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論文・技術情報
The Association Between Dexmedetomidine and Bradycardia: An Analysis of FDA Adverse Event Reporting System (FAERS) Data and Transcriptomic Profiles.
タグ:
FAERS
2025/6/26
SGLT2 Inhibitors May Increase Creatinine Clearance: Data Mining Utilizing the FDA Adverse Event Report System Database and Pharmacokinetic Study with Rats.
タグ:
FAERS
2025/6/26
Real-world pharmacovigilance reports of hepatitis A inactivated and hepatitis B (recombinant) vaccine: insights from disproportionality analysis of the vaccine adverse event reporting system.
タグ:
VAERS
FAERS
2025/6/25
A real-world pharmacovigilance study of lorazepam based on the FDA adverse event reporting system database.
タグ:
FAERS
2025/6/25
Safety evaluation of irinotecan: a real-world disproportionality analysis using FAERS and JADER databases during the time period 2004-2024.
タグ:
JADER
FAERS
2025/6/24
An integrated approach based on FDA adverse event reporting system, network pharmacology, molecular docking, and molecular dynamics simulation analysis to study the cardiac adverse reactions and mechanism of action of osimertinib.
タグ:
FAERS
2025/6/24
Postmarketing safety analysis of remimazolam: Identifying unlabelled serious events.
タグ:
JADER
FAERS
2025/6/24
Adverse events associated with gepants: a pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2025/6/24
Association Between Melatonin Receptor Agonists and Cardiac Arrhythmia; Disproportionality Analysis Studies Using Pharmacovigilance Databases.
タグ:
FAERS
2025/6/24
Beyond pain relief: the thrombosis threat of celecoxib.
タグ:
CVAR
JADER
FAERS
2025/6/24
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