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Epilepsy Drugs Double Suicide Risks

Keywords: Epilepsy| Suicide | Lawsuit | Lawyer | Felbatol | Neurontin | Lamictal | Keppra | Depakote

On January 31, 2008, the Food & Drug Administration (FDA) warned that people taking epilepsy drugs were twice as likely to suffer from suicidal thoughts and behavior as those taking a placebo. Millions of people take epilepsy drugs. Such anti-seizure medications are used for a variety of illnesses in addition to epilepsy, including migraines, certain nerve-pain disorders, and psychiatric diseases such as bipolar disorder that themselves carry a risk of suicide. The FDA said it would be working with manufacturers of marketed epilepsy drugs to include this new information about suicide risks in the labeling for these products

FDA Epilepsy Drug Suicide Study

The FDA began investigating if epilepsy drugs pose any suicide risk in 2005.  In doing so, the FDA analyzed almost 200 studies of 11 anti-seizure drugs, some that have been on the market for decades.  Even though the FDA only looked at 11 epilepsy medications, the agency said the suicide warning applied to all epilepsy drugs.  The FDA epilepsy drug analysis included the following drugs

The FDA studies tracked almost 28,000 people given epilepsy medications and another 16,000 given dummy pills.  According to the FDA, 0.43 percent of drug-treated patients experienced suicidal thoughts or behavior, compared with 0.22 percent of placebo-takers.  The higher risk of suicidal thoughts and behaviors was observed at one week after starting a drug and continued to at least 24 weeks. The results were generally consistent among all the different drug products studied and were seen in all demographic subgroups. There was no clear pattern of risk across age groups.

Overall, four people in the drug-treated groups committed suicide, and none in the placebo groups.  According to the FDA for every 1,000 patients, about two more patients taking epilepsy drugs experienced suicidal thoughts than those who took placebo.

Legal Help

If you or a loved one suffered from thoughts and/or behavior while taking epilepsy drugs, you may have valuable legal rights.  Please fill out the form at the right for a free case evaluation by a qualified drug side effects attorney.

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Suicide Warnings Approved for Epilepsy Drugs

May 6, 2009 | Parker Waichman Alonso LLP
Federal regulators have approved new suicide warnings for more than two dozen epilepsy drugs.  The Food & Drug Administration (FDA) had ordered the label update last December, when it issued a public-health advisory regarding the association between epilepsy drugs and suicidal thoughts and behavior.The new suicide warnings will appear on the labeling of Carbatrol, Celontin, Depakene, Depakote ER, Depakote sprinkles, Depakote tablets, Dilantin, Equetro, Felbatol, Gabitril, Keppra,...

Valproate Shouldn't be Taken by Pregnant Women, Medical Groups Say

Apr 28, 2009 | Parker Waichman Alonso LLP
The epilepsy drug valproate (Depacon) should not be taken by pregnant women, according to new guidelines issued by American Academy of Neurology and the American Epilepsy Society.  According to a report on medpagetoday.com, the groups have also recommended that expectant mothers who need them take only one epilepsy medication at a time.The groups, which published the new guidelines simultaneously in the journals Neurology and Epilepsia, said that in general, epileptic women can have safe...

Valproate During Pregnancy Linked to Children with Lower IQs

Apr 16, 2009 | Parker Waichman Alonso LLP
Valproate (sold under the brand names Depacon and Depakene) taken during pregnancy may cause children to have lower IQs, according to a new study published in The New England Journal of Medicine.  According to a report on Reuters.com, toddlers exposed to valproate in utero had IQs that were 6 to 9 points lower than children whose mothers took other epilepsy medications.The valproate IQ study, conducted by scientists at Emory University, is just the latest to show that the anti-seizure...

Zonegran Linked to Blood Disorder

Feb 23, 2009 | Parker Waichman Alonso LLP
The epilepsy drug zonisamide, sold both generically and under the brand name Zonegran, can cause a serious blood disorder called metabolic acidosis, the Food & Drug Administration (FDA) warned today.  The agency said it is working with the makers of zonisamide to revise the product labeling to reflect this new risk.According to the FDA, metabolic acidosis is a disturbance in the body's acid-base balance that results in excessive acidity of the blood.  Metabolic acidosis can result...

Valproate Use During Pregnancy Linked to Autism

Dec 2, 2008 | Parker Waichman Alonso LLP
Mothers who take the epilepsy drug valproate (sold under the brand names Depacon and Depakene) during pregnancy may face an increased risk of having a  child who will develop autism, a new study has found..  The British researchers who worked on the study, published in the journal Neurology, have recommended that pregnant women taking valproate be informed of the possible risks of autism and discuss the issue with their doctors.The valproate study, conducted by researchers at the...

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