中国药物警戒 ›› 2022, Vol. 19 ›› Issue (7): 770-774.
DOI: 10.19803/j.1672-8629.2022.07.16

• 安全与合理用药 • 上一篇    下一篇

107例利巴韦林不良反应分析

李美云1, 唐广良1, 陈志宏2, 何鑫1, 陈沈珏1, 李昕1, 刘丽华1,*   

  1. 1长沙市第三医院,湖南 长沙 410015;
    2长沙市市场监督管理局药品使用和不良反应监督管理处,湖南 长沙 410013
  • 收稿日期:2020-08-09 出版日期:2022-07-15 发布日期:2022-07-12
  • 通讯作者: *刘丽华,女,硕士,主任药师,临床药学。E-mail:tracyliu952@aliyun.com
  • 作者简介:李美云,女,硕士,主管药师,临床药学。
  • 基金资助:
    长沙市科学技术局项目(kq1907004)

Analysis of 107 reports of ADR induced by ribavirin

LI Meiyun1, TANG Guangliang1, CHEN Zhihong2, HE Xin1, CHEN Shenjue1, LI Xin1, LIU Lihua1,*   

  1. 1The Third Hospital of Changsha, Changsha Hunan 410015, China;
    2Changsha Administration for Market Regulation, Changsha Hunan 410013, China
  • Received:2020-08-09 Online:2022-07-15 Published:2022-07-12

摘要: 目的 分析利巴韦林药品不良反应(adverse drug reactions, ADR)特点,为促进临床用药安全提供参考。方法 对2015年1月22日至2020年2月28日湖南长沙地区的利巴韦林ADR报告进行统计与分析。结果 共有107例ADR,临床表现多样,涉及9种类型43种临床表现,在各年龄段均有分布,儿童和老年人所占比较高,男性略多于女性;静脉给药多于口服及局部给药;主要为全身性损害,胃肠系统损害;严重ADR 55例次;69例ADR发生时间在30 min内,停药或对症治疗后转归大多良好。结论 儿童和老年人、静脉给药时更易发生ADR,使用利巴韦林30 min内应密切监测ADR。

关键词: 利巴韦林, 药品不良反应, 特殊人群, 安全用药

Abstract: Objective To analyze the adverse drug reactions (ADR) of ribavirin in order to provide reference for the safety of clinical medications. Methods Adverse reaction reports of ribavirin collected between January 22, 2015 and February 28, 2020 in Changsha were statistically analyzed. Results The clinical manifestations of ADR caused by ribavirin were complicated and diverse, involving 107 patients. Forty-three different clinical manifestations of nine types of ADR were observed in various age groups. The proportion of children and the elderly was higher, and males slightly outnumbered females. Intravenous administration was more common than oral or inhaled administration. The main ADR were systemic damage and damage to the gastrointestinal system. There were 55 cases of severe ADR. ADR occurred within 30 minutes of medication in 69 patients, and most of them were relieved after drug withdrawal or symptomatic treatment. Conclusion Adverse reactions of ribavirin have various clinical manifestations, to which children, the elderly and patients receiving intravenous administration are more vulnerable. Adverse reactions should be closely monitored within 30 minutes of RBV administration.

Key words: ribavirin, adverse drug reaction, special populations, safe medication

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