4.6 Article

Infant Exposure to Armodafinil Through Human Milk Following Maternal Use of Modafinil

Journal

JOURNAL OF HUMAN LACTATION
Volume 39, Issue 2, Pages 218-222

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/08903344221134273

Keywords

armodafinil; breastfeeding; case study; human milk; modafinil; narcolepsy; relative infant dose

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In this case study, the concentration of armodafinil in human milk and infant plasma was measured to assess infant exposure. The findings suggest that relatively small amounts of armodafinil pass into human milk and have limited impact on the nursing infant. The use of modafinil or armodafinil during breastfeeding can be considered with proper monitoring of the infant.
Introduction Narcolepsy, a condition adversely affecting psychological, social, and cognitive function, is more prevalent in females of childbearing age than the general population. Modafinil and armodafinil are central nervous system stimulants approved for treatment of narcolepsy. Infant exposure to these agents through human milk has not been investigated. Poor quality medication safety information during lactation is associated with early cessation of breastfeeding and suboptimal healthcare for the breastfeeding family. Main Issue In this case study, we measured the concentration of armodafinil (the most active form of modafinil) in human milk and infant plasma to quantify infant exposure. Management The participant was a 30-year-old primipara with narcolepsy, taking modafinil (300 mg morning, 100 mg noon) while breastfeeding her 6-week-old infant despite the paucity of safety information. Armodafinil concentrations were measured in eight serial human milk samples collected over a 26-hr period and in single maternal and infant plasma samples using ultra performance liquid chromatography - tandem mass spectrometry. The average concentration of armodafinil in human milk was 1.96 mg/L; the relative infant dose was 4.85%; the theoretical infant dose was 0.294 mg/kg/day. Maternal and infant plasma concentrations of armodafinil were 12.02 mg/L and 0.19 mg/L, respectively. The participant continued to exclusively breastfeed the infant, who had normal growth and development. Conclusion Based on these findings, relatively small amounts of armodafinil pass into human milk, with consequent limited infant exposure. Consideration can be given to the use of modafinil or armodafinil during breastfeeding, provided the infant is monitored. Further studies are needed to confirm these findings.

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