FDA Drug Topics: An update to the FDA Adverse Event Reporting System (FAERS) Public Dashboard – October 9, 2018
FDA’s Division of Drug Information in the Center for Drug Evaluation and Research (CDER) is excited to present a series of educational webinars targeting the needs of all health care professionals and students, including physicians, physician assistants, nurses, pharmacists, and pharmacy technicians. Interact with FDA staff from a variety of divisions and learn more about the FDA and drug regulation!
On Tuesday, October 9, 2018, at 1pm (EDT), CDER's Office of Communication, Division of Drug Information (DDI) will host a webinar titled: FDA Drug Topics: An update to the FDA Adverse Event Reporting System (FAERS) Public Dashboard. 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, health care 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.
Activity Outline and Continuing Education Information: An update to the FDA Adverse Event Reporting System (FAERS) Public Dashboard (PDF - 167KB)
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