Active substanceTrimetazidineTrimetazidine
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  • Dosage form: & nbspfilm coated tablets
    Composition:

    1 tablet, film-coated, contains

    active substance: trimetazidine dihydrochloride 0.02 g

    Excipients: lactose (sugar milk), potato starch, copovidone, calcium stearate.

    sheath - Opadrai II (series 85): polyvinyl alcohol, partially hydrolysed, macrogol-3350, talc, titanium dioxide E 171.

    Description:

    The tablets covered with a film membrane of white color, round, biconcave, on a cross-section are visible two layers.

    Pharmacotherapeutic group:antihypoxic agent
    ATX: & nbsp

    C.01.E.B   Other drugs for the treatment of heart disease

    C.01.E.B.15   Trimetazidine

    Pharmacodynamics:

    Trimetazidine has antianginal, coronarodilating, antihypoxic and hypotensive effects.

    Directly affecting the cardiomyocytes and neurons of the brain, it optimizes their metabolism and function. Cytoprotective effect is due to - increased energy potential and activation of oxidative decarboxylation rationalization oxygen consumption (increasing aerobic glycolysis and fatty acid oxidation blockade).

    Supports contractility of the myocardium, prevents the reduction of intracellular (Content of adenosine triphosphate and phosphocreatinine, in conditions of acidosis normalizes the functioning of membrane ion channels, prevents accumulation of calcium and sodium in cardiomyocytes, normalizes the intracellular content of potassium ions, reduces intracellular acidosis and increased phosphate content due to myocardial ischemia and reperfusion .Prevents the damaging effect of free radicals, preserves the integrity of cell membranes, prevents the activation of neutrophils in the zone, ischemia, prolongs the duration of the electrical potential, reduces the yield of creatine phosphokinase from cells and the severity of myocardial ischemic damage.

    When angina pectoris reduces the frequency of attacks (reduces the consumption of nitrates), after 2 weeks of treatment increases tolerance to physical exertion, blood pressure. Improves hearing and results of vestibular samples in patients with pathology of ENT organs, reduces dizziness and tinnitus. In vascular pathology, the eye restores the functional activity of the retina.

    Pharmacokinetics:After taking trimetazidine quickly and almost completely absorbed in the gastrointestinal tract. Bioavailability is 90%. Time to reach the maximum concentration in blood plasma - 2 hours. The maximum concentration after a single dose of 20 mg of thymetazidine is about 55 ng / ml. The connection with plasma proteins is 16%. Easily penetrates through the histohematological barriers. The half-life is 4.5-5 hours. It is excreted by the kidneys (about 60% - unchanged).
    Indications:

    Ischemic heart disease, prevention of angina attacks (in complex therapy);

    Chorioretinal vascular disorders;

    Vertigo of vascular origin;

    Cohleo-vestibular disorders of ischemic nature (tinnitus, hearing impairment, Meniere's disease).

    Contraindications:

    Hypersensitivity to any of the components of the drug, including lactose intolerance; renal failure (creatinine clearance below 15 ml / min); severe liver dysfunction; pregnancy; lactation period; age to 18 years (efficacy and safety not established).

    Dosing and Administration:

    Inside, with food.

    The recommended dosage regimen is 1 tablet (20 mg) 2-3 times a day (40-60 mg per day). The course of treatment on the recommendation of a doctor.

    Side effects:

    Allergic reactions (skin itching). Rarely: headache, a feeling of strong palpitations; from the gastrointestinal tract - weak dyspeptic phenomena (nausea, vomiting, gastralgia).

    Overdose:

    At present, no cases of drug overdose have been reported.

    Interaction:

    Not described.

    Special instructions:

    Against the background of drug treatment in patients with coronary heart disease there is a significant decrease in the daily requirement for nitrates.

    Effect on the ability to drive transp. cf. and fur:

    The use of the drug does not affect the ability to drive a car and perform work that requires a high rate of psychomotor reactions.

    Form release / dosage:

    Tablets, film-coated, 20 mg.

    Packaging:

    For 10 tablets in a contour mesh box made of polyvinylchloride film and aluminum foil printed lacquered.

    2, 3 or 6 contour mesh packages together with the instruction for use are placed in a bundle.
    Storage conditions:

    In the dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:On prescription
    Registration number:LS-000452
    Date of registration:16.10.2009
    The owner of the registration certificate:VALENTA PHARM, PAO VALENTA PHARM, PAO Russia
    Manufacturer: & nbsp
    Information update date: & nbsp25.10.2015
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