What is the recommended tapering schedule for discontinuing Wellbutrin (bupropion)?

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Wellbutrin (Bupropion) Tapering Recommendations

For patients on bupropion 300 mg daily, taper to 150 mg once daily before complete discontinuation; no specific taper duration is mandated by the FDA label, but a gradual reduction over 1-2 weeks is reasonable to minimize potential withdrawal symptoms. 1

FDA-Approved Tapering Protocol

The FDA label for bupropion extended-release provides explicit guidance: 1

  • For patients on 300 mg daily: Decrease to 150 mg once daily before stopping completely 1
  • For patients on 150 mg daily: The label does not specify a required taper step, suggesting direct discontinuation may be acceptable 1
  • Timing: The label does not mandate a specific duration between dose reduction and complete cessation 1

Practical Tapering Approach

While the FDA label is brief, a conservative approach based on general antidepressant principles includes: 1, 2

  • Week 1-2: Reduce from 300 mg to 150 mg daily 1
  • Week 3-4: Continue 150 mg daily to assess tolerance 1
  • After Week 4: Discontinue if patient tolerates the 150 mg dose well 1

For patients experiencing withdrawal symptoms (anxiety, irritability, insomnia, mood changes), consider: 2, 3

  • Extending the 150 mg phase to 4-6 weeks before discontinuation 2
  • For severe symptoms, some patients may benefit from alternating 150 mg daily with 150 mg every other day for 1-2 weeks before stopping 4, 2

Key Differences from Other Antidepressants

Bupropion requires less aggressive tapering than SSRIs because: 1, 2

  • The FDA label only mandates one dose reduction step (300 mg → 150 mg) 1
  • Bupropion's mechanism (dopamine/norepinephrine reuptake inhibition) produces less severe withdrawal than serotonergic agents 5, 1
  • Research on hyperbolic tapering focuses primarily on SSRIs due to their serotonin transporter occupancy curves, which is less relevant for bupropion 2, 6

Monitoring During Discontinuation

Watch for these withdrawal symptoms: 2, 3

  • Mood changes: Irritability, anxiety, depressed mood 2
  • Physical symptoms: Headache, fatigue, dizziness 2
  • Sleep disturbances: Insomnia or vivid dreams 2
  • Cognitive symptoms: Difficulty concentrating 3

If significant symptoms emerge, return to the previous dose and slow the taper further. 2, 3

Critical Pitfalls to Avoid

  • Do not abruptly stop 300 mg daily dosing without first reducing to 150 mg, as this violates FDA guidance and increases withdrawal risk 1
  • Do not confuse withdrawal symptoms with depression relapse in the first 2-4 weeks after discontinuation; withdrawal symptoms typically emerge within days and resolve within 2-3 weeks, while relapse develops more gradually 2, 3
  • Do not use the same aggressive hyperbolic tapering strategies designed for SSRIs, as bupropion's pharmacology differs substantially 2, 6

Special Populations

Hepatic impairment: 1

  • Moderate to severe (Child-Pugh 7-15): Maximum dose is 150 mg every other day; taper by extending dosing interval further (every 3-4 days, then weekly, then stop) 1
  • Mild impairment (Child-Pugh 5-6): Consider slower taper with extended time at 150 mg daily 1

Renal impairment (GFR <90 mL/min): Consider extending the taper duration and monitoring more closely for withdrawal symptoms 1

References

Research

Strategies to reduce use of antidepressants.

British journal of clinical pharmacology, 2021

Guideline

Fluoxetine Tapering Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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