(PDF) Clustering Therapeutic Drugs Using FDA Adverse Event

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Proceedings for Annual Meeting of The Japanese Pharmacological Society

doi 10.1254/jpssuppl.93.0_3-p-388

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January 1, 2020

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Japanese Pharmacological Society

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Amanote Research

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Proceedings for Annual Meeting of The Japanese Pharmacological Society

doi 10.1254/jpssuppl.93.0_3-p-388

Full Text

Abstract

Date

Authors

Publisher

Related search

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Exploring the FDA Adverse Event Reporting System to Generate Hypotheses for Monitoring of Disease Characteristics

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Serious Adverse Drug Events Reported to the Food and Drug Administration (FDA): Analysis of the FDA Adverse Event Reporting System (FAERS) 2006-2011 Database

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