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U.S. Department of Health and Human Services

About FDA

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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 September 30, 2018

Fiscal Year - 2018

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TimeTargetNumber
Oct 2017N/A433,409
Nov 2017N/A442,998
Dec 2017N/A441,831
Jan 2018N/A403,447
Feb 2018N/A403,743
Mar 2018N/A398,488
Apr 2018N/A402,120
May 2018N/A400,318
Jun 2018N/A399,876
Jul 2018N/A385,798
Aug 2018N/A386,128
Sep 2018N/A384,769

FY 2018 Total: 384,769

Footnotes

  • The FDA subscriber email distribution system was replaced in FY 2017 Quarter 3. Subscriber data was reviewed and updated during this transition.”

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.

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