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Transparency and the Food and Drug Administration–a quantitative study.
タグ:
FAERS
2012/11/08
Underreporting of hemorrhagic and thrombotic complications of pharmaceuticals to the U.S. Food and Drug Administration: empirical findings for warfarin, clopidogrel, ticlopidine, and thalidomide from the Southern Network on Adverse Reactions (SONAR).
タグ:
FAERS
2012/10/23
Multinomial modeling and an evaluation of common data-mining algorithms for identifying signals of disproportionate reporting in pharmacovigilance databases.
タグ:
FAERS
2012/10/16
Causality assessment of adverse events reported to the Vaccine Adverse Event Reporting System (VAERS).
タグ:
VAERS
2012/10/16
Concomitant antibiotic usage does not augment the risk of inflammatory bowel disease with isotretinoin treatment for acne: a review of the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2012/10/12
Thrombotic events associated with C1 esterase inhibitor products in patients with hereditary angioedema: investigation from the United States Food and Drug Administration adverse event reporting system database.
タグ:
FAERS
2012/10/4
T-cell non-Hodgkin’s lymphomas reported to the FDA AERS with tumor necrosis factor-alpha (TNF-alpha) inhibitors: results of the REFURBISH study.
タグ:
FAERS
2012/10/4
Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season?
タグ:
VAERS
2012/10/2
Drug target prediction using adverse event report systems: a pharmacogenomic approach.
タグ:
FAERS
2012/9/11
Antipsychotics and torsadogenic risk: signals emerging from the US FDA Adverse Event Reporting System database.
タグ:
FAERS
2013/4/5
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