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Adverse event signal mining and severe adverse event influencing factor analysis of Lumateperone based on FAERS database.
タグ:
FAERS
2024/10/8
Adverse event profiles of CDK4/6 inhibitors: data mining and disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2024/10/8
Disproportionality analysis of reslizumab based on the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/10/9
A disproportionality analysis for assessing the safety of FLT3 inhibitors using the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/10/9
Mining and evaluation of adverse event signals for capmatinib based on the FAERS database.
タグ:
FAERS
2024/10/9
Development and validation of a clinical prediction model for osteonecrosis of the jaw in patients receiving zoledronic acid using FAERS and canadian databases.
タグ:
CVAR
FAERS
2024/10/9
Regional diversity in drug-induced lung diseases among the USA, European Union, and Japan.
タグ:
FAERS
2024/10/9
Signal detection of immune thrombocytopenia associated with immune checkpoint inhibitors.
タグ:
FAERS
2024/10/11
Adverse Event Assessment of Upadacitinib: A Pharmacovigilance Study Based on the FAERS Database.
タグ:
FAERS
2024/10/10
Real-world pharmacovigilance study of FDA adverse event reporting system events for finerenone.
タグ:
FAERS
2024/10/10
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