What is the starting dose for bupropion (Bupropion) in the treatment of Major Depressive Disorder (MDD) with anxiety?

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Starting Dose for Bupropion in MDD with Anxiety

For bupropion SR (sustained-release), start with 150 mg once daily in the morning for 3 days, then increase to 150 mg twice daily (300 mg total daily dose). 1, 2

Initial Dosing Strategy

  • The FDA-approved starting dose for bupropion XL (extended-release) in MDD is 150 mg once daily in the morning, with an increase to the target dose of 300 mg once daily after 4 days if tolerated. 2

  • For bupropion SR formulation, the American Family Physician recommends 150 mg once daily for the first 3 days, then titrating to 150 mg twice daily (300 mg total). 1

  • The second dose of bupropion SR should be administered before 3 PM to minimize insomnia risk, which is particularly important given the activating properties of this medication. 1

Special Considerations for Anxiety Comorbidity

  • While bupropion is FDA-approved for MDD, the presence of comorbid anxiety does not appear to significantly affect its comparative efficacy based on STAR*D trial analyses. 3

  • Bupropion's activating properties may theoretically worsen anxiety in some patients, so close monitoring for increased agitation is warranted during initiation. 1

  • The gradual dose titration (starting at 150 mg daily before increasing) helps minimize adverse effects including potential anxiety exacerbation. 2

Dosing Adjustments for Special Populations

  • For older adults, start with a lower dose of 37.5 mg every morning, increasing by 37.5 mg every 3 days as tolerated, with a maximum of 150 mg twice daily (300 mg total). 1, 4

  • For patients with moderate to severe hepatic impairment (Child-Pugh score 7-15), the maximum dose is 150 mg every other day. 2

  • For patients with renal impairment (GFR <90 mL/min), reduce the total daily dose by half. 1, 2

Critical Safety Monitoring

  • Bupropion is absolutely contraindicated in patients with seizure disorders, eating disorders (bulimia/anorexia), or those who have abruptly discontinued alcohol or benzodiazepines due to increased seizure risk. 1, 4, 2

  • Monitor blood pressure regularly, as bupropion should be avoided in patients with uncontrolled hypertension. 1, 4

  • Watch for neuropsychiatric symptoms, particularly in patients under 24 years old, as with all antidepressants. 1, 4

  • The maximum dose should not exceed 450 mg per day for XL formulation or 400 mg per day for SR formulation to minimize seizure risk. 1, 2

Administration Guidelines

  • Administer bupropion in the morning to leverage its activating properties and improve energy levels. 1

  • Tablets should be swallowed whole and not crushed, divided, or chewed to maintain the extended-release properties and minimize seizure risk. 4, 2

  • Bupropion may be taken with or without food. 4, 2

Efficacy Timeline

  • Evaluate treatment response after 6-8 weeks at an adequate dose; if no response is seen, consider alternative treatment strategies. 1, 4

  • The onset of action is typically 2 weeks, with full efficacy attained at 4 weeks of treatment. 5

References

Guideline

Bupropion Dosing and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Transitioning from Sertraline to Bupropion

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Other Antidepressants.

Handbook of experimental pharmacology, 2019

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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