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Risk of adverse events associated with co-administration of quetiapine and Bupleuri Radix: A population-based cohort
Xinya Mu1, Wenxin Tian1, Song Song1
1Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region of China.
Introduction:
Bupleuri Radix is a widely used herbal medicine in Asia. Experimental studies suggest it may modulate Cytochrome P450 3A4 (CYP3A4), the primary metabolic pathway of quetiapine, which is a first-line medication for psychosis, potentially altering drug exposure and raising concerns about pharmacokinetic interactions. We examined the risk of acute adverse events associated with concomitant use of Bupleuri Radix-containing formulations and quetiapine.
Methods:
We conducted a retrospective cohort study using a Japanese claims database. Individuals aged 18-75 years initiating quetiapine between 2014 and 2023 were eligible. Exposure was defined as dispensing of Bupleuri Radix-containing formulations during quetiapine use. Risk-set matching (1:4) was performed on age, sex, calendar time, duration of quetiapine exposure. The primary outcome was a composite of acute adverse events, including central nervous system (CNS) depression, orthostatic hypotension, tachycardia. Cox models with inverse probability of treatment weighting estimated hazard ratios (HRs) and 95% confidence intervals (CIs).
Results:
The matched cohort included 7552 exposed individuals and 30,091 controls. Weighted incidence rate of the composite outcome was 50.59 vs 32.21 per 1000 person-years in the concomitant-use and quetiapine-only groups. Concomitant use was associated with a statistically significant increased risk of the composite outcome (weighted HR 1.28, 95% CI 1.04-1.57) and CNS depression (HR 1.35, 95% CI 1.05-1.74).
Conclusion:
Concomitant use of Bupleuri Radix-containing formulations with quetiapine was associated with increased risk of acute adverse events, the absolute rate difference approached 2 additional events per 100 person-years, entailing clinical significance. Clinicians should consider this potential risk alongside expected treatment benefits.
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