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Neuropsychiatric adverse effects of oseltamivir in the FDA Adverse Event Reporting System, 1999-2012.
タグ:
FAERS
2013/7/25
Use of case reports and the Adverse Event Reporting System in systematic reviews: overcoming barriers to assess the link between Crohn’s disease medications and hepatosplenic T-cell lymphoma.
タグ:
FAERS
2013/7/6
Toxicity assessments of nonsteroidal anti-inflammatory drugs in isolated mitochondria, rat hepatocytes, and zebrafish show good concordance across chemical classes.
タグ:
FAERS
2013/7/3
Neurological events with tumour necrosis factor alpha inhibitors reported to the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2013/06/28
Pneumothorax as an adverse drug event: an exploratory aggregate analysis of the US FDA AERS database including a confounding by indication analysis inspired by Cornfield’s condition.
タグ:
FAERS
2013/6/27
Provider experiences with negative-pressure wound therapy systems.
タグ:
FAERS
2013/06/20
Traceability of biopharmaceuticals in spontaneous reporting systems: a cross-sectional study in the FDA Adverse Event Reporting System (FAERS) and EudraVigilance databases.
タグ:
EudraVigilance
FAERS
2013/6/19
Ramipril-induced liver injury: case report and review of the literature.
タグ:
FAERS
2013/06/12
The metoclopramide black box warning for tardive dyskinesia: effect on clinical practice, adverse event reporting, and prescription drug lawsuits.
タグ:
FAERS
2013/6/6
Application of information retrieval approaches to case classification in the vaccine adverse event reporting system.
タグ:
VAERS
2013/5/25
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