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Neuropsychiatric adverse events of SGLT2 inhibitors: a pharmacovigilance analysis of the FDA adverse event reporting system database.
タグ:
FAERS
2026/6/15
Signal mining and analysis of adverse events in children using growth hormones: A retrospective real-world study based on FAERS.
タグ:
FAERS
2026/6/16
Ketoacidosis Risk in Non-diabetic Patients Using Semaglutide Versus Tirzepatide for Obesity: A Disproportionality Analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/6/16
Analysis of ocular adverse events associated with SNRIs.
タグ:
FAERS
2026/6/15
A real-world retrospective study of vitiligo associated with immune checkpoint inhibitors based on FAERS and TCGA databases.
タグ:
FAERS
2026/6/16
Comprehensive analysis of cefuroxime-associated adverse events: Insights from JADER database (2004-2024) and comparison with FAERS database.
タグ:
JADER
FAERS
2026/6/16
Identification of Drug Associated Factors for Gingival Disorders: A Real-World Pharmacovigilance Study.
タグ:
FAERS
2026/6/17
Analysis signals of disproportionate reporting associated with donanemab: A retrospective pharmacovigilance study using the FAERS database.
タグ:
FAERS
2026/6/16
Adverse events of Alzheimer’s disease patients treated with memantine-based therapies: A disproportionality analysis of the FAERS database based on the MY FAERS platform.
タグ:
FAERS
2026/6/16
Pharmacovigilance evaluation of somatrogon-associated adverse events in real-world databases.
タグ:
FAERS
2026/6/17
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