Adverse drug events reported to FDA appear to have increased markedly

The number of serious adverse drug events reported to the U.S. Food and Drug Administration (FDA) more than doubled between 1998 and 2005, as did deaths associated with adverse drug events, according to a report in the September 10 issue of Archives of Internal Medicine, one of the JAMA/Archives journals.

If you want to include this story in your blog, copy and paste this formatted text: