Adding pharmacogenetics information to drug labels: Lessons learned

Abstract:

The US Food and Drug Administration approved a revised package insert for two cancer drugs to include information about the increased risk of severe adverse events owing to enzyme deficiencies caused by genetic variants. The label revisions stopped...

Type:
Journal Article
Date:
Authors and Contributors:
Susanne B. Haga Kenneth E. Thummel Wylie Burke
Pages:
847–854
Issue:
12
Volume:
16
Publication:
Pharmacogenetics and Genomics
LawSeqSM Record Last Modified:
08/07/2018