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Comprehensive post-marketing safety evaluation of atezolizumab: A disproportionality analysis based on individual case safety reports in the FAERS.
タグ:
FAERS
2026/3/3
Immunotherapy Safety in Thymic Epithelial Tumors: Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/2/25
QT-related adverse events with ondansetron and olanzapine: a real-world FAERS analysis with implications for oncology anti-emetic practice.
タグ:
FAERS
2026/3/9
Evaluating the Evolving Real-World Adverse Events of GLP-1RAs Using FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2026/3/9
Evaluation of Anticancer Therapy-Related Tumor Flare Reaction: Insights From Food and Drug Administration’s Adverse Event Reporting System Dataset.
タグ:
FAERS
2026/3/10
Leukotriene receptor antagonists and eosinophilic granulomatosis with polyangiitis: a disproportionality analysis from FAERS, JADER, CVAR databases integrated with network pharmacology.
タグ:
JADER
FAERS
2026/3/9
Ischemic optic neuropathy with semaglutide: global observational analysis of sex- and formulation-specific risk.
タグ:
FAERS
2026/3/11
Prioritization of adverse events related to integrase inhibitors and NNRTIs: a disproportionality analysis using data from the FAERS database.
タグ:
FAERS
2026/3/11
Adverse events associated with use of immunoglobulin in pediatric patients reported to the US Food and Drug Administration Adverse Event Reporting System, 2001-2023.
タグ:
FAERS
2026/3/11
Investigating tralokinumab-related adverse events in treating atopic dermatitis: insights from the FAERS database.
タグ:
FAERS
2026/3/11
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