Efficacy and safety of rufinamide in pediatric epilepsy

David T. Hsieh, Elizabeth A. Thiele*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

21 Scopus citations

Abstract

Rufinamide is a novel anticonvulsant medication approved by the US Food and Drug Administration (FDA) in 2008 for the treatment of seizures associated with Lennox–Gastaut syndrome in patients 4 years of age and older, based upon clinical trials demonstrating clinical efficacy and tolerability. Rufinamide is especially effective for tonic–atonic seizures in Lennox–Gastaut syndrome, but is subsequently proving to be safe and effective in clinical practice for a broad patient population with refractory epilepsy. Although further research and clinical experience is needed, rufinamide holds the promise to positively impact the care of children with epilepsy. In this review, we review the use of rufinamide in pediatric epilepsy, with a focus on efficacy and safety.

Original languageEnglish
Pages (from-to)189-198
Number of pages10
JournalTherapeutic Advances in Neurological Disorders
Volume6
Issue number3
DOIs
StatePublished - May 2013

Keywords

  • Lennox–Gastaut syndrome
  • anticonvulsants
  • epilepsy
  • rufinamide

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