print email comment close Adverse Event Reporting System (AERS) URL: http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/default.htm Description: AERS is a "database designed to support the FDA's post-marketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products." The site features quarterly reports, a table showing potential signals of serious risks identified by AERS, and related material. From the Food and Drug Administration (FDA). Publisher: Food and Drug Administration (FDA) LII Database Information: Record 26847 created by Maria Brandt on 09/07/2008 Last modification on 07/29/2009 Published: 09/11/2008   Funding agency: California State Library LII Item ID: http://lii.org/cs/lii/view/item/26847