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Ranking the Diabetes-related Safety Profile of Different Statin Drugs.
タグ:
FAERS
2025/9/24
Drug-drug interactions: A descriptive analysis of FDA adverse event reporting system.
タグ:
FAERS
2025/9/24
Post-marketing safety of solriamfetol: A retrospective pharmacovigilance study based on the us food and drug administration adverse event reporting system.
タグ:
FAERS
2025/9/22
Adverse Event Signals Associated with Beta-Lactamase Inhibitors: Disproportionality Analysis of USFDA Adverse Event Reporting System.
タグ:
FAERS
2025/9/22
Do PCSK9 Inhibitors Impair Memory? A Dual Approach Combining Real-World Data and Genetic Evidence.
タグ:
FAERS
2025/9/22
Linezolid-related Optic Nerve Disorders: Insight From a Pharmacovigilance Analysis of the US FDA Adverse Event Reporting System.
タグ:
FAERS
2025/9/22
Post-Marketing Safety Concerns with Efgartigimod alfa: A Pharmacovigilance Analysis Based on the Food and Drug Administration Adverse Event Reporting System Database.
タグ:
FAERS
2025/9/22
Integrative analysis of levofloxacin-induced liver injury: Insights from pharmacovigilance, human liver organoids, and extracellular vesicle proteomics.
タグ:
FAERS
2025/9/22
Drug-induced cough risk: A pharmacovigilance study of FDA adverse event reporting system database.
タグ:
FAERS
2025/9/21
Exploring Definity-related adverse reaction: A real-world pharmacovigilance study via FAERS database analysis.
タグ:
FAERS
2025/9/20
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