Prazosin
Brand names: Hypovase
Prazosin is a selective alpha-1 adrenoceptor antagonist used in hypertension, Raynaud's phenomenon and benign prostatic hyperplasia.
Adult dose
Dose adjustments
Patients with moderate to severe grades of renal impairment: evidence to date shows that prazosin does not further compromise renal function when used in patients with renal impairment. As some patients in this category have responded to small doses, it is recommended that therapy be initiated at 500 micrograms daily and that dosage increases be instituted cautiously.
No information is available on use in patients with hepatic dysfunction. Since prazosin normally undergoes substantial first-pass metabolism and subsequent metabolism and excretion by the liver, it is recommended that therapy be initiated at 500 micrograms daily and that dosage increases be instituted cautiously.
Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance, to other quinazolines, to prazosin, or to any of the excipients
Side effects
- Common — dizziness, drowsiness, headache, faintness and syncope
- Common — depression and nervousness; uncommon insomnia; rare hallucinations; rare worsening of pre-existing narcolepsy
- Common — blurred vision and vertigo; uncommon eye pain, reddened sclera and tinnitus
- Common — palpitations; uncommon angina pectoris and tachycardia; rare bradycardia
- Rare — flushing, hypotension, orthostatic hypotension and vasculitis
- Common — dyspnoea and nasal congestion; uncommon epistaxis
- Common — constipation, diarrhoea, dry mouth, nausea and vomiting; uncommon abdominal discomfort and/or pain; rare pancreatitis and liver function abnormalities
- Common — rash; uncommon diaphoresis, pruritis and urticaria; rare alopecia and lichen planus
- Common — urinary frequency; rare incontinence; uncommon impotence; rare gynaecomastia and priapism
- Common — oedema, lack of energy and weakness; rare fever, pain and positive ANA titer; uncommon arthralgia; rare allergic reaction
- In patients managed for left ventricular failure with prazosin plus cardiac glycosides and diuretics, postural hypotension and impotence were common, along with dizziness, blurred vision, dry mouth and nausea
- INCOMPLETE LIST — the §4.8 section was cut at the source-fetch limit within the reporting-of-suspected-adverse-reactions paragraph; the tabulated reactions above were retrieved in full but confirm against the SPC.
Interactions
- Other antihypertensive therapy — prazosin may augment the efficacy of medicines known to lower blood pressure, so close observation is recommended; where control is inadequate on another antihypertensive, reduce that drug to a maintenance level and start prazosin at 500 micrograms in the evening. Adding prazosin to an ACE inhibitor, beta-adrenergic antagonist or calcium antagonist may bring about a substantial reduction in blood pressure, so the low initial dosage regimen is recommended.
- Other alpha-1 antagonists — prazosin should not normally be administered to patients already receiving another alpha-1-antagonist.
- Diuretics or other antihypertensive agents (US labelling — verify vs UK SPC) — additive hypotensive effect, which can be minimised by reducing the prazosin dose to 1 mg to 2 mg three times a day, introducing the additional antihypertensive cautiously, then retitrating prazosin based on clinical response.
- Phosphodiesterase-5 (PDE-5) inhibitors (US labelling — verify vs UK SPC) — additive blood-pressure-lowering effects and symptomatic hypotension; PDE-5 inhibitor therapy should be initiated at the lowest dose in patients taking prazosin.
- US labelling reports no adverse drug interaction in limited clinical experience with cardiac glycosides (digitalis, digoxin), hypoglycaemics (insulin, chlorpropamide, phenformin, tolazamide, tolbutamide), tranquillisers and sedatives (chlordiazepoxide, diazepam, phenobarbital), antigout agents (allopurinol, colchicine, probenecid), antiarrhythmics (procainamide, propranolol, quinidine), or analgesics, antipyretics and anti-inflammatories (propoxyphene, aspirin, indometacin, phenylbutazone).
- Read §4.5 of the SPC for the complete UK interaction list.
- This interaction list may be incomplete — check the full SPC.
Monitoring
- Blood pressure, particularly on initiation and at each dose increase — a very small percentage of patients respond in an abrupt and exaggerated manner to the initial dose, with postural hypotension, dizziness and weakness or rarely loss of consciousness reported especially at the commencement of therapy
- In benign prostatic hyperplasia, careful monitoring of blood pressure during initial administration and dose adjustment is recommended, since many such patients are elderly; prazosin is not recommended for patients with a history of micturition syncope
- In congestive cardiac failure, monitor for weight gain or peripheral oedema indicating fluid retention if clinical efficacy diminishes after several months, and adjust diuretic dosage according to clinical condition
- NOTE: §4.4 was truncated at the source-fetch limit part-way through the hypertension first-dose paragraph, so the complete first-dose precautions were not retrieved — read them from the SPC
Clinical monograph
How it works
It selectively blocks postsynaptic alpha-1 adrenoceptors, causing arterial and venous vasodilatation and reducing peripheral vascular resistance.
Prescribing in practice
- A pronounced first-dose hypotensive effect with collapse can occur, so the first dose should be low and taken on retiring to bed, with caution on subsequent up-titration.
- Use with caution in patients prone to postural hypotension and in the elderly.
- It may cause or worsen urinary incontinence, particularly in women.
Monitoring
Monitor lying and standing blood pressure, especially after the first dose and during dose increases.
Counselling the patient
- Take the first dose at bedtime as it may make you dizzy or faint.
- Stand up slowly, particularly when starting or increasing the dose.
- Be cautious with activities such as driving until you know how it affects you.
Evidence & guidelines
Prazosin is a long-established selective alpha-1 blocker with a recognised first-dose hypotensive effect.
Reference: BSR/BHPR Raynaud's Guidelines; MHRA Drug Safety Update (IFIS); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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