Serveur d'exploration sur les relations entre la France et l'Australie

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Epoetin‐associated pure red cell aplasia: past, present, and future considerations

Identifieur interne : 008830 ( Main/Exploration ); précédent : 008829; suivant : 008831

Epoetin‐associated pure red cell aplasia: past, present, and future considerations

Auteurs : June M. Mckoy [France] ; Robin E. Stonecash [France] ; Denis Cournoyer [France] ; Jerome Rossert [France] ; Allen R. Nissenson [France] ; Dennis W. Raisch [France] ; Nicole Casadevall [France] ; Charles L. Bennett [France]

Source :

RBID : ISTEX:62C8628A4EF21823C8B13711A62B018C7EA8D332

Descripteurs français

English descriptors

Abstract

BACKGROUND: Since 1988, millions of patients have received epoetin products intravenously (IV) and subcutaneously. In 1998, epoetin‐associated pure red cell aplasia (PRCA) was first reported and causation was attributed to formulations without human serum albumin (HSA), subcutaneous administration, and uncoated rubber stoppers.

Url:
DOI: 10.1111/j.1537-2995.2008.01749.x


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title level="j" type="main">Transfusion</title>
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<term>Academic investigators</term>
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<term>Amgen</term>
<term>Antierythropoietin</term>
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<term>Aplasia</term>
<term>Assay</term>
<term>August</term>
<term>Beta</term>
<term>Canadian prca focus group</term>
<term>Casadevall</term>
<term>Cell aplasia</term>
<term>Chronic kidney disease</term>
<term>Chronic kidney disease patients</term>
<term>Class effect</term>
<term>Darbepoetin</term>
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<term>Epoetin</term>
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<term>Epoetin beta</term>
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<term>Immunosuppressive therapy</term>
<term>Incidence rates</term>
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<term>Ndings</term>
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<term>Nephrol dial transplant</term>
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<term>Neutralizing antibodies</term>
<term>Other countries</term>
<term>Polysorbate</term>
<term>Prca</term>
<term>Prca cases</term>
<term>Prca patients</term>
<term>Pure aplasia</term>
<term>Pure red cell aplasia</term>
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<term>Rare instances</term>
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<term>Regulatory approval</term>
<term>Regulatory authorities</term>
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<term>Stopper</term>
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<term>Uncoated</term>
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<term>Epoétine</term>
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<term>Transfusion</term>
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<term>Neutralizing antibodies</term>
<term>Other countries</term>
<term>Polysorbate</term>
<term>Prca</term>
<term>Prca cases</term>
<term>Prca patients</term>
<term>Pure aplasia</term>
<term>Radar group</term>
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<front>
<div type="abstract">BACKGROUND: Since 1988, millions of patients have received epoetin products intravenously (IV) and subcutaneously. In 1998, epoetin‐associated pure red cell aplasia (PRCA) was first reported and causation was attributed to formulations without human serum albumin (HSA), subcutaneous administration, and uncoated rubber stoppers.</div>
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