The Adverse Event
The Adverse Event Reporting System (AERS) is FDA's computerized database. AERS contains all mandatory adverse drug event reports from pharmaceutical companies, voluntary reports from health care providers and consumers through MedWatch and medication error reports obtained through MedWatch and the Institute for Safe Medication Practices. There are more than 6 million reports in AERS.
Lesson status: Incomplete (0% done)
Topic: page 1 of 5 (Lesson: page 24 of 52)