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Development of a drug safety ePlatform for physicians, pharmacists, and consumers based on post-marketing adverse events

Using Real Wold Data from the FDA Adverse Event Reporting System (FAERS)

Development of a drug safety ePlatform for physicians, pharmacists, and consumers based on post-marketing adverse events

The FDA’s sizeable repository of patient case reports linking AEs to approved drugs is the Adverse Event Reporting System (FAERS). We believe that open and user-friendly access to the millions of case reports in FAERS would help advance the field of post-marketing pharmacovigilance.

 

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