Publication | Open Access
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for <i>CYP2C9</i> and <i>HLA‐B</i> Genotypes and Phenytoin Dosing: 2020 Update
163
Citations
27
References
2020
Year
Toxic Epidermal NecrolysisTherapeutic Drug MonitoringTranslational PharmacologyClinical TherapeuticAntiepileptic DrugPhenytoin DosingInherited Metabolic DiseaseGenetic EpidemiologyClinical TrialsPharmacologyStevens-johnson SyndromePharmacotherapyPharmacogenomicsMedicineGenomic MedicineGenetic MedicineAdverse Drug ReactionMolecular Medicine
Phenytoin is an antiepileptic drug with a narrow therapeutic index and large interpatient pharmacokinetic variability, partly due to genetic variation in CYP2C9. Furthermore, the variant allele HLA-B*15:02 is associated with an increased risk of Stevens-Johnson syndrome and toxic epidermal necrolysis in response to phenytoin treatment. We summarize evidence from the published literature supporting these associations and provide therapeutic recommendations for the use of phenytoin based on CYP2C9 and/or HLA-B genotypes (updates on cpicpgx.org).
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