Adverse Event Profiles of Platinum Agents: Data Mining of the Public Version of the FDA Adverse Event Reporting System, AERS, and Reproducibility of Clinical Observations

<p><b>Objective:</b> Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were reviewed to confirm platinum agent-associated adverse events, and to clarify the rank-order of these drugs in terms of susceptibility.</p><p><b>Methods:&l...

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Bibliographic Details
Main Author: Toshiyuki Sakaeda, Kaori Kadoyama, Yasushi Okuno
Format: Article
Language:English
Published: Ivyspring International Publisher 2011-01-01
Series:International Journal of Medical Sciences
Online Access:http://www.medsci.org/v08p0487.htm