Lv31
240 积分 2024-11-16 加入
Direct-acting antiviral agent use and gastrointestinal safety in patients with chronic hepatitis C: a pharmacovigilance study based on FDA Adverse Event Reporting System
5小时前
待确认
Infection and infestation-related adverse events of biologics in psoriasis: insights from the food and drug administration adverse event reporting system (FAERS)
4个月前
已完结
A real-world study of antifibrotic drugs-related adverse events based on the United States food and drug administration adverse event reporting system and VigiAccess databases
5个月前
已完结
Infection and infestation-related adverse events of biologics in psoriasis: insights from the food and drug administration adverse event reporting system (FAERS)
5个月前
已完结
A disproportionality analysis of FDA adverse event reporting system (FAERS) events for ticagrelor
5个月前
已完结
Comparison of the safety profiles for pirfenidone and nintedanib: a disproportionality analysis of the US food and drug administration adverse event reporting system
5个月前
已完结
Pharmacovigilance analysis of orlistat adverse events based on the FDA adverse event reporting system (FAERS) database
5个月前
已完结
Drug-induced hypoglycemia: a disproportionality analysis of the FAERS database
5个月前
已完结
Safety assessment of Brexpiprazole: Real-world adverse event analysis from the FAERS database
5个月前
已完结
Major adverse cardiovascular events related to phosphodiesterase 5 inhibitors: analysis of real-life data from Eudra-Vigilance database
6个月前
已完结
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