Active substanceTrimetazidineTrimetazidine
Similar drugsTo uncover
  • Angiosyl® retard
    pills inwards 
  • Antisthene
    pills inwards 
    OZONE, LLC     Russia
  • Antisthene MB
    pills inwards 
    OZONE, LLC     Russia
  • Vero-Trimetazidine
    pills inwards 
    VEROPHARM SA     Russia
  • Deprenorm® MB
    pills inwards 
  • Deprenorm® MB
    pills inwards 
  • Predisin®
    pills inwards 
    GEDEON RICHTER, OJSC     Hungary
  • Preductal® MB
    pills inwards 
    SERVICE, CJSC     Russia
  • Preductal® OD
    capsules inwards 
    SERVICE, CJSC     Russia
  • Precard
    pills inwards 
  • Romekor
    pills inwards 
  • Romekor MB
    pills inwards 
  • Triducard®
    pills inwards 
    NORTH STAR, CJSC     Russia
  • Trimectal® MB
    pills inwards 
    VERTEKS, AO     Russia
  • Tremet
    pills inwards 
  • Trimetaside
    pills inwards 
  • Trimetazidine
    pills inwards 
    ZIO-HEALTH, JSC     Russia
  • Trimetazidine
    pills inwards 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Trimetazidine
    pills inwards 
  • Trimetazidine
    pills inwards 
  • Trimetazidine
    pills inwards 
  • Trimetazidine
    capsules inwards 
    VERTEKS, AO     Russia
  • Trimetazidine
    pills inwards 
    ALSI Pharma, ZAO     Russia
  • Trimetazidine
    pills inwards 
    VALENTA PHARM, PAO     Russia
  • Trimetazidine MB
    pills inwards 
  • Trimetazidine MB
    pills inwards 
    ATOLL, LLC     Russia
  • Trimetazidine MB
    pills inwards 
    VALENTA PHARM, PAO     Russia
  • Trimetazidine MB
    pills inwards 
  • Trimetazidine MB-Teva
    pills inwards 
  • Trimetazidine-Biocom MB
    pills inwards 
    BIOKOM, CJSC     Russia
  • Trimetazidine-Teva
    pills inwards 
  • Trimittard MB
    pills inwards 
    ROMFARMA, OOO     Russia
  • Dosage form: & nbspmodified release tablets coated with a film coating
    Composition:

    One tablet contains:

    active substance: trimetazidine dihydrochloride 35 mg

    Excipients: hypromellose (Methocel K100M) 42 mg, hypromellose (Methocel K15M) 42 mg, silicon dioxide colloid (aerosil) 1.4 mg, magnesium stearate 1.4 mg, microcrystalline cellulose 158.2 mg; Opadrai II pink - 8,4 mg (talc - 1,2432 mg, macrogol - 1,6970 mg, titanium dioxide - 2,0360 mg, polyvinyl alcohol - 3,3600 mg, iron oxide yellow - 0,0311 mg, iron oxide red - 0.0302 mg, iron oxide black - 0.0025 mg).

    Description:Round biconvex tablets, covered with a film coating of pink color. On the cross section, the nucleus is white or almost white in color.
    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:

    Has antihypoxic effect.

    By directly affecting cardiomyocytes and neurons of the brain, the drug optimizes their metabolism and function. The cytoprotective effect is due to an increase in the energy potential, activation of oxidative decarboxylation, and rationalization of oxygen consumption (enhancement of aerobic glycolysis and fat oxidation blockade).

    Trimetazidine supports myocardial contractility, prevents the reduction of intracellular adenosine triphosphatase (ATP) and phosphocreatine. Under acidosis, it normalizes the functioning of ion channels of membranes, prevents the accumulation of potassium and sodium ions 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 ischemia zone, prolongs the duration of the electrical potential, reduces the yield of creatine phosphokinase (CK) from cells and the severity of ischemic myocardial damage.

    Trimetazidine reduces the frequency of angina attacks, reduces the need for nitrates, after 2 weeks of use increases exercise tolerance, and sharp fluctuations in blood pressure (BP) decrease. Reduces dizziness and tinnitus. In vascular pathology, the eye improves the functional activity of the retina.

    Pharmacokinetics:

    After taking the drug inside trimetazidine quickly and almost completely absorbed in the gastrointestinal tract (GIT). Bioavailability is 90%. Time to reach the maximum concentration in blood plasma - 3-5 hours.

    The stable state is reached after 60 hours. The volume of distribution is 4.8 l / kg, which implies good distribution, diffusion, distribution in tissues.

    The connection with blood plasma proteins is 16%.

    Trimetazidine is excreted from the body mainly by the kidneys (about 60% - unchanged). Half-life of about 7 hours, in patients older than 65 years - about 12 hours.

    Renal clearance of trimetazidine directly correlates with the clearance of creatinine (CC), the hepatic clearance decreases with age.

    Easily penetrates through the histohematological barriers.

    Indications:

    Ischemic heart disease: prevention of angina attacks (in complex therapy).

    Vestibulo-cochlear disorders of ischemic etiology (dizziness, tinnitus, hearing impairment).

    Chorioretinal disorders with ischemic component.

    Contraindications:

    - hypersensitivity to any component of the drug;

    - renal failure (QC less than 15 ml / min.);

    - severe liver dysfunction;

    - pregnancy;

    - lactation period

    - age to 18 years (efficacy and safety not established).

    Pregnancy and lactation:

    The drug is contraindicated in pregnancy due to the lack of clinical data on the safety of its use. It is not known whether trimetazidine with breast milk. Therefore, if it is necessary to prescribe the drug during lactation,should stop breastfeeding.

    In experimental studies, no installationteratogenic effect of threemetazidine.

    Dosing and Administration:

    Inside, during a meal.

    Trimitar MV is prescribed 1 tablet 2 times a day (morning and evening).

    The course of treatment is recommended by a doctor.

    Side effects:

    The incidence of side effects is given in the following gradation: very often (> 1/10); often (> 1/100, <1/10); infrequently (> 1/1000, <1/100); rarely (> 1/10000, <1/1000); very rarely (<1/10000), including individual messages.

    From the digestive system: often - abdominal pain, diarrhea, indigestion, nausea, vomiting.

    Common violations: often - asthenia.

    From the central nervous system: often - dizziness, headache; very rarely - extrapyramidal symptoms (tremor, rigidity, akinesia), reversible after drug withdrawal.

    From the skin: often - skin rash, itching, hives.

    From the cardiovascular system: rarely - orthostatic hypotension, "tides" of blood to the skin of the face.

    Overdose:

    Data on overdose are limited; In case of an overdose, symptomatic therapy should be given.

    Interaction:

    There is no information.

    Special instructions:

    Do not use to stop angina attacks!

    The drug is not indicated for the initial course of therapy for unstable angina or myocardial infarction.

    In the case of an attack of angina pectoris, the treatment should be reviewed and adapted.

    If you skip one or more doses of the drug, you can not take a higher dose to the next dose!

    Effect on the ability to drive transp. cf. and fur:It is advisable to use caution when driving vehicles and engaging in other potentially dangerous activities that require increased concentration and speed of psychomotor reactions.
    Form release / dosage:

    Tablets with prolonged release, film-coated, 35 mg.

    Packaging:

    10 tablets per contour cell packaging made of polyvinylchloride film and aluminum foil.

    6 contour squares with instructions for use are placed in a pack of cardboard.

    Storage conditions:

    In a place protected from moisture 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:LP-000795
    Date of registration:03.10.2011
    The owner of the registration certificate:ROMFARMA, OOO ROMFARMA, OOO Russia
    Manufacturer: & nbsp
    LEKFARM, SOOO Republic of Belarus
    Information update date: & nbsp24.10.2015
    Illustrated instructions
      Instructions
      Up