WebNov 2, 2024 · Zofran (ondansetron) ... CYP2D6, CYP1A2), inducers or inhibitors of these enzymes may change the clearance and, hence, the half-life of ondansetron. In patients treated with potent inducers of CYP3A4 (i.e., phenytoin, carbamazepine, and rifampin), the clearance of ondansetron was significantly increased and ondansetron blood … WebNov 9, 2024 · Only two of the prior studies included ondansetron efficacy and CYP2D6 metabolizer status in children, neither of which assessed PONV; these studies have conflicting results. 13, 14 CYP2D6 expression rapidly rises within 24 h after birth, achieves about 50% of adult levels of enzyme activity by 1 month of age, and is close to 100% of …
Ondansetron - StatPearls - NCBI Bookshelf
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Zofran: Uses, Dosage, Side Effects, Interactions, …
WebBecause ondansetron is metabolized by hepatic cytochrome P450 drug-metabolizing enzymes (CYP3A4, CYP2D6, CYP1A2), inducers or inhibitors of these enzymes may change the clearance and, hence, the half-life of ondansetron. WebAug 24, 2014 · CYP2D6 activates hydrocodone to hydromorphone, 2 inactivates ondansetron, 15 and plays a minimal role in the analgesic efficacy of oxycodone 12, 16, 17 (Figure 1 ). Figure 1 Open in figure viewer PowerPoint Primary metabolic fate of oxycodone, hydrocodone, and ondansetron. Effectiveness Measure Webondansetron turnover, CYP3A4 played the predominant role. Because of the multiplicity of metabolic enzymes capable of metabolizing ondansetron, it is likely that inhibition or loss of one enzyme (e.g., CYP2D6 genetic deficiency) will be compensated by others and may result in little change in overall rates of ondansetron elimination. phoenix az building inspections