BMJ 2004;329:31-34 (3 July), doi:10.1136/bmj.329.7456.31
Clinical review
Balancing benefits and harms: the example of non-steroidal anti-inflammatory drugs
Paul Dieppe, professor1,
Christopher Bartlett, research assistant1,
Peter Davey, professor2,
Lesley Doyal, professor3,
Shah Ebrahim, professor1
1 Medical Research Council Health Services Research Collaboration, Department of Social Medicine, University of Bristol, Bristol BS8 2PR,
2 Medicines Monitoring Unit (MEMO), Divisions of Community Health Sciences and Medicine and Therapeutics, University of Dundee, Dundee,
3 School for Policy Studies, University of Bristol
Correspondence to: P Dieppe p.dieppe@bristol.ac.uk
| The first 150 words of the full text of this article appear below. |
Introduction
To provide safe and effective interventions for people, reliable
and valid evidence is needed. This is most easily produced by
undertaking trials in samples of people who are as homogeneous
as possible and applying the results to similar, well defined
groups of patients. To be equitable, however, appropriate care
needs to be provided for everyone in the diverse community using
health services. Therefore, there is a tension between obtaining
scientific evidence that is reliable but which can be applied
only to a small subset of the population, and distributive justice
that requires that all in need are treated equally appropriately.
Drugs have potential harms as well as benefits. Doctors would like to be able to balance any risks against benefits to derive a therapeutic ratio for each patient, but this is difficult. Formal trials can tell a lot about the efficacy of a drug in a specific context, but unless . . . [Full text of this article]
Risks and benefits of NSAIDs in treating joint pain
MethodsResultsCommunity cohort
Validity of trials
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Adverse event reportingRisk benefit ratioDifferent indicationsThe need for record linkage

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