中国药物警戒 ›› 2023, Vol. 20 ›› Issue (3): 334-338.
DOI: 10.19803/j.1672-8629.20220188

• 安全与合理用药 • 上一篇    下一篇

84例新型抗肿瘤药品不良反应报告分析

杨岩1, 周德喜2, 吴欣俐1, 薛淑雅1, 丁海华1, 张泉1, 张云玲1,*   

  1. 1安徽省胸科医院药剂科,安徽 合肥 230022;
    2皖南医学院第一附属医院,安徽 芜湖 241001
  • 收稿日期:2020-04-22 出版日期:2023-03-15 发布日期:2023-03-17
  • 通讯作者: * 张云玲,女,硕士,副主任药师,临床药学。E-mail:yl1525@126.com
  • 作者简介:杨岩,女,硕士,主管药师,临床药学。
  • 基金资助:
    安徽省自然科学基金资助项目(2008085QH355)

Eighty-four cases of adverse drug reactions caused by novel anti-tumor drugs

YANG Yan1, ZHOU Dexi2, WU Xinli1, XUE Shuya1, DING Haihua1, ZHANG Quan1, ZHANG Yunling1,*   

  1. 1Department of Pharmacy, Anhui Chest Hospital, Hefei Anhui 230022, China;
    2Department of Pharmacy, the First Affiliated Hospital of Wannan Medical College, Wuhu Anhui 241001, China
  • Received:2020-04-22 Online:2023-03-15 Published:2023-03-17

摘要: 目的 研究我院新型抗肿瘤药物引起的药品不良反应(adverse drug reaction, ADR)发生特点及规律,为临床合理用药提供参考。方法 收集我院 2020年1月1日至2021年12月31日上报至国家药品不良反应监测系统的新型抗肿瘤药物ADR,对 ADR 类型、患者年龄和疾病类型、药品种类、累及系统-器官、严重 ADR 的主要药品及临床表现等方面进行分析。结果 84例新型抗肿瘤药物ADR中,中老年患者居多;累及系统-器官主要是消化系统和皮肤及其附件系统;严重ADR占比34.52%。9例患者存在超说明书用药的问题。结论 临床医师和药师应重视新型抗肿瘤药物致ADR,加强患者药学监护,为临床用药安全以及药品上市后再评价提供参考依据。

关键词: 药品不良反应, 新型抗肿瘤药, 靶向药物, 免疫检查点抑制剂, 药学监护

Abstract: Objective To analyze the characteristics and regularity of adverse drug reactions (ADR) caused by novel anti-tumor drugs in Anhui Chest Hospital so as to provide reference for rational use of drugs. Methods A total of 84 cases of ADR of novel anti-tumor drugs reported by our hospital to the national ADR Monitoring System from January 1, 2020 to December 31, 2021 were collected. These ADR were analyzed in terms of types, age and diseases of patients, types of drugs used, organs and/or systems involved, main drugs and clinical manifestations of severe ADR. Results Most of these patients were middle-aged and elderly ones (≥45 years old). The organs and/or systems at the highest risk of ADR were the digestive system and the skin and its accessory system. 34.52% of the cases were serious ADR and there were 9 cases of off-label drug use. Conclusion Clinicians and pharmacists should be alert to ADR caused by novel anti-tumor drugs, and the course of medication should be rigorously monitored so as to provide data for clinical drug safety and re-evaluation of drugs after marketing.

Key words: adverse drug reaction, novel anti-tumor drugs, targeted medicine, immunocheckpoint inhibitor, pharmaceutical care

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