The new FDA label for erythropoietin treatment: how does it affect hemoglobin target?

Abstract:

:The erythropoietin analogs have been an important advance for the treatment of the anemia of kidney disease, resulting in reduced need for blood transfusion and improved quality of life. Recent studies, however, have indicated risks associated with targeting higher levels of hemoglobin (Hb). As a result, in March 2007, the US Food and Drug Administration (FDA) substantially changed prescribing information for these drugs to alert clinicians to these risks. In this review, we consider the recent literature, the change in FDA warnings, and new National Kidney Foundation Anemia Guidelines. Suggestions for new Hb targets during erythropoiesis-stimulating agent treatment are presented.

journal_name

Kidney Int

journal_title

Kidney international

authors

Fishbane S,Nissenson AR

doi

10.1038/sj.ki.5002401

subject

Has Abstract

pub_date

2007-10-01 00:00:00

pages

806-13

issue

7

eissn

0085-2538

issn

1523-1755

pii

S0085-2538(15)52739-7

journal_volume

72

pub_type

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