Classes
DEA Class; Rx
Common Brand Names; Tambocor
- Antidysrhythmics, Ib
Description
Oral, Class IB, local anesthetic-type antiarrhythmic; similar to lidocaine and tocainide; used to treat life-threatening ventricular arrhythmias; associated with proarrhythmic effects; also used successfully to treat neuropathic pain due to diabetic neuropathy.
Indications
Indicated Oral, Class IB, local anesthetic-type antiarrhythmic; similar to lidocaine and tocainide; used to treat life-threatening ventricular arrhythmias; associated with proarrhythmic effects; also used successfully to treat neuropathic pain due to diabetic neuropathy.
Contraindications
Hypersensitivity to mexiletine
Cardiogenic shock, preexisting 2°/3° AV block without pacemaker
Adverse Effects
- Nausea (40%)
- Vomiting (40%)
- Heartburn (40%)
- Ataxia (20%)
- Dizziness (20-25%)
- Lightheadedness (11-25%)
- Tremor (13%)
- Coordination difficulties (10%)
- Palpitation (4-7%)
- Hypotension (4-8%)
- Angina (2%)
- Headache (5-7%)
- Depression (2%)
- Xerostomia (3%)
- Proarrhythmia (10-15%)
- Rash (4%)
- Insomnia (5-7%)
- Confusion (5-7%)
- Chest pain (3-8%)
- Abdominal pain (1%)
- Dyspnea (3%)
- Constipation or diarrhea (4-5%)
- Premature ventricular contractions (1-2%)
- Blurred vision (5-7%)
- Nystagmus (6%)
- Edema
- Exacerbation of CHF
- Pulmonary fibrosis
- Proarrhythmia
- Convulsions
- Mouth sores
- Tinnitus
- Systemic lupus erythematosus
Warnings
Use caution in CHF, hypotension, history of seizures
Monitor and adjust dose to prevent QTc prolongation
Patients with second or third-degree heart block may be treated if continuously monitored; use caution when used in such patients or in patients with pre-existing sinus node dysfunction or intraventricular conduction abnormalities
Use in less severe arrhythmias not recommended; avoid in treatment of asymptomatic ventricular premature contractions or conduction disturbances
Some abnormal liver function tests reported in first few weeks of therapy; most have been observed in setting of congestive heart failure or ischemia; patients with liver disease should be followed carefully while receiving therapy; caution should also be observed in patients with hepatic dysfunction secondary to congestive heart failure
Rare instances of severe liver injury, including hepatic necrosis, reported in association with treatment; recommended that patients in whom an abnormal liver test has occurred, or who have signs or symptoms suggesting liver dysfunction, be carefully evaluated; if persistent or worsening elevation of hepatic enzymes is detected, consider discontinuing therapy
Prior to use electrolyte imbalances (especially hypokalemia or hypomagnesemia) must be corrected
Avoid concurrent drug therapy or dietary regimens which may markedly alter urinary pH during therapy; the minor fluctuations in urinary pH associated with normal diet do not affect excretion of drug
Marked leukopenia, agranulocytosis and mild depressions of leukocytes and thrombocytopenia reported (rare); If significant hematologic changes observed, patient should be carefully evaluated, and, if warranted, therapy should be discontinued; blood counts usually return to normal within one month of discontinuation
Pregnancy and Lactation
Pregnancy Category: C
Lactation: enters breast milk at concs comparable to maternal plasma (AAP Committee states compatible w/ nursing)
Maximum Dosage
1200 mg/day PO.
1200 mg/day PO.
1200 mg/day PO or 15 mg/kg/day PO, whichever is less.
15 mg/kg/day PO.
How supplied
Mexiletine hydrochloride
capsule
- 150mg
- 200mg
- 250mg