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DOI 10.1080/14740338.2024.2327502

Медицинская библиотека · Expert opinion on drug safety · 2024

Hemorrhage induced by antithrombotic agents: new insights from a real-world pharmacovigilance study.

Guo Kangyuan, Wang Ganyi, Zhang Li, Feng Zhanchun, Xia Xudong, Sun Xiaobo, Yan Ziqi, Jiao Zhiming, Feng Da

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Аннотация

BACKGROUND

Hemorrhage represents the most common and serious side effect of antithrombotic agents. Many studies have compared the risk of bleeding between different antithrombotic agents, but analysis of time-to-onset for hemorrhage induced by these drugs is yet sparse.

METHODS

We conducted a retrospective study based on the adverse drug reaction reports on antithrombotic agents collected by the Henan Adverse Drug Reaction Monitoring Center. We assessed the reporting odds ratio to determine the disproportionate reporting signals for bleeding and the Weibull shape parameter was used to evaluate the time-to-onset data.

RESULTS

In the signal detection, crude low molecular weight heparin-hemorrhage was found as a positive signal. The hemorrhage for most antithrombotic agents was random failure profiles. In particular, the hazard of hemorrhage decreased over time for warfarin and clopidogrel and increased for alteplase, nadroparin, and dipyridamole.

CONCLUSION

We found that the risk of bleeding in patients taking Crude low molecular weight heparins was significantly higher compared to other antithrombotic agents, but with a small magnificence, which may be attributed to the severely irrational use of this medication under improper management. Statistics in days, results showed that the risk of bleeding decreased over time for warfarin and clopidogrel and increased for alteplase, nadroparin, and dipyridamole.

Для цитирования: Guo Kangyuan, Wang Ganyi, Zhang Li, Feng Zhanchun, Xia Xudong, Sun Xiaobo, Yan Ziqi, Jiao Zhiming, Feng Da. Hemorrhage induced by antithrombotic agents: new insights from a real-world pharmacovigilance study.. Expert opinion on drug safety. 2024. DOI: 10.1080/14740338.2024.2327502.

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