Mental Health Center of Jiangnan University, Central Rehabilitation Hospital, Wuxi, Jiangsu, 214151, China.
BMC Psychiatry. 2024 May 16;24(1):371. doi: 10.1186/s12888-024-05813-0.
This study aims to conduct an exhaustive evaluation of Vilazodone's safety in clinical application and to unearth the potential adverse event (AE) risks associated with its utilization based on FDA Adverse Event Reporting System (FAERS) database.
This research employed data spanning from the first quarter of 2011 to the third quarter of 2023 from the FAERS database. Various signal detection methodologies, including the Reporting Odds Ratio (ROR), Proportional Reporting Ratio (PRR), Bayesian Confidence Propagation Neural Network (BCPNN), and Empirical Bayesian Geometric Mean (EBGM), were utilized to ascertain the correlation between Vilazodone and specific AEs.
The study compiled a total of 17,439,268 reports of drug AEs, out of which 5,375 were related to Vilazodone. Through signal mining, 125 Preferred Terms (PTs) encompassing 27 System Organ Classes (SOCs) were identified. The findings indicated a higher prevalence among females and patients within the 45 to 65 age bracket. The principal categories of AEs included Psychiatric disorders, Nervous system disorders, and Gastrointestinal disorders, with prevalent incidents of Diarrhoea, Nausea, and Insomnia. Moreover, the study identified robust signals of novel potential AEs, notably in areas such as sleep disturbances (Sleep paralysis, Hypnagogic hallucination, Rapid eye movements sleep abnormal, Sleep terror, Terminal insomnia, Tachyphrenia), sexual dysfunctions (Female orgasmic disorder, Orgasm abnormal, Disturbance in sexual arousal, Spontaneous penile erection, Anorgasmia, Sexual dysfunction, Ejaculation delayed), and other symptoms and injuries (Electric shock sensation, Violence-related symptom, Gun shot wound).
Although Vilazodone presents a positive prospect in the management of MDD, the discovery of AEs linked to its use, particularly the newly identified potential risks such as sleep and sexual dysfunctions, necessitates heightened vigilance among clinicians.
本研究旨在对维拉唑酮的临床应用安全性进行全面评估,并基于 FDA 不良事件报告系统(FAERS)数据库挖掘其潜在的不良反应(AE)风险。
本研究使用了 FAERS 数据库中 2011 年第一季度至 2023 年第三季度的数据。采用报告比值比(ROR)、比例报告比值(PRR)、贝叶斯置信传播神经网络(BCPNN)和经验贝叶斯几何均值(EBGM)等多种信号检测方法,确定维拉唑酮与特定 AE 之间的相关性。
研究共汇总了 17439268 例药物不良反应报告,其中 5375 例与维拉唑酮相关。通过信号挖掘,共发现 125 个包括 27 个系统器官类别(SOC)的首选术语(PT)。研究结果显示,女性和 45 至 65 岁年龄段的患者中 AE 发生率较高。主要的 AE 类别包括精神障碍、神经系统障碍和胃肠道疾病,常见的不良反应有腹泻、恶心和失眠。此外,研究还发现了一些新的潜在 AE 的强信号,特别是在睡眠障碍(睡眠瘫痪、催眠幻觉、快速眼动睡眠异常、睡眠恐怖症、终末失眠、心动过速)、性功能障碍(女性性功能障碍、性高潮异常、性唤起障碍、自发性阴茎勃起、性欲缺失、性功能障碍、射精延迟)和其他症状和损伤(电击感、与暴力相关的症状、枪伤)等方面。
虽然维拉唑酮在治疗 MDD 方面具有积极的前景,但与使用相关的 AE 发现,特别是新发现的睡眠和性功能障碍等潜在风险,需要临床医生提高警惕。