Can stopping Lamictal (lamotrigine) trigger Stevens-Johnson Syndrome (SJS)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: June 3, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

Stopping Lamictal (lamotrigine) abruptly does not typically trigger Stevens-Johnson Syndrome (SJS). SJS is a rare but serious skin reaction that is associated with starting lamotrigine, particularly when the medication is initiated at too high a dose or increased too quickly 1. The risk of SJS is highest during the first 2-8 weeks of treatment with lamotrigine. However, suddenly discontinuing lamotrigine can cause other problems, including seizure recurrence in people with epilepsy or mood destabilization in those with bipolar disorder. For this reason, lamotrigine should generally be tapered off gradually under medical supervision, typically over at least 2 weeks, with the exact schedule determined by your doctor based on your current dose and medical condition 1. If you are concerned about skin reactions or need to stop lamotrigine, contact your healthcare provider immediately rather than stopping on your own. The mechanism behind lamotrigine-induced SJS involves an immune-mediated hypersensitivity reaction to the drug or its metabolites, which is why the risk is present when introducing the medication to your system, not when removing it 1.

Some key points to consider when managing SJS/TEN include:

  • Discontinuing any potential culprit drug immediately 1
  • Establishing peripheral venous access and commencing appropriate intravenous fluid resuscitation if clinically indicated 1
  • Assessing the patient's ability to maintain adequate hydration and nutrition orally, and inserting a nasogastric tube if necessary 1
  • Inserting a urinary catheter when urogenital involvement is indicated 1
  • Using a patient-appropriate validated pain tool to assess pain in all conscious patients at least once daily 1

It's also important to note that the UK guidelines for the management of SJS/TEN in adults recommend a multidisciplinary approach to care, including daily reviews by a specialist team and the use of supportive therapeutic measures such as analgesia, wound care, and nutritional support 1.

In terms of specific treatments, the guidelines recommend the use of ocular lubricants, topical corticosteroids, and broad-spectrum topical antibiotics as needed, as well as the use of white soft paraffin ointment to the lips and urogenital skin and mucosae 1.

Overall, while stopping lamotrigine abruptly does not typically trigger SJS, it's still important to approach discontinuation with caution and under medical supervision to minimize the risk of other complications. Lamotrigine should be tapered off gradually, over at least 2 weeks, to minimize the risk of seizure recurrence or mood destabilization.

From the Research

Stevens-Johnson Syndrome (SJS) and Lamotrigine

  • Stevens-Johnson Syndrome (SJS) is a life-threatening, blistering mucocutaneous disease that can be triggered by various factors, including certain medications like lamotrigine 2, 3, 4, 5, 6.
  • The available evidence does not directly address whether stopping lamotrigine can trigger SJS, but it does indicate that SJS is a potential adverse reaction associated with the use of lamotrigine 2, 3, 4, 5, 6.
  • Studies suggest that the risk of SJS is higher when lamotrigine is started, and the condition is often characterized by a delayed-type hypersensitivity reaction 2, 3, 4, 5, 6.
  • The Federal Food and Drug Administration recommends testing HLA subtypes for those associated with SJS prior to starting lamotrigine, and a strict re-challenge dosing regimen can be used to facilitate successful reintroduction of lamotrigine in patients who have previously experienced SJS 4.
  • It is essential to monitor patients for possible systemic and cutaneous adverse effects of lamotrigine, especially during the initial treatment phase, and to discontinue treatment if any rash appears 5.

Risk Factors and Prevention

  • Certain genetic factors, such as specific HLA genotypes, can increase the risk of SJS in patients taking lamotrigine 4.
  • The risk of SJS recurrence can be minimized by considering the timing of re-dose and initial rash severity when reintroducing lamotrigine 4.
  • Prime candidates for lamotrigine re-challenge are those with mild initial rash that has not occurred within the previous 4 weeks 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Stevens Johnson Syndrome associated with Lamotrigine.

Pakistan journal of medical sciences, 2013

Research

Lamotrigine and Stevens-Johnson Syndrome Prevention.

Psychopharmacology bulletin, 2021

Research

[Lamotrigine and its relationship with Stevens-Johnson syndrome and toxic epidermal necrolysis].

Revista medica del Instituto Mexicano del Seguro Social, 2020

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.