Active substanceCholine alfoscerateCholine alfoscerate
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  • Dosage form: & nbsporal solution
    Composition:

    1 bottle 7 ml contains:

    Active substance: choline alphoscerate, in terms of 100% of the substance - 600 mg.

    Excipients: methyl parahydroxybenzoate - 8.0 mg, propyl parahydroxybenzoate - 2.4 mg, purified water - up to 7.0 ml.

    Description:A clear, colorless solution.
    Pharmacotherapeutic group:Nootropic remedy
    ATX: & nbsp

    N.07.A.X.02   Choline alfoscerate

    Pharmacodynamics:

    Choline alfoscerate (L-α-glycerylphosphorylcholine) is a prodrug, from which the choline precursor of acetylcholine is released by hydrolysis. The latter is an agonist of all subtypes of cholinergic receptors.

    Choline alphoscerate contains 40.5% choline by weight, released from the compound in the brain; Choline is involved in the biosynthesis of acetylcholine, is a donor of the methyl groups, and participates in other plastic reactions in the body. Alphoscerate ion is metabolized to the glycerophosphate ion.

    Acetylcholine directly participates in the transmission of a nerve impulse, both in the central and peripheral nervous system. Glycerophosphate is included in various metabolic pathways, including participates in the synthesis of phosphatidylcholine (one of the phospholipids of cell membranes). Thus, the drug acts on the cholinergic transmission of the nerve impulse, the plasticity of the neuron membrane.

    It is assumed that the drug reduces cognitive impairment in degenerative and cardiovascular lesions of the brain (including cerebrovascular insufficiency and some forms of dementia).

    Pharmacokinetics:

    Suction and distribution

    After ingestion, absorption is about 95%.

    Easily penetrates the blood-brain barrier, accumulates mainly in the brain (concentration reaches 45% of the level in the blood plasma), lungs and liver.

    Metabolism and excretion

    Choline and glycerophosphate ion are included in the total metabolism, therefore it is not possible to trace their real elimination from the body. However, it is known that they are metabolized to carbon dioxide, water, phosphates and nitrogen-containing products.

    Indications:

    Violations of cerebral circulation according to the ischemic type (acute and recovery period) and hemorrhagic type (recovery period). Psycho-organic syndrome on the background of involutional and degenerative processes of the brain.

    The consequences of cerebrovascular insufficiency, including cerebral blood flow disorders, or primary and secondary cognitive impairment in the elderly, characterized by memory impairment, confusion, disorientation, decreased motivation and initiative, decreased concentration of attention.

    Violations of behavior and affective sphere in old age; emotional lability, increased irritability, decreased interest; senile pseudomelanchia.

    Multi-infarct dementia.

    Contraindications:

    Hypersensitivity to the components of the drug, hemorrhagic stroke (acute stage), pregnancy, breastfeeding, children under 18 years of age (efficacy and safety not established).

    Pregnancy and lactation:

    The use of the drug during pregnancy and breastfeeding is contraindicated.

    Dosing and Administration:Inside before eating, drinking water, 1 bottle of 600 mg (7 ml), 2 times a day.Duration of treatment the doctor determines individually, depending on the clinical picture and features of the course of the disease, age and tolerability of the drug.
    Side effects:

    Impaired nervous system:

    short-term confusion (in this case, you need to reduce the dose of the drug).

    Disorders from the gastrointestinal tract:

    nausea (which is mainly a consequence of secondary dopaminergic activation); abdominal pain.

    The drug is well tolerated even with prolonged use.

    Overdose:

    Symptoms: nausea.

    It is possible to increase the severity of dose-dependent side effects.

    Treatment: symptomatic therapy. The effectiveness of dialysis is not established.
    Interaction:Drug interaction is not established.
    Effect on the ability to drive transp. cf. and fur:

    Care should be taken when driving vehicles or engaging in other activities that require increased concentration and / or speed of psychomotor reactions.

    Form release / dosage:

    Solution for ingestion 600 mg / 7 ml.

    Packaging:

    For 7 ml of solution, in bottles of brown glass, sealed with polyethylene caps with the control of the first opening. For 10 vials with instructions for use in a pack of cardboard.

    Storage conditions:

    In the dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children!

    Shelf life:3 years. Do not use the drug after the expiration date.
    Terms of leave from pharmacies:On prescription
    Registration number:LP-004777
    Date of registration:03.04.2018
    Expiration Date:03.04.2023
    The owner of the registration certificate:Berezovsky Pharmaceutical Plant, ZAO Berezovsky Pharmaceutical Plant, ZAO Russia
    Manufacturer: & nbsp
    Information update date: & nbsp25.04.2018
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