Abstract
Taking into account the high frequency of adverse drug reactions (ADRs) in the clinic and taking into account the growing knowledge of the genetic mechanisms underlying some of these ADRs, we believe that every clinician should know at least the basic principles of pharmacogenetics. However, our experience is that many clinicians are unaware of the potential contribution of pharmacogenetic testing and have not implemented this new modality in their daily practice. We present a case of Stevens-Johnson syndrome in a patient treated with carbamazepine. Following the pathways of clinical reasoning, we describe the possibilities of pharmacogenetic testing in the clinic (HLA-B*1502 and HLA-A*3101 in our patient). We describe the pharmacological and pharmacogenetic aspects relevant for the clinician's daily practice (the existence of ADR subtypes, cytochrome P450, drug-drug interactions, genetic variations, CYP450 and HLA genotyping). Based on the Dutch top 100
Original language | Undefined/Unknown |
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Pages (from-to) | 145-152 |
Number of pages | 8 |
Journal | Netherlands Journal of Medicine |
Volume | 71 |
Issue number | 3 |
Publication status | Published - 2013 |
Research programs
- EMC MM-01-25-01
- EMC MM-04-39-05
- EMC OR-01-34-01