What is the recommended dosage of Keppra (levetiracetam) for patients with seizures?

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Recommended Dosage of Levetiracetam (Keppra) for Seizures

For adult patients with seizures, levetiracetam (Keppra) should be initiated at 1000 mg/day (500 mg twice daily) with incremental increases of 1000 mg/day every 2 weeks to a maximum recommended daily dose of 3000 mg. 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
  • Higher doses (>3000 mg/day) have been used in open-label studies but without evidence of additional benefit 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
  • Lower doses have not been adequately studied 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 every 2 weeks
  • Recommended dose: 60 mg/kg/day (30 mg/kg twice daily)
  • Mean daily dose in clinical trials: 52 mg/kg 1

Ages 6 to <16 Years (Primary Generalized Tonic-Clonic Seizures)

  • Initial dose: 20 mg/kg/day in 2 divided doses (10 mg/kg twice daily)
  • Titration: Increase by 20 mg/kg every 2 weeks
  • Recommended dose: 60 mg/kg/day (30 mg/kg twice daily) 1

Status Epilepticus Dosing

IV Loading Dose for Status Epilepticus

  • 30-50 mg/kg IV at 100 mg/min 2
  • For non-convulsive status epilepticus: 40 mg/kg (maximum 2,500 mg) IV bolus 2
  • For convulsive status epilepticus: 40 mg/kg (maximum 2,500 mg) IV bolus 2

Maintenance Dosing After Status Epilepticus

  • For non-convulsive status epilepticus: 15 mg/kg (maximum 1,500 mg) IV every 12 hours 2
  • For convulsive status epilepticus: 30 mg/kg IV every 12 hours or increase prophylaxis dose by 10 mg/kg (to 20 mg/kg) IV every 12 hours (maximum 1,500 mg) 2

Special Considerations

Critically Ill Patients

  • Higher doses (750-1000 mg twice daily) are more effective than lower doses (500 mg twice daily) in critically ill patients
  • Higher doses are more than twice as likely to achieve target serum levels (12-46 μg/mL) and reduce seizure odds by 68% compared to lower doses 3

Renal Impairment

  • Dose adjustments required for patients with renal impairment
  • Maximum daily dose of 1000 mg for severe impairment (CrCl <30 mL/min)
  • 500-1000 mg every 24h with 250-500 mg supplemental dose following dialysis for ESRD patients 4

Administration

  • Can be given orally with or without food 1
  • For oral loading, 1500 mg as a single dose has been shown to be well-tolerated and rapidly achieves therapeutic serum concentrations 5

Efficacy and Safety

  • Dose-response relationship has been demonstrated, with higher doses providing greater seizure reduction 6
  • Approximately 15% of patients taking 1000 mg/day and 20-30% of patients taking 3000 mg/day achieve ≥50% reduction in seizure frequency 6
  • Most common adverse effects are somnolence and asthenia, which increase with higher doses 7
  • Levetiracetam has a low incidence of hypotension and respiratory depression when given as an IV load 2

Monitoring

  • Monitor renal function and adjust doses accordingly as levetiracetam is primarily renally eliminated 4
  • For status epilepticus, continuous EEG monitoring is recommended if seizures are refractory 2

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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