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Gabapentinoids-Related Delirium Adverse Events: A Real-World Study from 2004 to 2022 Based on FAERS.
タグ:
FAERS
2024/8/12
Muscular toxicity of colchicine combined with statins: a real-world study based on the FDA adverse event reporting system database from 2004-2023.
タグ:
FAERS
2024/8/12
Adverse events associated with inclisiran: a real-world disproportionality analysis based on the FAERS database.
タグ:
FAERS
2024/8/12
Ocular Adverse Effects of Over-the-Counter Cosmetics and Personal Care Products Reported to the Food and Drug Administration.
タグ:
FAERS
2024/8/13
Safety profiles of doxycycline, minocycline, and tigecycline in pediatric patients: a real-world pharmacovigilance analysis based on the FAERS database.
タグ:
FAERS
2024/8/13
Differences in hypersensitivity reactions and gadolinium deposition disease/symptoms associated with gadolinium exposure to gadolinium-based contrast agents: new insights based on global databases VigiBase, FAERS, and IQVIA-MIDAS.
タグ:
VigiBase
FAERS
2024/8/13
Post-marketing safety concerns with relugolix: a disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2024/8/12
Cardiovascular adverse events associated with PARP inhibitors for ovarian cancer: a real world study (RWS) with Bayesian disproportional analysis based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/8/12
A pharmacovigilance study assessing risk of angioedema with angiotensin receptor blockers using the US FDA Adverse Event Reporting System.
タグ:
FAERS
2024/8/14
Real-world safety profile of eculizumab: an analysis of FDA adverse event reporting system and systematic review of case reports.
タグ:
FAERS
2024/8/14
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