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Analysis and comparison of adverse events of colistin administered by different routes based on the FAERS database.
タグ:
FAERS
2025/3/27
Safety Profile and Hepatotoxicity of Anaplastic Lymphoma Kinase Tyrosine Kinase Inhibitors: A Disproportionality Analysis Based on FDA Adverse Event Reporting System Database.
タグ:
FAERS
2025/3/27
Risk assessment of the top 50 drugs associated with drug-induced orthostatic hypotension: a disproportionality analysis of the FAERS and JADER databases.
タグ:
JADER
FAERS
2025/3/26
Disproportionality analysis on semaglutide and nonarteritic anterior ischemic optic neuropathy in the FDA adverse event reporting system: An emerging pharmacovigilance signal?
タグ:
FAERS
2025/3/26
Detection of Clinically Significant Drug-Drug Interactions in Fatal Torsades de Pointes: Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2025/3/25
Safety assessment of sodium zirconium cyclosilicate: A FAERS-based disproportionality analysis.
タグ:
FAERS
2025/3/25
Toxicities Associated with Sacituzumab Govitecan: Data from Clinical Trials and a Real-World Pharmacovigilance Database.
タグ:
FAERS
2025/3/25
Correlation of atorvastatin with subjective memory deficits: a study from the NHANES and FAERS databases.
タグ:
FAERS
2025/3/25
Safety of sulfamethoxazole-trimethoprim for the treatment of bacterial infection in outpatient settings: A systematic review and meta-analysis with active comparator disproportionality analysis.
タグ:
FAERS
2025/3/25
Pharmacovigilance study and genetic target prediction analysis of FDA adverse event reports (FAERS) for drug-induced sinusitis.
タグ:
FAERS
2025/3/25
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