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J Med Ethics 2004;30:608-609
© 2004 BMJ Publishing Group Ltd & Institute of Medical Ethics


LETTER

Non-compliance: a side effect of drug information leaflets

F Verdú, A Castelló

Department of Legal Medicine, College of Medicine and Odontology, University of Valencia, Valencia, Spain

Correspondence to:
Dr F Verdú
Department of Legal Medicine, College of Medicine and Odontology, University of Valencia E G, Av/ Blasco Ibañez, n°15, 46010-Valencia (Spain); Fernando.Verdu@uv.es

Keywords: non-compliance; side effect; informed consent

The first 150 words of the full text of this article appear below.

The problem of non-compliance with treatment and its repercussions on the clinical evolution of different conditions has been widely investigated.1–4 Non-compliance has also been shown to have significant economic implications, not only as a result of product loss but also indirectly through the complication of disease management and its subsequent healthcare and social costs.5–7


Non-compliance as a health problem
The term "non-compliance" might be taken to refer both to the failure to follow a drug regimen and to the failure to adopt other measures that contribute to improvement in health—for example, changes in lifestyle or diet. This letter focuses on the former.

Non-compliance with a drug regimen can be the result of a number of different factors9–11 and a variety of techniques have been developed in an attempt to control it.12,13 Of these, the few techniques that have been shown to be effective have only managed to solve the problem in specific situations over short . . . [Full text of this article]







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