How to ascertain drug safety in the context of benefit. Controversies and concerns

Publication type
Journal article
Authors
Simon LS, Strand V, Boers M, Brooks PM, Tugwell P, Bombardier C, Fries JF, Henry D, Goldkind L, Guyatt GH, Laupacis A, Lynd L, Macdonald T, Mamdani M, Moore A, Saag KS, Silman AJ, Stevens R, Tyndall A
Date published
2009 Sep 01
Journal
Journal of Rheumatology
Volume
36
Issue
9
Pages
2114-2121
Open Access?
No
Abstract

There is great concern about clearly defining benefit and risk in the context of both drug development and clinical practice. In view of this pressure, the OMERACT Executive identified the need to bring together clinical trialists, pharmacoepidemiologists, clinicians, clinical epidemiologists, statistical experts, and regulatory representatives to discuss different approaches to define risk and perhaps improved ways to express it. Each attendee spoke on a given topic and the group was charged to consider the issue of risk in the context of formally posed questions. This article provides a summary of the presentations and outlines the discussions that followed