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Thursday, July 9, 2009
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FDA adds suicide warning to anti-seizure drugs

(WBOC-TV 16) UPDATED 2008-12-16
The U.S. Food and Drug Administration (FDA) has added a label warning about an increased suicide risk to anti-seizure drugs such as Klonopin, Dilantin, and Topamax. The FDA's move comes in response to a recommendation by one of its expert advisory panels last summer, but it stops short of the strongest "black box" warning label. FDA officials say patients taking these medications should be monitored for signs of depression, for suicidal thoughts or behavior, or for any other unusual changes in mood or behavior. Anti-seizure medicines are used to treat a number of conditions, including epilepsy, migraines, and bipolar disorder.   Read full story >
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