|Browse All Terms|
|Beginning With||By Language|
|A B C D E F G H I J K L M N O P Q R S T U V W X Y Z :: All||
AERS is a computerized database containing reports of adverse events. It supports FDA’s post-market safety surveillance program for all approved drugs and therapeutic biologics.
Publication Source: Guide to Drug Safety Terms at FDA
Publication Date: 2008
Do you have a term that should be included in the glossary?
Submit a term for review