Reasons for the wide range in reported adverse drug event rates include discrepancies in the definitions and data collection methods used. Great care must be taken when interpreting the results of studies of adverse drug events and other types of medical harm, and standardised methods and definitions are needed to compare adverse drug event rates.
CITATION STYLE
Dean, B. (2003). Adverse drug events: What’s the truth? Quality and Safety in Health Care. BMJ Publishing Group. https://doi.org/10.1136/qhc.12.3.165
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