Tag: adverse event reporting
Adverse Event Monitoring for Biosimilars: How Safety Surveillance Works Today
Biosimilars require specialized safety monitoring due to their complex biology. Learn how adverse event reporting, traceability, and real-world surveillance systems ensure patient safety while expanding access to affordable biologic treatments.
How to Report Adverse Events to the FDA for Medications: A Step-by-Step Guide
Learn how to report medication side effects to the FDA through MedWatch. Step-by-step guide for patients, caregivers, and healthcare providers to ensure drug safety and help prevent future harm.