Epoetin alfa (Procrit)

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General information

Class/mechanism: Erythropoiesis-stimulating agent (ESA), stimulates division and differentiation of erythroid precursors.[1][2][3][4]
Route: SC, IV
Extravasation: no information

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Patient drug information

History of changes in FDA indication

  • 6/1/1989: Initial FDA approval

Also known as

Ceriton Dynepo Epoch Epoetin Epoetin Alfa Epoetin Beta Epoetin Delta Epoetin Zeta
Epofer Epogen Epogin Epoimmun Epomax Epopen Epox Epoyet
Eprex Eritrelan Erypo Erypo FS Erythropoetin Erythropoietin Erythropoietin Human Erythrostim
Espo Espo Kirin Espo Sankyo Globuren Hemapo Hemax KE Long YI BAO LG Espogen
Procrit Recormon Recormon N Recormon NEU Recormon PS Recormon S Recormon SE Vepox
Vintor Wepox


  1. 1.0 1.1 1.2 Epoetin alfa (Procrit) package insert
  2. Epoetin alfa (Procrit) package insert (locally hosted backup)
  3. Procrit manufacturer's website
  4. As of 4/14/2017, use of this medication in patients with oncologic diagnoses no longer requires enrollment in the ESA APPRISE Risk Evaluation and Mitigation Strategy (REMS) Program
  5. Epoetin alfa (Procrit) patient instructions for use
  6. Epoetin alfa (Procrit) patient instructions for use (locally hosted backup)
  7. Epoetin alfa (Procrit) patient drug information (Chemocare)
  8. Epoetin alfa (Procrit) patient drug information (UpToDate)