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Feasibility of matching vaccine adverse event reporting system and poison center records.
タグ:
VAERS
2013/09/05
Adverse events after Fluzone (R) Intradermal vaccine reported to the Vaccine Adverse Event Reporting System (VAERS), 2011-2013.
タグ:
VAERS
FAERS
2013/9/3
Adverse drug and device reactions in the oral cavity: surveillance and reporting.
タグ:
FAERS
2013/8/31
Triptans and serious adverse vascular events: data mining of the FDA Adverse Event Reporting System database.
タグ:
FAERS
2013/08/08
Standardizing drug adverse event reporting data.
タグ:
FAERS
2013/08/08
Building a knowledge base of severe adverse drug events based on AERS reporting data using semantic web technologies.
タグ:
FAERS
2013/08/08
Physicians’ knowledge and attitude towards adverse event reporting system and result to intervention–randomized nested trial among Bulgarian physicians.
タグ:
FAERS
2013/7/31
Dabigatran-dronedarone interaction in a spontaneous reporting system.
タグ:
FAERS
2013/7/31
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
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