Active substanceCholine alfoscerateCholine alfoscerate
Similar drugsTo uncover
  • Alphofolin-Lekpharm
    solution w / m in / in 
    LEKFARM, SOOO     Republic of Belarus
  • Glacer
    solution w / m in / in 
    EKOFARMPLUS, CJSC     Russia
  • Gliatilin
    solution w / m d / infusion 
    Italfarmaco SpA     Italy
  • Gliatilin
    capsulessolution inwards w / m in / in 
    Italfarmaco SpA     Italy
  • Gliatilin
    capsulessolution inwards w / m in / in 
    Italfarmaco SpA     Italy
  • Gliatilin
    solution inwards 
    Italfarmaco SpA     Italy
  • Delecite
    solution w / m d / infusion 
    ITF, LLC     Russia
  • Delecite
    capsules inwards 
    ITF, LLC     Russia
  • Noochlin Rompharm
    solution w / m in / in 
  • Choline alfoscerate
    solution w / m in / in 
    Company DEKO, LLC     Russia
  • Choline alfoscerate
    solution w / m in / in 
    PharmIntelekt, OOO     Russia
  • Choline alfoscerate
    solution w / m in / in 
  • Choline alfoscerate
    solution w / m in / in 
    ATOLL, LLC     Russia
  • Choline alfoscerate
    solution w / m d / infusion 
    BIOSINTEZ, PAO     Russia
  • Choline alfoscerate
    solution inwards 
  • Holilitil
    solution w / m in / in 
    Company DEKO, LLC     Russia
  • Holilitil
    capsules inwards 
    ARTLIFE, LLC     Russia
  • Cerepro®
    solution w / m in / in 
    VEROPHARM SA     Russia
  • Cerepro
    capsulessolution inwards w / m in / in 
    VEROPHARM SA     Russia
  • Cereton®
    solution w / m in / in 
  • Cereton
    capsules inwards 
  • Cereton®
    solution inwards 
  • Dosage form: & nbsporal solution
    Composition:

    One 7 ml bottle contains:

    Active substance: choline alfoscerate - 600 mg;

    Excipients: methylparahydroxybenzoate 8.0 mg; propyl parahydroxybenzoate 2.4 mg; sodium saccharinate - 3.0 mg; orange flavoring - 29.0 mg; purified water - up to 7 ml.

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

    N.07.A.X.02   Choline alfoscerate

    Pharmacodynamics:
    Choline alphoscerate (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. connections in the brain, head; Choline participates in the biosynthesis of acetylcholine, is the 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 the nerve impulse in both 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 vascular lesions of the brain (including cerebrovascular insufficiency and some forms of dementia).
    Pharmacokinetics:Absorption on ingestion of 95%. Penetrates through the blood-brain barrier (concentration in the brain - 45% of that in the plasma). Both 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:
    As part of complex therapy:
    - Psycho-organic syndrome in the background of degenerative diseases and involuntary processes of the brain or cerebrovascular insufficiency, including primary and secondary senile cognitive impairments.
    - Multi-infarct dementia.
    Contraindications:
    Hypersensitivity to the drug, hemorrhagic stroke (acute phase), pregnancy; breastfeeding, children's age.
    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. The duration of therapy is 3-6 months.
    Side effects:
    From the digestive system: gastritis, peptic ulcer, constipation, diarrhea, mucosal dryness of the mouth, throat.
    From the nervous system: headache, drowsiness, insomnia, aggression, anxiety, cerebral ischemia, convulsions, hyperkinesia, dizziness.
    From the skin: rash.
    Other: increased frequency of urination, allergic reactions.
    Overdose:
    There is no information about overdose.
    When an overdose is shown: gastric lavage, taking adsorption drugs (for example, activated charcoal), 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 oral administration 600 mg / 7 ml.
    Packaging:By 7 ml of the solution in bottles of brown glass (type III, Hept. F.) sealed with polyethylene caps with the control of the first autopsy. For 10 vials with instructions for use in a pack of cardboard.
    Storage conditions:At a temperature of no higher than 25 ° C. Keep out of the reach of children!
    Shelf life:3 years. Do not use after expiry date.
    Terms of leave from pharmacies:On prescription
    Registration number:LP-001540
    Date of registration:27.02.2012 / 10.10.2016
    Expiration Date:27.02.2017
    The owner of the registration certificate:Italfarmaco SpAItalfarmaco SpA Italy
    Manufacturer: & nbsp
    Representation: & nbspCBS CJSC LTDCBS CJSC LTDItaly
    Information update date: & nbsp26.04.2017
    Illustrated instructions
      Instructions
      Up