reactions (skin rash, itching) are possible.
How to take, course of administration and dosage
Locally.
Apply in a thin layer to the affected area and around it 2-3 times a day, evenly spreading over the skin surface with light rubbing movements until completely absorbed.
The course of treatment is 2-3 weeks.
The need for further treatment is determined by the attending physician, based on the severity of the pathological process and the results of clinical tests.
In case of recurrence of the disease, the course of treatment can be carried out 2-3 times a year.
In case of trophic ulcers with weak exudation, before using the drug, the wound surface is cleaned of exudate and necrotic tissues, if necessary, washed with a solution of hydrogen peroxide 3%, furacilin 1: 5000 or chlorhexidine bigluconate 0.05% and dried.
The gel is applied in a uniform thin layer so that the entire affected surface is covered with the preparation, and a sterile gauze bandage is applied.
Dressings are changed once a day.
With an open method of treatment, the drug is applied 1–2 times a day.
The duration of treatment is determined by the dynamics of epithelialization.
Special instructions
Venolife is not intended for use in ophthalmology, for intravaginal and rectal administration.
Release form
Gel for external use
Storage conditions
At a temperature of 15-25 ° C
Shelf life
2 years
Active substance
Heparin sodium, Dexpanthenol, Troxerutin
Terms of dispensing from pharmacies
Without recipe
Name ENG
VENOLIFE
Clinical and pharmacological group
The drug with antithrombotic, angioprotective, venotonic and improving tissue regeneration action for external use
ATX code
Heparin in combination with other drugs
Dosage
0.25% + 5% + 2% x 100g
Structure
Active ingredients: troxerutin 2g
dexpanthenol 5 g
sodium heparin 0.25 g (30,000 IU)
Excipients: phenylethyl alcohol, propylene glycol, carbomer 940 or 980, trometamol, purified water.
Indications
Edematous 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 the granulation and epithelization of trophic ulcers in the regeneration phase (in the absence of pronounced exudation).
Contraindications
Hypersensitivity to Venolife components, open infected wounds or wounds with profuse exudation.
Storage conditions and periods
At a temperature of 15-25 degrees.
Expiration date: 2 years
INN / Active ingredient
troxerutin, dexpanthenol, sodium heparin
Specifications
Scope of the drug
Heart, vessels, blood
Release form
Gel
Manufacturer country
Russia
Package quantity, pcs
one
Way of introduction
On the skin
Vacation conditions
Without recipe
Brand name
Akrikhin
The amount of the dosage form in the primary package
100 g
Primary packaging type
Tuba
Type of consumer packaging
Pack of cardboard
Anatomical and therapeutic characteristics
C05BA53 Heparin sodium, in combination with other drugs
Dosage form
Gel for external use
Expiration date in days
730
Package weight, g
45
Category
:
Improving blood circulation
,
Angioprotectors and microcirculation correctors
,
Lipid-lowering drugs
,
Hematopoietic stimulants
Mode of application
:
The drug is used externally. < br> < br> The gel is applied in a thin layer to the affected area 2-3 times / day, evenly spreading over the skin surface with light rubbing movements until completely absorbed. The course of treatment is 2-3 weeks. The need for further treatment is determined by the attending physician, based on the severity of the pathological process and the results of clinical tests. < br> < br> In case of relapse of the disease, the course of treatment can be carried out 2-3 times a year. < br> < br> In trophic ulcers with weak exudation before using the drug, the wound surface is cleaned of exudate and necrotic tissues, if necessary, washed with 3% hydrogen peroxide solution, furacilin solution 1: 5000 or 0.05% chlorhexidine bigluconate solution and dried. The gel is applied in an even thin layer so thatso that the entire affected surface is covered with the drug, and a sterile gauze bandage is applied. Dressings are changed once a day. With an open method of treatment, the drug is applied 1-2 times / day. The duration of treatment is determined by the dynamics of epithelialization.
Pharmaco-therapeutic group
:
Direct-acting anticoagulant for topical use + other drugs
Dosage (volume) of the substance in the preparation
:
sodium heparin in terms of dry matter 0.25 g (30,000 IU) < IR> dexpanthenol in terms of 100% substance 5 g < IR> troxerutin in terms of 100% substance 2 g
Information on technical characteristics, delivery set, country of manufacture