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epoetin alfa (Eprex®)

 

Following non-submission

AWMSG advice

Status: Not endorsed (Statement of Advice)

In the absence of a submission from the holder of the marketing authorisation, epoetin alfa (Eprex®) cannot be endorsed for use within NHS Wales for the treatment of symptomatic anaemia (haemoglobin concentration of ≤ 10 g/dL) in adults with low- or intermediate-1-risk primary myelodysplastic syndromes (MDS) who have low serum erythropoietin (< 200 mU/mL).

 Statement of Advice (SOA): epoetinalfa (Eprex) 3138 (PDF, 113Kb)

Medicine details

Medicine name epoetin alfa (Eprex®)
Formulation 2000 IU/ml, 4000 IU/ml, 10000 IU/ml and 40000 IU/ml solution for injection
Reference number 3138
Indication

Treatment of symptomatic anaemia (haemoglobin concentration of ≤ 10 g/dL) in adults with low- or intermediate-1-risk primary myelodysplastic syndromes (MDS) who have low serum erythropoietin (< 200 mU/mL).

Company Janssen-Cilag Ltd
BNF chapter Nutrition & blood
Submission type Non-submission
Status Not endorsed (Statement of Advice)
Date of issue 13/07/2017
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