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U.S. Department of Health and Human Services

About FDA

Number of mandatory adverse event reports from the dietary supplement industry entered into CAERS in the month

Dictionary: FDA’s Center for Food Safety and Applied Nutrition Adverse Event Reporting System (CAERS) captures data on adverse events and product complaints reported about food, dietary supplements or cosmetics. These reports come from consumers, health professionals, the industry or others. Information from reports on adverse events experienced by individuals aids FDA in detecting problems with the safety of these products.

Fiscal Year - 2011

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TimeTargetNumber
Oct 2010N/A88
Nov 2010N/A114
Dec 2010N/A136
Jan 2011N/A65
Feb 2011N/A145
Mar 2011N/A182
Apr 2011N/A134
May 2011N/A321
Jun 2011N/A117
Jul 2011N/A149
Aug 2011N/A172
Sep 2011N/A154

FY 2011 Total: 1,777

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.