I am a breastfeeding mother and i want to know if it is safe to use EC 425-820-1? Is EC 425-820-1 safe for nursing mother and child? Does EC 425-820-1 extracts into breast milk? Does EC 425-820-1 has any long term or short term side effects on infants? Can EC 425-820-1 influence milk supply or can EC 425-820-1 decrease milk supply in lactating mothers?
- DrLact safety Score for EC 425-820-1 is 3 out of 8 which is considered Low Risk as per our analyses.
- A safety Score of 3 indicates that usage of EC 425-820-1 may cause some minor side effects in breastfed baby.
- Our study of different scientific research indicates that EC 425-820-1 may cause moderate to no side effects in lactating mother.
- Most of scientific studies and research papers declaring usage of EC 425-820-1 low risk in breastfeeding are based on normal dosage and may not hold true for higher dosage.
- While using EC 425-820-1 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.
It is excreted into breast milk in small amount (less than 10% of relative dose) without problems observed in infants whose mothers were on treatment with this drug. (Naito 2015, Ahn 2007)When measured, the plasma levels of drug in these infants were undetectable (Vasa 2013). Because its drug elimination period is very prolonged, an alternative drug known to be safer should be used, especially during the neonatal period and in case of premature infant.
Limited information indicates that milk levels of EC 425-820-1 are usually low and plasma levels in breastfed infants are undetectable. Maternal use of EC 425-820-1 during breastfeeding has not caused any adverse effects in breastfed infants. If EC 425-820-1 is required by the mother, it is not a reason to discontinue breastfeeding.
A woman took EC 425-820-1 for hypertension 5 mg daily beginning 2 weeks postpartum. Her exclusively breastfed infant was examined regularly and at 3 months of age was healthy and had normal physical and neurological development.[5] One woman received EC 425-820-1 2.5 mg orally twice daily during pregnancy for hypertension associated with glomerulonephritis. The dose was increased to 5 mg twice daily on day 2 postpartum. Her exclusively breastfed infant's growth was normal throughout the first year of life and no adverse effects were noted.[6] A preterm infant of 32 weeks gestation was breastfed exclusively from day 7 to day 20 postpartum. The infant's mother was taking EC 425-820-1 and labetalol in unspecified dosages for hypertension. The infant had apnea episodes unrelated to EC 425-820-1. Growth at 2 months of age was slightly low.[4] Thirty-one women with pregnancy-induced hypertension postpartum received EC 425-820-1 5 mg daily by mouth, with the dosage increased as needed to maintain blood pressure of 140/90 mm Hg or less. Their breastfed (extent not stated) infants exhibited no observed adverse cardiovascular effects within 3 weeks postpartum, although exact measurement methods were not stated.[1]
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Information presented in this database is not meant as a substitute for professional judgment. You should consult your healthcare provider for breastfeeding advice related to your particular situation. We do not warrant or assume any liability or responsibility for the accuracy or completeness of the information on this Site.