Office of New Drugs, the Office of Drug Evaluation III, the Division of Bone, Reproductive, and Urologic Products, the Office of Surveillance and Epidemiology, the Office of Pharmacovigilance and Epidemiology, and the Division of Pharmacovigilance II, U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Silver Spring, Maryland.
Obstet Gynecol. 2017 Jun;129(6):1054-1058. doi: 10.1097/AOG.0000000000002033.
This commentary serves to raise health care provider awareness about the regulatory status and available evidence regarding domperidone for insufficient lactation. Breastfeeding provides significant health benefits for mothers and infants, and insufficient milk production remains the most common reason for early weaning. Domperidone, a dopamine receptor antagonist that may increase milk production, is not approved for any human use in the United States. It is approved in some countries for certain gastrointestinal disorders, but is not approved in any country for lactation enhancement. Domperidone is associated with serious cardiac arrhythmias. The U.S. Food and Drug Administration (FDA) issued an import alert in 2004, updated in 2012, explaining that the importation of domperidone is illegal with limited exceptions, including when imported pursuant to an investigational new drug application. The FDA also issued a public safety warning regarding the use of domperidone for lactation. Nonetheless, domperidone is sometimes being obtained illegally and used in attempts to increase milk production in lactating mothers. There is limited quality evidence for the effectiveness of domperidone for lactation enhancement. In contrast, considerable information exists on domperidone's cardiac risks including QT prolongation, torsades de pointes, and sudden cardiac death, including among lactating women. In light of limited efficacy data that do not offset safety concerns from a public health perspective, we continue to caution against using domperidone for lactation enhancement. Research and drug development are needed to address the significant unmet medical need for lactation disorders.
这篇评论旨在提高医疗保健提供者对多潘立酮在泌乳不足方面的监管状况和现有证据的认识。母乳喂养为母亲和婴儿提供了显著的健康益处,而乳汁不足仍然是早期断奶的最常见原因。多潘立酮是一种多巴胺受体拮抗剂,可能增加乳汁产量,但未获得美国任何用途的批准。它在某些国家被批准用于某些胃肠道疾病,但在任何国家都未被批准用于促进泌乳。多潘立酮与严重的心律失常有关。美国食品和药物管理局(FDA)于 2004 年发布了一项进口警报,并于 2012 年进行了更新,解释说多潘立酮的进口是非法的,但有一些有限的例外情况,包括根据新药研究申请进口。FDA 还就多潘立酮用于泌乳发布了公共安全警告。尽管如此,多潘立酮仍有时被非法获取并用于尝试增加哺乳期母亲的乳汁产量。多潘立酮对泌乳增强的有效性的证据质量有限。相比之下,关于多潘立酮的心脏风险存在大量信息,包括 QT 延长、尖端扭转型室性心动过速和心脏性猝死,包括哺乳期妇女。鉴于从公共卫生角度来看,疗效数据有限,无法抵消安全性问题,我们继续警告不要将多潘立酮用于泌乳增强。需要进行研究和药物开发,以解决对哺乳期疾病的重大未满足的医疗需求。