Benign prostatic hypertrophy (BPH) - Medications

alfuzosin (UroXatral ®) doxazosin (Cardura ®)
dutasteride (Avodart ®) finasteride (Proscar ®):
tamsulosin (Flomax ®): terazosin (Hytrin ®):

alfuzosin (UroXatral ®) top of page icon

Oral: Adults:
BPH
: 10 mg once daily

Dosage adjustment in renal impairment: Bioavailability and maximum serum concentrations are increased by ~50% with mild, moderate, or severe renal impairment

Note: Safety has not been evaluated in patients with creatinine clearances <30 mL/minute.

Dosage adjustment in hepatic impairment:
Mild hepatic impairment: Use has not been studied.
Moderate or severe hepatic impairment (Child-Pugh class B and C): Clearance is decreased 1 /3 to 1 /4 and serum concentration is increased three- to fourfold; use is contraindicated

Administration
Tablet should be swallowed whole; do not crush or chew. Administer once daily (with a meal); should be taken at the same time each day.

[ Supplied: 10mg extended release tablet.]

doxazosin (Cardura ®)   top of page icon

Mechanism of Action
Competitively inhibits postsynaptic alpha-adrenergic receptors which results in vasodilation of veins and arterioles and a decrease in total peripheral resistance and blood pressure; approximately 50% as potent on a weight by weight basis as prazosin

Oral:  Adults: 1 mg once daily in morning or evening; may be increased to 2 mg once daily. Thereafter titrate upwards, if needed, over several weeks, balancing therapeutic benefit with doxazosin-induced postural hypotension

Hypertension: Maximum dose: 16 mg/day

BPH: Goal: 4-8 mg/day; maximum dose: 8 mg/day

Elderly: Initial: 0.5 mg once daily

[Supplied 1 mg, 2 mg, 4 mg, 8 mg tablets]

dutasteride (Avodart ®)  top of page icon

Mechanism: competitive, selective inhibitor of both reproductive tissues (type 2) and skin and hepatic (type 1) 5alpha-reductase. This results in inhibition of the conversion of testosterone to dihydrotestosterone and markedly suppresses serum dihydrotestosterone levels.

Adult (usual) - (BPH): 0.5 mg orally once daily.

[Supplied: 0.5 mg capsule]

finasteride (Proscar ®):  top of page icon

Use - Propecia®: Treatment of male pattern hair loss in men only . Safety and efficacy were demonstrated in men between 18-41 years of age.
Proscar®: Treatment of symptomatic benign prostatic hyperplasia (BPH); can be used in combination with an alpha blocker, doxazosin
Mechanism of Action- Finasteride is a competitive inhibitor of both tissue and hepatic 5-alpha reductase. This results in inhibition of the conversion of testosterone to dihydrotestosterone and markedly suppresses serum dihydrotestosterone levels

Dosing -  Oral: Adults:
Male:  Benign prostatic hyperplasia (Proscar®): 5 mg/day as a single dose; clinical responses occur within 12 weeks to 6 months of initiation of therapy; long-term administration is recommended for maximal response
Male pattern baldness (Propecia®): 1 mg daily
Female hirsutism (unlabeled use): 5 mg/day

Supplied
Tablet [film coated]:
Propecia®: 1 mg
Proscar®: 5 mg

tamsulosin  (Flomax ®): top of page icon

Mechanism of Action
Tamsulosin is an antagonist of alpha1A adrenoreceptors in the prostate. Smooth muscle tone in the prostate is mediated by alpha1A adrenoreceptors; blocking them leads to relaxation of smooth muscle in the bladder neck and prostate causing an improvement of urine flow and decreased symptoms of BPH. Approximately 75% of the alpha1 receptors in the prostate are of the alpha1A subtype.

Dosage - Oral: Adults:   BPH:   0.4 mg once daily ~30 minutes after the same meal each day; dose may be increased after 2-4 weeks to 0.8 mg once daily in patients who fail to respond. If therapy is interrupted for several days, restart with 0.4 mg once daily.

Dosage adjustment in renal impairment:
Clcr >/= 10 mL/minute: No adjustment needed
Clcr<10 mL/minute: Not studied

[Supplied: 0.4 mg capsule]

terazosin (Hytrin ®):  top of page icon

Mechanism of Action
Alpha1-specific blocking agent with minimal alpha2 effects; this allows peripheral postsynaptic blockade, with the resultant decrease in arterial tone, while preserving the negative feedback loop which is mediated by the peripheral presynaptic alpha2-receptors; terazosin relaxes the smooth muscle of the bladder neck, thus reducing bladder outlet obstruction

Oral: Adults:
Hypertension: Initial: 1 mg at bedtime; slowly increase dose to achieve desired blood pressure, up to 20 mg/day; usual dose range (JNC 7): 1-20 mg once daily

Dosage reduction may be needed when adding a diuretic or other antihypertensive agent; if drug is discontinued for greater than several days, consider beginning with initial dose and retitrate as needed; dosage may be given on a twice daily regimen if response is diminished at 24 hours and hypotensive is observed at 2-4 hours following a dose

Benign prostatic hyperplasia: Initial: 1 mg at bedtime, increasing as needed; most patients require 10 mg day; if no response after 4-6 weeks of 10 mg/day, may increase to 20 mg/day

[Supplied 1, 2, 5, 10 mg capsule]
 

Disclaimer

Listed dosages are for - Adult patients ONLY. PLEASE READ THE DISCLAIMER CAREFULLY BEFORE ACCESSING OR USING THIS SITE. BY ACCESSING OR USING THIS SITE, YOU AGREE TO BE BOUND BY THE TERMS AND CONDITIONS SET FORTH IN THE DISCLAIMER. GlobalRPH does not directly or indirectly practice medicine or provide medical services and therefore assumes no liability whatsoever of any kind for the information and data accessed through the Service or for any diagnosis or treatment made in reliance thereon.

David F. McAuley, Pharm.D., R.Ph.  GlobalRPh Inc.