Lucetam® (Tablets, Solution) Instructions for Use
ATC Code
N06BX03 (Piracetam)
Active Substance
Piracetam (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Nootropic drug
Pharmacotherapeutic Group
Nootropic agent
Pharmacological Action
Nootropic agent. It has a positive effect on metabolic processes and cerebral circulation.
It increases glucose utilization, improves the course of metabolic processes, improves microcirculation in ischemic areas, and inhibits aggregation of activated platelets.
It has a protective effect in brain damage caused by hypoxia, intoxication, and electric shock. It improves the integrative activity of the brain.
It does not have a sedative or psychostimulant effect. It reduces the duration of provoked vestibular neuronitis.
It inhibits increased aggregation of activated platelets and, in the case of pathological rigidity of erythrocytes, improves their deformability and filtration ability.
Pharmacokinetics
When taken orally, it is rapidly and almost completely absorbed from the gastrointestinal tract. The bioavailability is about 100%.
Cmax in plasma is reached in approximately 30 minutes, in cerebrospinal fluid – in 2-8 hours. The apparent Vd is 0.6 L/kg. It does not bind to plasma proteins.
It is distributed in all organs and tissues, penetrates the blood-brain barrier and the placental barrier.
It selectively accumulates in the tissues of the cerebral cortex, mainly in the frontal, parietal, and occipital lobes, in the cerebellum and basal ganglia.
T1/2 from plasma is 4-5 hours, from cerebrospinal fluid – 6-8 hours. It is excreted by the kidneys unchanged.
In renal failure, T1/2 increases.
Indications
Memory disorders, dizziness, decreased concentration, emotional lability, dementia due to cerebrovascular disorders (ischemic stroke), brain injuries, in Alzheimer’s disease, in old age, intellectual-mnestic disorders, cortical myoclonus; coma of vascular, traumatic or toxic origin; treatment of withdrawal and psychoorganic syndrome in chronic alcoholism; learning disabilities in children, not associated with inadequate learning or family environment (as part of combination therapy); sickle cell anemia (as part of combination therapy).
ICD codes
| ICD-10 code | Indication |
| D57 | Sickle-cell disorders |
| F00 | Dementia in Alzheimer's disease |
| F01 | Vascular dementia |
| F03 | Unspecified dementia |
| F07 | Personality and behavioral disorders due to disease, damage or dysfunction of the brain |
| F10.2 | Chronic alcoholism |
| F10.3 | Withdrawal state |
| F81 | Specific developmental disorders of scholastic skills |
| G25.3 | Myoclonus |
| G45 | Transient cerebral ischemic attacks [TIAs] and related syndromes |
| I63 | Cerebral infarction |
| I69 | Sequelae of cerebrovascular diseases |
| R40.2 | Coma, unspecified |
| R42 | Dizziness and giddiness |
| T90 | Sequelae of injuries of head |
| ICD-11 code | Indication |
| 3A51.Z | Sickle-cell disorders or other haemoglobinopathies, unspecified |
| 6A03.Z | Developmental learning disorder, unspecified |
| 6C40.2Z | Alcohol dependence, unspecified |
| 6C40.4Z | Alcohol withdrawal syndrome, unspecified |
| 6C40.Z | Disorders due to alcohol use, unspecified |
| 6D80.Z | Dementia due to Alzheimer's disease, onset unknown or unspecified |
| 6D81 | Dementia due to cerebrovascular disease |
| 6D8Z | Dementia, unknown or unspecified cause |
| 6E68 | Secondary emotionally labile personality disorder |
| 6E6Z | Unspecified secondary mental or behavioral syndromes |
| 8A06.Z | Myoclonic disorders, unspecified |
| 8B10.Z | Transient ischemic attack, unspecified |
| 8B11 | Cerebral ischemic stroke |
| 8B25.Z | Sequelae of cerebrovascular disease, unspecified |
| 8D44.Y | Other specified alcohol-related neurological disorders |
| 8E20 | Persistent vegetative state |
| 8E21 | Permanent vegetative state |
| MB20.1 | Coma |
| MB48.Z | Dizziness and giddiness, unspecified |
| NA0Z | Head injury, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Tablets, Solution
It is used orally, intramuscularly or intravenously. The dose, method and scheme of application, duration of therapy are determined individually, depending on the indications, clinical situation, patient’s age and the dosage form used.
Parenteral administration of piracetam is prescribed when oral forms cannot be used (unconsciousness, difficulty swallowing). Intravenous administration is preferred.
Adverse Reactions
From the blood coagulation system: frequency unknown – bleeding.
From the immune system: frequency unknown – anaphylactoid reactions, hypersensitivity reactions.
From the psyche: frequent – nervousness; infrequent – depression; frequency unknown – agitation, anxiety, confusion, hallucinations.
From the nervous system: frequent – hyperactivity; infrequent – drowsiness; frequency unknown – ataxia, balance disorders, exacerbation of epilepsy, headache, insomnia, tremor.
From the hearing organ and labyrinth: frequency unknown – vertigo.
From the cardiovascular system: rare – thrombophlebitis; with parenteral administration – arterial hypotension.
From the digestive system: frequency unknown – abdominal pain, diarrhea, nausea, vomiting.
From the skin and subcutaneous tissues: frequency unknown – angioedema, dermatitis, pruritus, urticaria.
Local reactions: rare – pain at the injection site.
Other: frequent – weight gain; infrequent – asthenia, fever (only with parenteral administration); frequency unknown – increased sexual desire.
Contraindications
Hypersensitivity to piracetam; Huntington’s chorea, acute cerebrovascular accident (hemorrhagic stroke), end-stage chronic renal failure; children’s age – depending on the dosage form.
Use in Pregnancy and Lactation
During pregnancy, it should be used only as prescribed by a doctor, in cases where the intended benefit to the mother outweighs the potential risk to the fetus.
If it is necessary to use during lactation, the issue of stopping breastfeeding should be decided.
Use in Hepatic Impairment
No dose adjustment is required for patients with impaired liver function.
Use in Renal Impairment
Contraindicated in severe renal failure. Use with caution in patients with renal failure; during the use of piracetam, monitoring of creatinine clearance is necessary. Dose adjustment is recommended in accordance with creatinine clearance values.
Pediatric Use
It can be used in children of the appropriate age categories strictly according to the indications, in recommended doses, regimens and dosage forms. It is necessary to strictly follow the instructions in the piracetam drug labels regarding contraindications for the use of specific piracetam dosage forms in children of different ages.
Geriatric Use
During long-term treatment of elderly patients, regular monitoring of creatinine clearance is necessary; dose adjustment may be required.
Special Precautions
Due to the antiplatelet effect of piracetam, it should be prescribed with caution to patients with severe hemorrhagic disorders, risk of bleeding (for example, with gastric ulcer), hemostasis disorders, in patients with surgical interventions, including dental interventions, in patients taking anticoagulants and antiplatelet agents, including low doses of acetylsalicylic acid.
Since Piracetam is excreted by the kidneys, caution should be exercised when prescribing it to patients with renal failure.
During long-term treatment of elderly patients, regular monitoring of creatinine clearance is necessary; dose adjustment may be required.
Piracetam penetrates through the filtering membranes of hemodialysis machines.
When treating cortical myoclonus, abrupt interruption of treatment should be avoided, as this may cause recurrence of seizures.
If sleep disorders occur, it is recommended to cancel the evening dose of piracetam, adding this dose to the daytime dose.
Effect on the ability to drive vehicles and mechanisms
During the use of piracetam, patients should be careful when driving vehicles and mechanisms, as well as when engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Drug Interactions
With simultaneous use of piracetam and thyroid extract (triiodothyronine + thyroxine), confusion, irritability and sleep disturbance were noted.
With simultaneous use with thyroid hormone drugs, the development of central effects is possible – tremor, anxiety, irritability, sleep disorders, confusion.
With simultaneous use with CNS stimulants, an increase in the psychostimulant effect is possible.
With simultaneous use with neuroleptics, an increase in extrapyramidal disorders is observed.
Storage Conditions
Store at 15°C (59°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Film-coated tablets, 400 mg: 60 pcs.
Marketing Authorization Holder
Egis Pharmaceuticals PLC (Hungary)
Dosage Form
| Lucetam® | Film-coated tablets, 400 mg: 60 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets white or almost white, oval, biconvex, with a bevel, with an engraving “E 241” on one side, odorless.
| 1 tab. | |
| Piracetam | 400 mg |
Excipients: magnesium stearate – 3 mg, povidone K-30 – 25 mg.
Shell composition: dibutyl sebacate – 0.7 mg, ethylcellulose (in the form of an aqueous dispersion) – 3.5 mg, Opadry white (macrogol 6000 – 0.25 mg, titanium dioxide – 0.75 mg, talc – 1 mg, hypromellose – 3.8 mg).
15 pcs. – blisters (4) – cardboard packs.
60 pcs. – brown glass jars (1) with a polyethylene cap with first opening control and a bellows cushion – cardboard packs.
Film-coated tablets, 800 mg: 30 pcs.
Marketing Authorization Holder
Egis Pharmaceuticals PLC (Hungary)
Dosage Form
| Lucetam® | Film-coated tablets, 800 mg: 30 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets white or almost white, oval, biconvex, with a bevel, with a score on both sides, with an engraving “E 242” on one side of the tablet, odorless.
| 1 tab. | |
| Piracetam | 800 mg |
Excipients: magnesium stearate – 6 mg, povidone K-30 – 50 mg.
Shell composition: dibutyl sebacate – 1.4 mg, ethylcellulose (in the form of an aqueous dispersion) – 7 mg, Opadry white (macrogol 6000 – 0.5 mg, titanium dioxide – 1.5 mg, talc – 2 mg, hypromellose – 7.6 mg).
15 pcs. – blisters (2) – cardboard packs.
30 pcs. – brown glass jars (1) with a polyethylene cap with first opening control and a bellows cushion – cardboard packs.
Film-coated tablets, 1200 mg: 20 or 60 pcs.
Marketing Authorization Holder
Egis Pharmaceuticals PLC (Hungary)
Dosage Form
| Lucetam® | Film-coated tablets, 1200 mg: 20 or 60 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets white or almost white, oval, biconvex, with a bevel, with an engraving “E 243” on one side of the tablet, odorless.
| 1 tab. | |
| Piracetam | 1200 mg |
Excipients: magnesium stearate – 9 mg, povidone K-30 – 75 mg.
Shell composition: dibutyl sebacate – 1.82 mg, ethylcellulose (in the form of an aqueous dispersion) – 9.1 mg, Opadry white (macrogol 6000 – 0.65 mg, titanium dioxide – 1.95 mg, talc – 2.6 mg, hypromellose – 9.88 mg).
10 pcs. – blisters (2) – cardboard packs.
20 pcs. – brown glass jars (1) with a polyethylene cap with first opening control – cardboard packs.
60 pcs. – brown glass jars (1) with a polyethylene cap with first opening control – cardboard packs.
Solution for intravenous and intramuscular administration 200 mg/1 ml: amp. 5 ml 10 pcs.
Marketing Authorization Holder
Egis Pharmaceuticals PLC (Hungary)
Dosage Form
| Lucetam® | Solution for intravenous and intramuscular administration 200 mg/1 ml: amp. 5 ml 10 pcs. |
Dosage Form, Packaging, and Composition
Solution for intravenous and intramuscular administration transparent, colorless or with a slight greenish tint, odorless.
| 1 ml | 1 amp. | |
| Piracetam | 200 mg | 1000 mg |
Excipients: sodium acetate trihydrate – 5 mg, glacial acetic acid – to pH 5.8, water for injections – up to 5 ml.
5 ml – ampoules of colorless glass with a break point and two red rings (5) – plastic cell packs (2) – cardboard packs.
Solution for intravenous and intramuscular administration 200 mg/1 ml: amp. 15 ml 4 or 20 pcs.
Marketing Authorization Holder
Egis Pharmaceuticals PLC (Hungary)
Dosage Form
| Lucetam® | Solution for intravenous and intramuscular administration 200 mg/1 ml: amp. 15 ml 4 or 20 pcs. |
Dosage Form, Packaging, and Composition
Solution for intravenous and intramuscular administration transparent, colorless or with a slight greenish tint, odorless.
| 1 ml | 1 amp. | |
| Piracetam | 200 mg | 3000 mg |
Excipients: sodium acetate trihydrate – 15 mg, glacial acetic acid – to pH 5.8, water for injections – up to 15 ml.
15 ml – ampoules of colorless glass with a break point (4) – contour cell packs (1) – cardboard packs.
15 ml – ampoules of colorless glass with a break point (4) – contour cell packs (5) – cardboard packs.
