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Real-World Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System Database for Asciminib.
タグ:
FAERS
2024/8/6
Adverse event profile of memantine and donepezil combination therapy: a real-world pharmacovigilance analysis based on FDA adverse event reporting system (FAERS) data from 2004 to 2023.
タグ:
FAERS
2024/8/5
Signal mining of adverse reactions in the antiemetic drug ondansetron during pregnancy: A real-world analysis of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/8/5
Post-marketing safety concerns with montelukast: A pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/8/5
Tinnitus after COVID-19 vaccination: Findings from the vaccine adverse event reporting system and the vaccine safety datalink.
タグ:
VAERS
FAERS
2024/8/4
Adverse events related to neuromuscular blocking agents: a disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2024/8/8
A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for sunitinib.
タグ:
FAERS
2024/8/8
Signal mining and analysis of trifluridine/tipiracil adverse events based on real-world data from the FAERS database.
タグ:
FAERS
2024/8/7
An investigation of broad-spectrum antibiotic-induced liver injury based on the FDA Adverse Event Reporting System and retrospective observational study.
タグ:
FAERS
2024/8/7
Lost needles, pads and where to find them.
タグ:
FAERS
2024/8/6
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