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

Main

Number of mandatory adverse event reports from the dietary supplement industry entered into CAERS in the monthFDA’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.

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2010

FY 2010 Total: 830

Oct 200984Nov 200940Dec 200948Jan 201060Feb 201069Mar 201090Apr 201077May 2010103Jun 201076Jul 201076Aug 201069Sep 201038

2011

FY 2011 Total: 1,777

Oct 201088Nov 2010114Dec 2010136Jan 201165Feb 2011145Mar 2011182Apr 2011134May 2011321Jun 2011117Jul 2011149Aug 2011172Sep 2011154

2012

FY 2012 YTD: 489

Oct 2011149Nov 2011165Dec 2011175Jan 2012Feb 2012Mar 2012Apr 2012May 2012Jun 2012Jul 2012Aug 2012Sep 2012

http://www.fda.gov/AboutFDA/Transparency/track/ucm206221.htmFDA-TRACK CFSAN Dashboardhttp://www.fda.gov/downloads/Food/DietarySupplements/GuidanceComplianceRegulatoryInformation/UCM267417.pdfFor Industry At a Glance: Dietary Supplements – Reporting an Adverse Event

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