Adverse events with quetiapine and clarithromycin coprescription: A population‐based retrospective cohort study

Author:

Yau Kevin1ORCID,McArthur Eric23,Jeyakumar Nivethika23,Tsobo Muanda Flory24,Kim Richard B.35,Clemens Kristin K.2367,Wald Ron128,Garg Amit X.2379

Affiliation:

1. Division of Nephrology Temerty Faculty of Medicine Toronto Ontario Canada

2. Institute for Clinical Evaluative Sciences Ontario Canada

3. London Health Sciences Centre Lawson Health Research Institute London Ontario Canada

4. Department of Physiology & Pharmacology Western University London Ontario Canada

5. Division of Clinical Pharmacology, Department of Medicine Western University London Ontario Canada

6. Division of Endocrinology, Department of Medicine Western University London Ontario Canada

7. Department of Epidemiology & Biostatistics Western University London Ontario Canada

8. Li Ka Shing Knowledge Institute St. Michael's Hospital Toronto Ontario Canada

9. Division of Nephrology, Department of Medicine Western University London Ontario Canada

Abstract

AbstractBackground and AimsQuetiapine is an atypical antipsychotic predominantly metabolized by the cytochrome P450 3A4 (CYP3A4) enzyme. We studied the risk of adverse events following coprescription of clarithromycin (a strong CYP3A4 inhibitor) versus azithromycin (not a CYP3A4 inhibitor) in quetiapine users.Materials and MethodsThis was a population‐based retrospective cohort study from 2004 to 2020 in Ontario, Canada in adult quetiapine users newly co‐prescribed clarithromycin (n = 16,909) or azithromycin (n = 25,267). The primary outcome was the composite of hospital encounters with encephalopathy (defined as a diagnosis of delirium, disorientation, transient alteration of awareness, transient ischemic attack, or unspecified dementia), a fall, or a fracture within 30 days of new coprescription. Secondary outcomes were individual components of the composite outcome, hospital encounter with computed tomography (CT) head scan, and all‐cause mortality.ResultsCoprescription of clarithromycin versus azithromycin with quetiapine was associated with a higher risk of the primary composite outcome (365 of 16,909 clarithromycin users [2.2%] vs. 309 of 16,929 azithromycin users [1.8%]; absolute risk increase, 0.34% [95% confidence interval, CI, 0.04–0.63]; relative risk [RR], 1.19 [95% CI, 1.02–1.38]). This was primarily driven by an increase in fragility fractures (78 of 16,909 clarithromycin users [0.5%] vs. 45 of 16,923 azithromycin users [0.3%]; absolute risk increase, 0.20% [95% CI, 0.07–0.32]; RR, 1.74 [95% CI, 1.21–2.52]). Hospital encounters with a CT head scan were higher in clarithromycin users (220 of 16,909 [1.3%] vs. 175 of 16,923 azithromycin users [1.0%]; absolute risk increase, 0.27% [95% CI, 0.04–0.50]; RR, 1.26 [95% CI, 1.04–1.54]), but there was no difference in hospital encounters with encephalopathy, falls, or all‐cause mortality between macrolide groups.ConclusionAmong adults taking quetiapine, concurrent use of clarithromycin compared with azithromycin was associated with a small but statistically greater 30‐day risk of a hospital encounter for encephalopathy, falls, or fracture, which was predominantly related to a higher rate of fragility fractures.

Publisher

Wiley

Subject

General Medicine

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