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46 积分 2026-06-07 加入
Drug-specific differences in fatal adverse events among PARP inhibitors: a FAERS pharmacovigilance study
5小时前
待确认
Immune-related adverse events associated with immune checkpoint inhibitors: An updated comprehensive disproportionality analysis of the FDA adverse event reporting system
1个月前
已完结
Chinese guidelines for diagnosis and treatment of neuromyelitis optica spectrum disorders (2025 edition)
2个月前
已完结
The spectrum of neuromyelitis optica
2个月前
已完结
Comparing the efficacy of efgartigimod and intravenous immunoglobulin on AQP4-IgG-positive neuromyelitis optica spectrum disorder during acute attacks
2个月前
已完结
An integrated approach based on FDA adverse event reporting system, network pharmacology, molecular docking, and molecular dynamics simulation analysis to study the cardiac adverse reactions and mechanism of action of osimertinib
3个月前
已完结
Evaluation of the post-marketing safety of eculizumab from 2007 to 2025: A real-world pharmacovigilance study and signal analysis based on the FAERS database
3个月前
已完结
Inebilizumab for the treatment of neuromyelitis optica spectrum disorder (N-MOmentum): a double-blind, randomised placebo-controlled phase 2/3 trial
3个月前
已完结
Trial of Satralizumab in Neuromyelitis Optica Spectrum Disorder
3个月前
已完结
Chinese guidelines for diagnosis and treatment of neuromyelitis optica spectrum disorders (2025 edition)
3个月前
已完结
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