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[Validation of an adverse event reporting system in primary care].
タグ:
FAERS
2016/4/23
Acute pancreatitis in patients with type 2 diabetes mellitus treated with dipeptidyl peptidase-4 inhibitors.
タグ:
FAERS
2016/4/1
An Empirical Examination of the FDAAA-Mandated “Toll-Free Statement” for Consumer Reporting of Side Effects in Direct-to-Consumer Television Advertisements.
タグ:
FAERS
2016/4/1
A Pharmacovigilance Signaling System Based on FDA Regulatory Action and Post-Marketing Adverse Event Reports.
タグ:
FAERS
2016/3/8
[Evaluation of the Association of Hand-Foot Syndrome with Anticancer Drugs Using the US Food and Drug Administration Adverse Event Reporting System (FAERS) and Japanese Adverse Drug Event Report (JADER) Databases].
タグ:
FAERS
JADER
2016/3/5
The Risk of Glioblastoma with TNF Inhibitors.
タグ:
FAERS
2016/3/5
Post-licensure surveillance of quadrivalent inactivated influenza (IIV4) vaccine in the United States, Vaccine Adverse Event Reporting System (VAERS), July 1, 2013-May 31, 2015.
タグ:
FAERS
VAERS
2016/3/27
Linking MedDRA((R))-Coded Clinical Phenotypes to Biological Mechanisms by the Ontology of Adverse Events: A Pilot Study on Tyrosine Kinase Inhibitors.
タグ:
FAERS
2016/3/24
Fluoroquinolone-related neuropsychiatric and mitochondrial toxicity: a collaborative investigation by scientists and members of a social network.
タグ:
FAERS
2016/3/10
An Integrative Data Science Pipeline to Identify Novel Drug Interactions that Prolong the QT Interval.
タグ:
FAERS
2016/2/11
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