Question

I am a breastfeeding mother and i want to know if it is safe to use EINECS 200-023-8? Is EINECS 200-023-8 safe for nursing mother and child? Does EINECS 200-023-8 extracts into breast milk? Does EINECS 200-023-8 has any long term or short term side effects on infants? Can EINECS 200-023-8 influence milk supply or can EINECS 200-023-8 decrease milk supply in lactating mothers?

EINECS 200-023-8 lactation summary

EINECS 200-023-8 usage has low risk in breastfeeding
  • DrLact safety Score for EINECS 200-023-8 is 3 out of 8 which is considered Low Risk as per our analyses.
  • A safety Score of 3 indicates that usage of EINECS 200-023-8 may cause some minor side effects in breastfed baby.
  • Our study of different scientific research indicates that EINECS 200-023-8 may cause moderate to no side effects in lactating mother.
  • Most of scientific studies and research papers declaring usage of EINECS 200-023-8 low risk in breastfeeding are based on normal dosage and may not hold true for higher dosage.
  • While using EINECS 200-023-8 We suggest monitoring child for possible reactions. It is also important to understand that side effects vary largely based on age of breastfed child and time of medication in addition to dosage.
  • Score calculated using the DrLact safety Version 1.2 model, this score ranges from 0 to 8 and measures overall safety of drug in lactation. Scores are primarily calculated using publicly available case studies, research papers, other scientific journals and publically available data.

Answer by Dr. Ru: About EINECS 200-023-8 usage in lactation

A natural Estrogen that is marketed for oral, injection and topical administration (skin and vaginal).On the chemical form of valerate, it is used in association with a progestin as a combined birth-control compound (e.g. EINECS 200-023-8 + Dienogest) EINECS 200-023-8 is excreted into breast milk in clinically non-significant amount (Nilson 1978) and no problems have been observed in infants whose mothers were treated (Pinheiro 2016). Plasma levels of these infants were undetectable or very low (Pinheiro 2016). After administration in the form of transdermal patches milk levels have been undetectable (Pinheiro 2016, Perheentupa 2004). Despite these data, an older publication associated the use of transdermal EINECS 200-023-8 with a case of jaundice and poor weight gain (Ball 1999).There is greater passage to milk when the administration is vaginal. There is evidence (albeit inconsistent) that estrogen-containing pills may decrease milk production, especially during the first few weeks postpartumThey may reduce the protein content of the milk. No problems have been observed in infants whose mothers were treated, except some cases of transient gynecomastia in infants whose mothers were receiving a higher dose than usual. Estrogen exposure in childhood or adolescence, does not influence the subsequent production of milk. The American Academy of Pediatrics states that this medication is usually compatible with breastfeeding.

Answer by DrLact: About EINECS 200-023-8 usage in lactation

Limited information on the use of EINECS 200-023-8 during breastfeeding indicates that the route of administration and dosage form have influences on the amount transferred into breastmilk. Vaginal administration results in measurable amounts in milk, but transdermal patches do not. Maternal doses of up to 200 mcg daily transdermally do not increase EINECS 200-023-8 or estriol in breastfed infants or cause any adverse effects in breastfed infants. Vaginal administration results in unpredictable peak times for EINECS 200-023-8 in breastmilk, so timing of the dose with respect to breastfeeding is probably not useful. A case report of inadequate milk production and inadequate infant weight gain was possibly caused by transdermal EINECS 200-023-8 initiated on the first day postpartum, but 2 small studies found no such effect when the drug was initiated after lactation was well established.

EINECS 200-023-8 Side Effects in Breastfeeding

A mother who had severe postpartum depression with 2 previous infants was prescribed a transdermal EINECS 200-023-8 patch that released 50 mcg daily beginning on day 1 postpartum to prevent recurrence of depression. At 11 days of age, the infant was jaundiced and had gained only 60 grams since birth. With more frequent nursing, weight gain improved, but remained inadequate until day 28 when the EINECS 200-023-8 was discontinued. The infant then experienced above average weight gain through day 66 postpartum. The delayed and reduced weight gain was possibly caused by EINECS 200-023-8.[4] Six nursing mothers received transdermal EINECS 200-023-8 as part of a study comparing EINECS 200-023-8 to sertraline and placebo for postpartum depression. The mothers received EINECS 200-023-8 dosages between 50 and 200 mcg daily (mean 133 mcg daily) at the time of serum level analysis at 4 and 8 weeks of therapy. Four of the 6 infants were exclusively breastfed and the other two were more than 50% breastfed. There was no difference in infant length, weight, and head circumference nor in the average daily gains in any of these parameters between treatments.[3]

EINECS 200-023-8 Possible Effects in Breastfeeding

Thirteen women who were 12 weeks postpartum and fully breastfeeding their infants were given a transdermal patch that released 100 mcg of EINECS 200-023-8 daily. The average number of breast feeds per day did not change significantly during 3 days of patch application.[5] Nineteen women who were 6 weeks postpartum, using a barrier contraceptive method and breastfeeding their infants were randomized to transdermal patches that released EINECS 200-023-8 50 mcg daily or placebo patches for 12 weeks. An additional control group received no patches. The number of breast feeds per day decreased in all groups over the course of the study, but there were no important differences among the groups.[6] A retrospective cohort study compared 371 women who received high-dose estrogen (either 3 mg of diethylstilbestrol or 150 mcg of ethinyl EINECS 200-023-8 daily) during adolescence for adult height reduction to 409 women who did not receive estrogen. No difference in breastfeeding duration was found between the two groups, indicating that high-dose estrogen during adolescence has no effect on later breastfeeding.[7]

Synonyms of EINECS 200-023-8

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