Complementing the US Food and Drug Administration Adverse Event Reporting System With Adverse Drug Reaction Reporting From Social Media: Comparative Analysis.

JMIR Public Health Surveill · 2020 · PMC7557434 · PMID 32996889

Europe PMC DOI

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might not be significantno p-value reported

This situation could potentially be resolved by extending the time frame to more than 1 year; however, the extent of sample size improvement might not be significant given the low number of social media users when studying specific drugs such as atorvastatin and amlodipine.

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