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Delayed immune-related adverse events profile associated with immune checkpoint inhibitors: a real-world analysis.
タグ:
FAERS
2024/11/26
Real-world study of adverse events associated with triptan use in migraine treatment based on the U.S. Food and Drug Administration (FDA) adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/11/26
Risk of ophthalmic adverse drug reactions in patients prescribed glucagon-like peptide 1 receptor agonists: a pharmacovigilance study based on the FDA adverse event reporting system database.
タグ:
FAERS
2024/11/23
A real-world pharmacovigilance study of FDA Adverse Event Reporting System events for pralsetinib.
タグ:
FAERS
2024/11/27
A Disproportionality Analysis of Treprostinil Based on FDA Adverse Event Reporting System Database.
タグ:
FAERS
2024/11/27
Investigating Osteomyelitis as a Rare Adverse Effect of Vaccination in the Pediatric Population.
タグ:
VAERS
FAERS
2024/11/27
Off-Label Use of Monoclonal Antibodies for Eosinophilic Esophagitis in Humans: A Scoping Review.
タグ:
FAERS
2024/11/27
Evaluation of pitolisant, sodium oxybate, solriamfetol, and modafinil for the management of narcolepsy: a retrospective analysis of the FAERS database.
タグ:
FAERS
2024/11/26
Advanced AI-Driven Prediction of Pregnancy-Related Adverse Drug Reactions.
タグ:
FAERS
2024/11/29
Association between different GLP-1 receptor agonists and acute pancreatitis: case series and real-world pharmacovigilance analysis.
タグ:
FAERS
2024/11/28
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