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Social Media “Revolution” Expected In Adverse Events Signal Detection

 
• By Sarah Karlin-Smith

Technology is ready now, and the agency anticipates Twitter and Facebook will become part of the “key instruments” of pharmacovigilance in the next five years, says Henry Francis, CDER’s data mining chief.

FDA expects advances in information technology to vastly expand how the agency collects and analyzes adverse event information on social media platforms like Twitter and Facebook.

While FDA currently relies on a single system of adverse event reporting to detect drug safety signals post-market, that is going to change, says Henry Francis, director for data mining and informatics evaluation and research in

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More from North America

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• By Sue Sutter

Some advisory committee members said adding quantitative data on misuse, abuse, opioid use disorder and overdose to labeling would be helpful, but others worried the two epidemiological studies were not sufficiently generalizable to a broader population.

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• By Dean Rudge

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• By Jessica Merrill

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