Discontinuing Lamotrigine 100mg Daily for Mood Regulation
Taper lamotrigine by reducing the dose by 25-50mg every 1-2 weeks over a minimum of 4-6 weeks, never stopping abruptly, as discontinuation over 10-14 days limits withdrawal symptoms for mood stabilizers. 1
Critical Safety Considerations
Abrupt discontinuation of lamotrigine is never appropriate and can lead to severe withdrawal symptoms, including rebound mood episodes, anxiety, irritability, and potentially seizures. While the evidence specifically addresses antidepressant discontinuation protocols 1, the same principles apply to mood stabilizers like lamotrigine, which require gradual tapering to prevent withdrawal phenomena.
Key Risks During Discontinuation
- Risk of mood destabilization: Lamotrigine is effective at preventing depressive episodes in bipolar disorder, and stopping it may precipitate a depressive relapse 2, 3
- Withdrawal symptoms: Similar to other psychotropic medications, sudden cessation can cause dizziness, headache, irritability, anxiety, insomnia, and mood instability 1
- Seizure risk: Although lamotrigine is an anticonvulsant, abrupt withdrawal in patients taking it for any indication carries theoretical seizure risk
Recommended Tapering Protocol
Standard Taper Schedule
Reduce lamotrigine by 25mg every 1-2 weeks, which represents a 25% reduction of the current dose initially, then progressively smaller absolute reductions 1, 4:
- Week 1-2: Reduce from 100mg to 75mg daily (25% reduction)
- Week 3-4: Reduce from 75mg to 50mg daily (33% reduction of current dose)
- Week 5-6: Reduce from 50mg to 25mg daily (50% reduction of current dose)
- Week 7-8: Reduce from 25mg to 0mg (complete discontinuation)
Alternative Slower Taper for Long-Term Users
For patients who have been on lamotrigine for more than 1 year, consider extending the taper to 10% of the current dose per month rather than the faster schedule above 4:
- Month 1: 100mg to 90mg daily
- Month 2: 90mg to 81mg daily
- Month 3: 81mg to 73mg daily
- Continue this pattern until complete discontinuation
This slower approach may require splitting tablets or using liquid formulations to achieve precise dosing.
Monitoring Requirements
Follow up at least monthly during the taper, with more frequent contact during difficult phases 4:
- Assess for withdrawal symptoms: Headache, dizziness, irritability, anxiety, insomnia, mood changes 1
- Monitor for mood destabilization: Screen for emerging depression, hypomania, or mania 4
- Watch for suicidal ideation: Increased risk during medication changes 1
- Evaluate functional status: Sleep quality, work performance, relationships 4
Managing Withdrawal Symptoms
Non-Pharmacological Support
Integrate cognitive behavioral therapy (CBT) during the taper, as this significantly increases success rates 4:
- Mindfulness and relaxation techniques 4
- Sleep hygiene education 4
- Exercise and fitness training 4
- Patient education about expected withdrawal symptoms and their time course 4
Pharmacological Adjuncts (If Needed)
- For insomnia: Trazodone 25-50mg at bedtime can be used for short-term management without abuse potential 4
- For anxiety: Consider buspirone 5mg twice daily, though it requires 2-4 weeks to become effective 1, 4
- For headache/muscle aches: NSAIDs or acetaminophen 4
Do not substitute another mood stabilizer or anticonvulsant during the taper unless there is a clear clinical indication, as this may complicate the discontinuation process and create new dependencies 4.
When to Slow or Pause the Taper
The taper rate must be determined by the patient's tolerance, not a rigid schedule, and pauses in the taper are acceptable and often necessary when withdrawal symptoms emerge 4:
- Clinically significant withdrawal symptoms signal the need to further slow the taper rate 4
- Emerging mood symptoms (depression, hypomania) require holding at current dose and reassessing 4
- Patient request: If the patient feels the taper is too fast, slow down or pause 4
Tapers may be considered successful as long as the patient is making progress, with the goal of durability of the taper, not speed 4.
Special Considerations for Lamotrigine
Risk of Mood Episode During Discontinuation
Lamotrigine is particularly effective at preventing depressive episodes but has limited antimanic effects 2, 3. Therefore:
- Higher risk of depressive relapse than manic relapse during discontinuation 2, 3
- Monitor closely for emerging depressive symptoms: Low mood, anhedonia, fatigue, suicidal thoughts 4
- Consider maintaining other mood stabilizers if the patient is on combination therapy 2, 3
Patients at Higher Risk for Complications
Immediate specialist referral is indicated for 4:
- Patients with bipolar I disorder with history of severe manic episodes 5
- Patients with history of rapid cycling or mixed episodes 5
- Patients with co-occurring substance use disorders 4
- Patients with unstable psychiatric comorbidities 4
- Previous unsuccessful tapering attempts 4
Common Pitfalls to Avoid
Never taper too quickly 4:
- Research shows that even aggressive tapers result in high failure rates 4
- Slower is always safer, even if it takes 6-12 months 4
Never abandon the patient 4:
- Even if tapering is unsuccessful, maintain the therapeutic relationship 4
- Consider maintenance therapy if discontinuation proves impossible 4
- Reassess the reasons for discontinuation and whether they outweigh the risks 4
Do not reduce by a fixed amount each time 4:
- Always reduce by a percentage of the current dose, not the original dose 4
- This prevents disproportionately large final reductions that often cause the most severe withdrawal 4
Realistic Timeline and Expectations
The taper will likely take a minimum of 4-8 weeks, and possibly longer for patients on lamotrigine for extended periods 1, 4:
- Patient agreement and interest in tapering is a key component of success 4
- Use shared decision-making and explain the risks of continued use versus benefits of discontinuation 4
- Set realistic expectations about withdrawal symptoms and their duration 4
Successful withdrawal is typically followed by improved psychomotor and cognitive functioning, particularly in memory and daytime alertness, though mood stability depends on the underlying condition 4.