Pharmacovigilance study of the association between progestogen and depression based on the FDA adverse event reporting System (FAERS) by Hui Gao, Xiaohan Zhai, Yan Hu, Hang Wu

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Evaluate the renal system damage caused by zoledronic acid: a comprehensive analysis of adverse events from FAERS by Zhaojun Wang, Xin Su, Donglei Shi, Li Wei

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Adverse events in the nervous system associated with blinatumomab: a real-world study by Wen Gao, Jingwei Yu, Yifei Sun, Zheng Song, Xia Liu, Xue Han, Lanfan Li, Lihua Qiu, Shiyong Zhou, Zhengzi Qian, Xianhuo Wang, Huilai Zhang

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Cardiovascular toxicity of tisagenlecleucel in children and adolescents: analysis of spontaneous reports submitted to FAERS by Ganggang Wang, Lin Su, Yanjun Liu, Xiaohan Yang, Yi Li, Qi Mei, Qi Mei, Wen Gao

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Mogamulizumab‐Associated Autoimmune Diseases: Insights From FAERS Database Analysis by Genshan Zhang, Haokun Zhang, Jie Fu, Zhixin Cao

Subjects: “…Food and Drug Administration Adverse Event Reporting System…”
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Quality of the record of drug-related problems in a database for voluntary adverse event reporting by Maria Teresa Aznar-Saliente, Laura Roca-Aznar, Amparo Talens-Bolós, Paola Herraiz-Robles, Manuel Bonete-Sánchez, Laia Pons-Martínez, Borja Marcos-Ribes

Subjects: “…Adverse event reporting system…”
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Progressive multifocal leukoencephalopathy reports in rheumatoid arthritis concerning different treatment patterns-an exploratory assessment using the food and drug administration... by Takeshi Honma, Kenji Onda, Koichi Masuyama

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Antibiotics-induced pulmonary embolism: A disproportionality analysis in Food and Drug Administration database of Adverse Event Reporting System using data mining algorithms by Pramod Kumar Adusumilli, Foujia Begum, Ankita Ashok Sangnure, Jeesa George

Subjects: “…food and drug administration database of adverse event reporting system…”
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Drug-induced retinal vein occlusion: a disproportionality analysis from the FDA adverse event reporting system (2004–2023) by Xiao-Dong Chen, Xiao-Dong Chen, Xiao-Dong Chen, Kun-Hong Xiao, Chao-Bing Zhou, Chao-Bing Zhou

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Real-world study of adverse events associated with triptan use in migraine treatment based on the U.S. Food and Drug Administration (FDA) adverse event reporting system (FAERS) dat... by Wen-Hui Liu, Hui-Min Hu, Chen Li, Qing Shi, Chun-Hua Liu, An-Xiang Liu, Yi-Fan Li, Yi Zhang, Peng Mao, Bi-Fa Fan

Subjects: “…Food and drug administration adverse event reporting system…”
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A real−world pharmacovigilance study of FDA Adverse Event Reporting System events for pralsetinib by Yi Yin, Fengli Sun, Youpeng Jin

Subjects: “…FDA Adverse Event Reporting System (FAERS)…”
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Precision Adverse Drug Reactions Prediction with Heterogeneous Graph Neural Network by Yang Gao, Xiang Zhang, Zhongquan Sun, Payal Chandak, Jiajun Bu, Haishuai Wang

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Assessing hemorrhagic risks in combination therapy: implications of angiogenesis inhibitors and immune checkpoint inhibitors by Yuhui Yang, Yuhui Yang, Yuhui Yang, Pingping Long, Pingping Long, Ying Tuo, Ying Tuo, Xiaoxiao Wang

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Fatal outcome related to drug reaction with eosinophilia and systemic symptoms: a disproportionality analysis of FAERS database and a systematic review of cases by Chunsu Liang, Chunsu Liang, Pengjiao An, Pengjiao An, Yizhou Zhang, Yizhou Zhang, Xin Liu, Xin Liu, Bo Zhang, Bo Zhang

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Comparisons of adverse events associated with immune checkpoint inhibitors in the treatment of non-small cell lung cancer: a real-world disproportionality analysis based on the FDA... by Ruichen Gao, Wenjun Liang, Jintao Chen, Mingxia Yang, Xiaowei Yu, Xiaohua Wang

Subjects: “…FDA adverse event reporting system…”
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Association of incretin-based therapies with hepatobiliary disorders among patients with type 2 diabetes: a case series from the FDA adverse event reporting system by Yankun Liang, Zhenpo Zhang, Jingping Zheng, Yuting Wang, Jiaxin He, Juanzhi Zhao, Ling Su

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