Ren Landong, Zhao Kaidi, Wang Bingqing, Xiao Shengxiang, Liu Jiashu, Tu Chen
Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, China.
Department of Dermatology, Xi'an Children's Hospital, Xi'an, 710000, China.
Arch Dermatol Res. 2025 Apr 7;317(1):684. doi: 10.1007/s00403-025-04193-z.
Apremilast, a unique oral immunomodulatory phosphodiesterase 4 inhibitor, has been approved by the U.S. Food and Drug Administration (FDA) for the treatment of psoriasis and psoriatic arthritis (PsA). But there is a lack of real-world studies on the safety of apremilast in large numbers of people. This research employs the FAERS database to assess the real-world safety profile of apremilast to evaluate the association between apremilast and adverse events, which can guide drug monitoring and clinical practice. Our study collected adverse event reports listing apremilast as the primary suspect drug from the first quarter of 2012 to the first quarter of 2024. We utilized multiple disproportionality analysis methods, including reporting odds ratio (ROR), proportional reporting ratio (PRR), Bayesian confidence propagation neural network (BCPNN), and multi-item gamma Poisson shrinker (MGPS), to evaluate adverse events associated with apremilast. A comprehensive analysis yielded 124,734 reports identifying apremilast as the primary suspect drug, encompassing 252,677 preferred terms (PT) for adverse reactions distributed across 27 system organ class (SOC) categories. Apart from the adverse reactions already mentioned in the drug label, this study identified some new clinically valuable potential adverse reactions, such as vomiting, depression, suicidal ideation, weight decreased, decreased appetite, nasopharyngitis, dyspepsia, abdominal pain, gastrooesophageal reflux disease, abdominal distension, migraine, insomnia, memory impairment, muscle spasms, musculoskeletal stiffness and so on. Our study provide new safety information for the clinical use of apremilast and establish a framework and insights for its further safety evaluation.
阿普米拉斯是一种独特的口服免疫调节磷酸二酯酶4抑制剂,已被美国食品药品监督管理局(FDA)批准用于治疗银屑病和银屑病关节炎(PsA)。但目前缺乏关于阿普米拉斯在大量人群中安全性的真实世界研究。本研究利用FAERS数据库评估阿普米拉斯的真实世界安全性,以评估阿普米拉斯与不良事件之间的关联,从而指导药物监测和临床实践。我们的研究收集了2012年第一季度至2024年第一季度将阿普米拉斯列为主要可疑药物的不良事件报告。我们使用了多种不成比例分析方法,包括报告比值比(ROR)、比例报告比(PRR)、贝叶斯置信传播神经网络(BCPNN)和多项目伽马泊松收缩器(MGPS),来评估与阿普米拉斯相关的不良事件。综合分析产生了124,734份将阿普米拉斯列为主要可疑药物的报告,其中包括252,677个不良反应的首选术语(PT),分布在27个系统器官类别(SOC)中。除了药物标签中已经提到的不良反应外,本研究还确定了一些新的具有临床价值的潜在不良反应,如呕吐、抑郁、自杀意念、体重减轻、食欲减退、鼻咽炎、消化不良、腹痛、胃食管反流病、腹胀、偏头痛、失眠、记忆障碍、肌肉痉挛、肌肉骨骼僵硬等。我们的研究为阿普米拉斯的临床应用提供了新的安全信息,并为其进一步的安全性评估建立了框架和见解。