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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 December 31, 2014

Fiscal Year - 2015

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Oct 2014N/A298,876
Nov 2014N/A300,332
Dec 2014N/A302,516
Jan 2015N/ATBD
Feb 2015N/ATBD
Mar 2015N/ATBD
Apr 2015N/ATBD
May 2015N/ATBD
Jun 2015N/ATBD
Jul 2015N/ATBD
Aug 2015N/ATBD
Sep 2015N/ATBD

FY 2015 YTD: 302,516


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.