What disease-modifying therapy (DMT) for multiple sclerosis (MS) is safe to take while breastfeeding?

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Last updated: November 7, 2025View editorial policy

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MS Disease-Modifying Therapies Compatible with Breastfeeding

Glatiramer acetate and interferon-beta are the safest and most evidence-supported DMTs for use during breastfeeding, with glatiramer acetate having the strongest real-world safety data in breastfed infants. 1, 2

First-Line Options During Breastfeeding

Glatiramer Acetate (Copaxone®)

  • Most strongly recommended DMT for breastfeeding mothers based on real-world safety data from the COBRA study showing no increase in adverse events, hospitalizations, or antibiotic use in breastfed offspring compared to controls 2
  • Available as 20 mg daily subcutaneous injection or 40 mg three times weekly 3
  • Large polar molecule with minimal passage into breast milk 1
  • Only MS DMT with FDA pregnancy category B designation, supporting its favorable safety profile 3
  • Safety demonstrated in offspring breastfed for durations ranging from 6 to >574 days 2

Interferon-Beta

  • Likely safe for breastfeeding due to large molecular size preventing clinically significant transfer into breast milk 1, 4
  • Observational data support safety during lactation 4
  • Can be continued or initiated while breastfeeding without interruption 1

Monoclonal Antibodies: Use with Caution

Natalizumab

  • May be considered during breastfeeding with likely low transfer into breast milk 4
  • For women with highly active MS requiring aggressive therapy, natalizumab represents a reasonable option 4
  • Limited but emerging data suggest compatibility with breastfeeding 5, 4

Rituximab and Other Anti-CD20 Therapies

  • Could be given before conception for women with highly active MS 4
  • Limited data on use during breastfeeding itself, but monoclonal antibodies generally have low breast milk transfer 4

Medications to Avoid During Breastfeeding

Oral DMTs

  • Dimethyl fumarate, teriflunomide, fingolimod, and other oral agents lack sufficient safety data for breastfeeding 1, 4
  • Should be discontinued or avoided until breastfeeding is complete 4

Immune-Depleting Therapies

  • Alemtuzumab and cladribine should not be used during breastfeeding due to their profound immunosuppressive effects 1

Corticosteroids for Acute Relapses

Prednisone Dosing Guidelines

  • ≤20 mg daily: Continue breastfeeding without interruption 6
  • >20 mg daily: Delay breastfeeding or discard milk for 4 hours after administration 7, 6
  • Low-dose corticosteroids are compatible with breastfeeding per the American Academy of Pediatrics 7

Clinical Decision Algorithm

Step 1: Assess Disease Activity Risk

  • Low relapse risk postpartum → Consider breastfeeding without DMT or with injectable DMTs 4
  • High relapse risk → Strongly consider glatiramer acetate or interferon-beta 4
  • Highly active MS → Consider natalizumab or cell-depleting therapy before conception 4

Step 2: Select Appropriate DMT

  • First choice: Glatiramer acetate (strongest safety evidence) 2
  • Second choice: Interferon-beta (likely safe, less robust data) 1, 4
  • Third choice: Natalizumab (for highly active disease only) 4

Step 3: Encourage Breastfeeding

  • Breastfeeding itself is associated with decreased postpartum relapse risk 4
  • The benefits of maternal MS treatment with compatible DMTs outweigh potential risks to breastfed offspring 2

Key Pitfalls to Avoid

  • Do not unnecessarily discontinue glatiramer acetate or interferon-beta when breastfeeding, as these are safe options and disease control is important 1, 2
  • Do not use oral DMTs (dimethyl fumarate, fingolimod, teriflunomide) during breastfeeding due to insufficient safety data 4
  • Do not discourage breastfeeding in women with MS, as it provides protective effects against postpartum relapses 4
  • Do not administer high-dose corticosteroids (>20 mg prednisone daily) without timing considerations for breastfeeding 6

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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