domingo, 9 de septiembre de 2018

Pharmacogenetic Labeling of FDA-Approved Drugs: A Regulatory Retrospective. - PubMed - NCBI

Pharmacogenetic Labeling of FDA-Approved Drugs: A Regulatory Retrospective. - PubMed - NCBI



 2018 Aug 28;3(4):545-549. doi: 10.1016/j.jacbts.2018.06.001. eCollection 2018 Aug.

Pharmacogenetic Labeling of FDA-Approved Drugs: A Regulatory Retrospective.

Abstract

The U.S. Food and Drug Administration recently marked 10 years since first updating the labeling for warfarin (often referred to as the "poster child" of pharmacogenomics) to include information regarding the potential impact of CYP2C9 and VKORC1 genetic variation on warfarin dosing requirements and risks. Herein, we opine on the experience updating the warfarin labeling, highlighting more generally the enabling factors and challenges encountered when considering incorporation of pharmacogenomic information into the prescribing recommendations for already approved drugs. We also provide a historical perspective of implemented changes in regulatory policies related to personalized medicine.

KEYWORDS:

drug labeling; pharmacogenomics; precision medicine; regulatory perspective; warfarin

PMID:
 
30175278
 
PMCID:
 
PMC6115648
 
DOI:
 
10.1016/j.jacbts.2018.06.001

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