Stronger Warnings Urged for Tamiflu

By Admin on November 28, 2007 | Last updated on March 21, 2019

Manufacturer Roche Laboratories, Inc. should update Tamiflu labeling to include stronger warnings regarding the risk of psychiatric problems in users of the flu medicine, according to a U.S. Food and Drug Administration (FDA) committee. The FDA Pediatric Advisory Committee made its recommendations after evaluating reports of adverse events associated with use of the prescription influenza medication -- including delusions, confusion, and self-injury -- especially in children. The New York Times reports that "nearly 600 cases of psychiatric problems in Tamiflu patients have been reported, with 75 percent of them from Japan."

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