January 06, 2009
FDA Decides Against Warnings on Epilepsy Medication Suicide Risk
The FDA has decided against placing new warning labels on anti-seizure medications used to treat epilepsy, in spite of recent findings that those drugs can increase a patient's risk of suicide. In January, the FDA raised the possibility of labeling 11 anti-seizure drugs with "black box" warnings, after numerous studies linked them to increased risks of suicidal behavior: carbamazepine (marketed as Carbatrol, Equetro, Tegretol and Tegretol XR), felbamate (marketed as Felbatol), gabapentin (marketed as Neurontin), lamotrigine (marketed as Lamictal), levetiracetam (marketed as Keppra), oxcarbazepine (marketed as Trileptal), pregabalin (marketed as Lyrica), tiagabine (marketed as Gabitril), topiramate (marketed as Topamax), valproate (marketed as Depakote, Depakote ER, Depakene and Depacon) and zonisamide (marketed as Zonegran).Click Here For The Full Story......
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