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Expert Opinion on Drug Safety|December 9, 2024
Post-marketing safety of panitumumab: a real-world pharmacovigilance studyHeli Wen, Yuqing Lei, Lingjie Mao
Expert Opinion on Drug Safety|December 24, 2024
Metoprolol adverse events and literature analyses: case/non-case analyses using the FDA Adverse Event Reporting System (FAERS)Yikuan Du, Mengting Zhang, Ziyi Luo, et al.
Expert Opinion on Drug Safety|December 21, 2024
A real-world pharmacovigilance analysis for agalsidase beta: findings from the FDA adverse event reporting databaseWen-Long Xie, Hou-Hong Li, Di Li, et al.
Expert Opinion on Drug Safety|December 23, 2024
Role of gliflozins on hepatocellular carcinoma progression: a systematic synthesis of preclinical and clinical evidenceLivia Basile, Rossella Cannarella, Paolo Magni, et al.
Expert Opinion on Drug Safety|December 18, 2024
A real‑world pharmacovigilance study of raloxifene based on the FDA adverse event reporting system (FAERS)Hao Liu, Wei Yan, Di Luo, et al.
Expert Opinion on Drug Safety|December 18, 2024
The antidepressants and sexual dysfunction: a pharmacovigilance-pharmacodynamic study of the FDA adverse event reporting systemYu Cheng, Youjun Chen, Xue Zhao, et al.
Expert Opinion on Drug Safety|December 10, 2024
Oral anticoagulants-induced intracranial hemorrhage: a real-world pharmacovigilance study over 2008-2024Jiale Chen, Ling Wang, Guoquan Chen, et al.
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