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Drug-induced hepatitis B virus reactivation: insights from FAERS database analysis.
タグ:
FAERS
2024/12/4
Investigating Sodium-Glucose Cotransporter 2 Inhibitors Versus Other Glucose-Lowering Drugs on Ventricular Arrhythmias or Sudden Cardiac Death Using the US FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/4
Adverse event profiles of selpercatinib: a real-world pharmacovigilance analysis based on FAERS database.
タグ:
FAERS
2024/12/4
Exploring the dark side of diagnostic dyes with a focus on Indocyanine green’s adverse reactions.
タグ:
FAERS
2024/12/4
Data Mining and Analysis for Iodinated Contrast Media Adverse Event Signals Based on the Food and Drug Administration Adverse Event Reporting System Database.
タグ:
FAERS
2024/12/4
Comparison of the pharmacovigilance signals of cardiac and renal adverse events associated with sacubitril/valsartan and valsartan alone based on the FAERS database.
タグ:
FAERS
2024/12/3
Analysis of literature-derived duplicate records in the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2024/12/2
Levetiracetam and severe cutaneous adverse reactions: insights from FAERS database analysis.
タグ:
FAERS
2024/12/2
Adverse events of mepolizumab in the treatment of nasal polyps: A FDA database evaluation.
タグ:
FAERS
2024/12/1
Sex differences of fall-risk-increasing drugs in the middle-aged and elderly: a descriptive, cross-sectional study of FDA adverse event reporting system.
タグ:
FAERS
2024/11/30
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