Cardiovascular Toxicities of Ibrutinib: A Pharmacovigilance Study Based on the United States Food and Drug Administration Adverse Event Reporting System Database.

Pharmaceuticals (Basel, Switzerland)(2023)

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摘要
This pharmacovigilance study systematically explored the adverse cardiovascular events of ibrutinib and provided new safety signals based on past safety information. Attention should be paid to some high-risk signals.
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关键词
FAERS,cardiovascular events,disproportionality analysis,ibrutinib,pharmacovigilance study
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