. "A Workshop Agenda." Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals: Workshop Summary. Washington, DC: The National Academies Press, 2007.
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Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals - Workshop Summary
Saira A. Jan, PharmD, MS
Horizon Blue Cross Blue Shield of New Jersey
Rutgers Ernest Mario School of Pharmacy
9:30 am
Discussion
10:45 am
Break
Topic 2: Once rare event reports have been received, how to identify possible signal and distinguish it from noise.
11:00 am
Anne E. Trontell, MD, MPH
U.S. Food and Drug Administration
David Hunt, MD, FACS
CMS Quality Improvement Group
11:20 am
Discussion
12:15 pm
Lunch
COMMON EVENTS AND THE MODULATION OFTHEIR FREQUENCY BY DRUGS
Topic 1: It is possible that drugs can modify the frequency of occurrence of a relatively common event. How can these events be detected?
