Last update May 31, 2024
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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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フマル酸 ; フマル酸ジメチル is Dimethyl Fumarate in Japanese.
Is written in other languages:フマル酸 ; フマル酸ジメチル is also known as
フマル酸 ; フマル酸ジメチル belongs to these groups or families:
Main tradenames from several countries containing フマル酸 ; フマル酸ジメチル in its composition:
Variable | Value | Unit |
---|---|---|
Molecular weight | 144 | daltons |
Protein Binding | 27 - 40 | % |
VD | 0.7 - 1.2 | l/Kg |
Tmax | 2 - 3 | hours |
T½ | 0.75 - 1 | hours |
Theoretical Dose | 0.0004 - 0.001 | mg/Kg/d |
Relative Dose | 0.005 - 0.01 | % |
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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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Anti-inflammatory and immunomodulatory used in the treatment of psoriasis and in relapsing forms of multiple sclerosis. Topical and oral administration every 12 hours.
Its pharmacokinetic data, wide volume of distribution and short half-life, explain (Almas 2016) the negligible passage to breast milk observed. (Ciplea 2020)
Dimethyl fumarate is not found in plasma as it is immediately converted to monomethyl fumarate, an active drug with a half-life of about 1 hour. (Almas 2016)
Possible side effects are rare and generally not serious (gastrointestinal and leukopenia), without presenting immunosuppressive effects or a higher frequency of infections.(AEMPS 2015, EMA 2017)
Various medical societies and/or expert consensus consider the use of this medication during breastfeeding possibly safe (Hale, Alroughani 2016, Briggs 2015), although others differ. (Langer 2019).
Exposure can be minimized by 90% by waiting 3 hours to breastfeed again after taking the drug.
Until more published data is known about this drug in relation to breastfeeding, known safer alternatives may be preferable (Langer 2019, Cree 2013), especially during the neonatal period and in the case of prematurity.
Given the strong evidence that exists on the benefits of breastfeeding for the development of babies and the health of mothers, it is convenient to evaluate the risk-benefit of any maternal treatment, including chemotherapy, individually advising each mother who wishes to continue with breastfeeding. (Koren 2013)
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