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
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.