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Cardiovascular · Drug monograph

Mexiletine: veterinary dose and monograph

Mexiletine is a veterinary cardiovascular drug. Oral class IB antiarrhythmic — essentially an orally available analogue of lidocaine — used in dogs for chronic suppression of VENTRICULAR tachyarrhythmias (ventricular premature complexes, ventricular tachycardia), commonly in dilated… Indications include ventricular premature complexes / ventricular tachycardia (chronic oral control); ventricular arrhythmias of dilated cardiomyopathy (often Boxer/Dobermann/large breeds); combination antiarrhythmic therapy (with sotalol/atenolol) for refractory ventricular ectopy. This monograph lists 2 reference doses for dogs, each with route, frequency and source.

At a glance

Drug class
Cardiovascular
Also known as
Mexitil, Mexilen
Species with doses
Dogs
General dose range
5–8 mg/kg PO q8h — check the species tables for the indication
Routes
PO
Last reviewed
1 October 2026

Indications

  • Ventricular premature complexes / ventricular tachycardia (chronic oral control)
  • Ventricular arrhythmias of dilated cardiomyopathy (often Boxer/Dobermann/large breeds)
  • Combination antiarrhythmic therapy (with sotalol/atenolol) for refractory ventricular ectopy

Mexiletine dose by species

Doses are per administration unless stated. mg/kg doses scale with body weight; per-animal, per-quarter and infusion-rate doses are shown as the reference writes them.

Dogs

Mexiletine doses for dogs
IndicationDoseRouteFrequencyDuration
Ventricular arrhythmia (chronic)5–8 mg/kgPOq8h—
Neuropathic pain / myotonia4–10 mg/kgPOq8h—
  • Ventricular arrhythmia (chronic): Plumb’s p.833: 5–8 mg/kg PO q8h (Fox); 4–10 mg/kg q8h (Hogan); Boxers 5–7.5 mg/kg three times daily with sotalol 1.5–3 mg/kg twice daily, or 5–8 mg/kg q8h with atenolol. Papich 5e: 6 mg/kg q8–12h PO. Always give with food. No safe cat dose (Papich).
  • Neuropathic pain / myotonia: Papich 5e: chronic pain from nerve injury 4–10 mg/kg PO q8h. Plumb’s p.833 (Lorenz 2007): myotonia congenita / myokymia 8.3 mg/kg PO q8h.

Contraindications

High-grade AV block / severe bradyarrhythmia without pacing. Cardiogenic shock. Significant hepatic impairment (hepatic metabolism). Seizure disorders (CNS effects). Known hypersensitivity. Caution combining multiple antiarrhythmics.

Adverse effects

  • GI upset (vomiting, anorexia) — give with food
  • CNS: tremor, ataxia, disorientation (lidocaine-like)
  • Proarrhythmia (less than many agents)
  • Rare: thrombocytopenia, hepatopathy

Drug interactions

  • Sotalol / atenolol: synergistic ventricular arrhythmia control (common, beneficial combination)
  • Hepatic enzyme inducers (phenobarbital, rifampin): lower mexiletine levels
  • CYP inhibitors / cimetidine: raise levels
  • Other antiarrhythmics: additive cardiac and proarrhythmic effects

Pregnancy and lactation

Limited data; use only if the maternal arrhythmia risk outweighs potential fetal risk.

Monitoring

  • ECG / Holter for efficacy and proarrhythmia
  • GI tolerance (give with food)
  • CNS signs (tremor/ataxia)
  • Liver values on long-term therapy

Toxicity and overdose

Overdose causes CNS toxicity (tremor, ataxia, disorientation, seizures) and cardiac effects (bradycardia, hypotension, proarrhythmia). GI upset is the common nuisance at therapeutic doses. Narrow-ish margin warrants titration and ECG follow-up.

Management: No specific antidote. Supportive — control seizures with benzodiazepines, IV fluids, ECG monitoring and cardiovascular support; manage bradyarrhythmia conventionally. Effects abate as the drug is metabolised.

Clinical pearls

  • Think "oral lidocaine" — the practical way to chronically suppress ventricular ectopy after lidocaine has controlled it acutely
  • Frequently combined with sotalol (or atenolol) for synergistic ventricular arrhythmia control in DCM/Boxer ARVC
  • Give with food to limit GI upset; titrate with Holter monitoring
  • Watch for lidocaine-like CNS signs (tremor, ataxia) as the toxicity cue

Mechanism of action

Class IB antiarrhythmic that blocks fast voltage-gated sodium channels (preferentially in depolarised/ischaemic tissue), shortening the action potential and effective refractory period and suppressing abnormal ventricular automaticity and re-entry — with minimal effect on normal conduction or the ECG intervals. Its oral bioavailability gives the chronic-therapy advantage lidocaine lacks.

Formulations and products

  • 50 mg capsule
  • 150 mg capsule
  • Mexitil — 50 / 150 mg capsule, Capsule (human-label)

Storage

Capsules: 15–30 °C, dry, protect from light.

Before you use this dose

Reference doses for veterinary professionals. Confirm the dose against the product label, the patient’s condition, current guidance and local regulations before use; the attending veterinarian remains responsible for every clinical decision.

Frequently asked questions

What is the dose of Mexiletine for dogs?

Reference doses for Mexiletine in dogs: 5–8 mg/kg PO q8h (Ventricular arrhythmia (chronic)); 4–10 mg/kg PO q8h (Neuropathic pain / myotonia). Confirm against the label and the patient before use.

When should Mexiletine not be used?

High-grade AV block / severe bradyarrhythmia without pacing. Cardiogenic shock. Significant hepatic impairment (hepatic metabolism). Seizure disorders (CNS effects). Known hypersensitivity. Caution combining multiple antiarrhythmics.

What are the side effects of Mexiletine in animals?

GI upset (vomiting, anorexia) — give with food; CNS: tremor, ataxia, disorientation (lidocaine-like); Proarrhythmia (less than many agents); Rare: thrombocytopenia, hepatopathy.

Sources

  • Plumb's Veterinary Drug Handbook
  • Merck Veterinary Manual, 11th edition
  • Papich, Papich Handbook of Veterinary Drugs, 5th edition

Last reviewed · VetMasterJi