Propranolol Dosing for Anxiety in Adults
For situational or performance anxiety with prominent somatic symptoms (tremor, palpitations, sweating), take propranolol immediate-release 10–20 mg as a single dose 30–60 minutes before the anxiety-provoking event, with a maximum single dose of 40 mg. 1, 2
Patient Selection: Who Benefits Most
Propranolol is effective only for situational anxiety with physical manifestations—not for chronic daily anxiety or generalized anxiety disorder. 1
Best candidates: Adults facing infrequent, predictable performance situations (public speaking, auditions, presentations) whose primary symptoms are autonomic hyperactivity—tremor, rapid heartbeat, sweating, palpitations. 1, 2
Poor candidates: Individuals with chronic daily anxiety, predominantly psychological symptoms (worry, rumination), or need for continuous treatment should receive SSRIs/SNRIs instead. 1
The Japanese Society of Anxiety and Related Disorders explicitly deprecates propranolol for generalized social anxiety disorder based on negative evidence, endorsing it only for performance-type situations. 1
Dosing Strategies
For Infrequent Performance Anxiety (Preferred Approach)
Take 10–20 mg immediate-release propranolol 30–60 minutes before the event; do not exceed 40 mg as a single situational dose. 1
This "as-needed" strategy is appropriate when anxiety-provoking situations occur infrequently (less than weekly). 1
No baseline daily dosing is required for purely situational use. 1
For Frequent Anxiety Episodes (Chronic Daily Dosing)
If performance situations occur multiple times weekly and warrant continuous coverage:
Start immediate-release propranolol 40 mg twice daily (total 80 mg/day). 1, 3
Titrate to 80–160 mg/day in two divided doses based on symptom control and heart rate response. 1, 3
Alternative: Long-acting propranolol 80 mg once daily, titrating to 120–160 mg once daily for maintenance. 1, 3
Historical data from a 1976 study of 513 anxiety patients found that 80–320 mg daily sufficed for most cases, with rare patients requiring up to 1200 mg temporarily for unusually intense symptoms. 4 However, contemporary guidelines recommend the 80–160 mg range as standard maintenance. 1
Hybrid Dosing (For Patients Also Requiring Antihypertensive Therapy)
- Maintain a baseline antihypertensive dose (e.g., 80 mg/day in divided doses) and add a supplemental 10–20 mg immediate-release dose 30–60 minutes before known anxiety-provoking events; the maximum single situational dose remains 40 mg. 1
Mandatory Pre-Treatment Screening
Before prescribing any dose of propranolol, screen for absolute contraindications—failure to do so risks life-threatening complications. 1, 2
Absolute Contraindications
Asthma or any obstructive airway disease (COPD, reactive airway disease): Non-selective β₂-blockade can precipitate fatal bronchospasm. 1, 2
Second- or third-degree atrioventricular block without a pacemaker: Risk of complete heart block. 1, 2
Decompensated heart failure or cardiogenic shock: Further reduction in cardiac output. 1, 2
Sinus node dysfunction or sinus bradycardia without a pacemaker: Risk of profound heart rate slowing. 1, 2
Severe hypotension (systolic BP < 90 mm Hg). 1
Recent or ongoing hypoglycemic episodes. 1
Required Baseline Assessment
Perform cardiovascular examination with auscultation to detect murmurs, gallops, or irregular rhythms. 1, 2
Screen history for:
Routine laboratory work (CBC, renal, liver, thyroid), ECG, or echocardiogram are NOT required in otherwise healthy adults without cardiac concerns. 1, 2
Critical Safety Warnings
Hypoglycemia Masking in Diabetic Patients
Propranolol blocks adrenergic warning signs of low blood glucose (tremor, rapid heartbeat, sweating); diabetic patients must monitor glucose more frequently and rely on non-adrenergic cues such as hunger, confusion, or sweating to detect hypoglycemia. 1, 2
- Take propranolol with food to reduce hypoglycemia risk. 1
Drug Interactions
Avoid combining propranolol with non-dihydropyridine calcium channel blockers (diltiazem, verapamil)—this combination markedly increases the risk of severe bradycardia and heart block. 1, 3, 2
- Caution is also required when combining with digoxin, amiodarone, or ivabradine due to additive bradycardic effects. 1
Discontinuation Protocol
Never abruptly stop propranolol after regular use—taper gradually over 1–3 weeks to prevent rebound hypertension, tachycardia, or angina. 1, 3, 2
Exception: For purely situational use (single doses taken infrequently), no taper is required when stopping. 1
Temporary hold during acute illness: If the patient develops vomiting, reduced oral intake, or wheezing requiring treatment, propranolol may be held temporarily without taper; restart at a lower dose once oral intake normalizes. 1
Signs of Excessive Beta-Blockade
Monitor patients for:
- Dizziness or light-headedness 1
- Marked fatigue 1
- Heart rate below 50 beats/min 1
- Systolic blood pressure below 90 mm Hg 1
- New or worsening shortness of breath or wheezing 1
Monitoring Requirements
For Situational Use (As-Needed Dosing)
No routine follow-up visits or vital sign monitoring required if the patient remains asymptomatic and uses the medication infrequently. 1
Schedule evaluation only if symptoms of excessive beta-blockade develop. 1
For Chronic Daily Dosing
During dose titration: Monitor for hypotension and bradycardia, especially with dose escalation. 1, 3
Once stable on maintenance therapy: Routine heart rate and blood pressure checks between appointments are not required if the patient is asymptomatic. 1
Common Pitfalls and How to Avoid Them
Pitfall 1: Prescribing for Chronic Generalized Anxiety
Error: Using propranolol as first-line treatment for chronic daily anxiety or generalized anxiety disorder.
Correction: Propranolol is ineffective for chronic anxiety; SSRIs (escitalopram, sertraline) or SNRIs (venlafaxine) are first-line. 1
Pitfall 2: Failing to Screen for Asthma
Error: Prescribing propranolol without asking about wheezing or obstructive airway disease.
Correction: Even mild asthma is an absolute contraindication; if beta-blockade is essential, use a cardioselective agent (metoprolol) at reduced doses with extreme caution. 1
Pitfall 3: Combining with Diltiazem or Verapamil
Error: Co-prescribing propranolol with non-dihydropyridine calcium channel blockers.
Correction: This combination causes severe bradycardia and heart block; avoid routine co-administration. 1, 3
Pitfall 4: Abrupt Discontinuation
Error: Stopping propranolol suddenly after weeks of daily use.
Correction: Taper gradually over 1–3 weeks to prevent rebound hypertension, tachycardia, or angina. 1, 3, 2
Alternative Beta-Blockers When Propranolol Is Unsuitable
If propranolol is contraindicated but beta-blockade is still desired:
| Alternative Agent | Typical Dose | Notes |
|---|---|---|
| Metoprolol tartrate | 25–50 mg per day | β₁-selective; less effective for peripheral tremor; still contraindicated in active asthma. [1] |
| Atenolol | 25–50 mg per day | β₁-selective with renal dosing considerations; same asthma contraindication; not recommended for anxiety due to weaker evidence. [1] |
Both agents are cardioselective (β₁-specific), reducing but not eliminating pulmonary risk. 1
Propranolol's non-selective β₂-blockade is advantageous for anxiety because it attenuates peripheral manifestations (tremor, sweating, palpitations) more effectively than cardioselective agents. 1
Evidence Strength
The recommendation to use propranolol for situational anxiety is supported by strong guideline consensus from the American College of Cardiology, American Heart Association, and Japanese Society of Anxiety and Related Disorders. 1, 2
Dosing ranges (10–40 mg situational; 80–160 mg daily maintenance) reflect Class I evidence from cardiovascular guidelines extrapolated to off-label anxiety use. 1
The 1976 long-term study of 513 anxiety patients provides historical support, though contemporary guidelines favor lower maintenance doses. 4