Semaglutide Levels and Effects while Breastfeeding
Summary of Use during Lactation
Semaglutide was not detectable in the milk of mothers taking the drug subcutaneously. Their breastfed infants experienced no adverse effects. Some brands of oral semaglutide, such as Rybelsus, contain the absorption enhancer salcaprozate sodium, which may enter milk and accumulate in infants. Only injectable forms of semaglutide should be used during breastfeeding.
Drug Levels
Maternal Levels. Eight nursing mothers who were using subcutaneous semaglutide in doses ranging from 0.25 to 1 mg weekly donated milk samples at 0,12 and 24 hours after a dose. None of the samples contained any measurable semaglutide (<1.7 mcg/L). The authors calculated that if milk had contained semaglutide at the detection limit, the relative infant dose would have averaged only 1.12%.[1] This does not take into consideration that the drug is poorly absorbed orally, with a maximum bioavailability of 1% in adults.
Infant Levels. Relevant published information was not found as of the revision date.
Effects in Breastfed Infants
Eight nursing mothers were using subcutaneous semaglutide in doses ranging from 0.25 to 1 mg weekly. Their infants ranged in age from 4 to 23 months of age and were mixed fed. They were fed breastmilk for 3 to 9 weeks while their mothers were taking semaglutide. All of the infants were reported to have normal growth and development by their mothers.[1]
Effects on Lactation and Breastmilk
Relevant published information was not found as of the revision date.
Diab H, Fuquay T, Datta P, et al. Subcutaneous semaglutide during breastfeeding: Infant safety regarding drug transfer into human milk. Nutrients 2024;16:2886. [PMC free article: PMC11397063] [PubMed: 39275201]
Substance Identification
Substance Name
Semaglutide
CAS Registry Number
910463-68-2
Drug Class
Breast Feeding
Lactation
Milk, Human
Hypoglycemic Agents
Incretins
Glucagon-Like Peptide-1 Agonists
GLP-1 Agonists
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