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Characterizing the FDA Adverse Event Reporting System (FAERS) as a Network to Improve Pattern Discovery.
タグ:
VAERS
FAERS
2025/9/16
Negative outcomes associated with tyrosine kinase inhibitors during management of gastrointestinal stromal tumors: examination of data from the FDA adverse event reporting system.
タグ:
FAERS
2025/9/15
Alopecia as an Emerging Adverse Effect Associated With Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists for Weight Loss: A Scoping Review.
タグ:
FAERS
2025/9/15
Adverse drug events associated with tiotropium: a real-world pharmacovigilance study of FDA adverse event reporting system database.
タグ:
FAERS
2025/9/15
A real-world pharmacovigilance assessment of drug-related carcinoembryonic antigen increase.
タグ:
FAERS
2025/9/17
A real-world data analysis of Ozanimod in the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2025/9/17
Exploring drug-induced pemphigus findings from the FDA adverse event reporting system database.
タグ:
FAERS
2025/9/17
Mechanistic insights into taxane-induced psychiatric adverse events: a global pharmacovigilance and experimental investigation.
タグ:
VigiBase
FAERS
2025/9/17
Pharmacovigilance-Based Identification and Mechanistic Exploration of Periodontitis-Related Drugs.
タグ:
FAERS
2025/9/17
Adverse events of ursodeoxycholic acid: a real-world pharmacovigilance study using FAERS (2004-2023).
タグ:
FAERS
2025/9/18
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