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Pining for Pete in the Pain Clinic

Fatal Forty DDI: nortriptyline, paroxetine, CYP2D6

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A Case Approach to Perioperative Drug-Drug Interactions

Abstract

This case discusses the interaction of nortriptyline and paroxetine. Nortriptyline is a tricyclic antidepressant (TCA) that is a cytochrome P450 2D6 substrate and paroxetine is a 2D6 inhibitor. The interaction resulted in TCA toxicity. The metabolism of other TCAs is discussed.

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References

  1. Leucht S, Hackl HJ, Steimer W, et al. Effect of adjunctive paroxetine on serum levels and side-effects of tricyclic antidepressants in depressive inpatients. Psychopharmacology (Berl). 2000;147(4):378–83.

    Article  CAS  Google Scholar 

  2. Venkatakrishnan K, von Moltke LL, Greenblatt DJ. Nortriptyline E-10-hydroxylation in vitro is mediated by human CYP2D6 (high affinity) and CYP3A4 (low affinity): implications for interactions with enzyme-inducing drugs. J Clin Pharmacol. 1999;39(6):567–77.

    Article  PubMed  CAS  Google Scholar 

  3. Olesen OV, Linnet K. Hydroxylation and demethylation of the tricyclic antidepressant nortriptyline by cDNA-expressed human cytochrome P-450 isozymes. Drug Metab Dispos. 1997;25:740–4.

    PubMed  CAS  Google Scholar 

  4. A new antidepressant of the tricyclic group: nortriptyline hydrochloride (aventyl hydrochloride). JAMA. 1965;194:727–8.

    Google Scholar 

  5. Crewe HK, Lennard MS, Tucker GT, et al. The effect of selective serotonin re-uptake inhibitors on cytochrome P4502D6 (CYP2D6) activity in human liver microsomes. Br J Clin Pharmacol. 1992;34:262–5.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. von Moltke LL, Greenblatt DJ, Court MH, et al. Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective serotonin reuptake inhibitor antidepressants. J Clin Psychopharmacol. 1995;15(2):125–31.

    Article  Google Scholar 

  7. Bertilsson L. Metabolism of antidepressant and neuroleptic drugs by cytochrome p450s: clinical and interethnic aspects. Clin Pharmacol Ther. 2007;82:606–9.

    Article  PubMed  CAS  Google Scholar 

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Liu, S.S., Weingarten, T.N., Marcucci, C. (2015). Pining for Pete in the Pain Clinic. In: Marcucci, C., et al. A Case Approach to Perioperative Drug-Drug Interactions. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-7495-1_65

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  • DOI: https://doi.org/10.1007/978-1-4614-7495-1_65

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4614-7494-4

  • Online ISBN: 978-1-4614-7495-1

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