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Indications

REMS


Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: atrial fibrillation/flutter, bradycardia, heart block, syncope, VENTRICULAR ARRHYTHMIAS

Derm: DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), rash, STEVENS-JOHNSON SYNDROME (SJS), TOXIC EPIDERMAL NECROLYSIS

EENT: diplopia

GI: nausea, vomiting

Hemat: AGRANULOCYTOSIS

Neuro: dizziness, headache, ataxia, hallucinations, SUICIDAL THOUGHTS, syncope, vertigo

Misc: physical dependence, psychological dependence

Interactions

Drug-drug:

Availability

(Generic available)

Route/Dosage

Partial-Onset Seizures

Renal Impairment

Hepatic Impairment

Primary Generalized Tonic-Clonic Seizures

Renal Impairment

Hepatic Impairment

US Brand Names

Motpoly XR, Vimpat

Action

  • Mechanism is not known, but may involve enhancement of slow inactivation of sodium channels with resultant membrane stabilization
Therapeutic effects:
  • Decreased incidence and severity of partial-onset seizures generalized tonic-clonic seizures.

Classifications

Therapeutic Classification: anticonvulsants

Pharmacokinetics

Absorption: 100% absorbed following oral administration; IV administration results in complete bioavailability.

Distribution: Unknown.

Protein Binding: <15%.

Metabolism/Excretion: Partially metabolized by the liver; 40% excreted in urine as unchanged drug; 30% as a metabolite.

Half-Life: 13 hr.

Contr. Subst. Schedule

Schedule V (C-V)

Time/Action Profile

(plasma concentrations)

ROUTEONSETPEAKDURATION
PO-IRunknown1–4 hr12 hr
PO-XRunknown7 hr24 hr
IVunknownend of infusion12 hr



Patient/Family Teaching

Pronunciation

la-KOSE-a-mide