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US Food and Drug Administration (FDA) Adverse Event (AE) Reporting System (FAERS) is a major source of data for monitoring drug safety. However, there is not general procedure to systematically… Click to show full abstract
US Food and Drug Administration (FDA) Adverse Event (AE) Reporting System (FAERS) is a major source of data for monitoring drug safety. However, there is not general procedure to systematically compare drugs group. We present a statistical method, which can effectively identify significant differences in AE rates among drugs and estimates the differences in age and gender distributions.
Keywords:
effects among;
comparing different;
different adverse;
among multiple;
adverse effects;
multiple drugs
Journal Title: Studies in health technology and informatics
Year Published: 2017
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Journal Title: Studies in health technology and informatics
Year Published: 2017
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!