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BFS-Galantamine

Ảnh sản phẩm

Active Element: Galantamin HBr 5mg/5ml

Dosage Form:

Composition

Galantamin HBr 5mg/5ml

Dosage Form

Solution for injection

Indication

indicated during the convalescence and residual phase of poliomyelitis; in neuritis, radiculitis, polyneuritis; spastic paresis and paralysis; myopathy, myasthenia gravis, progressive muscular dystrophy; infantile cerebral paralysis, birth paralysis, nocturnal enuresis, residual paresis following a cerebral hemorrhage, and for elimination of the effect of nondepolarizing neuromuscular blockers. As an antidote in poisoning with Morphinum hydrochloricum. Mild to moderate dementia of Alzheimer's type (tablets).

Dosage Adminstration

The solution for injections is applied subcutaneously, intramuscularly or intravenously. The treatment starts at the lowest effective dose that is gradually increased. The maximum single dose in adults is 10 mg, and the maximum daily dose - 20 mg.
In children it is applied subcutaneously at the following daily doses: aged from 1 to 2 years: 0.25-1 mg; from 3 to 5 years: 0.5-5 mg; from 6 to 8 years: 0.75-7.5 mg; from 9 to 11 years: 1-10 mg; from 12 to 15 years: 1.25-12.5 mg; over 15 years: 12.5-15 mg.
As an anticurare agent, Nivalin is applied intravenously at the following doses: Children aged from 1 to 2 years: 1-2 mg; from 3 to 5 years: 1.5-3 mg; from 6 to 8 years: 2-5 mg; from 9 to 11 years: 3-8 mg; from 12 to 15 years: 5-10 mg. Adults - from 10 to 20 mg.
May be applied by electrophoresis in a quantity of 1-2 ml 0.25% solution.
The course of treatment continues for 1-2 months, and in degenerative diseases of CNS the treatment may continue up to 1 year

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