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Assessment of drug induced hyperuricemia and gout risk using the FDA adverse event reporting system.
タグ:
FAERS
2025/7/2
MDDC: An R and Python package for adverse event identification in pharmacovigilance data.
タグ:
VigiBase
EudraVigilance
FAERS
2025/7/2
Pharmacovigilance study of drug-induced eye movement disorder based on FDA adverse event reports from 2004 to 2024.
タグ:
FAERS
2025/7/2
Disproportionality analysis of adverse events associated with ipilimumab and nivolumab combination therapy based on FAERS database.
タグ:
FAERS
2025/7/2
An investigation of drug-induced mental disorders in the children and adolescents population utilizing the FDA adverse event reporting system.
タグ:
FAERS
2025/7/2
A disproportionality analysis of cardiac arrhythmia associated with bisphosphonates based on the FAERS database.
タグ:
FAERS
2025/7/2
Disproportionality analysis and risk factor assessment of drug-associated thyroid dysfunction adverse events: a study based on the FAERS database.
タグ:
FAERS
2025/7/1
Hypoparathyroidism induced by immune checkpoint inhibitors: a review of literature reports and real-world pharmacovigilance data.
タグ:
FAERS
2025/7/1
Real-world safety of carboplatin in non-small cell lung cancer: a retrospective signal detection and subgroup analysis based on the FAERS database.
タグ:
FAERS
2025/7/1
PD-1/PD-L1 inhibitor-induced hyponatremia: a real-world pharmacovigilance analysis using FAERS database.
タグ:
FAERS
2025/7/1
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