Propranolol Dosing Recommendations
For most indications, propranolol should be dosed between 2-3 mg/kg per day in pediatric patients for infantile hemangiomas, and 120-160 mg daily for adults with hypertension, angina, or migraine. 1, 2
Adult Dosing by Indication
Hypertension
- Initial dose: 80 mg once daily with extended-release capsules 2
- Maintenance dose: 120-160 mg once daily 2
- Maximum dose: Up to 640 mg may be required in some cases 2
- Most of the antihypertensive effect occurs at relatively low doses (80-160 mg daily) 3
Angina Pectoris
- Starting dose: 80 mg once daily with extended-release capsules 2
- Typical effective dose: 160 mg once daily 2
- Maximum dose: 320 mg daily (higher doses have not been established as safe or effective) 2
- Dose should be gradually increased at 3-7 day intervals until optimal response 2
Migraine Prophylaxis
- Initial dose: 80 mg once daily with extended-release capsules 2
- Effective dose range: 160-240 mg once daily 2
- Treatment should be discontinued if no satisfactory response after 4-6 weeks at maximal dose 2
Hypertrophic Subaortic Stenosis
- Usual dosage: 80-160 mg once daily with extended-release capsules 2
Pediatric Dosing for Infantile Hemangiomas
- Recommended dose: 2-3 mg/kg per day 1
- Starting dose: 1 mg/kg per day with gradual titration 1
- FDA-approved formulation (Hemangeol): Starting at 0.6 mg/kg twice daily, increasing over 2 weeks to maintenance dose of 1.7 mg/kg twice daily (3.4 mg/kg/day total) 1
- Duration: Minimum 6 months of therapy is superior to 3 months, with many experts recommending continuing until at least 1 year of age 1
Administration Considerations
- Immediate-release formulations: Typically administered 3-4 times daily due to short half-life (3-6 hours) 4
- Extended-release formulations: Administered once daily 2
- When switching from immediate-release to extended-release, retitration may be necessary as they are not mg-for-mg equivalent 2
- Propranolol should be administered with or after feeding, especially in pediatric patients 1
- Doses should be held during times of diminished oral intake or vomiting to reduce hypoglycemia risk 1
Special Populations and Considerations
- Lower doses may be required for patients with:
- For high-risk patients requiring treatment:
Safety Monitoring
- Blood pressure and heart rate should be monitored during treatment, particularly at initiation 4
- Contraindications include asthma, obstructive airway disease, decompensated heart failure, and certain cardiac conduction abnormalities 4
- Severe toxicity risk increases with doses ≥2,000 mg in overdose situations 5