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FDA Launches Searchable Adverse Event Database for Drugs and Biologics By Michael Mezher - Published 29 September 2017

The US Food and Drug Administration (FDA) on Wednesday launched a new searchable public dashboard for its adverse event database for drugs and biologics.

Categories: News, US, FDA, Biologics and biotechnology, Drugs, Postmarket surveillance

Tags: FAERS, Public Dashboard, Adverse Event Reports