CPC A61K 31/165 (2013.01) | 26 Claims |
1. A method for decreasing the potential for adverse events from solriamfetol in an infant fed breast milk obtained from a human subject treated with solriamfetol comprising:
administering solriamfetol orally at a once-daily dose of about 75 mg to the subject; and
feeding the infant breast milk from the subject at least about 5 hours after administering the solriamfetol to the subject,
and the cumulative amount of solriamfetol excreted in breast milk over 8 hours is about 0.26 mg or lower.
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