Last update Oct. 17, 2024
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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Alogliptin .Alogliptin Benzoate in other languages or writings:
Alogliptin .Alogliptin Benzoate belongs to these groups or families:
Main tradenames from several countries containing Alogliptin .Alogliptin Benzoate in its composition:
Variable | Value | Unit |
---|---|---|
Oral Bioavail. | 70 - 100 | % |
Molecular weight | 462 | daltons |
Protein Binding | 20 - 30 | % |
VD | 4.3 - 6 | l/Kg |
Tmax | 1 - 2 | hours |
T½ | 21 | hours |
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e-lactancia is a resource recommended by Academy of Breastfeeding Medicine - 2015 of United States of America
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It promotes pancreatic insulin secretion by inhibiting the DPP-4 enzyme that degrades the GLP-1 and GIP intestinal hormones involved in the physiological regulation of glucose, which are activated by eating (EMA 2016, Baetta 2011, Scheen 2011). Administered orally, once a day.
Since the last update we have not found published data on its excretion in breast milk.
Its pharmacokinetic data (EMA 2015, Scheen 2011): low molecular weight, low protein binding, very long half-life, make passage into milk likely in quantity that could be significant, but its high volume of distribution would make this difficult
Infant's blood glucose should be monitored during maternal treatment with alogliptin. (Berlin 2005)
Until there is more published data on this drug in relation to breastfeeding, safer known alternatives may be preferable, especially during the neonatal period and in case of prematurity.
Diet, exercise, and breastfeeding improve blood sugar levels.
Common side effects are upper respiratory tract infections, urinary tract infections, gastrointestinal disorders, rash and headaches(EMA, 2015, Scheen 2011) . Low risk of hypoglycemia in monotherapy (EMA, 2015, Scheen 2011). Doses up to 16 times higher than normal for 2 weeks did not produce side effects. (EMA, 2015)
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