What is the significance of the FDA's Adverse Event Reporting System (FAERS)?
FAERS is a vital post-market surveillance tool used by the FDA to monitor the safety of drugs and biologics. It collects information on adverse events and medication errors, which helps identify potential safety concerns. Through data analysis, the FDA can identify new risks associated with a product, leading to updated safety information, label changes, or even product recalls. This system highlights the FDA's commitment to public health protection by continuously evaluating product safety even after market approval.
