Discover how post-marketing pharmacovigilance detects rare drug side effects missed in clinical trials. Learn about global monitoring systems, AI advancements, and how your reports contribute to safer medicines.
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Learn how to report side effects and adverse reactions to the FDA using MedWatch. This guide explains who can report, what counts as serious, how to fill out the form, and why your report matters for public safety.
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Serious adverse events from generic drugs are underreported due to confusing labeling, lack of resources, and systemic gaps. Learn how to report correctly, why the system fails, and what’s being done to fix it.
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