Literature DB >> 16414038

Negative urine opioid screening caused by rifampin-mediated induction of oxycodone hepatic metabolism.

Hong-Kee Lee1, Lionel D Lewis, Gregory J Tsongalis, Matthew McMullin, Bernard C Schur, Steven H Wong, Kiang-Teck J Yeo.   

Abstract

INTRODUCTION: Oxycodone has become widely used in the clinic for the treatment of chronic pain. This reflects its favorable pharmacokinetics and side effect profiles. CASE REPORT: We report a 60-y-old man who had a clinically significant drug interaction between rifampin and oxycodone, resulting in 3 consecutive negative urine oxycodone screens in a 2-month period, suggesting non-adherence. A combination of urine opioid metabolite quantification by GC/MS and CYP genotyping confirmed that he was compliant with his oxycodone therapy. Determination of the complete oxycodone metabolite profile and the CYP3A4/5 and 2D6 genotype allowed the physician to be confident that the patient was compliant with the medication (and not diverting it) and to increase his oxycodone dose to optimize his pain control.
CONCLUSION: This case demonstrates how the combination of analytical toxicology and pharmacogenetic analyses enhances a physician's ability to personalize drug therapy in patients with chronic pain syndromes.

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Year:  2006        PMID: 16414038     DOI: 10.1016/j.cca.2005.11.030

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  7 in total

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4.  The effects of CYP2D6 and CYP3A activities on the pharmacokinetics of immediate release oxycodone.

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Review 5.  Complex Drug-Drug-Gene-Disease Interactions Involving Cytochromes P450: Systematic Review of Published Case Reports and Clinical Perspectives.

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7.  Voriconazole drastically increases exposure to oral oxycodone.

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  7 in total

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