Tapering Bupropion (Wellbutrin) Before Discontinuation
When discontinuing bupropion, patients should taper by reducing to 150 mg once daily for 1-2 weeks before complete discontinuation to minimize withdrawal symptoms and neuropsychiatric side effects. 1
Recommended Tapering Protocol
The FDA-approved drug label for bupropion provides clear guidance on discontinuation:
- For patients on 300 mg daily: Decrease to 150 mg once daily for 1-2 weeks before complete discontinuation 1
- For patients already on 150 mg daily: May discontinue directly, though some clinicians still recommend taking the medication every other day for 1 week before stopping completely
Rationale for Tapering
Tapering bupropion is important for several reasons:
- Neuropsychiatric symptoms: Abrupt discontinuation may increase the risk of developing or worsening neuropsychiatric symptoms including depression and suicidal ideation 2, 3
- Withdrawal symptoms: Though less common than with SSRIs, some patients may experience withdrawal effects including irritability, anxiety, and mood disturbances
- Seizure risk: Bupropion carries a seizure risk (0.1% at therapeutic doses), and abrupt discontinuation could theoretically increase this risk in susceptible individuals 3
Monitoring During Tapering
During the tapering period, patients should be monitored for:
- Development or worsening of neuropsychiatric symptoms 2, 3
- Cognitive changes, as bupropion can affect concentration and memory 3
- Return of original symptoms (depression, if being used as an antidepressant, or nicotine cravings if used for smoking cessation) 2
Special Considerations
For Patients with Hepatic Impairment
- Patients with moderate to severe hepatic impairment already taking a reduced dose (150 mg every other day) should maintain this schedule for 1-2 weeks before stopping 1
For Patients with Renal Impairment
- Patients with renal impairment may need a more gradual taper due to altered drug clearance 1
Common Pitfalls to Avoid
- Abrupt discontinuation: Never stop bupropion suddenly, especially at higher doses
- Ignoring new symptoms: Any new or worsening neuropsychiatric symptoms during tapering require immediate medical attention
- Inadequate monitoring: Weekly assessment during the first month after dose reduction is recommended 3
- Failure to recognize formulation differences: The tapering schedule applies to all formulations (IR, SR, XL), though the pharmacokinetics differ slightly 4
By following this tapering protocol, patients can minimize the risk of adverse effects while safely discontinuing bupropion therapy.