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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
JADER
2025/12/10
Pharmacovigilance assessment of ropivacaine safety using FAERS data (2004-2024).
タグ:
FAERS
2025/12/10
Analyzing adverse event signals of aprepitant using FAERS database data in real-world settings: Broadening the adverse event spectrum of aprepitant and its clinical implications.
タグ:
FAERS
2025/12/10
Real-world safety profile of novel anti-multidrug-resistant tuberculosis drugs: a disproportionality analysis based on the FAERS database.
タグ:
FAERS
2025/12/9
Evaluating adverse events of antibacterials in infants: insights from FDA adverse event reporting system (FAERS) data.
タグ:
FAERS
2025/12/8
Comparative safety profile of levofloxacin versus moxifloxacin in first-line tuberculosis therapy: a pharmacovigilance study of the FAERS database.
タグ:
FAERS
2025/12/8
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