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INDI: a computational framework for inferring drug interactions and their associated recommendations.
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FAERS
2012/7/19
Omeprazole- and esomeprazole-associated hypomagnesaemia: data mining of the public version of the FDA Adverse Event Reporting System.
タグ:
FAERS
2012/6/30
Proarrhythmic potential of dronedarone: emerging evidence from spontaneous adverse event reporting.
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FAERS
2012/6/30
Adverse event reports after tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccines in pregnant women.
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VAERS
2012/6/26
Analysis of data from the CDC/FDA vaccine adverse event reporting system (1990-2009) on Guillain-Barre syndrome after hepatitis vaccination in the USA.
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VAERS
2012/6/19
A review on the association between glucagon-like peptide-1 receptor agonists and thyroid cancer.
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FAERS
2012/6/14
Assessing the association between omalizumab and arteriothrombotic events through spontaneous adverse event reporting.
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FAERS
2012/6/13
Adverse event profile of tigecycline: data mining of the public version of the U.S. Food and Drug Administration adverse event reporting system.
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FAERS
2012/6/13
A pre-marketing ALT signal predicts post-marketing liver safety.
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FAERS
2012/6/7
Novel adverse events of bevacizumab in the US FDA adverse event reporting system database: a disproportionality analysis.
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FAERS
2012/5/23
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