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Medications and the risk of perforated appendicitis: an adverse event report system (FAERS) database analysis.
タグ:
FAERS
2022/11/3
Potential cerebrovascular accident signal for risankizumab: A disproportionality analysis of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2022/11/3
Linezolid and the risk of QT interval prolongation: A pharmacovigilance study of the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/11/9
Impact of body mass index on in-hospital mortality for six acute cardiovascular diseases in Japan.
タグ:
DPC
2022/11/8
COVID-19 Vaccination as a Trigger of IgA Vasculitis: A Global Pharmacovigilance Study.
タグ:
VigiBase
2022/11/16
Benzonatate Exposure Trends and Adverse Events.
タグ:
FAERS
2022/11/16
A real-world pharmacovigilance study of severe cutaneous adverse reactions associated with antiepileptic drug combination therapy: data mining of FDA adverse event reporting system.
タグ:
FAERS
2022/11/15
Direct-acting antiviral agent use and gastrointestinal safety in patients with chronic hepatitis C: a pharmacovigilance study based on FDA Adverse Event Reporting System.
タグ:
FAERS
2022/11/14
Real-World Outcomes of Systemic Therapy in Japanese Patients with Cancer (Tokushukai REAl-World Data Project: TREAD): Study Protocol for a Nationwide Cohort Study.
タグ:
DPC
2022/11/12
GLP-1 receptor agonist-associated tumor adverse events: A real-world study from 2004 to 2021 based on FAERS.
タグ:
FAERS
2022/11/18
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