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Post-marketing safety signals of imatinib: pharmacovigilance insights from the FDA Adverse Event Reporting System (FAERS) and implications for clinical practice.
タグ:
FAERS
2025/7/8
Apixaban- and Rivaroxaban-Associated Bleeding: A Retrospective Analysis Using the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/7/8
Assessing post-marketing safety of PDE5Is in erectile dysfunction: real-world evidence from the FDA adverse event reporting system.
タグ:
FAERS
2025/7/8
Safety profile of ramelteon from the perspective of physicians and pharmacists: a 20-year real-world pharmacovigilance analysis based on the FAERS database.
タグ:
FAERS
2025/7/8
Cardiovascular safety of propranolol oral solution in infantile hemangiomas: a disproportionality analysis based on the FAERS database.
タグ:
FAERS
2025/7/8
Mifepristone-related foetal cardiac adverse events: findings from the postmarketing safety reports.
タグ:
FAERS
2025/7/7
HER2-targeted agents and interstitial lung disease: A real-world pharmacovigilance analysis using FAERS data.
タグ:
FAERS
2025/7/7
Real-World safety profile of Fenfluramine in refractory epilepsy: a pharmacovigilance study based on FAERS database.
タグ:
FAERS
2025/7/6
Comprehensive Cardiovascular Risk Profiling in People Living with HIV: Insights from the Japanese Adverse Drug Event Report Database.
タグ:
JADER
2025/7/11
Safety of Proton Pump Inhibitor in Paediatrics: A Study Based on EudraVigilance Data.
タグ:
EudraVigilance
2025/7/8
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