Terazosin (Hytrin) Dosage and Treatment Protocol for Hypertension and BPH
For benign prostatic hyperplasia (BPH), terazosin should be initiated at 1 mg at bedtime, then gradually titrated to 10 mg once daily for 4-6 weeks to achieve optimal clinical response. 1 For hypertension, terazosin should be started at 1 mg at bedtime and titrated to 1-5 mg once daily, with some patients requiring up to 20 mg daily. 2, 1
Dosing Protocol for BPH
Initial Dosing
- Start with 1 mg at bedtime (never exceed this initial dose) 1
- This low starting dose minimizes risk of severe hypotensive response
- If administration is discontinued for several days, restart with the initial 1 mg dosing regimen 1
Dose Titration for BPH
- Increase dose in stepwise fashion: 1 mg → 2 mg → 5 mg → 10 mg once daily 1
- Doses of 10 mg once daily are generally required for clinical response
- Minimum treatment duration of 4-6 weeks at 10 mg is needed to assess response 1
- Some patients may require up to 20 mg daily, though data supporting this dose is limited 1
Dosing Protocol for Hypertension
Initial Dosing
- Start with 1 mg at bedtime (never exceed this initial dose) 1
- This minimizes potential for severe hypotensive effects
Dose Titration for Hypertension
- Gradually increase dose to achieve desired blood pressure response
- Usual recommended dose: 1-5 mg once daily 1
- Some patients may benefit from doses up to 20 mg daily
- Doses over 20 mg provide no additional blood pressure benefit 1
- Monitor blood pressure at end of dosing interval to ensure 24-hour control
- Consider twice-daily dosing if response diminishes at 24 hours 1
Monitoring and Follow-up
For BPH Management:
- Closely follow patients during initial administration to minimize hypotensive risk 1
- Assess improvement in symptoms and flow rates after 4-6 weeks at target dose 3
- Use International Prostate Symptom Score (IPSS) to quantify symptom improvement 3
- Consider uroflowmetry to assess improvement in urinary flow rates 3
- Monitor for post-void residual volume to detect early signs of urinary retention 3
For Hypertension Management:
- Monitor blood pressure 2-3 hours after dosing to evaluate maximum response 1
- Assess for symptoms of excessive hypotensive response (dizziness, palpitations) 1
- Consider blood pressure measurement at end of dosing interval to ensure 24-hour control 1
Special Considerations and Precautions
Drug Interactions
- Use caution when administering with other antihypertensive agents, especially verapamil 1
- Dose reduction and retitration of either agent may be necessary with concomitant use 1
- Hypotension has been reported when used with PDE-5 inhibitors 1
Blood Pressure Effects
- In normotensive and controlled hypertensive patients, terazosin produces minimal clinically significant changes in blood pressure 4
- In untreated hypertensive patients, terazosin produces substantial decreases in both systolic and diastolic blood pressure 5
- Can be safely added to existing antihypertensive regimens, with greatest impact when added to diuretic therapy alone 6
Side Effects and Management
- Most common side effects: dizziness (2.0%) and headache (1.1%) 5
- Side effects are generally mild to moderate and resolve after stopping therapy 5
- Risk of orthostatic hypotension is low (only 4 of 636 patients or 0.6% experienced syncope in clinical trials) 5
- Advise patients to rise slowly from sitting or lying positions and take medication at bedtime 3
Common Pitfalls to Avoid
- Exceeding initial dose: Never start with more than 1 mg at bedtime to avoid severe hypotension 1
- Inadequate titration period: Allow 4-6 weeks at 10 mg daily to assess BPH response 1
- Failure to restart at initial dose: If therapy is interrupted for several days, restart with 1 mg 1
- Overlooking drug interactions: Use caution with other antihypertensives and PDE-5 inhibitors 1
- Inadequate monitoring: Follow blood pressure closely during initial administration and dose titration 1
Alpha blockers like terazosin are considered first-line therapy for BPH for rapid symptom relief, while for hypertension, they are generally not recommended as first-line agents unless the patient has specific indications. 2, 3