Adverse events reporting of Etelcalcetide: a real-word analysis from FAERS database.

IF 3.3 Q1 HEALTH POLICY & SERVICES
Journal of Pharmaceutical Policy and Practice Pub Date : 2025-03-31 eCollection Date: 2025-01-01 DOI:10.1080/20523211.2025.2479072
Dongdong Zhang, Ying Cai, Yixin Sun, Peiji Zeng, Wei Wang, Wenhui Wang, Chengfu Cai
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引用次数: 0

Abstract

Background: This study's main goal was to closely monitor and record adverse events (AEs) related to the medication Etelcalcetide, which is used to treat secondary hyperparathyroidism (SHPT, which is defined as elevated parathyroid hormone (PTH) levels in response to abnormalities in the calcium, phosphate, and vitamin D homeostasis). Optimising patient safety and offering evidence-based recommendations for the proper use of this medication are the ultimate goals.

Methods: A thorough collection and analysis of reports from the FDA Adverse Event Reporting System (FAERS) database was conducted, encompassing the first quarter of 2014 to the first quarter of 2024. Robust algorithms including as ROR, PRR, BCPNN, and EBGM were employed for proportional analysis, enabling efficient data mining to measure signals linked to AEs related to Etelcalcetide.

Results: Based on the reports gathered, the number of patients in the Etelcalcetide population was found to be 2,472 (5,435 AEs). As expected, the study's findings revealed the occurrence of Decreased blood calcium, Hypophosphatemia, among other AEs, which are in line with the instructions in the medication insert. Furthermore, unforeseen major AEs were noted at the preferred term (PT) level. These included hunt stenosis, Shunt aneurysm, Shunt occlusion, Shunt infection and Peripheral arterial occlusive disease (PAOD) and so on. These results point to the possibility of AEs that are not presently listed in the medication description.

Conclusion: This work successfully identified previously unidentified and novel signals linked to AEs associated with the administration of Etelcalcetide, offering crucial insights into the intricate relationship between AEs and Etelcalcetide use. In the context of Etelcalcetide therapy, the study's findings highlight the vital significance of diligent surveillance and ongoing monitoring for the prompt detection and efficient management of AEs and to enhance overall patient safety and well-being.

依替卡肽不良事件报告:来自FAERS数据库的实时分析。
背景:本研究的主要目的是密切监测和记录与用于治疗继发性甲状旁腺功能亢进(SHPT,定义为甲状旁腺激素(PTH)水平升高,以响应钙、磷酸盐和维生素D稳态异常)的药物依替卡肽相关的不良事件(ae)。优化患者安全并为正确使用该药物提供循证建议是最终目标。方法:对FDA不良事件报告系统(FAERS)数据库中2014年第一季度至2024年第一季度的报告进行全面收集和分析。采用ROR、PRR、BCPNN和EBGM等鲁棒算法进行比例分析,实现有效的数据挖掘,以测量与Etelcalcetide相关的ae相关的信号。结果:根据收集到的报告,发现Etelcalcetide人群中有2472例患者(5435例ae)。正如预期的那样,研究结果显示血钙降低、低磷血症等不良事件的发生与药物说明书中的说明一致。此外,在首选期限(PT)水平上记录了未预见的主要ae。包括狭窄、分流动脉瘤、分流闭塞、分流感染和外周动脉闭塞性疾病(PAOD)等。这些结果指出了目前在药物描述中没有列出的不良反应的可能性。结论:这项工作成功地识别了先前未被识别的和与Etelcalcetide管理相关的ae相关的新信号,为ae和Etelcalcetide使用之间的复杂关系提供了重要的见解。在Etelcalcetide治疗的背景下,研究结果强调了勤奋监测和持续监测对于及时发现和有效管理ae以及提高患者整体安全和福祉的重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pharmaceutical Policy and Practice
Journal of Pharmaceutical Policy and Practice Health Professions-Pharmacy
CiteScore
4.70
自引率
9.50%
发文量
81
审稿时长
14 weeks
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