Int. Journal of Clinical Pharmacology and Therapeutics, Volume 61 (2023) - April (148 - 158)

Association between hemorrhage and direct oral anticoagulants in combination with verapamil: Analysis of Japanese Adverse Drug Event Report database and electronic medical record data

Yuika Komatsu1, 2, Masahiro Yodoshi2, Manabu Takegami2, Satoshi Yokoyama1, Kouichi Hosomi1
1 Division of Drug Informatics, School of Pharmacy, Kindai University, Higashi-osaka, and 2 Division of Pharmacy, Kindai University Hospital, Osakasayama, Osaka, Japan

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DOI 10.5414/CP204310

Abstract

Objective: The aim of this study was to investigate the risk of hemorrhage in concomitant therapy with direct oral anticoagulants (DOACs) and class IV antiarrhythmic drugs.
Materials and methods: First, disproportionality analysis (DPA) was performed using the Japanese Adverse Drug Event Report (JADER) database to investigate the risk of hemorrhage with DOACs. Second, a cohort study was performed using electronic medical record data to confirm the results of the JADER analysis.
Results: In the JADER analysis, hemorrhage was significantly associated with treatment with edoxaban and verapamil (reporting odds ratio = 1.66; 95% confidence interval (CI) = 1.04 – 2.67). The cohort study revealed that hemorrhage incidence significantly differed between the verapamil-treated group and the bepridil-treated group, with a higher risk for hemorrhage in the verapamil group (log-rank test: p < 0.001). The multivariate Cox proportional hazards model also showed that the verapamil and DOAC combination was significantly associated with hemorrhage events compared with the bepridil and DOAC combination (hazard ratio (HR): 2.87, 95% CI: 1.17 – 7.07, p = 0.022). Furthermore, creatinine clearance (Ccr) ≥ 50 mL/min was significantly associated with hemorrhage events (HR: 2.72, 95% CI: 1.03 – 7.18, p = 0.043), and verapamil was significantly associated with hemorrhage in patients with Ccr ≥ 50 mL/min (HR: 3.58, 95% CI: 1.36 – 9.39, p = 0.010) but not in patients with Ccr < 50 mL/min.
Conclusion: Verapamil increases the risk of hemorrhage in patients on DOACs. Dose adjustment of DOACs based on renal function may prevent hemorrhage when verapamil is concomitantly administered.

Author Details

Authors

Departments

  • 1 Division of Drug Informatics, School of Pharmacy, Kindai University, Higashi-osaka, and
  • 2 Division of Pharmacy, Kindai University Hospital, Osakasayama, Osaka, Japan

Address

Kouichi Hosomi, PhD
Division of Drug Informatics, School of Pharmacy
Kindai University
3-4-1 Kowakae, Higashi-osaka
Osaka, 577-8502, Japan
Email: [email protected]

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Citation

Yuika Komatsu, Masahiro Yodoshi, Manabu Takegami, Satoshi Yokoyama, Kouichi Hosomi.Association between hemorrhage and direct oral anticoagulants in combination with verapamil: Analysis of Japanese Adverse Drug Event Report database and electronic medical record data
. Int J Clin Pharmacol Ther. 2023; 61: 148-158. doi: 10.5414/CP204310. Pubmed: https://pubmed.ncbi.nlm.nih.gov/36795612/; PMID: 36795612.

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