What is the risk of seizure when changing from Keppra (Levetiracetam) to Briviact (Brivaracetam)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 22, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Risk of Seizure When Changing from Keppra (Levetiracetam) to Briviact (Brivaracetam)

Switching from Keppra (levetiracetam) to Briviact (brivaracetam) carries a low risk of breakthrough seizures when done properly, with an overnight switch at a conversion ratio of 10:1 to 15:1 being feasible and potentially improving tolerability, especially regarding behavioral side effects.

Understanding the Medications

Both medications work through a similar mechanism:

  • Levetiracetam (Keppra) and brivaracetam (Briviact) are SV2A ligands
  • Brivaracetam has a higher affinity for SV2A receptors than levetiracetam
  • Both are used for seizure control in epilepsy patients

Conversion Strategy and Risk Assessment

Recommended Conversion Approach

  • An immediate overnight switch from levetiracetam to brivaracetam is feasible at a conversion ratio of 10:1 to 15:1 1
  • For example:
    • 1000 mg levetiracetam would convert to 100 mg brivaracetam
    • 1500 mg levetiracetam would convert to 100-150 mg brivaracetam

Seizure Risk Factors

  • The risk of breakthrough seizures appears to be low when switching between these specific medications
  • Studies have shown that brivaracetam may be better tolerated than levetiracetam, with 57.1% of patients reporting improved tolerability after switching 2
  • Patients with behavioral side effects from levetiracetam may particularly benefit from the switch 1, 2

Efficacy Considerations

Brivaracetam has demonstrated good efficacy in clinical trials:

  • Significant median seizure reduction rates of 30.5% to 53.1% for 50 mg/day
  • 50% responder rates of 32.7% to 55.8% for 50 mg/day 1
  • In a study of patients switched from levetiracetam to brivaracetam:
    • 32.6% were 50%-responders
    • 21.7% became newly seizure-free 2

Monitoring and Management

During Transition

  • Monitor closely for breakthrough seizures in the first few weeks after switching
  • Consider checking drug levels if available, especially if there are concerns about efficacy
  • Be alert for any new side effects, though brivaracetam is generally well-tolerated

Common Side Effects to Monitor

  • Main adverse events with brivaracetam are fatigue, dizziness, and somnolence 1
  • These are typically milder than with levetiracetam, especially behavioral side effects

Important Caveats and Pitfalls

Generic vs. Brand Considerations

  • There have been reports of breakthrough seizures when switching from brand-name to generic levetiracetam 3, 4
  • In one study, patients who experienced breakthrough seizures after switching to generic levetiracetam returned to seizure control when switched back to brand-name Keppra 3
  • This highlights the importance of consistency in formulation, regardless of which medication is chosen

Special Populations

  • While not directly related to the Keppra-to-Briviact switch, it's worth noting that the American Academy of Neurology recommends levetiracetam over older antiepileptic drugs to reduce side effects (level C recommendation) 5
  • This principle likely extends to brivaracetam, which has an even more favorable side effect profile

Conclusion

The transition from Keppra to Briviact carries a relatively low risk of breakthrough seizures when done with appropriate dosing conversion. The potential benefits of improved tolerability may outweigh the risks for many patients, particularly those experiencing behavioral side effects on levetiracetam.

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.