Discordance Between Availability of Pharmacogenetics Studies and Pharmacogenetics-Based Prescribing Information for the Top 200 Drugs
- 1 April 2006
- journal article
- Published by SAGE Publications in Annals of Pharmacotherapy
- Vol. 40 (4) , 639-644
- https://doi.org/10.1345/aph.1g464
Abstract
Background: Despite growing numbers of pharmacogenetics studies, little pharmacogenetics-based prescribing information is available to practitioners. It is possible that the lack of prescribing data for commonly used drugs is due to a paucity of evidence-based pharmacogenetics literature for these agents. Objective: To investigate the relationship between pharmacogenetics prescribing data in drug package inserts (Pls) and pharmacogenetics research literature for agents represented in the top 200 prescribed drugs for 2003. Methods: A PubMed search (to August 7, 2004) was performed to identify pharmacogenetics studies relevant to the top 200 drugs. These data were compared with Pls for drugs in the top 200 list that contained pharmacogenetics prescribing information. Results: Pharmacogenetics data in the literature were available for 71.3% of the top 200 drugs. The gene involved coded for a drug-metabolizing enzyme in 34.5% of the literature sampled. The remaining 65.5% of the pharmacogenetics studies contained information largely related to genetic variability in target proteins and drug transporters. Three drugs with Pls containing pharmacogenetics prescribing information deemed to be useful to guide therapy were in the top 200 list (celecoxib, fluoxetine, pantoprazole). There was no consensus on the strength of association between genetic variability and drug response for these agents. Conclusions: The lack of specific pharmacogenetics-based prescribing information in Pls for commonly used drugs does not seem to be related to a paucity of pharmacogenetics data in the research literature. Rather, other factors including, but not limited to, the uncertain clinical relevance of genetic associations may make practical prescribing recommendations difficult.Keywords
This publication has 21 references indexed in Scilit:
- Availability of pharmacogenomics-based prescribing information in drug package inserts for currently approved drugsThe Pharmacogenomics Journal, 2004
- CYP2C19 Polymorphism and Proton Pump InhibitorsBasic & Clinical Pharmacology & Toxicology, 2004
- Effect of CYP2D6 and CYP2C9 genotypes on fluoxetine and norfluoxetine plasma concentrations during steady-state conditionsEuropean Journal of Clinical Pharmacology, 2004
- No evidence of increased adverse drug reactions in cytochrome P450 CYP2D6 poor metabolizers treated with fluoxetine or nortriptylineHuman Psychopharmacology: Clinical and Experimental, 2004
- Polymorphisms in the CYP 2D6 Gene: Association with Plasma Concentrations of Fluoxetine and ParoxetineTherapeutic Drug Monitoring, 2003
- Cytochrome P450 2D6 genotype does not predict SSRI (fluoxetine or paroxetine) induced hyponatraemiaHuman Psychopharmacology: Clinical and Experimental, 2002
- Pharmacogenomics: The Inherited Basis for Interindividual Differences in Drug ResponseAnnual Review of Genomics and Human Genetics, 2001
- Stereoselective pharmacokinetics of pantoprazole, a proton pump inhibitor, in extensive and poor metabolizers of S-mephenytoinClinical Pharmacology & Therapeutics, 2001
- Fluoxetine-Related Death in a Child with Cytochrome P-450 2D6 Genetic DeficiencyJournal of Child and Adolescent Psychopharmacology, 2000
- Metabolic disposition of pantoprazole, a proton pump inhibitor, in relation to S-mephenytoin 4′-hydroxylation phenotype and genotype*Clinical Pharmacology & Therapeutics, 1997