Among the extensive family of nootropic agents, one preparation stands apart: its active ingredient is not a laboratory-synthesized molecule, but a naturally occurring brain metabolite. Aminalon delivers 250 mg of gamma-aminobutyric acid (GABA) in each tablet and is supplied in a pack of 100, calibrated for an extended therapeutic course. GABA is the primary inhibitory neurotransmitter of the central nervous system, and its additional exogenous supply can exert a complex influence on neuronal metabolism, cerebral hemodynamics, and cognitive processes.
Gamma-aminobutyric acid is an endogenous compound, normally synthesized within neurons from glutamic acid. Its physiological roles are multifaceted:
A notable peculiarity: in patients with diabetes mellitus, Aminalon tends to lower blood glucose levels, whereas under normoglycemic conditions it may induce a physiological increase — a bidirectional effect that mandates medical oversight.
The drug is indicated for adults and children aged 6 years and older as part of the treatment of the following conditions:
1. Cerebrovascular Pathology and Neurotrauma:
2. Chronic Encephalopathies of Diverse Origin:
3. Psychoorganic Syndrome — impairment of memory and intellectual productivity, affective lability, and fatigability of mental processes.
4. Pediatric Neurology (as part of complex treatment):
5. Kinetoses: prevention of sea and air sickness symptoms.
Tablets are taken orally, before meals. Dosage is differentiated by age and clinical task:
Adults:
Children:
Therapy Duration: The minimum course is 2–3 weeks; the optimal course ranges from 2 to 4 months. If necessary, courses may be repeated 1–2 times per year at the discretion of the treating physician.
Aminalon intake is absolutely ruled out in the following circumstances:
Special Considerations:
When therapeutic doses are respected, Aminalon is well tolerated. Possible undesirable effects include:
Intoxication develops exclusively upon the simultaneous ingestion of extremely high doses — exceeding 10–20 g. The clinical picture encompasses nausea, vomiting, epigastric pain, hyperthermia, headache, drowsiness, and bradycardia. No specific antidote exists. Management consists of immediate drug discontinuation, gastric lavage with activated charcoal, administration of coating agents, and supportive symptomatic therapy directed at resolving the resultant disturbances.
During the treatment period, caution is required when driving motor vehicles and performing tasks that demand heightened concentration and rapid psychomotor reactions.
Tablets must be kept in the original packaging, in a dry location inaccessible to children. The manufacturer does not stipulate specific temperature constraints; however, standard room temperature (15–25 °C / 59–77 °F) is considered optimal.

