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Safety of CDK4/6 inhibitors in older patients: A FAERS-based analysis of serious and fatal adverse events.
タグ:
FAERS
2025/12/12
Disproportionality analysis of adverse events associated with bimekizumab: a real-world study based on FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/12/11
Cardiotoxicity associated with antifungal agents: A pharmacovigilance analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/12/11
A pharmacovigilance study of Bruton’s tyrosine kinase inhibitors: a multidimensional analysis based on FAERS and VigiBase.
タグ:
VigiBase
2025/12/11
Pharmacovigilance assessment of adverse events following yellow fever vaccination: Disproportionality analysis of VAERS reports, 2015-2025.
タグ:
VAERS
2025/12/10
Disproportionality analysis of biliary adverse events associated with fibrates using the JADER and FAERS databases.
タグ:
JADER
2025/12/10
Drug-induced polycystic ovary syndrome: a real-world pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2025/12/10
Analysis of infection-related adverse events induced by proton pump inhibitors based on the FAERS and JADER databases.
タグ:
JADER
2025/12/10
The real-world safety profile and potential mechanism of isatuximab: Integration of pharmacovigilance and transcriptomic analysis.
タグ:
FAERS
2025/12/10
Systematic analysis of adverse reactions associated with dantrolene treatment: From clinical features to molecular mechanisms.
タグ:
CVAR
2025/12/10
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