menu

The FDA's Adverse Event Reporting System (FAERS) Public Dashboard

Be part of the knowledge.
Register

ReachMD is even better when
you join the community!
Registration is free and easy.

Register Now

The FDA's Adverse Event Reporting System (FAERS) Public Dashboard

    Dr. Janet Woodcock, Director of the FDA Center for Drug Evaluation and Research, discusses the new FAERS Dashboard's strengths and limitations.
    • Overview

      Many listeners may be familiar with the FDA's Adverse Event Reporting System or FAERS.  Data in FAERS supports the FDA's post-marketing safety surveillance program for drug products and therapeutic biologic products.  Recently, CDER's Office of Surveillance and Epidemiology created and released a tool that makes FAERS data easier to query and retrieve.  This new interactive dashboard is designed to expand access of FAERS data to the general public.

      Dr. Janet Woodcock, Director of the FDA Center for Drug Evaluation and Research, discusses the advantages of the tool as well as its limitations.

    Facebook Comments

    You must be in to display playlists.

    Get a Dose of ReachMD in Your Inbox
    and Practice Smarter Medicine

    Stay current with the best in medical education.