J Am Pharm Assoc (2003). 2021 May-Jun;61(3):293-298. doi: 10.1016/j.japh.2021.01.007. Epub 2021 Jan 11.
Given the increased use of hydroxychloroquine (HCQ), chloroquine (CQ), and azithromycin (AZM) during the early months of the coronavirus disease 2019 (COVID-19) pandemic, there is a need to evaluate the associated safety concerns. The objective of this study was to summarize the adverse drug events (ADEs) associated with HCQ, CQ, and AZM use during the national COVID-19 emergency and compare the results with known adverse reactions listed in the drugs' package inserts.
A cross-sectional study design was used. The publicly available Food and Drug Administration Adverse Event Reporting System quarterly data extract files from January 1, 2020 to June 30, 2020 were downloaded. A disproportionality analysis was conducted using the proportional reporting ratio to identify possible ADE signals. A Poisson regression was used to assess if the number of ADE reports for the 3 drugs increased over time.
There was a statistically significant increasing trend in the reported ADEs for both HCQ (P < 0.001) and AZM (P < 0.001). Before the declaration of the national emergency, there were 592 reported drug-ADE pairs for the 3 drugs compared with 2492 drug-ADE pairs reported after March 13, 2020. These 2492 drug-ADE pairs represented 848 ADEs across the 3 drugs, of which 114 (13.4%) were identified as potential signals including 55 (48.2%) that were not listed in the prescribing information.
Our results showed that the reported ADEs for HCQ and AZM have increased during the COVID-19 pandemic. Differences were observed in both the type of and frequency of the highest reported ADEs for the 3 selected drugs before and after the national emergency declaration. Although causation cannot be determined from ADE reports, further investigation of some reports may be warranted. Our results highlight the need for pharmacovigilance and education of health care professionals on the safety of these drugs when being used for COVID-19 prophylaxis or treatment.
鉴于在 2019 冠状病毒病(COVID-19)大流行的早期,羟氯喹(HCQ)、氯喹(CQ)和阿奇霉素(AZM)的使用有所增加,因此需要评估其相关的安全问题。本研究的目的是总结 HCQ、CQ 和 AZM 在国家 COVID-19 紧急情况下使用相关的不良药物事件(ADE),并将结果与药物说明书中列出的已知不良反应进行比较。
采用横断面研究设计。从 2020 年 1 月 1 日至 2020 年 6 月 30 日,下载了公开的美国食品和药物管理局不良事件报告系统季度数据提取文件。使用比例报告比值进行不相称性分析,以识别可能的 ADE 信号。采用泊松回归评估这 3 种药物的 ADE 报告数量是否随时间增加。
HCQ(P < 0.001)和 AZM(P < 0.001)的报告 ADE 数量呈统计学显著增加趋势。在宣布国家紧急状态之前,这 3 种药物报告的药物-ADE 对有 592 对,而 2020 年 3 月 13 日之后报告的药物-ADE 对有 2492 对。这 2492 对药物-ADE 对代表 3 种药物的 848 个 ADE,其中 114 个(13.4%)被确定为潜在信号,包括 55 个(48.2%)未在说明书中列出。
我们的结果表明,在 COVID-19 大流行期间,HCQ 和 AZM 的报告 ADE 增加。在宣布国家紧急状态之前和之后,3 种选定药物报告的最高 ADE 的类型和频率都存在差异。尽管不能从 ADE 报告中确定因果关系,但可能需要对一些报告进行进一步调查。我们的结果强调了在 COVID-19 预防或治疗中使用这些药物时,需要进行药物警戒和对医疗保健专业人员进行安全性教育。