Understanding and Reporting Adverse Reactions: How Do I Report Suspected Adverse Reactions?
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3 min read
The FDA receives over one million adverse event reports annually through its MedWatch program, a cornerstone of post-market surveillance. This system allows patients, consumers, and healthcare professionals to contribute vital data, directly addressing the key question of how do I report suspected adverse reactions. Your report helps identify new or rare side effects and potential safety issues with FDA-regulated products, ensuring a safer medical landscape for everyone.
