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42例利妥昔单抗药品不良反应/事件报告分析 被引量：11

Analysis on 42 Cases of Adverse Drug Reaction/Event Induced by Rituximab
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摘要 采用回顾性研究方法,对42例利妥昔单抗药品不良反应/事件(ADR/ADE)报告进行综合分析:有20例是急性输注反应,其中发生过敏性休克3例;血液系统、皮肤及附件损害各6例;肝损害5例;胃肠道损害3例,含1例出现胃肠穿孔;肾功能异常、高血压加重各1例。利妥昔单抗可引起严重ADR/ADE,须加强该药ADR/ADE的研究及防治。 A total of 42 adverse drug reactions/event （ADR/ADE） reports induced by rituximab in Jiangsu province were analyzed in order to investigate the epidemiological characteristics of ADR/ADE induced by rituximab. Among the ADR/ADE, 20 cases were acute infusion reactions, included three allergic shock cases; six cases in each were blood system lesions and the skin and appendages lesions; five cases were liver damages; three cases were gastrointestinal lesions, included one gastrointestinal perforation; one fbr each were renal dysfunction and increased hypertension. It should toe strengthened the observation and evaluation of rituximab ADR/ADE.
作者 甘戈 孙骏
机构地区 江苏省药品不良反应监测中心
出处 《药学与临床研究》 2012年第1期80-83,共4页 Pharmaceutical and Clinical Research
关键词 利妥昔单抗 急性输注反应 血液系统损害 肝损害 药品不良反应 Rituximab Infusion Reactions Blood system lesions Liver damage： Adverse drug reactions
分类号 R969.3 [医药卫生—药理学]
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参考文献13

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共引文献31

同被引文献94

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引证文献11

二级引证文献41

药学与临床研究
2012年 第1期

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