The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Perspective
PreviousPrevious
Volume 356:2448-2451 June 14, 2007 Number 24
NextNext

Erythropoietin, the FDA, and Oncology
Robert Steinbrook, M.D.

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

 Sign up for free e-toc
 

This Article
-Full Text
- PDF
-PDA Full Text
-Purchase this article

Commentary
-Perspective
 by Khuri, F. R.

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited
-E-mail When Letters Appear

More Information
-PubMed Citation
As has been the case for patients with chronic renal failure, treatment with erythropoiesis-stimulating agents (ESAs) has substantially raised the hemoglobin concentrations of hundreds of thousands of patients with cancer, diminishing their need for red-cell transfusions during chemotherapy. At the same time, use of these agents has raised safety concerns because they can cause thromboembolic events and increase "the risk for death and for serious cardiovascular events when administered to target a hemoglobin of greater than 12 g/dL," according to the black-box warning that the Food and Drug Administration (FDA) added to the prescribing information in March 2007.1 Therefore, the . . . [Full Text of this Article]


Source Information

Dr. Steinbrook (rsteinbrook@attglobal.net) is a national correspondent for the Journal.


This article has been cited by other articles:



HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.