Meldonium

Pharmstandard-Leksredstva, Russia

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$14 - $21
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Product Overview

Composition

Active ingredient:

meldonium dihydrate (trimethylhydrazinium propionate dihydrate) - 500 mg.

Excipients:

potato starch,

colloidal silicon dioxide (aerosil),

calcium stearate.

pharmachologic effect

Meldonium, an analogue of gamma-butyrobetaine, inhibits gamma-butyrobetaine hydroxinase, reduces the synthesis of carnitine and the transport of long-chain fatty acids through the cell membranes, prevents the accumulation of activated forms of non-oxidized fatty acids in cells - derivatives of acylcarnitine and acylcoenzyme A. -butyrobetaine, which has vasodilating properties.

Under conditions of ischemia, it restores the balance of the processes of oxygen delivery and its consumption in cells, prevents disruption of ATP transport; at the same time activates glycolysis, which proceeds without additional oxygen consumption.

The mechanism of action determines the variety of its pharmacological effects: increased efficiency, decreased symptoms of mental and physical stress, activation of tissue and humoral immunity, cardioprotective effect. In the case of acute ischemic myocardial damage, it slows down the formation of a necrotic zone, shortens the rehabilitation period.

In case of heart failure, it increases myocardial contractility, increases exercise tolerance, and reduces the frequency of angina attacks. In acute and chronic ischemic disorders of cerebral circulation, it improves blood circulation in the ischemic focus, promotes blood redistribution in favor of the ischemic area.

Effective in case of vascular and dystrophic pathology of the fundus. It is also characterized by a tonic effect on the central nervous system, elimination of functional disorders of the somatic and autonomic nervous systems in patients with alcoholism during the period of abstinence.

Indications

As part of the combined therapy of ischemic heart disease, chronic heart failure, cardialgia against the background of dyshormonal myocardial dystrophy.

Violations of the blood supply to the brain (stroke, cerebrovascular insufficiency). Complex therapy of alcohol withdrawal syndrome.

Reduced performance, chronic physical stress, postoperative period to accelerate the rehabilitation process.

Application during pregnancy and lactation

Not recommended during pregnancy (efficacy and safety have not been studied).
 
If necessary, the appointment of the drug during lactation should stop breastfeeding.

Contraindications

Hypersensitivity to the drug, increased intracranial pressure (in violation of venous outflow and intracranial tumors), pregnancy, lactation, age up to 18 years (efficacy and safety have not been established).

Side effects

Rarely - allergic reactions (skin redness, itching, swelling), dyspeptic symptoms, tachycardia, agitation, decreased blood pressure.

Interaction

Strengthens the effect of coronary dilating and some antihypertensive drugs, cardiac glycosides.

It can be combined with antianginal drugs, anticoagulants, antiplatelet agents, antiarrhythmics, diuretics, bronchodilators.

In view of the possible development of moderate tachycardia and arterial hypotension, caution should be exercised when combined with peripheral vasodilators and antihypertensive drugs (including nifedipine, alpha-blockers).

How to take, course of administration and dosage

Inside, before meals.

Stable angina pectoris, chronic heart failure - as part of complex therapy, 500-1000 mg per day, using the entire dose at once or dividing it by 2 times. The course of treatment is 4-6 weeks.

Cardialgia against the background of dyshormonal myocardial dystrophy - 250 mg 2 times a day (morning and evening). The course of treatment is 12 days.

Violations of the blood supply to the brain (stroke, cerebrovascular insufficiency) - 500-1000 mg per day, preferably in the morning. The course of treatment is 4-6 weeks. Withdrawal alcohol syndrome - 500 mg 4 times a day. The course of treatment is 7-10 days.

With a decrease in working capacity and chronic physical overstrain, in the postoperative period to accelerate the rehabilitation processes - 250 mg 4 times a day. The course of treatment is 10-14 days. If necessary, the treatment is repeated after 2-3 weeks. Athletes are prescribed 500-1000 mg 2 times a day before training. The duration of the course in the preparatory period is 14-21 days, during the competition period - 10-14 days.

Overdose

There is no information.

Special instructions

May test positive during doping control.

Storage conditions

In a dry place inaccessible to children at a temperature not higher than 25 for AS

Shelf life

4 years.

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