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Risk analysis of enfortumab vedotin: A real-world approach based on the FAERS database.
タグ:
FAERS
2024/9/23
Suspected adverse drug reactions of rivaroxaban reported in the United States food and drug administration adverse event reporting system database: a pharmacovigilance study.
タグ:
FAERS
2024/9/23
Low-Dose Oral Minoxidil and Associated Adverse Events: Analyses of the FDA Adverse Event Reporting System (FAERS) With a Focus on Pericardial Effusions.
タグ:
FAERS
2024/9/27
Post-marketing safety of tralokinumab: a real-world pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/9/26
Mining of adverse event signals associated with inclisiran: a post-marketing analysis based on FAERS.
タグ:
FAERS
2024/9/26
Tumor lysis syndrome signal with the combination of encorafenib and binimetinib for malignant melanoma: a pharmacovigilance study using data from the FAERS database.
タグ:
FAERS
2024/9/24
Clinical characteristics and influencing factors of anti-PD-1/PD-L1-related severe cardiac adverse event: based on FAERS and TCGA databases.
タグ:
FAERS
2024/9/28
The real-world analysis of adverse events with teduglutide: a pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2024/9/27
Safety assessment of sulfasalazine: a pharmacovigilance study based on FAERS database.
タグ:
FAERS
2024/9/27
A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for denosumab.
タグ:
FAERS
2024/9/27
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