Levetiracetam (Keppra) Dosage and Treatment Regimen for Seizures
For seizure treatment, levetiracetam should be initiated at 1000 mg/day (500 mg twice daily) for adults, with increases of 1000 mg/day every 2 weeks to a maximum recommended dose of 3000 mg/day. 1
Adult Dosing (16 years and older)
Partial Onset Seizures
- Initial dose: 1000 mg/day given as 500 mg twice daily
- Titration: Increase by 1000 mg/day every 2 weeks
- Maximum recommended dose: 3000 mg/day
- Administration: Can be taken with or without food 1
Myoclonic Seizures (12 years and older with juvenile myoclonic epilepsy)
- Initial dose: 1000 mg/day given as 500 mg twice daily
- Titration: Increase by 1000 mg/day every 2 weeks
- Recommended dose: 3000 mg/day 1
Primary Generalized Tonic-Clonic Seizures
- Initial dose: 1000 mg/day given as 500 mg twice daily
- Titration: Increase by 1000 mg/day every 2 weeks
- Recommended dose: 3000 mg/day 1
Pediatric Dosing
Ages 4 to <16 years (Partial Onset Seizures)
- Initial dose: 20 mg/kg/day in 2 divided doses (10 mg/kg twice daily)
- Titration: Increase by 20 mg/kg/day every 2 weeks
- Recommended dose: 60 mg/kg/day (30 mg/kg twice daily)
- Weight-based dosing:
- 20-40 kg: Start with 500 mg/day, target 1500 mg/day
40 kg: Start with 1000 mg/day, target 3000 mg/day 1
Ages 6 to <16 years (Primary Generalized Tonic-Clonic Seizures)
- Initial dose: 20 mg/kg/day in 2 divided doses
- Titration: Increase by 20 mg/kg/day every 2 weeks
- Recommended dose: 60 mg/kg/day (30 mg/kg twice daily) 1
Status Epilepticus Management
For status epilepticus, levetiracetam can be administered intravenously:
- Loading dose: 30-50 mg/kg IV (maximum 2,500 mg)
- Maintenance dose: 15-30 mg/kg every 12 hours (maximum 1,500 mg per dose) 2
In the ESETT trial, levetiracetam showed similar efficacy to fosphenytoin and valproate for benzodiazepine-resistant status epilepticus, with approximately 47% of patients achieving seizure cessation 3, 2.
Efficacy and Safety Profile
- Levetiracetam has demonstrated efficacy in reducing seizure frequency in multiple clinical trials, with median percentage reductions of 17-30% over placebo 4
- Responder rates (≥50% reduction in seizure frequency) range from 20.8% to 39.6% across different doses 4
- Common adverse effects include:
Practical Considerations
- Levetiracetam has high oral bioavailability and minimal metabolism
- Primarily eliminated through renal excretion
- Minimal drug-drug interactions, making it suitable for patients on multiple medications 5, 6
- For oral loading in patients who missed doses, a safety study showed good tolerability with minimal adverse effects 3
Monitoring
- Regular follow-up every 3-6 months is recommended to assess:
- Seizure control
- Medication tolerability
- Potential side effects 2
- Monitor for behavioral adverse effects, which can occur in some patients 5, 6
Levetiracetam's favorable pharmacokinetic profile, minimal drug interactions, and established efficacy make it a valuable option for seizure management across various seizure types and age groups.