(PDF) Spontaneous Reporting on Adverse Events by Consumers

Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

Drugs - Real World Outcomes - Switzerland

doi 10.1007/s40801-018-0134-0

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Abstract

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Date

May 3, 2018

Authors

Tadashi Toki

Shunsuke Ono

Publisher

Springer Science and Business Media LLC

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Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

Drugs - Real World Outcomes - Switzerland

doi 10.1007/s40801-018-0134-0

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

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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Adverse Events Associated With Colchicine Drug Interactions: Analysis of the Public Version of the Fda Adverse Event Reporting System

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Spontaneous Reporting of Adverse Drug Reactions

Adverse Events Associated With Pediatric Use of Proton Pump Inhibitors: Analysis of the Fda Adverse Event Reporting System

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