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Detecting drug-drug interactions between therapies for COVID-19 and concomitant medications through the FDA adverse event reporting system.
タグ:
FAERS
2022/8/9
Rituximab and Pyoderma Gangrenosum: An Investigation of Disproportionality Using a Systems Biology-Informed Approach in the FAERS Database.
タグ:
FAERS
2022/8/7
Immune checkpoint inhibitors increase the risk of kidney transplant rejection: a real-world pharmacovigilance study.
タグ:
FAERS
2022/8/6
Acute Cholecystitis Associated With the Use of Glucagon-Like Peptide-1 Receptor Agonists Reported to the US Food and Drug Administration.
タグ:
FAERS
2022/8/30
Machine Learning for Predicting Hyperglycemic Cases Induced by PD-1/PD-L1 Inhibitors.
タグ:
FAERS
2022/8/30
Identification of novel signal of clobazam-associated drug reaction with eosinophilia and systemic symptoms syndrome: A disproportionality analysis.
タグ:
FAERS
2022/8/28
Omeprazole Suppresses Oxaliplatin-Induced Peripheral Neuropathy in a Rodent Model and Clinical Database.
タグ:
FAERS
2022/8/27
Characteristics of adverse event reporting of Xeljanz/Xeljanz XR, Olumiant, and Rinvoq to the US Food and Drug Administration.
タグ:
FAERS
2022/8/25
Incidence and clinical characteristics of fall-related injuries among older inpatients at a tertiary grade a hospital in Shandong province from 2018 to 2020.
タグ:
FAERS
2022/8/2
Adverse Events of Axitinib plus Pembrolizumab Versus Lenvatinib plus Pembrolizumab: A Pharmacovigilance Study in Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/8/2
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