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Assessing the Association Between GLP-1 Receptor Agonist Use and Diabetic Retinopathy Through the FDA Adverse Event Reporting System.
タグ:
FAERS
2018/12/12
Unusual Neisseria species as a cause of infection in patients taking eculizumab.
タグ:
FAERS
2018/11/9
Retrospective Side Effect Profiling of the Metastatic Melanoma Combination Therapy Ipilimumab-Nivolumab Using Adverse Event Data.
タグ:
FAERS
2018/11/6
Stevens-Johnson syndrome and toxic epidermal necrolysis with antiepileptic drugs: An analysis of the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2018/11/6
Response to “Comment on: Botulinum Toxin Type A Overdoses: Analysis of the FDA Adverse Event Reporting System Database”.
タグ:
FAERS
2018/11/6
Comment on: Botulinum Toxin Type A Overdoses: Analysis of the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2018/11/6
Extraction of Information Related to Adverse Drug Events from Electronic Health Record Notes: Design of an End-to-End Model Based on Deep Learning.
タグ:
FAERS
2018/11/28
Influence of excess ligand on Nephrogenic Systemic Fibrosis associated with nonionic, linear gadolinium-based contrast agents.
タグ:
FAERS
2018/11/25
Dosing Recommendations for Quetiapine When Coadministered With HIV Protease Inhibitors.
タグ:
FAERS
2018/11/20
A characterization and disproportionality analysis of medication error related adverse events reported to the FAERS database.
タグ:
FAERS
2018/11/20
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