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Issue title: Health Care
Article type: Research Article
Authors: Vredenburgh, Alison G. | Zackowitz, Ilene B.
Affiliations: Vredenburgh & Associates, Inc., Human Factors, Safety, and Organizational Consulting, Carlsbad, CA, USA
Note: [] Address for correspondence: Alison G. Vredenburgh, PhD, CPE, Principal, Vredenburgh & Associates, Inc., Human Factors, Safety, and Organizational Consulting, 2588 El Camino Real, F-353, Carlsbad, CA 92008, USA. Tel.: +1 760 434 4741; E-mail: [email protected]
Abstract: Adverse drug events (ADE) are defined as any medication error with significant potential to harm a patient [13]. Often times, ADE occur due to inadequate or ineffective systems of labeling. These ADE often result in mistakes in prescription adherence (compliance) with the prescription instructions. These mistakes are costly and can be deadly. Potential problems with drug labeling can occur in both in-patient and out-patient environments. This paper discusses some of the key issues to consider in drug labeling and its impact on patient safety.
Keywords: Medication, adverse reaction, prescriptions, warnings, adverse drug event (ADE), patient safety
DOI: 10.3233/WOR-2009-0863
Journal: Work, vol. 33, no. 2, pp. 169-174, 2009
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