Development of an automated assessment tool for MedWatch reports in the FDA adverse event reporting system.

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ADEPt, a semantically-enriched pipeline for extracting adverse drug events from free-text electronic health records.

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Development of an automated assessment tool for MedWatch reports in the FDA adverse event reporting system.

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2017 nî lūn-bûn

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Development of an automated as ...... dverse event reporting system.

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Development of an automated as ...... dverse event reporting system.

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Development of an automated as ...... dverse event reporting system.

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Development of an automated as ...... dverse event reporting system.

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Development of an automated as ...... dverse event reporting system.

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Development of an automated as ...... dverse event reporting system.

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Carol A Pamer

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Lichy Han

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Robert Ball

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Scott Proestel

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P2860

Standardizing adverse drug event reporting data

The Unified Medical Language System (UMLS): integrating biomedical terminology.

Data mining of the public version of the FDA Adverse Event Reporting System

Perspectives on the use of data mining in pharmaco-vigilance.

Drug-versus-drug adverse event rate comparisons: a pilot study based on data from the US FDA Adverse Event Reporting System.

Drug-induced torsades de pointes: data mining of the public version of the FDA Adverse Event Reporting System (AERS).

The medical dictionary for regulatory activities (MedDRA).

Mining multi-item drug adverse effect associations in spontaneous reporting systems

The contribution of the vaccine adverse event text mining system to the classification of possible Guillain-Barré syndrome reports.

Large-scale combining signals from both biomedical literature and the FDA Adverse Event Reporting System (FAERS) to improve post-marketing drug safety signal detection.

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913-920

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scholarly article

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10.1093/JAMIA/OCX022

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Russ Altman

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2017-03-21T00:00:00Z

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28371826

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automation

Development of an automated assessment tool for MedWatch reports in the FDA adverse event reporting system.

about

P2860

P2860

Development of an automated assessment tool for MedWatch reports in the FDA adverse event reporting system.

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