中国药物警戒 ›› 2026, Vol. 23 ›› Issue (9): 1056-1058.
DOI: 10.19803/j.1672-8629.20250867

• 安全与合理用药 • 上一篇    下一篇

阿昔洛韦咀嚼片致急性重度肝损伤1例分析

孙玲玲1, 方薇1, 王雨廷1, 李进峰1, 杨依磊2,*   

  1. 1山东大学附属威海市立医院药剂科,山东 威海 264200;
    2山东第一医科大学第一附属医院(山东省千佛山医院)临床药学科,山东 济南 250014
  • 收稿日期:2025-12-01 出版日期:2026-09-15 发布日期:2026-09-15
  • 通讯作者: *杨依磊,男,博士,副主任药师,临床药学。E-mail: yileiyang@126.com
  • 作者简介:孙玲玲,女,硕士,主管药师,临床药学。
  • 基金资助:
    山东省药学会医疗机构药物警戒中青年学术课题(SDSYXH-43-2024-04)

One case of acute severe liver injury caused by chewable tablets of acyclovir

Sun Lingling1, Fang Wei1, Wang Yuting1, Li Jinfeng1, Yang Yilei2,*   

  1. 1Department of Pharmacy, Weihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai Shandong 264200, China;
    2Department of Clinical Pharmacy, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan Shandong 250014, China
  • Received:2025-12-01 Online:2026-09-15 Published:2026-09-15

摘要: 目的 探索阿昔洛韦咀嚼片致急性重度肝损伤病例,为临床合理用药提供参考。方法 分析1例成人患者服用阿昔洛韦咀嚼片导致急性重度肝损伤的案例,评价肝损伤与阿昔洛韦咀嚼片的相关性,通过文献回顾讨论阿昔洛韦致药物性肝损伤可能机制。结果 阿昔洛韦咀嚼片为患者入院前单独用药,入院后根据患者的临床表现、实验室检查及用药时间关联性评定,患者发生急性重度肝损伤很可能为阿昔洛韦咀嚼片所致,停用阿昔洛韦咀嚼片,并给予保肝治疗后,患者肝功能明显好转。结论 阿昔洛韦引起肝损伤的机制尚不明确,需进一步研究证实。临床应用阿昔洛韦应警惕发生药物性肝损伤的风险,加强其不良反应监护,保障患者用药安全。

关键词: 阿昔洛韦, 咀嚼片, 肝损伤, 黄疸, 药品不良反应

Abstract: Objective To analyze a case of acute severe liver injury caused by acyclovir (ACV) chewable tablets in order to provide a reference for rational clinical use of this drug. Methods One case of acute severe liver injury induced by ACV chewable tablets in an adult patient was analyzed before the causality between acyclovir exposure and liver injury was assessed based on the clinical course, laboratory findings and temporal association with drug administration. The potential mechanism of drug-induced liver injury related to acyclovir was explored via literature review. Results Prior to hospitalization, the patient was treated with ACV chewable tablets alone. Based on clinical manifestations, laboratory tests, and the temporal correlations with medication, it was determined that the acute severe liver injury in this patient was likely caused by acyclovir chewable tablets. After acyclovir chewable tablets were discontinued and liver-protecting therapy was initiated, the liver function of this patient improved significantly. Conclusion The underlying mechanism of acyclovir-induced hepatotoxicity remains elusive. When acyclovir is used clinically, the risk of drug-induced liver injury needs to be taken into consideration while adverse reactions should be monitored to make medication safer.

Key words: Acyclovir, Chewable Tablets, Liver Injury, Icterus, Adverse Drug Reaction

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