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Drug-induced retinal vein occlusion: a disproportionality analysis from the FDA adverse event reporting system (2004-2023).
タグ:
FAERS
2024/12/30
A real-world pharmacovigilance study of Sorafenib based on the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/1/1
Cardiovascular and Metabolic Adverse Events of Endocrine Therapies in Women with Breast Cancer: A Disproportionality Analysis of Reports in the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/1/1
Data mining of adverse drug event signals with Nirmatrelvir/Ritonavir from FAERS.
タグ:
FAERS
2025/1/1
Drug-Induced Spontaneous Intramural Hematoma of the Gastrointestinal Tract: A Real-World Pharmacovigilance Analysis.
タグ:
FAERS
2025/1/1
Real-world individual and comparative analysis of adverse event reporting for adalimumab and etanercept using public FDA adverse event reporting system data.
タグ:
FAERS
2025/1/1
Using multiple drug similarity networks to promote adverse drug event detection.
タグ:
FAERS
2025/1/3
Gabapentinoids related psychiatric disorders: an analysis based on the FAERS database from 2004 to 2023.
タグ:
FAERS
2025/1/3
Vertebral artery dissection in a patient with migraine treated with calcitonin gene-related peptide monoclonal antibody: a case report and FAERS database analysis.
タグ:
FAERS
2025/1/3
Drug-induced coagulopathies: a real-world pharmacovigilance study using the FDA adverse event reporting system.
タグ:
FAERS
2025/1/2
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