Last update Nov. 8, 2023
Likely Compatibility
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.
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Tirzepatide in other languages or writings:
Tirzepatide belongs to this group or family:
Main tradenames from several countries containing Tirzepatide in its composition:
Variable | Value | Unit |
---|---|---|
Oral Bioavail. | ≈ 0 | % |
Molecular weight | 4.814 | daltons |
Protein Binding | 99 | % |
VD | 0.14 | l/Kg |
Tmax | 8 - 72 | hours |
T½ | 120 | hours |
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e-lactancia is a resource recommended by Academy of Breastfeeding Medicine - 2015 of United States of America
Would you like to recommend the use of e-lactancia? Write to us at corporate mail of APILAM
Tirzepatide is a long-acting glucose-dependent insulinotropic polypeptide (GIP) receptor agonist and a glucagon-like peptide 1 (GLP-1) receptor agonist. It increases insulin sensitivity and secretion, suppresses glucagon secretion, and slows gastric emptying. It is used in the treatment of type 2 diabetes mellitus as an adjunct to diet and exercise. It is also used in the treatment of obesity. Weekly subcutaneous administration.
At the time of the last update, we found no published data on its excretion in breast milk.
Its very high molecular weight and high binding to plasma proteins make it very unlikely to pass into breast milk.
Due to its protein nature, it is inactivated in the gastrointestinal tract and is not absorbed (oral bioavailability is practically nil), which makes it difficult or impossible for it to pass into the infant's plasma from ingested breast milk, except in premature infants and in the immediate neonatal period, where there may be greater intestinal permeability.