Tag: FAERS
How the FDA Monitors Drug Safety After Medication Approval
The FDA uses a mix of reporting systems, real-time data analysis, and strict regulations to monitor drug safety after approval. Learn how FAERS, Sentinel, and REMS work together to catch hidden risks and protect patients.
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How to Report a Suspected Adverse Drug Reaction to the FDA
Learn how to report a suspected adverse drug reaction to the FDA using MedWatch. Step-by-step guide for patients, caregivers, and healthcare providers on what to report, how to file, and why it matters for drug safety.
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