Tag: FDA adverse events
MedWatch Reporting for Generics: How Safety Data Is Collected and Why It Matters
- By : Tamsin Riverton
- Date : Jan 11 2026
MedWatch is the FDA's system for collecting safety data on generic drugs, but underreporting and lack of manufacturer details make it hard to track problems. Learn how reports are filed, why therapeutic inequivalence matters, and how you can help improve generic drug safety.
