Betaxolol
Administration
- Type: Beta blocker
- Dosage Forms: 10, 20 mg
- Routes of Administration: Oral
- Common Trade Names: Kerlone
Adult Dosing
- 10-20 mg PO qd
- Start: 10 mg PO qd
- Max: 40 mg/day
- Consider starting 5 mg PO qd in elderly pts
- Taper dose over 2 weeks to D/C
Pediatric Dosing
N/A
Special Populations
- Pregnancy Rating: C; Caution advised in 2nd and 3rd trimesters. Risk of intrauterine growth restriction and neonatal adverse effects including bradycardia and hypoglycemia.
- Lactation risk: L3; Safety unknown
Renal Dosing
- Adult: Severe impairment: Start 5 mg PO qd. May increase by 5 mg/day q 2 weeks to max 20 mg/day.
- Pediatric: N/A
Hepatic Dosing
- Adult: No adjustement
- Pediatric: N/A
Contraindications
- Allergy to class/drug
- Sinus bradycardia
- 2nd or 3rd degree AV block
- Decompensated heart failure
- Cardiogenic shock
- Sick sinus syndrome w/o pacemaker
- Pheochromocytoma, untreated
- Avoid abrupt withdrawal
Adverse Reactions
Serious
- CHF
- Bradycardia, severe
- Heart block
- Angina exacerbation with abrupt D/C
- MI if abrupt D/C
- Ventricular arrhythmia if abrupt D/C
- Bronchospasm
- Hypersensitivity reaction
- Raynaud's phenomenon
- Psoriasis exacerbation
- Lupus erythematosus
Common
- Bradycardia
- Headache
- Dyspepsia
- Dizziness
- Arthralgia
- Fatigue
- Lethargy
- URI
- Dyspnea
- Chest pain
- Pharyngitis
- Diarrhea
Pharmacology
- Half-life: 14-22 hr
- Metabolism: Liver extensively; CYP450: Unknown
- Excretion: Urine > 80% (15% unchanged)
Mechanism of Action
Selectively antagonizes beta-1 adrenergic receptors.
