The FAERS Public Dashboard and its Value to the Pharmaceutical Industry
Jul 31, 2018 - 00:24:45
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Radio and PodcastLive Radio & PodcastsMany 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. Rece...
The FDA's Adverse Event Reporting System (FAERS) Public Dashboard is an episode from FDA Drug Information Updates by ReachMD. Many listeners may be familiar with the FDA's Adverse Event Reporting System or FAERS. Data in FAERS supports the...
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Published Oct 29, 2017, 00:09:22 long, audio available.
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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.
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The FDA's Adverse Event Reporting System (FAERS) Public Dashboard is an episode from FDA Drug Information Updates by ReachMD.
This episode is 00:09:22 long.
This episode was published on Oct 29, 2017.
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