Provigil Label Revised

Jamie G. Goldstein

Attorney
(866) 735-1102 Ext 626

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The FDA is notifying healthcare professionals about updates to the warning labels of the prescription drug Provigil. Provigil is used to help adult patients who suffer from sleep apnea, narcolepsy and other sleeping disorders. The revised label warns patients that Provigil may caused a serious rash that could include Stevens-Johnson Syndrome (SJS) and hypersensitivity reactions. It may also cause psychiatric symptoms. In some cases Toxic Epidermal Necrolysis may occur which may be life-threatening. This life-threatening rash along with Eosinophulia and Systemic Symptoms have been reported in adults and children since Provigil began being marketed. Angiodema and multi-organ hypersentivity reactions are also being reported as side effects to the medication.

If you or someone you know is suffering from or has suffered from any of the above side effects or similar side effects while taking Provigil, contact an attorney immediately. You may be able to recover from the manufacturer of the medication for these side effects that were not listed until the recent label change.

For more information on this subject, please refer to the section on Drugs, Medical Devices, and Implants.