Safety of triazole antifungals: a pharmacovigilance study from 2004 to 2021 based on FAERS.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Drug Safety Pub Date : 2022-01-01 DOI:10.1177/20420986221143266
Shuang Chai, Jing-Lun Zhan, Li-Mei Zhao, Xiao-Dong Liu
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引用次数: 2

Abstract

Background: Triazole antifungals are widely used as broad-spectrum antifungal activity; however, there are many undetected and unreported adverse events (AEs).

Methods: Data from the Food and Drug Administration Adverse Event Reporting System (FAERS) from the first quarter (Q1) of 2004 to the third quarter (Q3) of 2021 were selected for disproportionality analysis to assess the connection between antifungal triazoles, and AEs and important medical events (IMEs).

Results: A total of 22,566 records associated with triazole antifungals were identified, with 9584 triazole antifungal-IME pairs. The following system organ classes (SOCs) appeared as significant signals: 'Endocrine disorders' [reported odds ratio (ROR) = 167.94], 'Metabolism and nutrition disorders' (ROR = 46.30), and 'Skin and subcutaneous tissue disorders' (ROR = 21.37). Strong signals were observed with respiratory failure, rash, hepatic function abnormal, and hypokalemia. Uncommon security signals included a change in the QT interval, neurotoxicity, pseudoaldosteronism, and hallucinations.

Conclusion: Various triazole antifungals cause AEs of different types and intensities of association. Our results are broadly consistent with prescribing information and previous studies; however, additional pharmacoepidemiological studies are required to verify AEs with modest incidence but high signal.

Plain language summary: A study on the adverse effects of triazole antifungals Introduction: The triazole antifungals we studied include fluconazole, itraconazole, voriconazole, posaconazole, and isavuconazole. Triazole antifungals are widely used as broad-spectrum antifungals; however, there are many undetected and unreported adverse events (AEs).Materials and Methods: The Food and Drug Administration Adverse Event Reporting System (FAERS) database contains AEs reported to the FDA by different countries regarding post-marketing drugs. Through the FAERS database, we retrieved a total of 22,566 AE reports related to triazole antifungals. We not only counted information about patients' gender, age, weight, reporting country, outcome indicators, and indications but also analyzed the system organ classes (SOCs) of AEs, and the number of reported drug-related AEs and the degree of relevance.Results: We found a total of 22,566 records related to triazole antifungal agents, of which 9584 reports made important medical events (IMEs) about triazole antifungal agents, which are serious AEs. The following SOCs appear as important signals: 'endocrine disorders', 'metabolic and nutritional disorders', and 'skin and subcutaneous tissue disorders'. Triazole antifungals produce AEs, such as respiratory failure, rash, hepatic function abnormal, and hypokalemia. They also produce uncommon AEs, including changes in the QT interval, neurotoxicity, pseudoaldosteronism, and hallucinations.Conclusion: By analyzing data from the FAERS database, we identified more AEs associated with these five triazole antifungals than were indicated in the instructions and our findings provide additional insight into triazole-related AEs to inform clinicians before and during treatment.

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三唑类抗真菌药物的安全性:2004 - 2021年基于FAERS的药物警戒研究
背景:三唑类抗真菌药物因具有广谱抗真菌活性而被广泛应用;然而,有许多未被发现和未报告的不良事件(ae)。方法:选取2004年第一季度(Q1)至2021年第三季度(Q3)美国食品药品监督管理局不良事件报告系统(FAERS)的数据进行歧化分析,评估抗真菌三唑类药物与ae和重要医疗事件(IMEs)之间的关系。结果:共鉴定出与三唑类抗真菌药物相关的记录22566条,其中三唑类抗真菌药物- ime对9584对。以下系统器官类别(soc)出现为重要信号:“内分泌紊乱”[报道的优势比(ROR) = 167.94],“代谢和营养紊乱”(ROR = 46.30),以及“皮肤和皮下组织紊乱”(ROR = 21.37)。强烈信号表现为呼吸衰竭、皮疹、肝功能异常、低血钾。不常见的安全信号包括QT间期改变、神经毒性、假性醛固酮增多症和幻觉。结论:不同类型的三唑类抗真菌药物可引起不同类型和强度的ae。我们的结果与处方信息和以前的研究大致一致;然而,需要进一步的药物流行病学研究来证实发生率适中但信号较高的不良反应。摘要:三唑类抗真菌药物不良反应的研究简介:我们研究的三唑类抗真菌药物包括氟康唑、伊曲康唑、伏立康唑、泊沙康唑和异戊康唑。三唑类抗真菌药作为广谱抗真菌药被广泛应用;然而,有许多未被发现和未报告的不良事件(ae)。材料和方法:美国食品和药物管理局不良事件报告系统(FAERS)数据库包含不同国家向FDA报告的有关上市后药物的不良事件。通过FAERS数据库,我们共检索到22,566例与三唑类抗真菌药物相关的AE报告。我们不仅统计了患者的性别、年龄、体重、报告国家、结局指标和适应症等信息,还分析了ae的系统器官分类(soc)、报告的药物相关ae的数量和相关程度。结果:共发现与三唑类抗真菌药物相关的病历22566份,其中涉及三唑类抗真菌药物的重要医学事件(ime) 9584份,均为严重ae。以下soc表现为重要信号:“内分泌紊乱”、“代谢和营养紊乱”以及“皮肤和皮下组织紊乱”。三唑类抗真菌药物可产生不良反应,如呼吸衰竭、皮疹、肝功能异常和低钾血症。它们也会产生不常见的不良反应,包括QT间期改变、神经毒性、假性醛固酮增多症和幻觉。结论:通过分析FAERS数据库的数据,我们发现与这五种三唑类抗真菌药物相关的不良事件比说明书中指出的要多,我们的发现为三唑类相关的不良事件提供了更多的见解,可以在治疗前和治疗期间告知临床医生。
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来源期刊
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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