Development of a computerized adverse drug event monitor.

Adverse events during drug therapy are receiving renewed attention. Some adverse drug events (ADEs) are identified only after the widespread clinical use of a drug. The Food and Drug Administration advocates post-marketing surveillance systems to provide early warnings of previously undetected ADEs....

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Bibliografische gegevens
Hoofdauteurs: Evans, R. S., Pestotnik, S. L., Classen, D. C., Bass, S. B., Menlove, R. L., Gardner, R. M., Burke, J. P.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Medical Informatics Association 1991
Onderwerpen:
Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2247488/
https://ncbi.nlm.nih.gov/pubmed/1807594
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