Tag: FDA MedWatch

12 January 2026 9 Comments Tessa Marley

How to Report Adverse Drug Reactions to FDA MedWatch

Learn how to report adverse drug reactions to FDA MedWatch. Understand who can report, what counts as serious, and why your report matters for drug safety. Step-by-step guide for patients and professionals.

12 December 2025 12 Comments Tessa Marley

Serious Adverse Events: How to Report Generic Drug Reactions Correctly

Serious adverse events from generic drugs are underreported due to unclear manufacturer identification. Learn how to report reactions correctly, why the system fails, and what’s being done to fix it.

17 November 2025 8 Comments Tessa Marley

FDA MedWatch: How to Report Side Effects and Adverse Drug Reactions

Learn how to report side effects and adverse reactions to the FDA using MedWatch. Step-by-step guide for patients, caregivers, and healthcare providers on filing reports to improve drug and device safety.