MEDOTILIN
(Choline alfoscerate)




COMPOSITION

A capsule contains:

Active ingredients: choline alfoscerate (as choline alfoscerate hydrate) 400 mg.

Excipients: glycerin, purified water.

Composition of capsule coating: gelatin, sorbitans (D-sorbitol and 1.4-sorbitan), sodium ethyl parahydroxybenzoate, sodium propylparahydroxibenzoate, titanium dioxide, yellow iron oxide.

THERAPEUTIC INDICATIONS

- rehabilitation period after ischemic and hemorrhagic stroke, craniocerebral injury;

- degenerative and involutional psycho-organic syndromes and consequences of cerebrovascular insufficiency, such as primary or secondary disturbances of mnestic functions characterized by memory disturbances, confused consciousness, disorientation, lack of motivation and initiative, as well as ability to concentrate;

-emotional and behavioral changes: emotional lability, increased irritability, decreased interest; age-related pseudo melancholy;

- multi-infarction dementia.

CONTRAINDICATIONS

- Hypersensitivity to the drug or any drug components;

- pregnancy;

- lactation.

ADVERSE EFFECTS

Allergic reactions, nausea (the result of stimulation of dopaminergic).

As a rule, the drug is well-tolerated in case of long-term administration.

DOSAGE AND ADMINISTRATION

Medotilin is administered orally before the meals, 1 capsule 3 times daily. The duration of treatment is 3 to 6 months.

The duration of treatment is determined by the doctor with due regard to the peculiarities of the disease, achieved therapeutic effect and tolerability of drug.

SPECIAL INDICATIONS

If nausea develops after administration of Medotilin, the dose should be decreased.

PREGNANCY AND LACTATION

The administration of Medotilin during pregnancy is contraindicated. During the treatment lactation should be withdrawn.

MANUFACTURED FORM AND PACKAGE

Soft gelatin capsules

14 capsules in a blister.

1 or 2 blisters with a leaflet in a carton box.

Alimentary Tract and Metabolism

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