Application instruction:
Korvaltab – drug with vasodilating, sedative and moderately spasmolytic action.
Korvaltab release in the form of tablets: round, flat, with facets, almost white or white color with impregnations, with a specific smell (on 10 pieces in blisters, on 2 or 10 blisters in a cardboard pack).
Active ingredients are a part of 1 tablet:
Auxiliary components: magnesium stearate, microcrystallic cellulose, potato starch, beta cyclodextrin, monohydrate of lactose.
It is contraindicated to apply the medicines containing phenobarbital at a diabetes mellitus, an acute myocardial infarction, the expressed arterial hypotension, a depression, alcoholism, a myasthenia, medicinal and drug addiction, an obstructive syndrome, respiratory diseases with an asthma.
To the feeding and pregnant women Korvaltab do not appoint.
As lactose is a part of drug, patients with hereditary intolerance of lactose galactose are not recommended to accept it.
Korvaltab patients need to take with caution with arterial hypotension, hyperkinesias, a hyperthyroidism, a hypoadrenalism, acute and constant pains, acute intoxication medicines.
Korvaltab accept inside, to food.
The dosage and duration of a medical course is established by the doctor individually.
As a rule, Korvaltab appoint 2-3 times a day 1-2 tablets. The single dose increased to 3 tablets is applied at treatment of spasms of coronary vessels and tachycardia.
Korvaltab is usually had well.
In some cases development of the following side effects can be observed:
Long reception of the medicines containing bromine can lead to poisoning with bromine, characterized by such symptoms as: depressive mood, oppression of the central nervous system, ataxy, apathy, confusion of consciousness, conjunctivitis, dacryagogue, rhinitis, purpura or acne.
Usually these side effects take place at decrease in a dose of Korvaltab or the termination of therapy.
During treatment of the use of alcoholic drinks it is necessary to avoid.
The phenobarbital which is Korvaltab's part can result in risk of development of a syndrome of Stephens-Johnson and Layell (it is the most probable – in the first weeks of use).
Long therapy is not recommended as long administration of drug can cause medicamentous dependence, accumulation of bromine in an organism and, as a result, poisoning with it.
In cases if pains in heart after Korvaltab's reception do not pass, it is necessary to see a doctor for an exception of an acute coronary syndrome.
Korvaltab can cause dizziness and drowsiness therefore during therapy by the patient it is not recommended to work with dangerous mechanisms, to manage vehicles and to perform the works demanding bystry motor and mental reactions and special attention.
At simultaneous use of Korvaltab with some medicines there can be undesirable effects:
To store in the place, unavailable to children, at a temperature up to 25 °C.
Period of validity – 2 years.
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