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Research Article

Article
Association between dual orexin receptor antagonists (DORAs) and suicidality: reports to the united states food and drug administration adverse event reporting system (FAERS)
Roger S. McIntyre, Sabrina Wong, Angela T.H. Kwan, Taeho Greg Rhee, Kayla M. Teopiz, Roger Ho, Bing Cao, Rodrigo B. Mansur, Joshua D. Rosenblat & Gia Han Le
Accepted author version posted online: 28 May 2024
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Original Research

Article
Real-world safety profile of tetracyclines in children younger than 8 years old: an analysis of FAERS database and review of case report
Wei Dou, Xin Liu, Pengjiao An, Wei Zuo & Bo Zhang
Published online: 28 May 2024
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Original Research

Article
Risk of drug-induced delirium in older patients- a pharmacovigilance study of FDA adverse event reporting system database
Boying Jia, Shuang Zhou, Jiayu Li, Liyan Wan, Ying Zhou & Yimin Cui
Published online: 26 May 2024
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Original Research

Article
Neurological disorders following the use of tumor necrosis factor-α inhibitors in inflammatory bowel disease patients: a real-world pharmacovigilance analysis
Yi Zhao, Zelin Li, Kanghuai Zhang & Na Wang
Published online: 23 May 2024
  • 19 Views
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Original Research

Article
Safety assessment of clomiphene: a real-world pharmacovigilance analysis from the Food and Drug Administration adverse event reporting system
Yifeng Shao, Lisha Ma, Jianqing Zhou & Baicai Yang
Published online: 23 May 2024
  • 28 Views
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Original Research

Article
Comparison of four criteria for potentially inappropriate medications in older patients with newly diagnosed non-small cell lung cancer
Man Xu, Zhuo Ma, Xin Feng & Zhuoling An
Published online: 22 May 2024
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Original Research

Article
Adverse tumor events induced by ranitidine: an analysis based on the FAERS database
ManTing Liu, DongQiang Luo, JiaZhen Jiang, Ying Shao, DanDan Dai, YiNing Hou, XiangYun Dou, XiaoLu Gao, BoHui Zheng & Tian Liu
Published online: 21 May 2024
  • 44 Views
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Original Research

Article
Glass bead-activated clotting time (gb-ACT) for monitoring the anticoagulation effects in elderly patients with high risk of venous thromboembolism (VTE)
Pingan Peng, Yiwen Chen, Guang Yang, Mingzhao Qin, Xiaohan Xu & Yujie Zhou
Published online: 20 May 2024
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Original Research

Article
Post-marketing safety concerns with abrocitinib: a real-world pharmacovigilance analysis of the FDA adverse event reporting system
Zhou Zhu, Mingjuan Liu, Hanlin Zhang, Heyi Zheng & Jun Li
Published online: 17 May 2024
  • 116 Views
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Original Research

Article
Differences in ocular adverse events associated with phosphodiesterase-5 inhibitors: a real-world pharmacovigilance study
Guixiang Chen, Li Zhang, Si-Ting Zhao, Hao Huang & Zhiwen Fu
Published online: 16 May 2024
  • 88 Views
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Meta-analysis

Review Article
Hematological toxicity of cyclin-dependent kinase 4/6 inhibitors in patients with breast cancer: a network meta-analysis and pharmacovigilance study
Haiying Ding, Weiben Xu, Mengfei Dai, Shujing Li, Wenxiu Xin, Yinghui Tong, Chaoneng He, Xiufang Mi, Zhajun Zhan & Luo Fang
Published online: 16 May 2024
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Original Research

Article
Abrocitinib-associated adverse events: a real-world pharmacovigilance study using the FAERS database
Yu Sun, Tao Xu, Suyan Zhu & Hongbin Xu
Published online: 16 May 2024
  • 203 Views
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Review

Review Article
Underuse of GLP-1 receptor agonists in the management of type 2 diabetes despite a favorable benefit-safety profile
André J. Scheen
Published online: 13 May 2024
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Original Research

Article
Comparison of safety of acetaminophen and ibuprofen in minors: based on the FAERS database
Jing Wang, Guowen Feng, Dan Li, Xiaodan Zhou, Jia Chen, Fengdie Wang & Li Chen
Published online: 12 May 2024
  • 102 Views
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Original Research

Article
A real-world disproportionality analysis of the FDA adverse event reporting system events for ibuprofen
Yikuan Du, Zhuoming Guo, Bijun Xu, Yujia Yang, Mianda Hu, Yanghui Hu, Yurong Yang, Mengting Zhang, Zhenjie Wang, Xiaochun Guo, Yixing Huang, Jinfeng Zhu, Weichui Zhang & Chun Yang
Published online: 09 May 2024
  • 78 Views
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Original Research

Article
Evaluation of the safety and efficacy of biosimilar recombinant growth hormone in children with growth hormone deficiency: non-inferiority, randomized, parallel, multicentric and Phase III trial
Hossein Zaeri, Shahriar Omidvar, Nazli Servatian, Serajaddin Arefnia, Nasrin Khademolreza, Hossein Amini, Behnam Taghavi, Mahin Hashemipour, Peyman Eshraghi, Mahmoud Ghasemi, Robabeh Ghergherehchi, Elham Maleki, Hossein Moravej, Shahab Noorian, Fahimeh Soheilipour, Setila Dalili, Hosseinali Kharazmi, Abdollah Didban, Aliasghar Akhlaghi, Sina Ghaznavi & Majid Shahbazi
Published online: 08 May 2024
  • 39 Views
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Original Research

Article
Infectious events in patients with alopecia areata treated with JAK inhibitors: low burden and minimal impact on persistence in treatment
Giacomo Caldarola, Lorenzo Maria Pinto, Francesco Bellinato, Nicoletta Bernardini, Elena Campione, Andrea Chiricozzi, Laura Colonna, Clara De Simone, Laura Diluvio, Paolo Gisondi, Enrico Matteini, Eleonora Tomassetti, Ersilia Tolino, Luca Bianchi & Ketty Peris
Published online: 08 May 2024
  • 81 Views
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Original Research

Article
Analysis of Inclisiran in the US FDA Adverse Event Reporting System (FAERS): a focus on overall patient population and sex-specific subgroups
YuBin He, Xin Guan, YaYun Zhang, Zixiong Zhu, YanHui Zhang, Yue Feng & Xuewen Li
Published online: 07 May 2024
  • 143 Views
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Original Research

Article
Post-marketing safety concerns with elagolix: a disproportionality analysis of the FDA adverse event reporting system
En Chang, Yong-Fang Shi, Jin-Feng Liu & Wei Wei
Published online: 07 May 2024
  • 46 Views
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Original Research

Article
Safety of marketed biosimilar monoclonal antibody cancer treatments in the US: a disproportionality analysis using the food and drug administration adverse event reporting system (FAERS) database
Xiangzhong Xue & Jingjing Qian
Published online: 03 May 2024
  • 49 Views
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Original Research

Article
Development and validation of a machine learning model to improve precision prediction for irrational prescriptions in orthopedic perioperative patients
Weipeng Li, Nan Shang, Zhiqi Zhang, Yun Li, Xianlin Li & Xiaojun Zheng
Published online: 02 May 2024
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Original Research

Article
A real-world pharmacovigilance analysis of the FDA adverse event reporting system events for polatuzumab vedotin
Zhongliang Xu, Dan Huang, Qiusha Liu, Sha Liu, Jiating Liu, Hongli Wang & Zhengze Shen
Published online: 02 May 2024
  • 81 Views
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Original Research

Article
A pharmacovigilance study of adverse events associated with polymyxins based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database
Tingxi Wu, Yanfeng Shi, Chang Xu, Bin Zhu, Dandan Li, Zhe Li, Zhigang Zhao & Yang Zhang
Published online: 01 May 2024
  • 41 Views
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Original Research

Article
Analysis of new-onset seizures following use of COVID-19 vaccinations in children based on VAERS
Yanhui Liu, Jinyang He, Xiaozhu Zhou, Yi Wu, Heping Cai, Yuquan Sun & Xiangli Cui
Published online: 01 May 2024
  • 30 Views
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Original Research

Article
Signal detection of adverse reactions for bendamustine based on FDA adverse event reporting system
Qing Huang, Yuanbin Wu & Huimin Li
Published online: 30 Apr 2024
  • 243 Views
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Open Access

Original Research

Article
Immune checkpoint inhibitor related myositis: an observational, retrospective, pharmacovigilance study
Hui Yang, Zhexin Ding, Zhuoling An, Yong Zhao & Hezhe Lu
Published online: 24 Apr 2024
  • 63 Views
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Meta-analysis

Review Article
Efficacy and safety of bimekizumab in the treatment of psoriatic arthritis: a systematic review and meta-analysis
Qin-Yi Su, Liu Yang, Ting-Yu Cao, Hai-Ying Dang, Zhuo-Chen Han, Jia-Jing Cao, He-Yi Zhang, Ting Cheng, Sheng-Xiao Zhang & Yue-Hong Huo
Published online: 23 Apr 2024
  • 128 Views
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Original Research

Article
Comprehensive safety profile of dipeptidyl peptidase-4 inhibitors: a post-marketing study based on FAERS database using signal detection algorithms
Beema T Yoosuf, Muhammed Favas KT, Pinaki Dutta & Dipika Bansal
Published online: 23 Apr 2024
  • 113 Views
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Original Research

Article
Incidence and risk factors for potential drug-drug interactions in outpatients receiving opioid analgesics
Fei Chu, Yang Yao, Bei Gao, Mingzhi Huang & Lingti Kong
Published online: 23 Apr 2024
  • 46 Views
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Original Research

Article
Long-term safety of lanthanum carbonate in the real word: a 19-year disproportionality analysis from the FDA Adverse Event Reporting System
Mengjia Ying, Jian Shi, Yahao Ling, Tao Shi, Lele Liao & Linhui Cao
Published online: 15 Apr 2024
  • 62 Views
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Original Research

Article
Antibiotics-associated pseudomembranous colitis: a disproportionality analysis of the US food and drug administration adverse event reporting system (FAERS) database
Jinhua Chen, Weijiang Yu, Wancun Zhang, Cuicui Sun & Wenzhou Zhang
Published online: 11 Apr 2024
  • 52 Views
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Original Research

Article
Investigating bleeding adverse events associated with BTK inhibitors in the food and drug administration adverse event reporting system (FAERS)
Xianlin Li, Nan Shang, Qianci Yan, Xiunan Yue, Yang Liu & Xiaojun Zheng
Published online: 08 Apr 2024
  • 125 Views
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Original Research

Article
A real-world pharmacovigilance study of QT interval prolongation and Torsades de Pointes associated with CDK4/6 inhibitors in breast cancer patients: findings from the FDA adverse event reporting system
Yu Yan, Bin Wu & Ling Wang
Published online: 14 Mar 2024
  • 175 Views
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Original Research

Article
Adverse events associated with brolucizumab: a disproportionality analysis of the FDA adverse event reporting system (FAERS)
Xiaomei Xiong, Xiuwen Zhang, Xiaoxia Li & Taomin Huang
Published online: 27 Feb 2024
  • 149 Views
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Original Research

Article
Anticancer drug-induced interstitial lung disease: a critical appraisal of clinical practice guidelines and consensus statements
Yi Zhang, Zhuo Ma, Ximu Sun, Yuhui Zhang, Min Zhu, Shu Zhang, Xin Feng & Zhuoling An
Published online: 20 Feb 2024
  • 64 Views
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Original Research

Article
Reporting of tumor lysis syndrome with targeted therapy for hepatic cancer in the FDA adverse events reporting system
Ling Liu, Chengyi Zhang, Huihui Liu, Huan Luo, Rong Cao, Mingxuan Xiao, Pan Zou, Zhuzhu Xie, Hui Gong, Rui Ma, Miao Yan & Zhichao Jiang
Published online: 30 Jan 2024
  • 142 Views
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Original Research

Article
Utilizing temporal pattern of adverse event reports to identify potential late-onset adverse events
Jae Hyun Kim & Yun-Kyoung Song
Published online: 22 Jan 2024
  • 71 Views
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Original Research

Article
Hematological adverse events associated with anti-MRSA agents: a real-world analysis based on FAERS
Xiuheng Yu, Xiaodan Zhou, Min Li & Yu Zhao
Published online: 22 Jan 2024
  • 94 Views
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Meta-analysis

Review Article
Effects of adding adjuvants to propofol on the post-anesthesia cognitive function in patients undergoing gastroscopy/colonoscopy: a systematic review and meta-analysis
Liupu Zheng, Mengqian Ye, Jun Ma, Chen Jin, Yan Yang, Haoqi Li, Rongyuan Zheng & Yi Wang
Published online: 13 Jan 2024
  • 60 Views
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Original Research

Article
Safety of daratumumab in the real-world: a pharmacovigilance study based on FAERS database
Junlin Wu, Hanbiao Wu, Lili Chen, Haiping Liang, Guoning Huang, Sensen Yang, Bishan Chen, Yoshihiro Noguchi & Yonggang Shen
Published online: 18 Dec 2023
  • 140 Views
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Original Research

Article
Cognitive dysfunction following finasteride use: a disproportionality analysis of the global pharmacovigilance database
Yongtai Cho, Sungho Bea, Ji-Hwan Bae, Dong Hyun Kim, Jong Hee Lee & Ju-Young Shin
Published online: 19 Dec 2023
  • 100 Views
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Original Research

Article
Urinary tract infections and genital mycotic infections associated with SGLT‑2 inhibitors: an analysis of the FDA Adverse Event Reporting System
Ting Yang, Ying Zhou & Yimin Cui
Published online: 27 Nov 2023
  • 240 Views
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Original Research

Article
Long QT syndrome after using EGFR-TKIs in older patients with advanced non-small cell lung cancer
Joo-Young Byun, Sola Han, Aiham Qdaisat & Chanhyun Park
Published online: 13 Dec 2023
  • 91 Views
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Original Research

Article
Model driven method for exploring individual and confounding effects in spontaneous adverse event reporting databases
Bo Lv, Yuedong Li, Aiming Shi & Jie Pan
Accepted author version posted online: 11 Dec 2023
  • 68 Views
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Original Research

Article
A real-world analysis of safety profile of selexipag by using FDA adverse Event Reporting System (FAERS)
Jie Zhao, Mei Wang, Qing Yu, Yi Yang, Bin Zhang & Sanhua Zhan
Published online: 30 Nov 2023
  • 148 Views
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Original Research

Article
New exploration of signal detection of Regional Risks from the perspective of data mining: a pharmacovigilance analysis based on spontaneous reporting data in Zhenjiang, China
Yuan Liu, Xiaoli Xu, Jingfei Yang, Yuwei Zhang, Mengjiao He, Wenzhi Liao, Na Wang & Pengcheng Liu
Published online: 27 Nov 2023
  • 114 Views
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Original Research

Article
Newly identified adverse events for gemcitabine using the Food and Drug Administration Adverse Event Reporting System
Wei Zhang, Yuhong Wang, Xin Jiang, Hu Zhao, Xinli Jia, Qiye Wang, Yue Chen, Yuanfang Jiang, Zhifang Ma, Lina Chang & Xin Wang
Published online: 16 Nov 2023
  • 104 Views
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Original Research

Article
Hospital registration of adverse drug reactions in electronic health records: importance and contribution to pharmacovigilance
Roba Alloush, Jette van Lint, Rob J. van Marum, Walter W.A.J.J. Hermens & Naomi T. Jessurun
Published online: 14 Nov 2023
  • 154 Views
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Original Research

Article
Pneumatosis intestinalis associated with α-glucosidase inhibitors: a pharmacovigilance study of the FDA adverse event reporting system from 2004 to 2022
Yiqian Chen, Yao Xiao, Guanghui Lian, Jun Yi & Xiaowei Liu
Published online: 06 Nov 2023
  • 139 Views
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Original Research

Article
Drug-induced hypoglycemia: a disproportionality analysis of the FAERS database
Jie Li, Yilei Wang, Xiang Yang, Haohao Zhu & Zhitao Jiang
Published online: 01 Nov 2023
  • 255 Views
  • 0 CrossRef citations
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