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UCB Japan Obtains FDA Approval of Treatment Drug for Epilepsy Patients.


Tokyo, Japan, Aug 14, 2006 - (JCN JCN Japan Corporate News
JCN Journal of Cognitive Neuroscience
JCN Journal of Cardiovascular Nursing
JCN Journal of Christian Nursing
JCN Job Control Number
JCN Journal of Child Neurology
JCN joint communications network (US DoD) 
) - UCB UCB - University of California at Berkeley  Japan, a leading global biopharmaceutical company has obtained the approval of Keppra - generic name generic name
n.
1. The official nonproprietary name of a drug, under which it is licensed and identified by the manufacturer.

2.
 levetiracetam - 500mg/5mL (100mg/mL) from the U.S. Food and Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) for use as an adjunctive therapy for treatment of partial-onset seizures in adults with epilepsy.

The 15- minute intravenous infusion of Keppra offers an alternative for patients who find oral administration difficult or temporarily not feasible. The drug is prescribed to adults and children four years of age and older with epilepsy.

Keppra has already been approved in March 2006 from the European Commission.

Copyright [c] 2006 Japan Corporate News Network. All rights reserved.
COPYRIGHT 2006 Japan Corporate News Network K.K.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2006, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:JCNN News Summaries
Date:Aug 15, 2006
Words:109
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