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Alpha-1 Adrenoceptor Antagonist — Raynaud's Phenomenon / Hypertension Pregnancy: UK SPC §4.6 (this replaces the US 'Pregnancy Category C' text previously held on this draft — US pregnancy categories are not used in UK labelling). Pregnancy: prazosin hydrochloride was not teratogenic in rats and rabbits, but although no teratogenic effects were seen in animal testing the safety of prazosin during pregnancy has not yet been established. Use of prazosin with a beta-blocker for the control of severe hypertension in 44 pregnant women revealed no drug-related foetal abnormalities or adverse effects, with therapy continued for as long as 14 weeks; no foetal or neonatal abnormalities have been reported with the use of prazosin hydrochloride, and it has also been used alone or in combination with other hypotensive agents in severe hypertension of pregnancy. Prazosin should be used only when, in the opinion of the physician, potential benefit outweighs potential risk. Breast-feeding: prazosin has been shown to be excreted in small amounts in human milk, so caution should be exercised when it is administered to nursing mothers. Fertility: a decrease in fertility in male and female rats was observed at high, non-clinically relevant doses (225 times the usual maximum recommended human dose), with no adverse effects at doses up to 75 times that dose.

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: SCOPE — this dose text covers both indications named on this page. RAYNAUD'S PHENOMENON AND RAYNAUD'S DISEASE (the page's lead indication): starting dose 500 micrograms twice daily for a period of three to seven days, then adjusted according to the patient's clinical response; usual maintenance dosage is 1 mg or 2 mg twice daily. HYPERTENSION: the dosage range is 500 micrograms to 20 mg daily; initiate at the lowest dose, 500 micrograms twice or three times daily for three to seven days with the starting dose given in the evening, then increase to 1 mg twice or three times daily for a further three to seven days, then increase the daily dose gradually according to the blood-pressure-lowering response — most patients are likely to be maintained on up to 15 mg daily in divided doses, and the maximum recommended daily dosage for hypertension is 20 mg in divided doses. That 20 mg ceiling belongs to the hypertension regimen only: the SPC states no maximum for Raynaud's, where usual maintenance is 1 mg or 2 mg twice daily.
Route: Oral — Hypovase tablets are for oral administration only
Frequency: Raynaud's phenomenon: twice daily. Hypertension: twice or three times daily during initiation and titration.
MAXDOSE DELIBERATELY LEFT BLANK. The only numeric ceiling in the SPC (20 mg daily in divided doses) sits under the Hypertension heading and is the hypertension ceiling. This page leads on Raynaud's phenomenon, for which the SPC gives no maximum and a usual maintenance of only 1 mg or 2 mg twice daily — roughly 2 to 4 mg a day. Surfacing 20 mg/day as this page's maximum would present a 5- to 10-fold overshoot as if it were a Raynaud's target, so the ceiling has been left inside the dose text where it is labelled with the indication it belongs to. FIRST-DOSE HYPOTENSION: a very small percentage of patients may respond in an abrupt and exaggerated manner to the initial dose. Postural hypotension evidenced by dizziness and weakness, or rarely loss of consciousness, has been reported particularly at the commencement of therapy — hence the 500 microgram starting dose given in the evening. §4.4 was cut at the source-fetch limit part-way through this sentence, so the full first-dose precaution text was not retrieved and must be read from the SPC. OTHER INDICATIONS IN THE SAME SPC, RECORDED BUT NOT PART OF THIS PAGE'S PRIMARY DOSE: congestive cardiac failure — recommended starting dose 500 micrograms two, three or four times daily, increasing to 4 mg in divided doses, adjusted to clinical response with careful monitoring of cardiopulmonary signs and symptoms and, when indicated, haemodynamic studies; dosage may be adjusted as often as every two to three days under close medical supervision, and in severely ill decompensated patients rapid adjustment over one to two days may be indicated and is best done where haemodynamic monitoring is available; therapeutic dosages in clinical studies ranged from 4 mg to 20 mg daily in divided doses, with a usual daily maintenance dosage of 4 mg to 20 mg in divided doses. Benign prostatic hyperplasia — 500 micrograms twice daily for 3 to 7 days with the initial dose in the evening, then adjusted to clinical response; usual maintenance 2 mg twice daily, which should not be exceeded unless the patient also requires prazosin as antihypertensive therapy, and such patients should be treated only under the supervision of the practitioner responsible for their hypertension. PATIENTS ALREADY ON OTHER ANTIHYPERTENSIVE THERAPY WITH INADEQUATE CONTROL: reduce the other drug to a maintenance level and initiate prazosin at 500 micrograms in the evening, then continue with 500 micrograms twice or three times daily, increasing gradually according to response; there is evidence that adding prazosin to an ACE inhibitor, beta-adrenergic antagonist or calcium antagonist may produce a substantial reduction in blood pressure, so the low initial dosage regimen is recommended. ELDERLY: the elderly may be more susceptible to hypotension, so initiate therapy with the lowest possible dose. PAEDIATRIC: the SPC states prazosin is not recommended for the treatment of children under the age of 12 years since safe conditions for its use have not been established, and it gives no paediatric dose. Direct any under-18 use to a specialist and to current prescribing references.

Dose adjustments

Renal

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.

Hepatic

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.