Improving the Reporting of Adverse Drug Reactions in the Hospital Setting

Log in or subscribe to view full content.
Article is also available for purchase the article in one of the available formats.
Richard Pushkin, MD; Lynda Frassetto, MD; Candy Tsourounis, PharmD; Eleanor S. Segal, MD; and Stephanie Kim, MBA

Table of Contents

Postgraduate Medicine:

Volume 122 No. 6

Category:

Clinical Features

Purchase this article in one of the formats specified below:

DOI: 10.3810/pgm.2010.11.2233
Abstract: The US Food and Drug Administration (FDA) is perceived by the public as having a substantial responsibility to ensure drug safety; however, the FDA has limited resources for active surveillance and relies on voluntary reporting of adverse events and potential adverse drug reactions. Studies have shown that underreporting of adverse events and adverse drug reactions is widespread. Furthermore, a review of several studies demonstrates that most adverse drug reactions are reported by pharmacists and nurses, with physicians reporting the fewest. The hospital setting, with its clearly defined patient population observed around the clock, is an ideal setting in which to identify potential adverse drug reaction signals and to report them to either the drug manufacturer or the FDA. In this article we describe the present system for addressing adverse events, obstacles to reporting them, and the important role any hospital physician could play in reporting adverse events and potential adverse drug reactions.

Keywords: adverse drug reactions , adverse events , drug safety , hospital setting , pharmacovigilance