martedì, 27 luglio 2021
Medinews
3 Ottobre 2017

FDA improves access to reports of adverse drug reactions

September 28, 2017 – 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. “Tools like the FDA Adverse Event Reporting System are critical to the FDA’s ability to help ensure the … (leggi tutto)

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