Adverse Drug Reactions to Antifungals Used in the Management of COVID-19 Associated Rhino-Orbito-Cerebral Mucormycosis

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2022-06-01 DOI:10.1177/0976500X221105759
S. Tiwari, Zahaan Vakil
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Abstract

Objectives: To determine the incidence and frequency of adverse drug reactions (ADRs) to find out factors, if any contributing to the same, while also exploring the use of amphotericin B deoxycholate as a cheaper and safe alternative to liposomal amphotericin B. Materials and Methods: It was a cross-sectional observational study, with a study population of 50 conducted over three months after ethics approval. All adult patients admitted to a tertiary care center, in a metropolitan city of Maharashtra, diagnosed with Rhino-orbito-cerebral mucormycosis, with a history of previous COVID-19 infection and receiving antifungals for the treatment of the same were included in the study. Central Drugs Standard Control Organization (CDSCO) ADR reporting forms were used to collect data. Results: Electrolyte disturbances mainly hypokalemia were the most frequently encountered ADR with both Amphotericin formulations (39/50; 20.31%) followed by pain at the injection site (33/50; 17.19%). Nephrotoxicity occurred slightly more frequently with Amphotericin B Deoxycholate (19/29; 65%), compared to Liposomal Amphotericin B (11/19; 57%), while Posaconazole was mainly associated with gastrointestinal (GI) disturbances and hepatotoxicity. Conclusion: Amphotericin B Deoxycholate was associated most with ADRs, hypokalemia, and pain at the injection site being the most frequent. However, concerning nephrotoxicity, both Amphotericin formulations showed only a modest difference. Posaconazole was associated with the least number of ADRs and had a favorable safety profile.
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用于治疗新冠肺炎相关鼻眶脑毛霉菌病的抗真菌药物不良反应
目的:确定药物不良反应(adr)的发生率和频率,找出导致adr的因素,同时探索两性霉素B去氧胆酸盐作为两性霉素B脂质体更便宜、更安全的替代品的使用。材料和方法:这是一项横断面观察性研究,研究人群50人,在伦理批准后3个月内进行。所有在马哈拉施特拉邦一个大城市三级保健中心就诊、诊断为鼻-眶-脑毛霉菌病、既往有COVID-19感染史并接受抗真菌治疗的成年患者均被纳入研究。使用中央药品标准控制组织(CDSCO)的不良反应报告表收集数据。结果:两种两性霉素制剂最常见的不良反应是电解质紊乱,主要是低钾血症(39/50;20.31%),其次是注射部位疼痛(33/50;17.19%)。两性霉素B脱氧胆酸盐组的肾毒性发生率略高(19/29;65%),而脂质体两性霉素B (11/19;57%),泊沙康唑主要与胃肠道紊乱和肝毒性有关。结论:两性霉素B去氧胆酸酯与不良反应、低钾血症、注射部位疼痛最相关。然而,关于肾毒性,两种两性霉素制剂显示只有适度的差异。泊沙康唑与最少的不良反应相关,并且具有良好的安全性。
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