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These brands contain the same active ingredient (Prazosin Hydrochloride). Same strength and form. Confirm the switch with your doctor or pharmacist.
Alphapress XR
Rx2.5 mg • Tablet (Extended Release)
More from Alphapress XR
Other strengths and forms by Renata PLC
Indications & Uses
Prazosin Hydrochloride is used to treat all grades of essential (primary) hypertension, and all grades of secondary hypertension from varied causes. Doctors can give it as the first and only medicine, or as part of a treatment programme alongside a diuretic and/or other antihypertensive drugs, depending on how the patient responds. Long-term oral use does not impair renal blood flow or glomerular filtration rate, so it can be used safely in hypertensive patients with impaired renal function. It is also used for left ventricular failure. Here it can be added to the treatment of patients who have not responded satisfactorily, or who have become refractory, to conventional therapy with diuretics, with or without cardiac glycosides. Prazosin is indicated too for Raynaud's phenomenon and Raynaud's disease. In benign prostatic hyperplasia, it is used as an adjunct in the symptomatic treatment of urinary obstruction caused by the condition, and it is also of value in patients awaiting prostatic surgery.
Pharmacology
Prazosin lowers total peripheral vascular resistance. It does this by selectively blocking postsynaptic alpha-1-adrenoreceptors in the smooth muscle of blood vessels. In people with high blood pressure, it brings the pressure down both lying and standing, and the effect is stronger on the diastolic pressure. Blood pressure does not rebound upward if Prazosin therapy is stopped suddenly.
In congestive heart failure, Prazosin works by reducing left ventricular filling pressure and cardiac impedance, and by increasing cardiac output. It does not cause a reflex tachycardia in these patients, and in people with normal blood pressure the fall in pressure is minimal. In Raynaud's disease, Prazosin reduces the severity of the signs and symptoms, and also the frequency and duration of attacks.
At a low dose, Prazosin blocks alpha-1-receptors on the smooth muscle of the prostate and urethra. This has been shown to improve the urinary pressure profile in men and to ease the symptoms of benign prostatic hyperplasia. Clinical studies have also shown that Prazosin therapy is not linked with adverse changes in the serum lipid profile.
Dosage Reference
Reference Information Only
Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.
Adults:
Prazosin Tablet
Tolerance is best when treatment starts with a low dose. During the first week, adjust the Prazosin dosage to how well the patient tolerates it. After that, adjust the daily dosage according to the patient's response. If a response is going to occur at a particular dose, it is usually seen within one to 14 days. Once a response appears, continue at that dosage until the response has reached its optimum, and only then add the next increment.
Hypertension
For maximum benefit, keep making small increases until the desired effect is reached or the total daily dosage reaches 20 mg. A diuretic or adrenergic beta-blocking agent may be added to improve the effect. The maintenance dosage of Prazosin may be given twice or three times daily.
Patients Receiving No Antihypertensive Therapy
Start with 0.5 mg in the evening at bedtime, then 0.5 mg b.i.d. or t.i.d. for three to seven days. Unless poor tolerance suggests the patient is unusually sensitive, increase this to 1 mg b.i.d. or t.i.d. for a further three to seven days. After that, raise the dosage gradually, guided by how the patient's blood pressure responds, up to a total daily dosage of 20 mg given in divided doses.
Patients Receiving Diuretic Therapy With Inadequate Control of Blood Pressure
Reduce the diuretic to the maintenance dosage level for that particular agent. Then start Prazosin at 0.5 mg h.s. and go on to 0.5 mg b.i.d or t.i.d. After the initial period of observation, increase the Prazosin dosage gradually, as the patient's response decides.
Patients Receiving Other Antihypertensives But With Inadequate Control
Some additive effect is expected, so reduce the dosage level of the other agent (e.g. beta-adrenergic blocking agents, methyldopa, reserpine, lsnidine etc.) and start Prazosin at 0.5 mg h.s., then 0.5 mg b.i.d. or t.i.d. Later dosage increases depend on the patient's response. Adding Prazosin to beta-adrenergic blocking agents, calcium antagonists or ACE inhibitors may bring about a substantial reduction in blood pressure. For that reason, a low initial dosage regimen is strongly recommended.
Patients With Moderate to Severe Grades of Renal Impairment
Evidence to date shows that Prazosin does not further compromise renal function in patients with renal impairment. Some patients in this group have responded to small doses of Prazosin, so start at 0.5 mg daily and make dosage increases cautiously.
Left Ventricular Failure
The recommended starting dose is 0.5 mg two, three or four times a day. Titrate the dosage to the patient's clinical response, based on careful monitoring of cardiopulmonary signs and symptoms and, when indicated, hemodynamic studies. For patients under close medical supervision, titration steps may be done as often as every two or three days. Severely ill, decompensated patients may need rapid titration over one to two days, and this is best done when hemodynamic monitoring is available. Clinical studies used therapeutic dosages from 4 mg to 20 mg daily in divided doses. Some patients may need the dosage adjusted during Prazosin therapy to keep the best clinical improvement.
Suggested Starting Dosage: 0.5 mg b.i.d., t.i.d. or q.i.d. increasing to 4 mg in divided doses.
Usual Daily Maintenance Dosage: 4 mg once daily to 20 mg in divided doses.
Raynaud's Phenomenon And Raynaud's Disease
The recommended starting dosage is 0.5 mg b.i.d. for three to seven days. Adjust the dosage according to the patient's clinical response.
Suggested Starting Dosage: 0.5 mg b.i.d.
Usual Daily Maintenance Dosage: 1 mg or 2 mg b.i.d. Some patients may need doses up to 2 mg t.i.d.
Benign Prostatic Hyperplasia
The recommended starting dose is 0.5 mg twice daily for 3 to 7 days, and it should then be adjusted to the patient's clinical response. The usual maintenance dose is 2 mg twice daily. The safety and efficacy of a total daily dosage greater than 4 mg have not been established, so use total daily dosages above 4 mg with caution.
Prazosin XR Tablet
Prazosin XR Extended-Release Tablets must be swallowed whole. Don't bite or divide them. For hypertension, Prazosin XR must be started at 2.5 mg once daily, and the 5 mg dosage form is not for initial dosing. The dosage may be increased slowly, generally over a 7 to 14-day period, depending on the response to each dose level. Doses above 20 mg once daily have not been studied.
Maintenance Dose
The dosage may be increased as clinically indicated to 20 mg given once daily. Hypertensive patients controlled on Prazosin Tablets alone, or together with other antihypertensive medicines, may be switched to Prazosin XR Extended Release Tablets at the equivalent or nearest higher total daily dose, e.g. Prazosin Tablets 4 mg daily is equivalent to Prazosin XR Extended Release Tablets 5 mg once daily. Take blood pressure measurements at the end of the dosing interval, to confirm that blood pressure control is maintained throughout the 24-hour period. Some patients may need further titration. Adding a diuretic or another antihypertensive agent to prazosin has been shown to cause an additive hypotensive effect.
Side Effects
The most common reactions with Prazosin Hydrochloride are dizziness, headache, drowsiness, lack of energy, weakness, palpitations and nausea. In most cases these side effects have disappeared as treatment continued, or people have tolerated them without the dose being lowered. Other reactions have also been linked with the medicine: vomiting, diarrhoea, constipation, abdominal discomfort and/or pain, liver function abnormalities, pancreatitis, edema, orthostatic hypotension, dyspnea, faintness, tachycardia, nervousness, vertigo, hallucinations, depression, paresthesia, rash, pruritus, alopecia, lichen planus, urinary frequency, impotence, incontinence, priapism, blurred vision, reddened sclera, epistaxis, tinnitus, dry mouth, nasal congestion, diaphoresis, fever, positive ANA titre and arthralgia. Some of these have occurred rarely, and in many cases the exact causal relationship has not been established. Published reports link Prazosin Hydrochloride with a worsening of pre-existing narcolepsy. A causal relationship is uncertain in these cases. Patients being treated for left ventricular failure with Prazosin Hydrochloride, together with cardiac glycosides and diuretics, have shown the following: drowsiness, dizziness, postural hypotension, blurred vision, edema, dry mouth, palpitations, nausea, diarrhoea, impotence, headache and nasal congestion. In most cases these were mild to moderate in severity, and they either resolved as treatment continued or were tolerated without any decrease in the dose. In the treatment of Raynaud's Phenomenon/Disease, the side effect reported most often (though still infrequently) was mild dizziness.
Cautions & Contraindications
Warnings & Precautions
Hypertension A very small percentage of patients have reacted to the first dose of Prazosin Hydrochloride in a sudden and exaggerated way. Postural hypotension has been reported, shown by dizziness and weakness, or rarely loss of consciousness. It happens particularly at the start of therapy. It is easily avoided by starting treatment with a low dose of Prazosin Hydrochloride XR and increasing the dose in small steps during the first one to two weeks. When the effect does appear, it is not related to the severity of the hypertension and it settles by itself. In most patients it does not come back after the initial period of therapy or during later dose titration steps. With any effective antihypertensive medicine, the patient should be told how to avoid symptoms of postural hypotension and what to do if they develop. The patient should also be cautioned to avoid situations where an injury could result if dizziness or weakness occurs while Prazosin Hydrochloride is being started. Left Ventricular Failure Some patients with left ventricular failure have already had vigorous diuretic or other vasodilator treatment. When prazosin is first given to them, particularly in a dose higher than the recommended starting dose, left ventricular filling pressure falls. This may be linked with a significant drop in cardiac output and systemic blood pressure. In these patients it is especially important to keep to the recommended starting dose of prazosin and then titrate gradually (see dosage and administration). In occasional patients with left ventricular failure, the clinical efficacy of Prazosin Hydrochloride has been reported to lessen after several months of treatment. These patients usually show weight gain or peripheral edema, which points to fluid retention. Spontaneous deterioration may occur in such severely ill patients, so a causal relationship to prazosin therapy has not been established. As with all patients with left ventricular failure, the diuretic dose needs careful adjustment according to the patient's clinical condition, to prevent excessive fluid retention and consequent relief of symptoms. In patients with no sign of fluid retention whose clinical improvement has lessened, an increase in the dose of Prazosin Hydrochloride will usually restore clinical efficacy. Raynaud's Phenomenon and Raynaud's Disease Prazosin Hydrochloride lowers peripheral vascular resistance, so blood pressure should be monitored carefully during the first administration and during titration. Close observation is especially recommended for patients who already take medicines known to lower blood pressure. Benign Prostatic Hyperplasia Prazosin Hydrochloride lowers peripheral vascular resistance, and many patients with this disorder are elderly. Careful monitoring of blood pressure is therefore suggested during the first administration and while the dose is being adjusted. Close observation is especially recommended for patients taking medicines known to lower blood pressure.
Contraindications
Prazosin shouldn't be given to anyone who is known to be sensitive to quinazolines.
Pregnancy & Breastfeeding
Animal studies with prazosin showed no teratogenic effects, but its safety in pregnancy has not been established. In one report, prazosin was given with a beta-blocker to control severe hypertension in 44 pregnant women, and no drug-related fetal abnormalities or adverse effects were seen. Treatment with prazosin went on for as long as 14 weeks. Prazosin has also been used on its own, or with other hypotensive agents, for severe hypertension in pregnancy. No fetal or neonatal abnormalities have been reported with its use.
Still, there are no adequate and well controlled studies that establish the safety of prazosin in pregnant women. So it should be used during pregnancy only if the doctor judges that the potential benefit justifies the potential risk to the mother and the fetus.
Prazosin passes into human milk in small amounts. Caution should be taken when it is given to nursing mothers.
⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.
Use in Special Populations
Children
Prazosin Hydrochloride is not recommended for children under 12 years of age, because safe conditions for its use have not been established.
Left Ventricular Failure
Prazosin Hydrochloride should not be used to treat left ventricular failure that is caused by a mechanical obstruction. Examples are aortic valve stenosis, mitral valve stenosis, pulmonary embolism and restrictive pericardial disease. There isn't enough data yet to show that it works in patients whose left ventricular failure is due to a recent myocardial infarction.
Overdose
A two-year-old child who accidentally swallowed at least 50 mg of Prazosin Hydrochloride became very drowsy and had depressed reflexes. Blood pressure did not fall, and the child recovered without any problems.
If an overdose does cause low blood pressure, supporting the cardiovascular system comes first. Keeping the patient lying flat (supine) may be enough to bring blood pressure back and settle the heart rate. If that isn't enough, treat shock first with volume expanders. Vasopressors should be used after that, if needed. Kidney function should be monitored and supported as needed.
Laboratory data show that Prazosin Hydrochloride can't be removed by dialysis, because it is protein bound.
⚠️ In an emergency call 999 or go to the nearest hospital emergency department.
Storage
Store Prazosin Hydrochloride below 30°C, and keep it away from light and moisture. Keep it out of the reach of children.
Drug Interactions
Common questions about Alphapress XR 2.5 mg
What is Alphapress XR 2.5 mg Tablet (Extended Release)?
Alphapress XR 2.5 mg Tablet (Extended Release) is a medicine that contains Prazosin Hydrochloride. It is made by Renata PLC. It belongs to the Alpha adrenoceptor blocking drugs group of medicines.
What is Alphapress XR used for?
Prazosin Hydrochloride is used to treat all grades of essential (primary) hypertension, and all grades of secondary hypertension from varied causes. Doctors can give it as the first and only medicine, or as part of a treatment programme alongside a diuretic and/or other antihypertensive drugs, depending on how the patient responds.
What are the side effects of Alphapress XR?
The most common reactions with Prazosin Hydrochloride are dizziness, headache, drowsiness, lack of energy, weakness, palpitations and nausea. In most cases these side effects have disappeared as treatment continued, or people have tolerated them without the dose being lowered.
Can I take Alphapress XR during pregnancy or while breastfeeding?
Animal studies with prazosin showed no teratogenic effects, but its safety in pregnancy has not been established. In one report, prazosin was given with a beta-blocker to control severe hypertension in 44 pregnant women, and no drug-related fetal abnormalities or adverse effects were seen. Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.
What happens if I take too much Alphapress XR?
A two-year-old child who accidentally swallowed at least 50 mg of Prazosin Hydrochloride became very drowsy and had depressed reflexes. Blood pressure did not fall, and the child recovered without any problems. In an emergency call 999 or go to the nearest hospital emergency department.
How should I store Alphapress XR?
Store Prazosin Hydrochloride below 30°C, and keep it away from light and moisture. Keep it out of the reach of children.
Can I take other medicines with Alphapress XR?
Some medicines can interact with Prazosin Hydrochloride, for example: Insulin (Human) 30/70, Phenobarbitone, Aspirin, Indomethacin, Digoxin, Propranolol Hydrochloride. Tell your doctor or pharmacist about every medicine you take.
Is there a cheaper medicine with the same ingredient?
Alphalok XR by Opsonin Pharma Limited has the same ingredient and strength for ৳10.00 per unit, compared with ৳12.00 for Alphapress XR. Ask your doctor or pharmacist before switching.
Do I need a prescription for Alphapress XR?
Alphapress XR is a prescription (Rx) medicine. Take it as your doctor advises.