Metoprolol Succinate Dosing for Adults
For most adult indications, metoprolol succinate should be initiated at 50 mg once daily and titrated to a target maintenance dose of 200 mg once daily, with a maximum dose of 400 mg daily. 1, 2
Standard Dosing by Indication
Hypertension
- Initial dose: 50 mg once daily 2
- Maintenance dose: 50-200 mg once daily 2
- Maximum dose: 400 mg once daily 1, 2
- Titration interval: Every 1-2 weeks based on blood pressure response 2
Heart Failure with Reduced Ejection Fraction (HFrEF)
- Initial dose: 12.5-25 mg once daily (start lower in NYHA class III-IV patients) 2, 3, 4
- Target dose: 200 mg once daily 2, 3, 4
- Maximum dose: 400 mg once daily 1
- Titration schedule: Increase dose every 2 weeks if tolerated 2, 3
- Critical principle: At least 50% of target dose (100 mg daily) should be achieved for optimal mortality reduction 2
The MERIT-HF trial demonstrated that this dosing strategy produces a 34% reduction in all-cause mortality, 38% decrease in cardiovascular mortality, and 41% decrease in sudden death 2, 4
Atrial Fibrillation Rate Control
- Initial dose: 50 mg once daily 2
- Maintenance dose: 50-400 mg once daily 1, 2
- Target heart rate: 50-80 bpm (resting) 2
Supraventricular Tachycardia (SVT)
- Initial dose: 50 mg once daily 1
- Maintenance dose: 50-200 mg once daily 1
- Maximum dose: 400 mg once daily 1
Acute Myocardial Infarction Protocol
IV Phase (Early Treatment)
- Dose: 5 mg IV bolus over 1-2 minutes 2, 5
- Repeat: Every 5 minutes as needed 2, 5
- Maximum total IV dose: 15 mg (three 5 mg boluses) 2, 5
- Monitoring required: Continuous blood pressure, heart rate, and ECG during administration 5
Transition to Oral Therapy
- Timing: 15 minutes after last IV dose 2, 5
- Initial oral dose: 50 mg every 6 hours for 48 hours (if full IV dose tolerated) 2, 5
- Alternative: 25 mg every 6 hours if partial IV intolerance 5
- Maintenance dose: 100 mg twice daily after initial 48 hours 5
Critical contraindications before IV administration: Signs of heart failure, low output state, systolic BP <120 mmHg, heart rate >110 bpm or <60 bpm, PR interval >0.24 seconds, second or third-degree heart block, active asthma, or age >70 years with multiple risk factors 2
Special Population Considerations
Women
- Recommended dose reduction: 50% of standard doses on average 2
- Rationale: Metoprolol exposure is 50-80% higher in women than men, resulting in greater heart rate and blood pressure reduction 2
- Evidence: Women with heart failure achieve optimal outcomes at 50% of guideline-recommended doses, with 30% lower risk of death or heart failure hospitalization 2
Elderly Patients (>65 years)
- Initial dose: Start at low end of dosing range 5
- Titration: Cautious gradual dose escalation 5
- Rationale: Greater frequency of decreased hepatic, renal, or cardiac function 5
- Example: In elderly women, 25 mg produces similar drug exposure to 100 mg in healthy young men 2
Hepatic Impairment
- Approach: Initiate at low doses with cautious gradual titration 5
- Rationale: Metoprolol blood levels increase substantially in hepatic impairment 5
Renal Impairment
- Dose adjustment: None required 5
Pharmacokinetic Advantages of Extended-Release Formulation
The extended-release metoprolol succinate formulation delivers metoprolol at a near-constant rate for approximately 20 hours, producing even plasma concentrations over 24 hours without marked peaks and troughs 6. This leads to consistent beta1-blockade over 24 hours while maintaining cardioselectivity at doses up to 200 mg daily 6.
Critical Precautions and Contraindications
Absolute contraindications: 1, 2
- AV block greater than first degree or SA node dysfunction (without pacemaker)
- Decompensated systolic heart failure (for acute administration)
- Active asthma or reactive airway disease
- Cardiogenic shock
- Severe hypotension
Common adverse effects: Hypotension, bradycardia, bronchospasm, fatigue 1, 2
Common Pitfalls to Avoid
- Never abruptly discontinue metoprolol: This can cause severe exacerbation of angina, myocardial infarction, and ventricular arrhythmias, with 50% mortality rate in one study and 2.7-fold increased risk of 1-year mortality 2
- Never give full 15 mg IV dose rapidly or as single bolus: This significantly increases hypotension and bradycardia risk 2
- Do not skip gradual titration in heart failure: Treatment must be initiated at very low doses with gradual incremental increases every 2 weeks 2, 3
- Monitor closely during IV administration: Frequent checks of heart rate, blood pressure, continuous ECG monitoring, and auscultation for rales and bronchospasm are essential 2