GAO recommends, among other things, that FDA explore options to obtain poison center data, if determined to be useful; collect information on how it uses AERs; provide more information to the public about AERs; and establish a time frame to finalize guidance related to GAO's 2009 recommendations. FDA generally concurred with each of GAO's recommendations.Read the full GAO Report (PDF):
DIETARY SUPPLEMENTS - FDA May Have Opportunities to Expand Its Use of Reported Health Problems to Oversee Products
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