Metoprolol 50 mg Long-Acting: Side Effects and Management
Common Side Effects
The most frequently reported side effects of metoprolol include tiredness and dizziness (occurring in approximately 10% of patients), bradycardia and shortness of breath (approximately 3% of patients), and depression (approximately 5% of patients). 1
Cardiovascular Side Effects
- Bradycardia (heart rate <50 bpm) occurs in approximately 3% of patients and may require dose reduction if symptomatic 1
- Hypotension is usually asymptomatic but can cause dizziness, lightheadedness, or blurred vision 2
- Cold extremities and arterial insufficiency (Raynaud-type) occur in approximately 1% of patients 1
- Peripheral edema and congestive heart failure have been reported in about 1% of patients 1
Central Nervous System Effects
- Tiredness and dizziness are the most common, affecting 10% of patients 1
- Depression occurs in approximately 5% of patients 1
- Mental confusion, short-term memory loss, headache, nightmares, and insomnia have been reported 1
Respiratory Effects
- Bronchospasm and wheezing occur in approximately 1% of patients, particularly concerning in those with underlying reactive airway disease 1
- Dyspnea has been reported 1
Gastrointestinal Effects
- Diarrhea occurs in approximately 5% of patients 1
- Nausea, dry mouth, gastric pain, constipation, and vomiting are common occurrences 1
Other Side Effects
- Pruritus or rash occur in approximately 5% of patients 1
- Blurred vision, tinnitus, and musculoskeletal pain have been reported 1
- Rare reports include reversible alopecia, weight gain, and sexual dysfunction 1
Management of Side Effects
Bradycardia Management
If heart rate falls below 50 bpm with worsening symptoms (dizziness, lightheadedness, or syncope), halve the metoprolol dose immediately. 2
- Review other heart rate-slowing medications (digoxin, amiodarone, diltiazem, verapamil) and consider discontinuation 2
- Obtain an electrocardiogram to exclude heart block 2
- If heart rate remains <45 bpm consistently, hold the dose for 12 hours 3
- Seek specialist advice if symptoms persist after dose reduction 2
Hypotension Management
Asymptomatic low blood pressure does not require treatment changes. 2
For symptomatic hypotension (dizziness, lightheadedness, confusion):
- First, reconsider need for nitrates, calcium-channel blockers, and other vasodilators—reduce or stop these medications if possible 2
- Second, if no signs of congestion are present, consider reducing diuretic dose 2
- Third, if above measures fail, temporarily reduce metoprolol dose by 50% 2
- Never reduce metoprolol first—address other vasodilators and volume status before adjusting beta-blocker 2
Worsening Heart Failure
If increasing congestion develops (dyspnea, fatigue, edema, weight gain >1.5-2.0 kg over 2 days), increase diuretic dose first. 2
- Only halve metoprolol dose if increasing diuretic does not resolve congestion 2
- Monitor daily weights and adjust diuretics accordingly 2
- Rarely necessary to stop metoprolol completely 2
Fatigue Management
Marked fatigue typically resolves spontaneously within several weeks without treatment. 2
- If severe enough to limit function, halve the metoprolol dose 2
- Review patient in 1-2 weeks after dose reduction 2
- Consider reducing diuretic dose if volume depletion is suspected 2
- Discontinue only if fatigue is accompanied by evidence of peripheral hypoperfusion 2
Bronchospasm Management
Metoprolol should generally be avoided in patients with active asthma or severe reactive airway disease. 1
- If bronchospasm develops, ensure beta-2 agonist bronchodilators are readily available 1
- Use the lowest possible dose and consider dividing into three times daily dosing to avoid higher peak plasma levels 1
- Discontinue if severe bronchospasm occurs 1
Critical Warnings
Never Abruptly Discontinue
Abrupt discontinuation of metoprolol can cause severe exacerbation of angina, myocardial infarction, ventricular arrhythmias, and has been associated with 50% mortality in one study. 1, 2
- When discontinuation is necessary, taper gradually over 1-2 weeks 1
- Monitor closely for worsening angina or ischemia during tapering 1
- Beta-blocker withdrawal increases 1-year mortality risk 2.7-fold compared to continuous use 3
Contraindications Requiring Immediate Discontinuation
- Signs of decompensated heart failure or low output state 1, 2
- Second or third-degree heart block without a functioning pacemaker 1
- Cardiogenic shock 1
- Severe bradycardia (<50 bpm) with hemodynamic compromise 2
Drug Interactions to Monitor
- Other heart rate-slowing drugs (digoxin, amiodarone, diltiazem, verapamil) increase bradycardia risk 2
- Calcium channel blockers (especially diltiazem and verapamil) should be discontinued due to negative inotropic effects 2
- NSAIDs may reduce antihypertensive efficacy 2
Overdose Management
In metoprolol overdose, expect bradycardia, hypotension, bronchospasm, and potential cardiovascular collapse. 1, 4
- No specific antidote exists 1
- For hypotension: administer vasopressors (norepinephrine or dopamine) 1
- For bronchospasm: administer beta-2 agonists and/or theophylline 1
- For cardiac failure: consider dobutamine, isoproterenol, or glucagon 1
- Advanced cases may require intravenous lipid emulsion and hyperinsulinemia/euglycemia therapy 4
- Gastric lavage and activated charcoal if recent ingestion 4
Special Populations
Diabetes
Beta-blockers may mask tachycardia associated with hypoglycemia, though dizziness and sweating remain detectable. 1
Pheochromocytoma
Metoprolol must only be used in combination with an alpha-blocker, and only after the alpha-blocker has been initiated. 1