section name header

Pronunciation

la-MOE-tri-jeen audio

Indications

REMS

Action

Therapeutic Effects:

Pharmacokinetics

Absorption: 98% absorbed following oral administration.

Distribution: Enters breast milk. Highly bound to melanin-containing tissues (eyes, pigmented skin).

Metabolism/Excretion: Mostly metabolized by the liver via glucuronidation to inactive metabolites; 10% excreted unchanged by the kidneys.

Half-life: Children taking enzyme–inducing anticonvulsants: 7–10 hr; Children taking enzyme inducers and valproic acid: 15–27 hr; Children taking valproic acid: 44–94 hr; Adults: 25.4 hr (during chronic therapy of lamotrigine alone).

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: CARDIAC ARREST, arrhythmias, bradycardia, heart block, QRS interval prolongation.

Derm: DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), STEVENS-JOHNSON SYNDROME, photosensitivity, rash (higher incidence in children, patients taking valproic acid, high initial doses, or rapid dose increases).

EENT: blurred vision, double vision, rhinitis.

GI: HEPATIC FAILURE, nausea, vomiting.

GU: vaginitis.

Hemat: HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS.

MS: arthralgia.

Neuro: ASEPTIC MENINGITIS, SUICIDAL THOUGHTS, ataxia, dizziness, headache, behavior changes, depression, drowsiness, insomnia, tremor.

Interactions

Drug-Drug:

Route/Dosage

see Calculator

Epilepsy

In Combination with Other Antiepileptic Agents

Bipolar Disorder

Escalation Regimen

Implementation

US Brand Names

LaMICtal, LaMICtal ODT, LaMICtal XR

Classifications

Therapeutic Classification: anticonvulsants

Availability

(Generic available)

Time/Action Profile

(blood levels)

ROUTEONSETPEAKDURATION
POunknown1.4–4.8 hr; 4–10 hr (XR)unknown

Assessment

Lab Test Considerations:

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code*