Last update Sept. 23, 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.
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.
C6468H10016N1728O2012S47 is Lanadelumab in Molecular formula.
Is written in other languages:C6468H10016N1728O2012S47 belongs to these groups or families:
Main tradenames from several countries containing C6468H10016N1728O2012S47 in its composition:
Variable | Value | Unit |
---|---|---|
Oral Bioavail. | 0 | % |
Molecular weight | 146.000 | daltons |
VD | 0.17 - 0.23 | l/Kg |
Tmax | 168 | hours |
T½ | 331 -360 | hours |
Write us at elactancia.org@gmail.com
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
Lanadelumab is a human monoclonal antibody that inhibits plasma kallikrein, limiting the production of bradykinin, a potent vasodilator. It is used to treat and prevent attacks of hereditary angioedema. It is administered by subcutaneous injection every 2 weeks.
As of the last update, we found no published data on its excretion in breast milk.
Its very high molecular weight makes it unlikely to be excreted in breast milk.
Due to its protein nature, it is inactivated in the gastrointestinal tract and is not absorbed (oral bioavailability practically nil), which makes it difficult or impossible for it to pass into infant plasma from ingested breast milk, except in premature infants and in the immediate neonatal period, in which there may be greater intestinal permeability.
Pending further published data on this drug in relation to lactation, safer known alternatives may be preferable, especially during the neonatal period and in case of prematurity. (Yeich 2023, Bouillet 2015)