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Epoetin alfa

Colony-Stimulating Factor · Anemia treatment

Also known as EPREX

Colony-Stimulating FactorAnemia treatment
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
none in our sources
PREGNANCY
not curated

Mechanism

Erythropoietin (EPO) is a sialoglycoprotein hormone produced by peritubular cells of the kidney that is essential for normal erythropoiesis. Anemia and hypoxia induce rapid secretion of EPO, which acts on erythroid marrow to stimulate proliferation of colony-forming cells, induce hemoglobin formation, erythroblast maturation, and release reticulocytes. EPO binds to specific JAK-STAT-binding receptors on target cells, altering phosphorylation of intracellular proteins and activating transcription factors to regulate gene expression, thereby inducing erythropoiesis in a dose-dependent manner.

Indications

Symptomatic anaemia associated with chronic renal failure in patients on haemodialysisSymptomatic anaemia associated with chronic renal failure in adults on peritoneal dialysisSymptomatic anaemia associated with chronic renal failure in adults not on dialysisAnaemia in AIDS patients treated with zidovudineCancer chemotherapy induced anaemiaTo increase yield of autologous blood (to avoid homologous blood) in predonation programme in moderate anaemia either when large volume of blood required or when sufficient blood cannot be saved for elective major surgeryanemia due to chronic kidney diseaseanemia associated with surgeryanemia associated with AIDSanemia associated with cancer chemotherapyanemia of prematurityanemia associated with certain chronic inflammatory conditions

Dosing

Adult
Symptomatic anaemia associated with chronic renal failure (haemodialysis, peritoneal dialysis, or not on dialysis): Initially 50 units/kg 3 times a week by intravenous or subcutaneous injection. Adjust in steps of 25 units/kg 3 times a week, according to response at intervals of at least 4 weeks. Maintenance: 75–300 units/kg once weekly.…
Pediatric
Children less than 5 years of age generally require a higher dose in CKD. For anemia of prematurity, dosing is not explicitly provided but discussed as having limited efficacy.
Renal adjustment
For symptomatic anaemia associated with chronic renal failure: Reduce dose by approximately 25% if rise in haemoglobin concentration exceeds 2 g/100 mL over 4 weeks or if haemoglobin concentration exceeds 12 g/100 mL.…

Pharmacokinetics

Half-life
4 to 8 h (intravenous)

Contraindications

  • Not recommended when hemoglobin level exceeds 11 g/dL in patients with chronic kidney disease
  • Not to be used when cancer therapy is being given with curative intent
  • pre-existing uncontrolled hypertension

Side effects

Common
HypertensionThrombotic complicationsIncreased clot formation in A-V shunts (in dialysis patients)Hypertensive episodesSeizures (occasionally)Flu-like symptoms (lasting 2–4 hours)aggravation of hypertension (20-30% of patients)headachetachycardiaedemashortness of breathnauseavomitingdiarrheainjection site stingingflu-like symptoms (arthralgias, myalgias)
Serious
  • Serious cardiovascular events
  • Thromboembolic events
  • Stroke
  • Mortality (when hemoglobin levels exceed 11 g/dL)
  • Pure red cell aplasia (PRCA) accompanied by neutralizing antibodies to erythropoietin (especially with Eprex with polysorbate 80 stabilizer given subcutaneously for long periods)
  • Increased rate of all-cause mortality and venous thrombosis (in cancer patients)
  • thrombotic events
  • cancer recurrence (in cancer patients)
  • decreased on-study survival (in cancer patients)
  • hypertensive encephalopathy
  • seizures
  • death (if administered to target hemoglobin concentrations near normal physiological levels)

Drug interactions

Anticoagulants
Moderate
Textbook

During hemodialysis, patients receiving epoetin alfa may require increased anticoagulation.

Patients during hemodialysis may require increased anticoagulation. Monitoring for thrombotic events is recommended.

Source: G&G 14e · p902

Nandrolone Decanoate
Moderate
Database

Increased risk of polycythemia, hyperviscosity, and associated thrombotic events.

Monitor hemoglobin and hematocrit closely. Adjust dose of epoetin alfa as needed to maintain target hemoglobin levels. Ensure adequate hydration.

Related guidelines

Other Colony-Stimulating Factor drugs

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Sources: Goodman & Gilman 14e, Katzung, BNF, Harriet Lane·Verified: 2026-05-13 · House clinical team