National Academies of Sciences%2c Engineering%2c and Medicine

Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals: Workshop Summary

Adverse reactions to prescription drugs (adverse drug events, or ADEs) are quite common and usually do little harm to patients. But in a small percentage of cases, they can have serious consequences ...
The Scientist

The FDA's New Adverse Event Dashboard: More Data Doesn't Mean a Better Understanding

On March 11, the FDA launched the Adverse Event Monitoring System (AEMS), consolidating several fragmented reporting databases into a single real-time public dashboard with artificial intelligence ...