Author Affiliations: Jesse Brown VA Medical
Center/Mid-West Center for Health Services and Policy Research, Chicago, Ill
(Drs Bennett and Parada); Divisions of Hematology/Oncology (Ms Lyons, Drs
Bennett, Carson, Evens, Kuzel, and Tallman), Division of Cardiology (Dr Davidson),
Department of Emergency Medicine (Dr Yarnold), Division of General Internal
Medicine (Dr Belknap), Division of Geriatric Medicine (Dr McKoy), Department
of Dermatology (Dr West), Robert H. Lurie Comprehensive Cancer Center, Northwestern
University Feinberg School of Medicine, Chicago, Ill (Drs Bennett, Carson,
Evens, Kuzel, Tallman); Department of Pharmacy, Northwestern Memorial Hospital,
Chicago, Ill (Mr Trifilio); Institute for Health Services Research and Policy
Studies at Northwestern University, Evanston, Ill (Drs Carson and Bennett);
Center for Pharmacoeconomic Research, College of Pharmacy, University of Illinois
at Chicago, Chicago (Dr Schumock); San Antonio VA and the Department of Medicine
at the University of Texas at San Antonio, San Antonio (Dr Feldman); VA Cooperative
Studies Program Clinical Research Pharmacy Coordinating Center, University
of New Mexico, Albuquerque (Dr Raisch); University of Utah School of Medicine
and the Salt Lake City VA, Salt Lake City (Drs Nebeker and Samore); Departments
of Medicine and Oncology, McGill University, Montreal, Canada (Dr Cournoyer);
Stanley Scott Cancer Center and the Divisions of Hematology/Oncology of the
Louisiana State University School of Medicine, New Orleans (Dr Sartor).
Context In 1998, a multidisciplinary team of investigators initiated RADAR (Research
on Adverse Drug events And Reports), a clinically based postmarketing surveillance
program that systematically investigates and disseminates information describing
serious and previously unrecognized adverse drug and device reactions (ADRs).
Objective To describe the structure, operations, and preliminary findings from
the RADAR project and related dissemination efforts by pharmaceutical suppliers
and the US Food and Drug Administration (FDA).
Design After identifying a serious and unexpected clinical event suitable for
further investigation, RADAR collaborators postulated clinical hypotheses
and derived case series and incidence estimates from physician queries, published
and unpublished clinical trials, published case reports, FDA databases, and
manufacturer sales figures.
Results RADAR investigators identified 16 types of serious ADRs among 1699 patients,
of whom 169 (10%) died as a result of the reaction. Initial cases were identified
by 7 RADAR investigators, 4 collaborating physicians, 2 attorneys, and by
reviewing 3 published reports. Additional sources included queries of occupational
health programs and medical directors of interventional cardiology laboratories
(3 types of ADRs), published manuscripts and clinical trials (11 types of
ADRs), review of medical records at a RADAR site (2 types of ADRs), unpublished
clinical trial reports (3 types of ADRs), and reports from attorneys, family
members, or patients (4 types of ADRs). Incidence estimates, ranging from
0.4% to 33%, were derived from 5 clinical trial reports, 2 physician queries,
and 2 observational databases. Laboratory support for hypotheses included
identification of 3 neutralizing antibodies and 3 histopathological findings.
ADR reports were disseminated as 8 revised package inserts, 7 “dear
doctor” letters, and 9 peer-reviewed articles.
Conclusion A new, clinically based, hypothesis-driven approach to postmarketing
surveillance may supplement existing regulatory surveillance systems and improve
Bennett CL, Nebeker JR, Lyons EA, et al. The Research on Adverse Drug Events and Reports (RADAR) Project. JAMA. 2005;293(17):2131–2140. doi:https://doi.org/10.1001/jama.293.17.2131
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