FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA (U.S. Food and Drug Administration). The informatic...

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA (U.S. Food and Drug Administration). The informatic...

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA (U.S. Food and Drug Administration). The informatic...