Levetiracetam Injectable Dosing in Pediatric Patients
Levetiracetam injectable dosing in pediatric patients should be initiated at 20 mg/kg/day divided into two doses (10 mg/kg every 12 hours), with potential titration up to 60 mg/kg/day based on clinical response and tolerability. 1
Initial Dosing Strategy
- Start with 10 mg/kg per dose administered every 12 hours (total daily dose of 20 mg/kg/day) for pediatric patients requiring adjunctive therapy for partial onset seizures 1
- The dosing range studied in pediatric populations extends from 10 to 40 mg/kg/day, demonstrating efficacy as adjunctive therapy in children with refractory partial seizures 1
- Injectable levetiracetam can be substituted for oral formulations at the same total daily dose when oral administration is temporarily not feasible 2
Dose Titration and Optimization
- Increase the dose by 10-20 mg/kg/day every 1-2 weeks if seizure control is inadequate, up to a maximum of 60 mg/kg/day (or 3000 mg/day in adolescents approaching adult weight) 1
- Clinical response should be assessed within 48-72 hours of dose adjustments, with further investigation warranted if no improvement is observed 3
- The therapeutic approach should prioritize achieving seizure control while monitoring for concentration-related adverse effects, which may be minimized with gradual titration 2
Age and Weight Considerations
- Pediatric dosing must account for age-dependent pharmacokinetic differences, as children demonstrate more rapid drug clearance compared to adults, necessitating weight-based rather than fixed dosing 4, 5
- For children weighing more than 40 kg, consider transitioning to adult dosing protocols (typically 1000-3000 mg/day in divided doses) 3
- Twice-daily administration is essential in pediatric patients due to faster drug clearance rates compared to adults 5
Administration Guidelines
- Levetiracetam injection should be administered intravenously over 15 minutes when used as a substitute for oral therapy 2
- The injectable formulation provides identical bioavailability to oral administration, allowing seamless transition between routes 2
- Monitor for neuropsychiatric adverse effects including behavioral disturbances, agitation, and mood changes, which occur in approximately 13.3% of patients, though severe symptoms are less common 6
Safety Monitoring
- The most common adverse events include somnolence, irritability, dizziness, and asthenia, with an overall tolerability profile similar to placebo in controlled trials 2, 1
- Behavioral adverse effects can emerge beyond the initial titration period and may necessitate drug discontinuation in predisposed individuals 6
- No significant drug-drug interactions occur with levetiracetam due to minimal cytochrome P450 metabolism, making it suitable for combination therapy 2, 1
- Dose adjustment is not typically required based on hepatic function, though renal impairment may necessitate dosing modifications 2