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Corrects erythropoietic abnormalities caused by a deficiency of iron.

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The finding that the levels were highest in our patients with late responses or none could merely be a phenomenon of chance, but preliminary data on patients with other chronic diseases seem to corroborate our findings.

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Peginterferon-alpha2a and ribavirin combination therapy in chronic hepatitis C: a randomized study of treatment duration and ribavirin dose.

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Increases in blood pressure have been reported in clinical trials, often during the first 90 days of therapy.

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Bone marrow changes following treatment of renal anemia with erythropoietin.

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The number of BFU-E in the bone marrow was very low before erythropoietin treatment (median, 0; range, 0 to 7).

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Specific risk factors for thromboembolism have not been defined in these trials; therefore, clinicians should use caution and clinical judgment when considering use of these agents.

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To date, the EMA has approved 14 biosimilars within the product classes of human growth hormone, granulocyte stimulating factor and erythropoietin, for use in the EU, see Table below.

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Another type could prove to be the result of suppression or impairment of the bone marrow response to stimulation by erythropoietin; substitution treatment could not be expected to benefit patients with this type of anemia.

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In a randomized, double-blind, placebo-controlled study of 4038 patients, there was an increased risk of stroke when darbepoetin alfa was administered to patients with anemia, type 2 diabetes, and CRF who were not on dialysis.

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Three trials compared different weight-based doses of epoetin, and three compared different weight-based doses of darbepoetin; five compared different fixed doses of epoetin; one trial each compared weight-based versus fixed doses for epoetin and darbepoetin, respectively; two compared more versus less frequent dosing of epoetin; two compared front-loaded versus reduced or constant dosing of darbepoetin; and one compared titrated versus constant-dose regimens of epoetin.

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