Russom Mulugeta, Fitsum Yodit, Abraham Abiel, Savage Ruth L
Eritrean Pharmacovigilance Centre, National Medicines and Food Administration, Ministry of Health, Asmara, Eritrea.
Akordat Hospital, Ministry of Health, Akordat, Eritrea.
Drugs Real World Outcomes. 2021 Sep;8(3):263-275. doi: 10.1007/s40801-021-00240-z. Epub 2021 Mar 30.
Diclofenac, a nonsteroidal anti-inflammatory drug, is not a documented cause of rhabdomyolysis in the Summaries of Product Characteristics held by major regulators. There are, however, eight published single case reports that associate rhabdomyolysis with diclofenac.
Triggered by a serious local case report, this study was conducted to evaluate the evidence for a causal association between diclofenac and rhabdomyolysis.
A descriptive analysis of rhabdomyolysis associated with diclofenac was conducted by mining data from the WHO Global Database of Individual Case Safety Reports, VigiBase, and published case reports.
70 eligible cases were retrieved from VigiBase. The median age was 56.5 years (range 1-90). Where reported precisely (26 reports), the median time to onset of rhabdomyolysis following administration of diclofenac was 3 days. In 20 cases, diclofenac was reported as a sole suspect and was solely administered in 14 of these. In 30 cases, rhabdomyolysis abated following withdrawal of diclofenac. Seven of these cases fulfilled the WHO-UMC case-causality assessment criteria for 'probable'. Diclofenac was probably an indirect cause in another five reports where rhabdomyolysis ensued from injection-site necrosis. There were eight fatalities and intramuscular administration was over-represented in this group. In 27 patients taking lipid-lowering agents, the incidence of acute kidney injury with rhabdomyolysis was 62.9% compared with 37.1% for the whole cohort. Off-label use of diclofenac for minor or undiagnosed conditions was reported.
Currently available data suggests a causal link between diclofenac and rhabdomyolysis either directly or indirectly.
双氯芬酸是一种非甾体抗炎药,在主要监管机构持有的产品特性摘要中,它并非横纹肌溶解症的已记录病因。然而,有八篇已发表的单病例报告将横纹肌溶解症与双氯芬酸联系起来。
受一则严重的本地病例报告启发,开展本研究以评估双氯芬酸与横纹肌溶解症之间存在因果关联的证据。
通过挖掘世界卫生组织个体病例安全报告全球数据库(VigiBase)中的数据以及已发表的病例报告,对与双氯芬酸相关的横纹肌溶解症进行描述性分析。
从VigiBase中检索到70例符合条件的病例。中位年龄为56.5岁(范围1 - 90岁)。在精确报告的病例中(26份报告),服用双氯芬酸后发生横纹肌溶解症的中位时间为3天。在20例病例中,双氯芬酸被报告为唯一可疑药物,其中14例仅使用了双氯芬酸。在30例病例中,停用双氯芬酸后横纹肌溶解症有所缓解。其中7例符合世界卫生组织药物不良反应因果关系评估标准中的“可能”级别。在另外5份报告中,双氯芬酸可能是间接病因,横纹肌溶解症由注射部位坏死引发。有8例死亡病例,且该组中肌肉注射的情况占比过高。在27例服用降脂药的患者中,发生急性肾损伤合并横纹肌溶解症的发生率为62.9%,而整个队列的这一发生率为37.1%。报告了双氯芬酸用于轻微或未确诊病症的超说明书用药情况。
现有数据表明双氯芬酸与横纹肌溶解症之间存在直接或间接的因果联系。