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U.S. Department of Health and Human Services

About FDA

Number of MedWatch e-list subscribers (www.fda.gov/Safety/MedWatch) during the month

Dictionary: MedWatch is FDA's Safety Information and Adverse Event Reporting Program. It is the FDA gateway for clinically important safety information and reporting serious problems with FDA-regulated products. MedWatch offers many ways to help the public stay informed. It sends safety alerts directly to subscribers as soon as they appear on the website. OEA's Office of Health and Constituent Affairs (OHCA) oversees MedWatch as well as its subscriber base to assess its growth and change over time.

Information is current as of March 31, 2015

Fiscal Year - 2013

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Oct 2012N/AN/A
Nov 2012N/AN/A
Dec 2012N/AN/A
Jan 2013N/AN/A
Feb 2013N/AN/A
Mar 2013N/AN/A
Apr 2013N/A245,324
May 2013N/A247,973
Jun 2013N/A250,457
Jul 2013N/A254,680
Aug 2013N/A258,446
Sep 2013N/A261,395

FY 2013 Total: 261,395


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.