Emoksikard
Producer: JSC Borisovsky Plant of Medical Supplies Republic of Belarus
Code of automatic telephone exchange: C05CX
Release form: Liquid dosage forms. Solution for injections.
General characteristics. Structure:
Active ingredient: 150 mg of a metiletilpiridinol of a hydrochloride in 1 ampoule.
Excipients: sodium sulfite anhydrous, dinatrium phosphate a dihydrate, water for injections.
Pharmacological properties:
Pharmacodynamics. Metiletilpiridinol exerts beneficial effect on system of a blood coagulation: slows down aggregation of thrombocytes, reduces the general index of coagulation, extends a blood clotting time. Strengthens process of a fibrinolysis. Improves microcirculation. Reduces permeability of a vascular wall.
Metiletilpiridinol stabilizes membranes of cells of blood vessels and erythrocytes, increases resistance of erythrocytes to a mechanical injury and hemolysis. Has angioprotektorny properties.
Effectively inhibits free radical oxidation of lipids of biomembranes, increases activity of antioxidant enzymes. Stabilizes R-450 cytochrome, possesses anti-toxic action. In the extreme situations which are followed by strengthening of peroxide oxidation of lipids and a hypoxia optimizes biopower processes.
Metiletilpiridinol reduces symptoms of cerebral haemo dysfunction. Increases resistance of a brain to a hypoxia and ischemia. At disturbances of cerebral circulation (ischemic and hemorrhagic) promotes correction of vegetative dysfunctions, facilitates recovery of integrative activity of a brain, improves mnestichesky functions.
Has hypolipidemic effect, reduces synthesis of triglycerides.
Drug possesses the expressed cardioprotective action. Expands coronary vessels, reduces ischemic injury of a myocardium. At a myocardial infarction limits necrosis center size, accelerates reparative processes, contributes to normalization of metabolism of a myocardium. Exerts beneficial effect on the clinical course of a myocardial infarction, reducing the frequency of development of an acute heart failure. Promotes regulation of oxidation-reduction system at a circulatory unefficiency.
Pharmacokinetics. At intravenous administration in a dose of 10 mg/ml the low period of semi-elimination is noted (T1/2 — 18 min. that testifies to the high speed of elimination of drug from blood. Elimination constant size — 0,041 min.; the general clearance of Cl — 214,8 ml/min.; the seeming volume of distribution of Vkazh. — 5,2 l.
Drug quickly gets into bodies and fabrics where there is its deposition and metabolism. 5 metabolites of a metiletilpiridinol presented by the dialkylated and conjugated products of its transformation are revealed. Metabolites of a metiletilpiridinol are excreted by kidneys. In significant amounts in a liver 2-ethyl-6-methyl-3-oxypyridine-phosphate is found.
Indications to use:
In neurology and neurosurgery in complex therapy:
· hemorrhagic stroke,
· an ischemic stroke in the pool of an internal carotid artery and in vertebrobazilyarny system,
· passing disturbances of cerebral circulation,
· chronic insufficiency of cerebral circulation,
· the craniocereberal injury which is followed by brain bruises;
· the postoperative period at the patients with a craniocereberal injury operated concerning Epi - the subdural and intracerebral hematomas which are combined with brain bruises
· before - and the postoperative period at patients with arterial aneurisms and arteriovenous malformation of vessels of a brain.
In cardiology in complex therapy:
· acute myocardial infarction,
· prevention of "reperfusion syndrome",
· unstable stenocardia.
Route of administration and doses:
Doses, duration of a course of treatment are defined individually.
In neurology and neurosurgery apply intravenously kapelno in a daily dose 5-10 mg/kg within 10-12 days. Before introduction Emoksikard part in 200 ml of solution of sodium of chloride isotonic. Enter with a speed of 20-30 thaws a minute. In the subsequent 2 — 3 times a day within 10 — 30 days pass to intramuscular introduction 2-10 ml 30 mg/ml of solution (60 — 300 mg).
In cardiology begin with intravenous drop (20-40 drops a minute) introductions of 20 — 30 ml 30 mg/ml of solution of a metiletilpiridinol (600-900 mg) to 200 ml of solution of sodium of chloride of isotonic 1 — 3 time a day within 5 — 15 days depending on the course of a disease, with the subsequent transition to intramuscular introduction of 2 — 10 ml 30 mg/ml of solution of a metiletilpiridinol (60 — 300 mg) 2 — 3 times a day within 10 — 30 days.
Treatment methylethylpyrrolidinoscrap, in case of its intravenous and intramuscular administration, should be carried out under control of arterial pressure and a functional condition of coagulant and anticoagulative systems of blood.
Features of use:
It is necessary to control constantly during treatment the arterial pressure and coagulability of blood.
Medicine does not influence ability to manage vehicles and the machine equipment.
Side effects:
As a rule, adverse effects at use of drug are not observed.
At intravenous administration — a burning sensation on the vein course; increase in arterial pressure, excitement or drowsiness can be noted. At predisposition to allergic reactions emergence of an itch and erubescence is in rare instances observed.
Interaction with other medicines:
α-tocopherol acetate exponentiates antioxidant effect of a metiletilpiridinol.
Metiletilpiridinol is not recommended to mix with other injection means in one syringe.
Contraindications:
Individual intolerance, pregnancy, the lactation period, children's age up to 18 years.
Overdose:
At overdose strengthening of expressiveness of side effects of drug is possible.
Symptoms: increase in arterial pressure, excitement or drowsiness, a headache, pain in heart, nausea, discomfort in epigastric area. Disturbance of coagulability of blood is possible.
Treatment: drug withdrawal, performing symptomatic therapy, a specific antidote is not present.
Storage conditions:
In the place protected from light, at a temperature not over 30 ºС. To store in the place, unavailable to children. A period of validity - 2 years. Medicine cannot be used after the term specified on the label.
Issue conditions:
According to the recipe
Packaging:
In ampoules on 5 ml. On 10 ampoules together with a leaf insert place in a box from a cardboard; on 5 ampoules in the blister from a PVC film, on 2 blisters together with a leaf insert place in a pack from a cardboard; on 5 or 10 ampoules together with a leaf insert in a pack from a cardboard.