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Postmarketing safety of anaplastic lymphoma kinase (ALK) inhibitors: an analysis of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2021/12/6
Active-comparator restricted disproportionality analysis for pharmacovigilance signal detection studies of chronic disease medications: An example using sodium/glucose cotransporter 2 inhibitors.
タグ:
FAERS
2021/12/30
Potential Safety Signals for Rhabdomyolysis Associated With High-Potency Statin Use With or Without Sacubitril/Valsartan.
タグ:
FAERS
2021/12/30
Retrospective analysis and nursing management of inpatient falls: Case series.
タグ:
FAERS
2021/12/30
Analysis of anticholinergic adverse effects using two large databases: The US Food and Drug Administration Adverse Event Reporting System database and the Japanese Adverse Drug Event Report database.
タグ:
FAERS
JADER
2021/12/3
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
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