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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 - 2010

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TimeTargetNumber
Oct 2009N/A84
Nov 2009N/A40
Dec 2009N/A48
Jan 2010N/A60
Feb 2010N/A69
Mar 2010N/A90
Apr 2010N/A77
May 2010N/A103
Jun 2010N/A76
Jul 2010N/A76
Aug 2010N/A69
Sep 2010N/A38

FY 2010 Total: 830

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.