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FDA Warns Against Breast Milk Drug
Tracy Hampton, PhD
JAMA. 2004;292:322.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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The Food and Drug Administration (FDA) is cautioning breastfeeding women not to use an unapproved drug, domperidone, which may increase the secretion of prolactin and therefore increase milk production. Several published reports and case studies have linked domperidone to cardiac arrhythmias, cardiac arrest, and sudden death in patients receiving an intravenous form of the drug.
More than 2000 reports of adverse effects from 33 countries have been related to domperidone, and the drug has been withdrawn from marketing in a number of countries. Several nations, including Canada, have approved oral domperidone for gastric disorders, as it increases contractions of the stomach and bowel.
But domperidone is not approved in any country for enhancing breast milk production. It is not known if domperidone causes adverse effects in newborns, and drug labels on the oral form of the drug note that it is excreted in the milk of lactating . . . [Full Text of this Article]
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