Nonstimulant Medications for ADHD in Breastfeeding
Bupropion is the preferred nonstimulant option for breastfeeding mothers with ADHD, particularly when co-occurring depression is present, though caution is warranted due to limited data and two case reports of seizures in breastfed infants. 1
Primary Nonstimulant Options
Bupropion (First-Line Nonstimulant)
- Bupropion can be considered as an alternative for individuals requiring treatment for co-occurring ADHD and depression, given available safety data in the perinatal period. 1
- Start with 100-150 mg daily (SR formulation) or 150 mg daily (XL formulation), titrating to maintenance doses of 100-150 mg twice daily (SR) or 150-300 mg daily (XL), with a maximum of 450 mg per day. 1
- Bupropion is present in human milk and has been detected in infant serum at very low levels (sometimes undetectable). 1
- Very limited breastfeeding data exists (only 21 cases documented). 1
- Two case reports of seizures in breastfed infants have been documented, though causality remains uncertain. 1
- Generally, no adverse events have been reported in most cases. 1
- Monitor infants carefully for vomiting, diarrhea, jitteriness, sedation, and/or seizures. 1
- Important limitation: Bupropion is not as efficacious as stimulants for treating ADHD. 1
Atomoxetine (Use with Caution)
- Overall caution is advised for atomoxetine during breastfeeding. 1
- No published studies of atomoxetine use while breastfeeding exist. 1
- Based on pharmacokinetics (low molecular weight, long half-life), atomoxetine will likely be present in human milk. 1
- The effects on nursing infants are unknown, and current references advise caution. 1
- The FDA drug label confirms no data exists on atomoxetine presence in human milk or effects on breastfed children. 2
Alpha-2 Agonists (Limited Data, Use with Extreme Caution)
Clonidine:
- Overall caution is advised with very limited published data. 1
- Clonidine is found in human milk and detectable in infant serum following breastfeeding exposure. 1
- Milk-to-plasma (M:P) ratio reported as 2 with relative infant dose (RID) up to 7.1%. 1
- Majority of cases reported no adverse effects, but one case report documented an infant developing drowsiness, hypotonia, suspected generalized seizures, and episodes of apnea (exposed to 0.15 mg daily; symptoms resolved within 24 hours of breastfeeding cessation). 1
- Monitor infants for drowsiness, hypotonia, vomiting, diarrhea, jitteriness, sedation, and/or seizures. 1
Guanfacine:
- Overall caution is advised. 1
- No published studies of guanfacine use while breastfeeding exist. 1
- Alternative agents would be preferred. 1
Viloxazine:
- Overall caution is advised. 1
- No published studies of viloxazine use while breastfeeding exist. 1
- Not currently available in Canada; approved in the United States for children and adolescents aged 6 and older only. 1
Clinical Decision Algorithm
Step 1: Assess Clinical Need
- Determine if ADHD medication is essential for daily functioning during the postpartum period. 1
- Consider whether co-occurring depression is present. 1
Step 2: Select Medication Based on Clinical Profile
- If co-occurring depression: Bupropion is the preferred nonstimulant option. 1
- If ADHD only without depression: Consider methylphenidate (stimulant with excellent breastfeeding safety data, RID <1%) as an alternative to nonstimulants, as it may be safer than most nonstimulants. 1
- Avoid atomoxetine, guanfacine, and viloxazine due to complete absence of breastfeeding data. 1
Step 3: Implement Safety Monitoring
- For bupropion: Monitor infant for vomiting, diarrhea, jitteriness, sedation, and especially seizures. 1
- For clonidine (if used): Monitor for drowsiness, hypotonia, and respiratory symptoms. 1
- Ensure infants are gaining weight appropriately and meeting developmental milestones. 1
- Arrange early follow-up after hospital discharge. 3
Step 4: Optimize Dosing Strategy
- Use the lowest effective dose. 1
- Consider intermittent use on an as-needed basis to maximize functioning while reducing infant exposure. 1
- Time medication administration just after breastfeeding or before the infant's longest sleep period. 4, 5
Critical Caveats
Common Pitfall: Discontinuing necessary ADHD treatment due to fear of medication exposure can harm the mother-infant dyad more than continued treatment. 1 The consensus is that treatment should not be stopped if required for daily functioning. 1
Important Consideration: The evidence for nonstimulants during breastfeeding is substantially weaker than for stimulants (particularly methylphenidate). 1 If ADHD symptoms are severe and nonstimulants are insufficient, methylphenidate may actually represent a safer, better-studied option. 1
Bupropion Efficacy Limitation: While bupropion has the most breastfeeding data among nonstimulants, it is significantly less efficacious than stimulants for ADHD treatment. 1 Set realistic expectations with patients about symptom control.