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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Current status of adverse event profile of tacrolimus in patients with solid organ transplantation from a pharmacovigilance study
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Current status of adverse event profile of tacrolimus in patients with solid organ transplantation from a pharmacovigilance study

机译:药物警戒研究中他克莫司在实体器官移植患者中的不良事件概况现状

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Objective: The calcineurin inhibitor tacrolimus has been widely used to prevent allograft rejection after transplantation. The purpose of this study was to clarify the adverse events associated with tacrolimus in solid organ transplantation using a spontaneous reporting system database. Materials and methods: We performed a retrospective pharmacovigilance disproportionality analysis using the Japanese Adverse Drug Event Report (JADER) database. Adverse event reports submitted to the Pharmaceuticals and Medical Devices Agency were analyzed, and the reporting odds ratio (ROR) and 95 confidence interval (CI) for each adverse event were calculated. Results: The database comprised 26,620 reports associated with tacrolimus, of which 2,014, 1,988, and 725 reports involved heart, kidney, and liver transplantation, respectively. Infectious disorder was commonly detected in these transplant patients. There was a significant association between tacrolimus use and colon cancer in patients undergoing heart transplantation (ROR: 3.33, 95 CI: 2.18 - 5.08), but not kidney or liver transplantation. Tacrolimus use in those undergoing kidney transplantation is strongly associated with bronchitis (ROR, 8.95; 95 CI, 6.34 - 12.6). A signal for seizure was detected in liver transplant patients with tacrolimus (ROR, 4.12; 95 CI, 1.77 - 9.59). Conclusion: It was suggested that there is a diversity in the strength of the association between tacrolimus and adverse events in patients receiving heart, kidney, and liver transplantation. Our results may provide useful information for treatment with tacrolimus, although further research with more data is needed to clarify this.
机译:目的:钙调磷酸酶抑制剂他克莫司已广泛用于预防移植后的同种异体移植物排斥反应。本研究的目的是使用自发报告系统数据库阐明实体器官移植中与他克莫司相关的不良事件。材料和方法:我们使用日本药物不良事件报告(JADER)数据库进行了回顾性药物警戒不相称性分析。对提交给药品和医疗器械管理局的不良事件报告进行分析,并计算每个不良事件的报告比值比(ROR)和95%置信区间(CI)。结果:该数据库包含26,620份与他克莫司相关的报告,其中2,014份,1,988份和725份报告分别涉及心脏、肾脏和肝脏移植。在这些移植患者中,感染性疾病很常见。在接受心脏移植的患者中,他克莫司的使用与结肠癌之间存在显著相关性(ROR:3.33,95% CI:2.18 - 5.08),但与肾移植或肝移植无关。在接受肾移植的患者中使用他克莫司与支气管炎密切相关(ROR,8.95;95% CI,6.34 - 12.6)。在他克莫司肝移植患者中检测到癫痫发作信号(ROR,4.12;95% CI,1.77 - 9.59)。结论:在接受心脏、肾脏和肝脏移植的患者中,他克莫司与不良事件之间的关联强度存在差异。我们的研究结果可能为他克莫司的治疗提供有用的信息,尽管需要进一步研究更多的数据来阐明这一点。

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