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Amlodipine-Associated Angioedema: An Integrated Pharmacovigilance Assessment Using Disproportionality and Interaction Analysis and Case Reviews.
タグ:
FAERS
2025/2/26
Post-marketing safety surveillance of Amivantamab: a real world study based on the FDA adverse event reporting system.
タグ:
FAERS
2025/2/26
Haemorrhage-related adverse events profles of lenvatinib and pembrolizumab alone or in combination: a real-world pharmacovigilance study based on FAERS database.
タグ:
FAERS
2025/2/26
Oseltamivir-induced hepatotoxicity: A retrospective analysis of the FDA adverse event reporting system.
タグ:
FAERS
2025/2/25
Assessing hemorrhagic risks in combination therapy: implications of angiogenesis inhibitors and immune checkpoint inhibitors.
タグ:
FAERS
2025/2/25
Second-Generation Antipsychotic-Associated Serious Adverse Events in Women: An Analysis of a National Pharmacoepidemiologic Database.
タグ:
FAERS
2025/2/27
Severe Acute Respiratory Failure Associated With Trimethoprim/Sulfamethoxazole Among Adolescent and Young Adults: An Active Comparator-Restricted Disproportionality Analysis From the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/2/27
Fosfomycin-associated adverse events: A disproportionality analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/2/27
Disproportionality analysis of upadacitinib-related adverse events in inflammatory bowel disease using the FDA adverse event reporting system.
タグ:
FAERS
2025/2/26
Diabetic Ketoacidosis and the Use of New Hypoglycemic Groups: Real-World Evidence Utilizing the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2025/2/26
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