Clinical and pharmacological group: & nbsp

Nootropics

Included in the formulation
  • Noocleolin®
    solution inwards 
    PIK-PHARMA, LLC     Russia
  • АТХ:

    N.06.B.X   Other psychostimulants and nootropic drugs

    Pharmacodynamics:

    Nootropic drug, by chemical structure is close to natural metabolites of the brain (γ-aminobutyric acid, glutamic acid). It is also a precursor of choline, which is why it enhances the formation of acetylcholine. Has cerebroprotective effect, restores mental activity, improves learning, facilitates the processes of fixation, consolidation and reproduction of a memorable trace, stimulates tissue metabolism processes, improves ability to concentrate attention, positively influences neurotic states of senile age that develop against the background of organic brain insufficiency, with alcohol abstinence syndrome.

    Pharmacokinetics:

    It has high bioavailability. After 0.5-1 hour after oral administration, it is detected in the maximum concentration in the brain, liver, kidneys, blood plasma, heart. The therapeutic concentration in the central nervous system is reached in 30-60 minutes after taking the drug. Half-life is 24 hours. Eliminated by the kidneys.

    Indications:

    - Intellectual-mnestichesky infringements;

    - Tardive dyskinesia;

    - Neuroleptic syndrome;

    - Psychosomatic disorders;

    - Alcohol withdrawal syndrome;

    - Astheno-depressive conditions;

    - Vascular diseases of the brain;

    - The period of convalescence after a head trauma.

    V.F00-F09.F07   Personality and behavioral disorders due to illness, damage or dysfunction of the brain

    V.F00-F09.F07.2   Postcontasia syndrome

    V.F00-F09.F07.9   Organic personality and behavioral disorder due to illness, damage or dysfunction of the brain, unspecified

    V.F10-F19.F10.2   Mental and behavioral disorders caused by alcohol use - addiction syndrome

    V.F10-F19.F10.3   Mental and behavioral disorders caused by alcohol use - withdrawal symptoms

    V.F20-F29.F20   Schizophrenia

    V.F20-F29.F21   Chrysotile disorder

    V.F20-F29.F22   Chronic delusional disorders

    V.F20-F29.F23   Acute and transient psychotic disorders

    V.F20-F29.F25   Schizoaffective disorder

    V.F20-F29.F29   Inorganic psychosis, unspecified

    V.F30-F39.F32   Depressive episode

    V.F30-F39.F34.1   Dysthymia

    V.F40-F48.F45   Somatoform disorders

    V.F50-F59.F51.1   Drowsiness [hypersomnia] inorganic etiology

    IX.I60-I69.I67.2   Cerebral atherosclerosis

    IX.I60-I69.I69   Effects of cerebrovascular disease

    XI.K70-K77.K70   Alcoholic liver disease

    XI.K70-K77.K72.0   Acute and subacute liver failure

    XI.K70-K77.K73   Chronic hepatitis, not elsewhere classified

    XI.K70-K77.K74.6   Other and unspecified liver cirrhosis

    XI.K70-K77.K76.0   Fatty degeneration of the liver, not elsewhere classified

    XI.K80-K87.K83.1   Blockage of the bile duct

    Contraindications:

    Hypersensitivity, febrile states, psychotic conditions, epilepsy, pregnancy and lactation, infectious diseases of the central nervous system, blood diseases, chronic liver and kidney diseases, age up to 10 years.

    Carefully:

    In the period of treatment, abstinence from driving vehicles and controlling mechanisms is required, and one should refrain from occupations that are potentially dangerous and require special concentration of attention.

    Pregnancy and lactation:

    Category FDA not determined. Adequate and well-controlled studies on humans and animals have not been conducted. Do not apply.

    Dosing and Administration:

    Inside for 1 g (one teaspoon) 2-3 times a day; the last reception - no later than 16-18 hours. The average daily intake for adults is 4-6 g.The maximum single dose is 2 g, the maximum daily dose is 10 g; the duration of treatment is 1.5-2.5 months 2-3 times a year.

    Side effects:

    Hypersensitivity, depression (in people over 65 years), headaches, sleep disorders, constipation, weight loss, itching.

    Overdose:

    Increased side effects. Treatment is symptomatic.

    Interaction:

    With simultaneous reception with funds that stimulate the central nervous system, potentiation of the action of the drug is possible.

    Special instructions:

    At the time of taking the drug, it is necessary to observe the neurologist, monitoring the electroencephalogram.

    Instructions
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