Terazosin: Recommended Use and Dosage
Benign Prostatic Hyperplasia (BPH)
Terazosin is an appropriate and effective treatment option for men with lower urinary tract symptoms (LUTS) secondary to BPH, with a recommended titration starting at 1 mg at bedtime and escalating to 10 mg daily for optimal clinical response. 1, 2
Dosing Protocol for BPH
- Initial dose: 1 mg at bedtime—this starting dose must not be exceeded to minimize severe hypotensive response risk 2
- Titration schedule: Increase stepwise to 2 mg, 5 mg, or 10 mg once daily based on symptom improvement and flow rates 2
- Target dose: 10 mg once daily is generally required for clinical response 2
- Treatment duration: A minimum of 4-6 weeks at 10 mg is necessary to assess therapeutic benefit 2
- Maximum dose: Some patients may respond to 20 mg daily, though insufficient data exist to support routine use of higher doses 2
Expected Clinical Outcomes
- Terazosin produces an average 4-6 point improvement in the AUA Symptom Index, which patients perceive as meaningful symptom relief 1
- Peak urinary flow rates increase approximately 50% from baseline 3
- The medication is similarly effective to other alpha-blockers (alfuzosin, doxazosin, tamsulosin) for symptom relief 1
Key Safety Considerations for BPH Treatment
- Primary adverse events: Orthostatic hypotension, dizziness, asthenia, ejaculatory problems, and nasal congestion 1
- Discontinuation rate: Approximately 5% of patients discontinue due to adverse events 4
- Syncope risk: Only 0.6% of patients experience syncopal episodes, typically at initiation or dose escalation 5
- Blood pressure effects: Minimal reductions occur in normotensive patients and those with controlled hypertension; substantial decreases occur in untreated hypertensive patients 5
Critical Pitfall to Avoid
If terazosin administration is discontinued for several days or longer, therapy must be reinstituted using the initial 1 mg dosing regimen—never resume at the previous higher dose. 2
Hypertension
Terazosin should NOT be used as a first-line agent for hypertension management due to safety concerns and availability of more effective alternatives. 6
Dosing for Hypertension (When Used)
- Initial dose: 1 mg at bedtime—strictly observe this to minimize severe hypotensive effects 2
- Titration: Slowly increase to achieve desired blood pressure response 2
- Usual dose range: 1-5 mg once daily 2
- Maximum effective dose: Up to 20 mg daily may benefit some patients; doses over 20 mg provide no additional blood pressure effect 2
- Dosing frequency: Once daily is standard, though twice daily may be considered if 24-hour control is inadequate 2
Place in Hypertension Therapy
- The American College of Cardiology recommends alpha-1 blockers like terazosin are not first-line agents for hypertension 6
- May be considered as second-line agents in patients with concomitant BPH 6
- Critical safety concern: In men with hypertension and cardiac risk factors, alpha-blockers (including doxazosin, similar to terazosin) have been associated with higher incidence of congestive heart failure compared to other antihypertensive agents 1, 6
Important Clinical Caveat
Using an alpha-blocker to manage LUTS should not be assumed to constitute optimal management of concomitant hypertension—patients with hypertension and cardiac risk factors may require separate management with other antihypertensive agents. 1, 6
Drug Interactions
- Exercise caution when combining terazosin with other antihypertensive agents, especially calcium channel blockers like verapamil, to avoid significant hypotension 2
- Dosage reduction and retitration of either agent may be necessary with concomitant use 2
- Hypotension has been reported when terazosin is used with phosphodiesterase-5 (PDE-5) inhibitors 2
Monitoring Recommendations
- Measure blood pressure at the end of the dosing interval to ensure 24-hour control 2
- Consider measuring blood pressure 2-3 hours post-dose to assess maximum response and evaluate symptoms like dizziness or palpitations from excessive hypotensive response 2
- Patients should be closely followed during initial administration to minimize severe hypotensive response risk 2