Troxevasin 100g of 2% gel for topical application

The instruction for medical use of TROKSEVAZIN® medicine the Trade name of Troksevazin® the International unlicensed name Trokserutin Lekarstvennaya a form Gel for external use of 2% Structure of 100 g of gel contains active agent - trokserutin 2 g, excipients: carbomer, disodium EDTA salt, a benzalkoniya chloride, trietanolamine, water purified. The description Uniform gel from yellow till light brown color. Pharmacotherapeutic group Cardiovascular system. Vazoprotektora. Kapillyarostabiliziruyushchy means. Bioflavonoids. Trokserutin. The ATX C05CA04 code the Pharmacological Pharmacokinetics At properties topical administration of Troksevazin® gel active component of drug is easily released from a water-soluble basis of gel and gets through skin in 30–60 minutes, and into hypodermic fatty tissue — in several hours, creating high concentration in the inflamed fabrics. A pharmacodynamics of Troksevazin® – a complex of bioflavonoids which contains not less than 95% of a trokserutin. It reduces permeability and fragility of capillaries, raises a tone of unstriated muscles of venous vessels, has antiedematous effect, eliminates inflammation of paravenous fabrics. Stabilizes walls of capillaries and has moderate antiagregantny effect. Improves a trophicity of fabrics, reduces the pain and other pathological manifestations connected with venous insufficiency. Is an antagonist of vazodilatiruyushchy effects of a histamine, bradykinin, acetylcholine. In this connection, Troksevazin® shows venomotor, kapillyaroprotektorny, antiexudative and haemo static effects. Working as antioxidant, suppresses peroxide oxidation of lipids. Indications - the pains and hypostases of the lower extremities caused by chronic venous insufficiency - a varicosity - pains and hypostases of traumatic origin, a hematoma, dislocations, stretchings, bruises, muscular spasms. The route of administration and doses apply Gel in the morning and in the evening on affected areas of skin by means of the easy massing movements before its full absorption in skin. Gel can be used also for imposing of compresses. Gel should be applied to ensuring adequate therapeutic effect regularly before total disappearance of hypostases and other symptoms. Then treatment can be interrupted. At emergence of repeated symptoms the treatment should be resumed. The course of treatment is appointed by the doctor. If during drug use the expressiveness of symptoms of a disease does not decrease, it is necessary to consult with the doctor. Side effects Seldom - allergic skin reactions (urticaria, eczema, dermatitis) of the Contraindication - hypersensitivity to any component of drug - the I trimester of pregnancy - the children's age up to 15 years Medicinal interactions Strengthens effect of ascorbic acid on structure and permeability of a vascular wall. The special instructions Gel apply only on the damaged sites of skin. Not to apply on open wounds, eyes and mucous membranes. Use of drug at advanced age is possible. Pregnancy and the period of a lactation to Apply Troksevazin® during pregnancy (II and III trimesters) and in the period of a lactation perhaps if the expected advantage for mother exceeds potential risk for a fruit and the child. Features of influence of drug on ability to run the vehicle or potentially dangerous mechanisms Medicine does not influence performance of potentially dangerous types of activity requiring special attention and fast reactions. The overdose At external use of Troksevazina® the probability of overdose is absent. A form of release and packing On 40 g or 100 g of drug in tubas aluminum or laminatny. On 1 tuba together with the instruction for medical use in the state and Russian languages place in a pack from cardboard. Storage conditions In the place protected from light at a temperature not above 25 °C. Not to freeze! To store out of children's reach! Not to apply a period of storage of 5 years after an expiration date. Prescription status Without prescription ABP Balkanpharma-Troyan Producer Bulgaria, 5600. A trojan, St. Krayrechn 1 Owner of the Registration Certificate of Balkanpharma-Troyan of the ABP, Bulgaria the Name, the address and a contact information (phone, the fax, e-mail) of the organization in the territory of the Republic of Kazakhstan, the accepting claim (offer) on quality of medicines from consumers and responsible for post-registration observation of safety medicinal means: Ratiopharm Kazakhstan LLP, 050059 (A15E2P), Almaty, Al-Farabi Ave. 17/1, BC Nurly-Tau, 5B, 6 floor. Phone number: (727) 3251615, e-mail: safety.kazakhstan@tevapharm.com, web website: www.teva.kz