About FDA
Number of Adverse Events (AE) reported for drugs/biological products (15-day manufacture reports)
Dictionary: The FDA receives hundreds of thousands of AE reports each year. The AE reports are monitored very closely to determine whether or not a serious safety signal is observed and whether a regulatory action might be necessary.
Information is current as of December 31, 2017.
Fiscal Year - 2017
| Time | Target | Number |
|---|---|---|
| Oct 2016 | N/A | 67,805 |
| Nov 2016 | N/A | 73,397 |
| Dec 2016 | N/A | 75,414 |
| Jan 2017 | N/A | 75,733 |
| Feb 2017 | N/A | 72,852 |
| Mar 2017 | N/A | 83,383 |
| Apr 2017 | N/A | 72,402 |
| May 2017 | N/A | 80,430 |
| Jun 2017 | N/A | 79,900 |
| Jul 2017 | N/A | 75,854 |
| Aug 2017 | N/A | 80,126 |
| Sep 2017 | N/A | 77,183 |
FY 2017 Total: 914,479
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.
