Cereton (Choline alfoscerate) solution 250 mg
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Cereton (Choline alfoscerate) solution 250 mg

SKU:2340
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Cereton (Choline alfoscerate) solution
Active substance:Choline alfoscerate
Pharmacological group:Nootropic
Formulation:ampoules
Dosage mg:250
In stock
$26
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Instructions for Cereton (Choline alfoscerate) solution 250 mg

Cereton (Choline alfoscerate) solution 250 mg

English product name
Cereton

Release Form
250 mg/1 ml: amp. four ml 3, 5, 6 or 10 pcs.

Description Cereton

The solution for in/in and in/m injection is transparent, colorless.

1 ml 1 amp.
choline alfoscerate polyhydrate (in terms of anhydrous choline alfoscerate) 250 mg 1000 mg
Auxiliary substances: water d/i.

ATC codes
N07AX02 Choline alfoscerate

Clinical-pharmacological groups / Group affiliation
Nootropic drug. Central Action Cholinomimetic

Active substance
choline alfoscerate

Pharmaco-therapeutic group

Nootropic agent

Storage Conditions

The drug should be stored in a place inaccessible to children, protected from light at a temperature not higher than 25 ° C.

Best before date
The shelf life is five years.

Pharmacological effect Cereton

Nootropic drug. Central cholinovulator containing 40.5% metabolically protected choline.
Metabolic protection promotes the release of choline in the brain. Provides acetylcholine and phosphatidylcholine synthesis in neuronal membranes, improves blood flow and enhances metabolic processes in the CNS, activates the reticular formation.

Testimony Cereton

  • acute and recovery periods of severe head trauma and ischemic stroke, 
  • recovery period of hemorrhagic stroke, 
  • occurring with focal hemispheric symptoms or symptoms of brain stem lesions;
  • psychoorganic syndrome amid degenerative and involutive brain changes;
  • cognitive disorders (impairments in thought function, 
  • memory, confusion,
  • disorientation, 
  • decreased motivation, initiative, 
  • and ability to focus), including dementia and encephalopathy;
  • an old pseudo-melancholy.

Method of use, course and dosage Cereton

In the case of acute conditions, 1,000 mg (one ampoule) per day is injected into/into (slowly) or deeply into/into (slowly) the vessels for ten to fifteen days.

  • Nosology (ICD codes)
  • F01
  • Vascular dementia
  • F03
  • Dementia unspecified
  • F07
  • Personality and behavioural disorders caused by disease, damage or brain dysfunction
  • G92
  • Toxic encephalopathy
  • G93.4
  • Encephalopathy unrefined
  • I63
  • Brain infarction
  • I67.4
  • Hypertensive encephalopathy
  • I69
  • Effects of cerebrovascular disease
  • S06
  • Intracranial injury
  • T90
  • Effects of head injuries
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