PIRACETAM:
Class:             Antimyoclonic, Nootropic
Indications:       Enhance cognition in the elderly; cortical myoclonus; sickle cell anemia
Available dosage form in the hospital: CAP (400MG, 800MG), 1G /5ML INJ, 20MG/100ML SYRP
Dosage:
Cognitive disorders: Oral, I.V.: Dosage range: 1.2-4.8 g daily administered in 2-3 divided doses. May
 start at higher end of range according to initial severity of symptoms.
Cortical myoclonus, adjunctive: Oral, I.V.: Initial: 7.2 g daily administered in 2-3 divided doses. May
 increase total daily dose by 4.8 g every 3-4 days if needed (maximum daily dose: 24 g). Consider
 dosage reduction or gradual withdrawal of piracetam therapy every 6 months if symptoms are
 controlled; reduce daily dose by 1.2 g every 2 days (every 3-4 days for patients with Lance-Adams
 syndrome).
Vertigo: Oral, I.V.: 2.4-4.8 g daily administered in 2-3 divided doses
Hepatic impairment:
No dosage adjustment necessary.
Renal impairment:
Clcr >80 mL/minute: No dosage adjustment necessary.
Clcr 50-80 mL/minute: Initial and maximum dose: Decrease to 2/3 of the normal daily dose administered
  in 2-3 divided doses.
Clcr 30 to <50 mL/minute: Initial and maximum dose: Decrease to 1/3 of the normal daily dose
  administered in 2 divided doses.
Clcr 20 to <30 mL/minute: Decrease to 1/6 of the normal daily dose administered once daily.
Clcr <20 mL/minute: Use is contraindicated.
Common side effect:
Weight gain, nervousness, hyperkinesia; less commonly drowsiness, depression, asthenia,; also reported
 abdominal pain, nausea, vomiting, diarrhoea, headache, anxiety, confusion, hallucination, vertigo,
 ataxia, insomnia, and rash
Pregnancy Risk Factor :
Adverse events have not been observed in animal reproduction studies. Piracetam crosses placental
  barrier with neonatal levels ~70% to 90% of maternal levels. In general, higher risk of teratogenic
  effects may be associated with anticonvulsant polytherapy compared to monotherapy (Morrow, 2006).