Lacosamide – Vimpat

Lacosamide – VimpatR

Vimpat 50mg vimpat 100

Indication

Partial-Onset Seizures

Adjunctive therapy

Initial: 50 mg PO/IV q12hr

Increase by 100 mg/day qWeek

Maintenance: 200-400 mg/day PO divided q12hr

Mechanism of Action

Antiepileptic effects unknown; may slowly inactivate voltage-gated Na channels

Binds to collapsin response mediator protein-2 (CRMP-2), a phosphoprotein that is expressed mainly in the nervous system and is involved in neuronal differentiation and control of axonal outgrowth

Absorption

Bioavailability: ~100%

Peak plasma time: 1-4 hr

Distribution

Protein bound: <15%

Vd: 0.6 L/kg

Metabolism

By CYP2C19; major metabolite, O-desmethyl-lacosamide, is inactive

Elimination

Half-life: 13 hr

Excretion: Urine

Dialyzable: Yes (hemodialysis)

IV Preparation

May be administered without dilution or diluted in compatible solvents: NS; D5W; LR

IV Administration

Infuse over 30-60 min

Pregnancy category: C

Lactation: Unknown if distributed in breast milk; use caution

>10%

Dizziness (31%)

Headache (13%)

Diplopia (11%)

Nausea (11%)

1-10%

Vomiting (9%)

Ataxia (8%)

Blurred vision (8%)

Tremor (7%)

Nystagmus (5%)

Balance disorder (4%)

Diarrhea (4%)

Injection site discomfort (2.5%)

Depression (2%)

Memory impairment (2%)

Pruritus (2%)

Increased ALT (1%)

Local irritation (1%)

<1%

Anemia

Cerebellar syndrome

Dyspepsia

Hepatitis

Atrial fibrillation/flutter

Atrioventricular block

Mood changes

Muscle spasm

Hypoesthesia

Neutropenia

Xerostomia

Nephritis

Palpitation

Postmarketing Reports

Blood and lymphatic system disorders: Agranulocytosis

Cardiac disorders: Bradycardia

Psychiatric disorders: Hallucination

Skin and subcutaneous tissue disorders: Rash

Contraindications

Hypersensitivity

Cautions

FDA warning on potential suicidal behavior with antiepileptic drugs

Cardiac conduction disorder

Hepatic/renal impairment

Pregnancy

May impair ability to perform hazardous tasks

Withdraw gradually