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Methodological Considerations for Comparison of Brand Versus Generic Versus Authorized Generic Adverse Event Reports in the US Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2017/9/22
Identification and Characteristics of Time-Related Shifts in Suicide-Related Event Frequency During Smoking Cessation Treatment with Varenicline.
タグ:
FAERS
2017/09/20
Digoxin-induced anemia among patients with atrial fibrillation and heart failure: clinical data analysis and drug-gene interaction network.
タグ:
FAERS
2017/09/17
Acute pancreatitis in patients with type 2 diabetes mellitus treated with dipeptidyl peptidase-4 inhibitors.
タグ:
FAERS
2016/4/1
Safety Concerns Reported by Patients Identified in a Collaborative Signal Detection Workshop using VigiBase: Results and Reflections from Lareb and Uppsala Monitoring Centre.
タグ:
VigiBase
2017/9/22
Filing Sources after Oral P2Y12 Platelet Inhibitors to the Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2017/9/13
Levetiracetam-induced rhabdomyolysis: Analysis of reports from the Food and Drug Administration’s Adverse Event Reporting System database.
タグ:
FAERS
2017/9/10
Postmarketing safety surveillance of trivalent recombinant influenza vaccine: Reports to the Vaccine Adverse Event Reporting System.
タグ:
VAERS
2017/09/10
Etonogestrel implant migration to the vasculature, chest wall, and distant body sites: cases from a pharmacovigilance database.
タグ:
FAERS
2017/9/5
Influence of Japanese Regulatory Action on Denosumab-Related Hypocalcemia Using Japanese Adverse Drug Event Report Database.
タグ:
JADER
2017/9/5
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