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Development of a Network-Based Signal Detection Tool: The COVID-19 Adversome in the FDA Adverse Event Reporting System.
タグ:
FAERS
2021/12/28
Response to “Facial nerve palsy following the administration of COVID-19 mRNA vaccines: analysis of a self-reporting database” by Sato et al.
タグ:
FAERS
VAERS
2021/12/27
Cardiovascular safety profile of taxanes and vinca alkaloids: 30 years FDA registry experience.
タグ:
FAERS
2021/12/26
A New Criterion for Fluoroquinolone-Associated Disability Diagnosis: Functional Gastrointestinal Disorders.
タグ:
FAERS
2021/12/25
Postmarketing safety surveillance data reveals protective effects of botulinum toxin injections against incident anxiety.
タグ:
FAERS
2021/12/23
A real-world pharmacovigilance study of axitinib: data mining of the public version of FDA adverse event reporting system.
タグ:
FAERS
2021/12/18
Dupilumab Adverse Events in Nasal Polyp Treatment: Analysis of FDA Adverse Event Reporting System.
タグ:
FAERS
2021/12/18
Proton pump inhibitors and increased reporting odds of renal neoplasms: FAERS-based adverse event data mining and analysis.
タグ:
FAERS
2021/12/18
Case Report: Collapsing Focal Segmental Glomerulosclerosis After Initiation of Ado-Trastuzumab Emtansine Therapy.
タグ:
FAERS
2021/12/17
Common Immune-Related Adverse Events of Immune Checkpoint Inhibitors in the Gastrointestinal System: A Study Based on the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2021/12/17
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