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TAKE CONTROL TODAYAs of May 15, 2007, rufinamide has not been approved for use in the United States. The U.S. Food and Drug Administration is currently determining whether to approve rufinamide as 1) add-on therapy for partial seizures with or without secondary generalization in adults and adolescents 12 years of age and older, and 2) add-on therapy for Lennox-Gastaut syndrome in children ages 4 and over.
In the European Union countries, Inovelon® was approved in January 2007 as add-on therapy for the treatment of Lennox-Gastaut syndrome.
Reviewed by Steven C. Schachter, MD
Submitted: 05/16/07
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