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Lamotrigine-induced Stevens-Johnson syndrome
1Clinical Pharmacy Practice, St. John's University, 8000 Utopia Parkway, Queens, NY 11439, USA.
A case study highlights lamotrigine as a cause of Stevens-Johnson syndrome (SJS), a severe skin reaction. Prompt recognition and discontinuation of lamotrigine are crucial for managing SJS in patients.
Area of Science:
- Dermatology
- Pharmacology
- Neurology
Background:
- Stevens-Johnson syndrome (SJS) is a rare but severe adverse drug reaction.
- Lamotrigine is an anticonvulsant and mood stabilizer used for epilepsy and bipolar disorder.
- Schizoaffective disorder patients may be prescribed lamotrigine, increasing their risk for adverse reactions.
Observation:
- A 29-year-old woman with schizoaffective disorder developed a generalized skin reaction, including oral lesions and a full-body rash.
- The patient was taking lamotrigine, aripiprazole, and escitalopram; lamotrigine was the only recently initiated medication.
- Diagnosis of SJS was confirmed via punch biopsy, with lamotrigine identified as the suspected causative agent.
Findings:
- Lamotrigine was immediately discontinued, and the patient received treatment with oral prednisone, intravenous fluids, and symptomatic care.
- The patient showed significant improvement in skin manifestations and oral irritation within days of lamotrigine discontinuation.
- SJS developed despite appropriate dosing and dosage adjustment of lamotrigine.
Implications:
- This case underscores the potential for lamotrigine to induce SJS, even with correct dosing.
- Early identification and withdrawal of the offending drug are critical for mitigating SJS severity.
- Patient education regarding potential serious cutaneous reactions is vital for safe lamotrigine use.
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