2015
DOI: 10.1002/phar.1550
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Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome Probably Induced by a Lamotrigine-Ginseng Drug Interaction

Abstract: The likelihood of a drug reaction with lamotrigine is increased by dose escalation that is too rapid or drug interactions that increase the concentration of lamotrigine. There is a well-documented interaction between valproic acid and lamotrigine in which lamotrigine levels are increased, subsequently increasing the risk of a drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome. This syndrome is characterized by fever, lymphadenopathy, diffuse maculopapular rash, multivisceral involvement, eo… Show more

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Cited by 16 publications
(6 citation statements)
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“…Lamotrigine is an aromatic anticonvulsant drug that is hepatically eliminated through glucuronidation by the uridine diphosphate glucuronosyl transferase enzyme. 2 Valproate is a broad spectrum inhibitor of the uridine diphosphate glucuronosyl transferase enzyme. 3 When valproate is used in combination with lamotrigine, because of the inhibition of elimination, the half-life of lamotrigine prolongs and its serum levels elevate.…”
Section: Discussionmentioning
confidence: 99%
“…Lamotrigine is an aromatic anticonvulsant drug that is hepatically eliminated through glucuronidation by the uridine diphosphate glucuronosyl transferase enzyme. 2 Valproate is a broad spectrum inhibitor of the uridine diphosphate glucuronosyl transferase enzyme. 3 When valproate is used in combination with lamotrigine, because of the inhibition of elimination, the half-life of lamotrigine prolongs and its serum levels elevate.…”
Section: Discussionmentioning
confidence: 99%
“…Many studies have reported that VA in co-administration with Lamotrigine (LMT) increases the risk of Lamotrigine-induced ADRs [7,[22][23][24].…”
Section: Discussionmentioning
confidence: 99%
“…Over these studies, 32 aimed to highlight only PK mechanisms such as area under the curve, half-life, or clearance. Only five studies considered clinical effects rather than only PK parameters (CS 3,10,25,33,34) [46,49,55,61,73]. With such a limited number of studies describing clinical effects, interpretation is limited.…”
Section: Clinical Studiesmentioning
confidence: 99%