An update to the FDA Adverse Event Reporting System (FAERS) Public Dashboard

Activity: FDA Drug Topics
Tue, 10/9 2018: 1:00 PM  - 2:00 PM 
Regularly Scheduled Series 
FDA 
Credits:
This webinar will provide an updated overview of the changes in the FAERS Public Dashboard, a highly interactive web-based tool that allows for the querying of FAERS data in a user-friendly fashion. These changes includes displaying report counts by quarter and month, search by reactions and data export. The intention of this tool is to expand access to the FAERS data to the general public to search for information related to human adverse events reported to the FDA by the pharmaceutical industry, healthcare providers and consumers. FDA anticipates that this increased transparency will help to spur the submission of more detailed and complete reports from consumers, health care providers and other members of the public.

Objectives

Describe the FAERS public database and summarize the recent updates.|Demonstrate how to use the FAERS public dashboard to view information on adverse event reporting metrics.|Illustrate use of FAERS public dashboard to view adverse event information on a specific product. 

Faculty

Suranjan De, FDA

Activity Coordinator

Lesley Navin, FDA/CDER/DDI