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FDA improves access to reports of adverse drug reactions

FDA improves access to reports of adverse drug reactions

New online tool makes it easier for users to search the FDA Adverse Event Reporting System

The U.S. Food and Drug Administration today launched a new user-friendly search tool that improves access to data on adverse events associated with drug and biologic products through the FDA’s Adverse Event Reporting System (FAERS). The tool is designed to make it easier for consumers, providers, and researchers to access this information. Continue reading

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