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A real‑world pharmacovigilance study of raloxifene based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/12/18
Concomitant use of sodium-glucose co-transporter 2 inhibitors and metformin and the risk of osteomyelitis reporting: a disproportionality analysis based on FAERS database.
タグ:
FAERS
2024/12/22
Drug-Associated Risk of Subacute Cutaneous Lupus Erythematosus: A Pharmacovigilance Study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/22
Adverse event of ruxolitinib cream: a real-world analysis based on FDA Adverse Event Reporting System from 2021 to 2024.
タグ:
FAERS
2024/12/22
A real-world pharmacovigilance analysis for agalsidase beta: findings from the FDA adverse event reporting database.
タグ:
FAERS
2024/12/22
Adverse drug events associated with capecitabine: a real-world pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2024/12/23
DDI-GPT: Explainable Prediction of Drug-Drug Interactions using Large Language Models enhanced with Knowledge Graphs.
タグ:
FAERS
2024/12/23
Increasing Trends in the Pancreatitis Risk With Tumor Necrosis Factor Inhibitor Use.
タグ:
FAERS
2024/12/23
Drug-induced nephrolithiasis: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/23
Detection of risk signals for ustekinumab in the real world using the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/12/23
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