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Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006-.
CASRN: 14222-60-7
Drug Levels and Effects
Summary of Use during Lactation
Prothionamide (protionamide) is not approved for marketing in the United States by the U.S. Food and Drug Administration, but is available in other countries. No information is available on the use of prothionamide during breastfeeding. International sources consider breastfeeding to be acceptable during prothionamide use, but mothers should receive 100 mg of pyridoxine daily and the breastfed infant should receive pyridoxine 1 to 2 mg/kg once daily. Monitor the breastfed infant for gastrointestinal disturbances.[1]
Drug Levels
Maternal Levels. Relevant published information was not found as of the revision date.
Infant Levels. Relevant published information was not found as of the revision date.
Effects in Breastfed Infants
Relevant published information was not found as of the revision date.
Effects on Lactation and Breastmilk
Relevant published information was not found as of the revision date.
References
- 1.
- Anon. Ethionamide (Eto) or prothionamide (Pto). MSF Medical Guidelines 2026. https:
//medicalguidelines .msf.org/en/viewport /TUB/english/ethionamide-eto-or-prothionamide-pto-20324029 .html#section-target-3.
Substance Identification
Substance Name
Prothionamide
CAS Registry Number
14222-60-7
Disclaimer: 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. The U.S. government does not warrant or assume any liability or responsibility for the accuracy or completeness of the information on this Site.
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