Lamotrigine: Risk of hemophagocytic lymphohistiocytosis (HLH)


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Background of Safety Issue

The United States Food and Drug Administration (US FDA) warned that lamotrigine can cause a very rare but serious reaction called Hemophagocytic Lymphohistiocytosis (HLH), that excessively activates the body’s infection-fighting immune system. HLH typically presents as a persistent fever and it can lead to severe problems with blood cells and affects organs such as the liver, kidneys, and lungs2. The Japan Pharmaceuticals and Medical Devices Agency (PMDA) also issued out a similar alert following one reported case of HLH3.

Diagnosis is often complicated because early signs and symptoms such as fever and rash are not specific. HLH may also be confused with other serious immune-related adverse reactions such as drug reaction with eosinophilia and systemic symptoms (DRESS). The time to onset can occur within 4 weeks after initiation of lamotrigine.

A diagnosis of HLH can be established if a patient has at least five (5) of the following signs or symptoms2:


Adverse Drug Reaction Reports

Since year 2000, NPRA has received 272 reports and 496 adverse events suspected to be associated with lamotrigine use. Out of these reports, no case of HLH had been reported to NPRA4.


Advice for Healthcare Professionals


A directive [Ruj. Kami: (3) dlm. BPFK/PPP/07/25 Jld. 3] has been issued by NPRA for updates to the local product packaging insert and consumer medication information leaflet (Risalah Maklumat Ubat untuk Pengguna) related to this safety issue. Please refer to the directive for more information.



  1. The QUEST 3+ database, NPRA [Accessed: 1 November 2018]
  2. United States Food and Drug Administration (USFDA). FDA Drug Safety Communication: FDA warns of serious immune system reaction with seizure and mental health medicine lamotrigine (Lamictal).
  3. The Japan Pharmaceuticals and Medical Devices Agency (PMDA). Summary of Investigation Results- Lamotrigine.
  4. The Malaysian Adverse Drug Reactions database, NPRA [Accessed: 31 May 2018].



This publication is aimed at health professionals. The information is meant to provide updates on medication safety issues, and not as a substitute for clinical judgement. While reasonable care has been taken to verify the accuracy of the information at the time of publication, the NPRA shall not be held liable for any loss whatsoever arising from the use of or reliance on this publication.