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Phenytoin intoxication associated with omeprazole administration in a child with defective CYP2C9
M Marano1,2, F Nicoletti3,4, S Pro5
1DEA Paediatric Intensive Care Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy. marco.marano@opbg.net.
Insights
Adverse drug reactions are common in children, especially with antiepileptic drugs like phenytoin. A case study highlights phenytoin intoxication in a child with a defective CYP2C9 gene after omeprazole administration.
Area of Science:
- Pharmacogenomics
- Pediatric Pharmacology
- Drug Metabolism
Background:
- Adverse drug reactions (ADRs) are prevalent in hospitalized children, often linked to antiepileptic drugs.
- Phenytoin, a common antiepileptic, is metabolized by CYP2C9, an enzyme encoded by a polymorphic gene.
- Other frequently used drugs, like proton pump inhibitors, can interfere with drug metabolism pathways.
Abstract:
Adverse drug reactions occur at a high rate in hospitalized children, frequently due to antiepileptic drug administration. Phenytoin is a commonly used drug, and its metabolism is mediated by a specific cytochrome-P450 isoform, CYP2C9, which is encoded by a polymorphic gene. It is worth noting that very frequently administered drugs, such as proton pump inhibitors, compete with phenytoin for CYP2C19-mediated metabolism. Here we describe a case of phenytoin intoxication in a child with defective CYP2C9, after omeprazole administration.
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