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Adverse events in different administration routes of amiodarone: a pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2025/2/11
Assessment the real-world safety of intravitreal dexamethasone implant (Ozurdex): novel insights from a comprehensive pharmacovigilance analysis utilizing the FAERS database.
タグ:
FAERS
2025/2/11
Antibiotic-induced IgA vasculitis: insights from a real-world retrospective analysis and pharmacovigilance assessment.
タグ:
FAERS
2025/2/11
Assessment of adverse events of tasimelteon: a real-world pharmacovigilance study based on FAERS.
タグ:
FAERS
2025/2/10
The impact of the COVID-19 pandemic on adverse events associated with ACEIs and ARBs: a real-world analysis using the FDA adverse event reporting system.
タグ:
FAERS
2025/2/10
Data mining and safety analysis of voriconazole in patients with a hematological malignant tumor based on the FAERS database: differences between children and adults.
タグ:
FAERS
2025/2/10
Post-marketing safety evaluation of zanubrutinib: a real-world pharmacovigilance analysis based on the FAERS database.
タグ:
FAERS
2025/2/10
Adverse event profile of setmelanotide in obesity: an integrated assessment and systematic review using disproportionality analysis, case reports and meta-analysis.
タグ:
FAERS
2025/2/10
Ezetimibe-associated rhabdomyolysis: A comprehensive assessment of the USFDA adverse event reporting system using disproportionality analysis, case reviews, and meta-analysis of randomized clinical trials.
タグ:
FAERS
2025/2/10
Improving entity recognition using ensembles of deep learning and fine-tuned large language models: A case study on adverse event extraction from VAERS and social media.
タグ:
VAERS
FAERS
2025/2/10
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