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Fetal exposure to Depakote needs further study, FDA panel says
25 June 2009
Nancy Faigen

nancy.faigen@informausa.com

At a June 23rd meeting, the US FDA's paediatric advisory committee unanimously concurred, by a vote of 11-0, with a report from agency safety researchers recommending further study of developmental delay reported in children whose mothers took Abbott Laboratories' anti-epileptic Depokote (divalproex...



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