Last update March 6, 2025

Молграмостим

Likely Compatibility

Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.

Granulocyte and macrophage colony stimulating factor (GM-CSF) obtained by recombinant technology. Practically identical to the natural product found in breast milk. Indicated in neutropenia secondary to antineoplastic therapy and in bone marrow autotransplantation.

At the date of last update we found no published data on its excretion in breast milk.

Its high molecular weight makes it unlikely to be excreted in milk in significant quantities.

Its low oral bioavailability makes it difficult for it to pass into infant plasma from ingested breast milk since, due to its protein nature, it is degraded in the gastrointestinal tract and is not absorbed. (Calhoun 2003)

Other substances similar in composition and action such as Filgrastim and Lenograstim are excreted in milk in negligible amounts and have been used to treat sepsis and necrotizing enterocolitis in newborns and premature infants. (Canpolat 2006, Carr 2003, Bedford 2001, Gillan 1994)

It is a drug with very few bibliographic references and marketed in few countries.

Until more data on this drug in relation to breastfeeding are known, safer alternatives may be preferable, especially during the neonatal period and in case of prematurity.


See below the information of these related products:

  • Bone Marrow Donation (Safe product and/or breastfeeding is the best option.)
  • Maternal Cancer; Maternal Neoplasia (Unsafe. Moderate/severe adverse effects. Compatible under certain circumstances. Follow-up recommended. Use safer alternative or discontinue breastfeeding from 5 to 7 T ½ . Read Commentary.)

Alternatives

  • Filgrastim (Safe product and/or breastfeeding is the best option.)
  • Lenograstim (Safe product and/or breastfeeding is the best option.)

Suggestions made at e-lactancia are done by APILAM team of health professionals, and are based on updated scientific publications. It is not intended to replace the relationship you have with your doctor but to compound it. The pharmaceutical industry contraindicates breastfeeding, mistakenly and without scientific reasons, in most of the drug data sheets.

Jose Maria Paricio, Founder & President of APILAM/e-Lactancia

Your contribution is essential for this service to continue to exist. We need the generosity of people like you who believe in the benefits of breastfeeding.

Thank you for helping to protect and promote breastfeeding.

José María Paricio, founder of e-lactancia.

Other names

Молграмостим is Molgramostim in Cyrillic.

Is written in other languages:

Group

Молграмостим belongs to this group or family:

Tradenames

Main tradenames from several countries containing Молграмостим in its composition:

Pharmacokinetics

Variable Value Unit
Molecular weight 14.478 daltons
Tmax 3 - 46 hours
1 - 3 hours

References

  1. Canpolat FE, Yurdakök M, Korkmaz A, Yiğit S, Tekinalp G. Enteral granulocyte colony-stimulating factor for the treatment of mild (stage I) necrotizing enterocolitis: a placebo-controlled pilot study. J Pediatr Surg. 2006 Abstract
  2. Carr R, Modi N, Doré C. G-CSF and GM-CSF for treating or preventing neonatal infections. Cochrane Database Syst Rev. 2003 Abstract
  3. Calhoun DA, Maheshwari A, Christensen RD. Recombinant granulocyte colony-stimulating factor administered enterally to neonates is not absorbed. Pediatrics. 2003 Abstract
  4. Bedford Russell AR, Emmerson AJ, Wilkinson N, Chant T, Sweet DG, Halliday HL, Holland B, Davies EG. A trial of recombinant human granulocyte colony stimulating factor for the treatment of very low birthweight infants with presumed sepsis and neutropenia. Arch Dis Child Fetal Neonatal Ed. 2001 Abstract Full text (link to original source) Full text (in our servers)
  5. EMA. Molgramostin. Ficha técnica. 2000 Full text (in our servers)
  6. EMA. Molgramostin. Drug Summary 2000 Full text (in our servers)
  7. Gillan ER, Christensen RD, Suen Y, Ellis R, van de Ven C, Cairo MS. A randomized, placebo-controlled trial of recombinant human granulocyte colony-stimulating factor administration in newborn infants with presumed sepsis: significant induction of peripheral and bone marrow neutrophilia. Blood. 1994 Abstract Full text (link to original source) Full text (in our servers)

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