Safety Alerts for Drugs, Biologics, Devices, and Dietary
Supplements (last revised 10/29/2004)
Medical product safety alerts, Class
I recalls,
market withdrawals, public health advisories
Vaccine Adverse Event Reporting
System (VAERS)
VAERS is a cooperative program for vaccine
safety of the Centers for Disease Control and Prevention (CDC)
and the Food and Drug Administration (FDA). VAERS collects
information about adverse events that occur after the administration
of U.S. licensed vaccines.
Manufacturer
and User Facility Device Experience Database (MAUDE)
Search database information of all voluntary
reports since June, 1993, user facility reports since 1991,
distributor reports since 1993, and manufacturer reports since
August, 1996. (MDR Data files, 1992-1996)