Abstract:
:Pharmacogenomics is one of the first clinical applications of the postgenomic era. It promises personalized medicine rather than the established "one size fits all" approach to drugs and dosages. The expected reduction in trial and error should ultimately lead to more efficient and safer drug therapy. In recent years, commercially available pharmacogenomic tests have been approved by the Food and Drug Administration (FDA), but their application in patient care remains very limited. More generally, the implementation of pharmacogenomics in routine clinical practice presents significant challenges. This article presents specific clinical examples of such challenges and discusses how obstacles to implementation of pharmacogenomic testing can be addressed.
journal_name
PLoS Medjournal_title
PLoS medicineauthors
Swen JJ,Huizinga TW,Gelderblom H,de Vries EG,Assendelft WJ,Kirchheiner J,Guchelaar HJdoi
10.1371/journal.pmed.0040209subject
Has Abstractpub_date
2007-08-01 00:00:00pages
e209issue
8eissn
1549-1277issn
1549-1676pii
07-PLME-RIT-0029journal_volume
4pub_type
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