(PDF) A Computerized System for Reporting and Analysis of

A Computerized System for Reporting and Analysis of Incidents, Errors or Adverse Events: Results of 2014

Clinical Therapeutics - United States

doi 10.1016/j.clinthera.2015.05.391

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August 1, 2015

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Elsevier BV

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A Computerized System for Reporting and Analysis of Incidents, Errors or Adverse Events: Results of 2014

Clinical Therapeutics - United States

doi 10.1016/j.clinthera.2015.05.391

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

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

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

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

Association Between Myocarditis and Other Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitor Use: Analysis of the FDA Adverse Events Reporting System (FAERS)

Preventing Medication Errors and Adverse Drug Events

Computerized Surveillance of Adverse Drug Events in Hospital Patients

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