mexiletine

REMS

Prophylaxis/treatment of serious ventricular arrhythmias, including ventricular tachycardia.

Unlabeled Use:

Management of chronic neuropathic pain.

Contraind./Precautions ⬆ ⬇

Contraindicated in:

Hypersensitivity;
Cardiogenic shock;
2nd- or 3rd-degree heart block (if a pacemaker has not been inserted);
Lactation: Lactation.

Use Cautiously in:

Sinus node or intraventricular conduction abnormalities;
Hypotension;
HF;
Severe hepatic impairment (dosage ↓ suggested);
OB: Pedi: Safety not established.

Adv. Reactions/Side Effects ⬆ ⬇

CV: palpitations, ARRHYTHMIAS, chest pain, edema

Derm: rash

EENT: tinnitus, blurred vision

GI: nausea, heartburn, vomiting, HEPATIC NECROSIS

Hemat: blood dyscrasias

Neuro: dizziness, nervousness, tremor, coordination difficulties, confusion, fatigue, headache, paresthesia, sleep disorder

Resp: dyspnea

Interactions ⬆ ⬇

Drug-drug:

Opioid analgesics, atropine, and antacids may slow absorption.
Metoclopramide may speed absorption.
Phenytoin, rifampin, cigarette smoking, orphenobarbital may ↑ metabolism and ↓ effectiveness.
Cimetidine may ↑ levels.
May ↑ levels and risk of toxicity from theophylline.
Additive cardiac effects may occur with other antiarrhythmics.
Drugs that drastically alter urine pH may alter blood levels (alkalinization ↑ reabsorption and blood levels; acidification ↑ excretion and ↓ levels).

Drug-Food:

Foods that drastically alter urine pH may alter blood levels. Alkalinization ↑ reabsorption and ↑ levels. Acidification ↑ excretion and may ↓ effectiveness (see Food Sources for Specific Nutrients).

Availability ⬆ ⬇

(Generic available)

Capsules: 100 mg; 150 mg; 200 mg; 250 mg

Route/Dosage ⬆ ⬇

PO (Adults ): 400-mg loading dose initially, then 200 mg 8 hr later, then 200–400 mg q 8 hr; dosage alterations of 50–100 mg may be made q 2–3 days. If controlled on ≤300 mg q 8 hr, can give same daily dose at 12-hr intervals (not to exceed 1200 mg/day). Some patients may require q 6 hr dosing.

US Brand Names ⬆ ⬇

Action ⬆ ⬇

Decreases the duration of the action potential and effective refractory period in cardiac conduction tissue by altering transport of sodium across myocardial cell membranes.
Has little or no effect on heart rate.

Therapeutic effects:

Control of ventricular arrhythmias.

Classifications ⬆ ⬇

Therapeutic Classification: antiarrhythmics (class IB)

Pharmacokinetics ⬆ ⬇

Absorption: Well absorbed from the GI tract.

Distribution: Enters breast milk in concentrations similar to plasma.

Metabolism/Excretion: Mostly metabolized by the liver; 10% excreted unchanged by the kidneys.

Half-Life: 10–12 hr.

Time/Action Profile ⬆ ⬇

(antiarrhythmic effects‡)

ROUTE	ONSET	PEAK	DURATION
PO	30 min–2 hr	2–3 hr	8–12 hr

‡Provided a loading dose has been given.

Patient/Family Teaching ⬆ ⬇

Advise patient to take medication exactly as directed, at evenly spaced intervals, even if feeling well. Missed doses should be taken within 4 hr or omitted. Do not skip or double up on missed doses.
Teach patients to monitor pulse. Advise patient to contact health care professional if pulse rate is <50 bpm or becomes irregular.
May cause dizziness and light-headedness. Caution patient to avoid driving and other activities requiring alertness until response to medication is known.
Instruct patient to avoid changes in diet that may drastically acidify or alkalinize the urine (see Food Sources for Specific Nutrients for foods included).
Advise patient to notify health care professional of disease process and medication regimen prior to treatment or surgery.
Advise patient to notify health care professional if general tiredness, yellowing of the skin or eyes, fever, sore throat, or persistent side effects occur.
Patient should carry identification describing disease process and medication regimen at all times.

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Indications ⬇