Grassley Highlights Unexpected FDA Panel Move on Attention Deficit Medicines

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Grassley Highlights Unexpected FDA Panel Move on Attention Deficit Medicines

The following press release was published by the United States Committee on Finance Ranking Member’s News on Feb. 9, 2006. It is reproduced in full below.

Earlier this week, Sen. Chuck Grassley, chairman of the Committee on Finance, wrote to the Food and Drug Administration (FDA) urging a comprehensive, more timely review of the safety risks associated with Attention Deficit Hyperactivity Disorder medications. More than 2.5 million children under the age of 17 use these drugs, and many adults use them as well. Today the FDA’s Drug Safety and Risk Management Advisory Committee voted to recommend that the FDA include its strongest “black box" warning alerting both adults and children using Attention Deficit Hyperactivity Disorder medications of possible cardiovascular side effects. Grassley made the following comment on today’s development.

“Today’s unexpected action shows an urgency to warn consumers of safety risks with these medicines. It’s a surprising turn of events for a meeting that was only supposed to consider how to further study the risks of these drugs. It’ll be interesting to see whether the FDA will act on the committee's recommendations."

Source: Ranking Member’s News

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