Michigan Inventors Coalition: Pharma Insights

Tag: postmarket surveillance

How the FDA Monitors Drug Safety After Medication Approval

By Joe Barnett    On 2 Feb, 2026    Comments (0)

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The FDA doesn't stop monitoring drugs after approval. Using FAERS, Sentinel, AI tools, and REMS programs, it tracks side effects in millions of real-world patients to catch hidden risks and protect public health.

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