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Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006-.
CASRN: 1513857-77-6
Drug Levels and Effects
Summary of Use during Lactation
No information is available on the clinical use of pemigatinib during breastfeeding. The manufacturer recommends that breastfeeding be discontinued during pemigatinib therapy and for 1 week after the last dose.
Drug Levels
Maternal Levels. Relevant published information was not found as of the revision date.
Infant Levels. Relevant published information was not found as of the revision date.
Effects in Breastfed Infants
Relevant published information was not found as of the revision date.
Effects on Lactation and Breastmilk
Relevant published information was not found as of the revision date.
Substance Identification
Substance Name
Pemigatinib
CAS Registry Number
1513857-77-6
Drug Class
Breast Feeding
Milk, Human
Antineoplastic Agents
Enzyme Inhibitors
Protein Kinase Inhibitors
Signal Transduction Inhibitors
Disclaimer: Information presented in this database is not meant as a substitute for professional judgment. You should consult your healthcare provider for breastfeeding advice related to your particular situation. The U.S. government does not warrant or assume any liability or responsibility for the accuracy or completeness of the information on this Site.
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- [Pharmacological characteristics and clinical study results of Pemigatinib (Pemazyre(®) Tablets), a selective fibroblast growth factor receptor (FGFR) inhibitor].[Nihon Yakurigaku Zasshi. 2021][Pharmacological characteristics and clinical study results of Pemigatinib (Pemazyre(®) Tablets), a selective fibroblast growth factor receptor (FGFR) inhibitor].Kabu K, Takei S, Kondo M, Kitazawa K, Harada T. Nihon Yakurigaku Zasshi. 2021; 156(6):392-402.
- INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models.[PLoS One. 2020]INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models.Liu PCC, Koblish H, Wu L, Bowman K, Diamond S, DiMatteo D, Zhang Y, Hansbury M, Rupar M, Wen X, et al. PLoS One. 2020; 15(4):e0231877. Epub 2020 Apr 21.
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