Tag: adverse event reporting

Toby Rotman
20 Mar, 2026

How to Report Adverse Drug Events to FDA MedWatch: Step-by-Step Guide for Patients and Providers

Learn how to report dangerous drug side effects to the FDA's MedWatch system. Step-by-step guide for patients and providers on filling out forms, what to include, and why your report matters.

Toby Rotman
7 Feb, 2026

Accessing FDA Adverse Event Databases: Transparency and Tools

The FDA's FAERS database provides public access to millions of drug side effect reports. Learn how to use the Public Dashboard, OpenFDA API, and quarterly data extracts - and why this tool matters for patient safety.

Toby Rotman
4 Jan, 2026

MedWatch System Explained: How FDA Tracks Drug and Device Safety

MedWatch is the FDA's system for collecting safety reports on drugs, devices, and other medical products. Learn how it works, who reports, why underreporting is a problem, and how your report can help save lives.

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