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I have been suffering from anemia for more than 6 years now. I have bloodclots that went into my eyes, because of them I lost most of the sight in my right eye. Our family doctor said that my eyesight might never come back but I decided not to give up. I have my laser treatment every 2 weeks. He prescribed me with Epogen and the drug has greatly improved my condition. My eyesight is better and I'm not in panic anymore. In addition my general symptoms have gone milder; I don't get tired that easily and don't look too pale. Epogen is great for me.
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I have been on Epogen for years and it has helped me a lot with my anemia. Now the doctors have stared me on another drug and i feel terrible. I am going to ask for another prescription of Epogen as it is the only medication that allows me to feel ok and live normal life.

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Procrit (epoetin alfa) is prescribed by doctors every year to help patients who suffer from anemia as part of their CKD.

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Oral adsorbent AST-120 potentiates the effect of erythropoietin-stimulating agents on Stage 5 chronic kidney disease patients: a randomized crossover study.

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If the patient shows no response within an initial trial period of 6-8 weeks, treatment should be considered a failure and discontinued (rule out and treat deficient iron stores).

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Interaction between Epoetin Alfa and Eprex: There is no known interaction between Epoetin Alfa and Eprex in our records.

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Potential beneficial interactions between HAART and HCV include a slowing of HCV-related liver disease in patients on HAART.

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If you have bad anemia resulting from your chemotherapy and radiation cancer treatments, but your physician doesn't believe that taking iron would help you, he may prescribe a medication called epoetin alfa instead.

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Therapeutic administration of erythropoietin seems to affect a complex, dynamic system that apparently is highly susceptible to disturbances in its balance.

The systematic review performed by CCO identified 13 trials of epoetin (12 unique trials) and two trials of darbepoetin ( to provide details of the review).

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This observation provided the basis for a warning on the label for darbepoetin alfa (and eventually a stronger warning on the label for epoetin alfa) regarding excessive rates of increase in hemoglobin concentrations.

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The recommendation is based on a randomized, double-blind, placebo-controlled trial of ESA therapy in patients with low-risk MDS, which was reviewed in the 2002 guideline; and on a second randomized open-label phase III clinical trial of EPO and G-CSF versus best supportive care reported in 2004.

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