Electronic Submission of Adverse Event Reports to FDA FAERS
Electronic Submission of Adverse Event Reports to FDA FAERS
Apr 28, 2019
fda.gov
FDA starts 'real-time reporting of adverse event data' for first time
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How the Vaccine Adverse Event Reporting System (VAERS) works
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The Med Safety App is a tool to improve reporting of Adverse Drug Reactions (ADRs), Adverse Events Following Immunization (AEFI) and side effects to medical products (incl. vaccines) used for the prevention and management of COVID-19. The Med Safety App can be used to: - Report a suspected side effect to a medicine, including vaccines, herbal products, and homeopathic remedies. - Stay up to date with all the latest safety information published by NAFDAC using the newsfeed. - Create watchlists fo
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