Terazosin (Monograph)
Drug class: alpha-Adrenergic Blocking Agents
Introduction
Postsynaptic α1-adrenergic blocking agent; quinazoline derivative.1 2 3 4 5 6 8 9 10
Uses for Terazosin
Hypertension
Management of hypertension alone or in combination with other classes of antihypertensive agents.1 3 4 6 8 11 12 13 14 30 31 32 1200
Not considered a preferred agent for initial management of hypertension according to current evidence-based hypertension guidelines, but may be useful in the management of resistant hypertension as a component of combination therapy.501 502 503 504 1200
Most effective when used in combination with a diuretic; beneficial effects of α1-blockers on blood glucose and lipid concentrations also may mitigate some adverse metabolic effects of diuretics.504
Some experts state that an α1-blocker may be a second-line agent in antihypertensive treatment regimens in men with coexisting benign prostatic hyperplasia (BPH);504 1200 however, the American Urology Association (AUA) states that monotherapy with these drugs is not optimal in hypertensive patients with lower urinary tract symptoms (LUTS) or BPH and that such conditions should be managed separately.230
Individualize choice of therapy; consider patient characteristics (e.g., age, ethnicity/race, comorbidities, cardiovascular risk) as well as drug-related factors (e.g., ease of administration, availability, adverse effects, cost).501 502 503 504 515 1200 1201
A 2017 ACC/AHA multidisciplinary hypertension guideline classifies BP in adults into 4 categories: normal, elevated, stage 1 hypertension, and stage 2 hypertension.1200 (See Table 1.)
Source: Whelton PK, Carey RM, Aronow WS et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Hypertension. 2018;71:e13-115.
Individuals with SBP and DBP in 2 different categories (e.g., elevated SBP and normal DBP) should be designated as being in the higher BP category (i.e., elevated BP).
Category |
SBP (mm Hg) |
DBP (mm Hg) |
|
---|---|---|---|
Normal |
<120 |
and |
<80 |
Elevated |
120–129 |
and |
<80 |
Hypertension, Stage 1 |
130–139 |
or |
80–89 |
Hypertension, Stage 2 |
≥140 |
or |
≥90 |
The goal of hypertension management and prevention is to achieve and maintain optimal control of BP.1200 However, the BP thresholds used to define hypertension, the optimum BP threshold at which to initiate antihypertensive drug therapy, and the ideal target BP values remain controversial.501 503 504 505 506 507 508 515 523 526 530 1200 1201 1207 1209 1222 1223 1229
The 2017 ACC/AHA hypertension guideline generally recommends a target BP goal (i.e., BP to achieve with drug therapy and/or nonpharmacologic intervention) of <130/80 mm Hg in all adults regardless of comorbidities or level of atherosclerotic cardiovascular disease (ASCVD) risk.1200 In addition, an SBP goal of <130 mm Hg generally is recommended for noninstitutionalized ambulatory patients ≥65 years of age with an average SBP of ≥130 mm Hg.1200 These BP goals are based upon clinical studies demonstrating continuing reduction of cardiovascular risk at progressively lower levels of SBP.1200 1202 1210
Other hypertension guidelines generally have based target BP goals on age and comorbidities.501 504 536 Guidelines such as those issued by the JNC 8 expert panel generally have targeted a BP goal of <140/90 mm Hg regardless of cardiovascular risk, and have used higher BP thresholds and target BPs in elderly patients501 504 536 compared with those recommended by the 2017 ACC/AHA hypertension guideline.1200
Some clinicians continue to support previous target BPs recommended by JNC 8 due to concerns about the lack of generalizability of data from some clinical trials (e.g., SPRINT study) used to support the 2017 ACC/AHA hypertension guideline and potential harms (e.g., adverse drug effects, costs of therapy) versus benefits of BP lowering in patients at lower risk of cardiovascular disease.1222 1223 1224 1229
Consider potential benefits of hypertension management and drug cost, adverse effects, and risks associated with the use of multiple antihypertensive drugs when deciding a patient's BP treatment goal.1200 1220 1229
For decisions regarding when to initiate drug therapy (BP threshold), the 2017 ACC/AHA hypertension guideline incorporates underlying cardiovascular risk factors.1200 1207 ASCVD risk assessment is recommended by ACC/AHA for all adults with hypertension.1200
ACC/AHA currently recommend initiation of antihypertensive drug therapy in addition to lifestyle/behavioral modifications at an SBP ≥140 mm Hg or DBP ≥90 mm Hg in adults who have no history of cardiovascular disease (i.e., primary prevention) and a low ASCVD risk (10-year risk <10%).1200
For secondary prevention in adults with known cardiovascular disease or for primary prevention in those at higher risk for ASCVD (10-year risk ≥10%), ACC/AHA recommend initiation of antihypertensive drug therapy at an average SBP ≥130 mm Hg or an average DBP ≥80 mm Hg.1200
Adults with hypertension and diabetes mellitus, chronic kidney disease (CKD), or age ≥65 years are assumed to be at high risk for cardiovascular disease; ACC/AHA state that such patients should have antihypertensive drug therapy initiated at a BP ≥130/80 mm Hg.1200 Individualize drug therapy in patients with hypertension and underlying cardiovascular or other risk factors.502 1200
In stage 1 hypertension, experts state that it is reasonable to initiate drug therapy using the stepped-care approach in which one drug is initiated and titrated and other drugs are added sequentially to achieve the target BP.1200 Initiation of antihypertensive therapy with 2 first-line agents from different pharmacologic classes recommended in adults with stage 2 hypertension and average BP >20/10 mm Hg above BP goal.1200
Benign Prostatic Hyperplasia
Reduction of urinary obstruction and relief of associated manifestations in patients with symptomatic BPH.1 5 9 17 18 21 23 25 33
Although drug therapy usually is not as effective as surgical therapy, it may provide adequate symptomatic relief with fewer and less serious adverse effects compared with surgery.59
May consider combined therapy with an α1-adrenergic blocker and 5α-reductase inhibitor for men with bothersome moderate to severe BPH and demonstrable prostatic enlargement.59 Has been more effective than therapy with either drug alone in preventing long-term BPH symptom progression.59 Men at risk for BPH progression are most likely to benefit from combination therapy.59
Terazosin Dosage and Administration
General
BP Monitoring and Treatment Goals
-
Monitor BP regularly (i.e., monthly) during therapy and adjust dosage of the antihypertensive drug until BP controlled.1200
-
If unacceptable adverse effects occur, discontinue drug and initiate another antihypertensive agent from a different pharmacologic class.1216
-
If adequate BP response not achieved with a single antihypertensive agent, either increase dosage of single drug or add a second drug with demonstrated benefit and preferably a complementary mechanism of action (e.g., ACE inhibitor, angiotensin II receptor antagonist, calcium-channel blocker, thiazide diuretic).1200 1216 Many patients will require ≥2 drugs from different pharmacologic classes to achieve BP goal; if goal BP still not achieved with 2 antihypertensive agents, add a third drug.1200 1216
Administration
Oral Administration
Food may delay time to peak plasma concentrations by about 40 minutes but has little effect on extent of absorption.1 28 Manufacturer makes no specific recommendations regarding administration with meals.1
Hypertension
Administer initial dose at bedtime; may administer maintenance doses in the morning.1
Administer once daily or, if needed for optimal BP control, in 2 divided doses at 12-hour intervals.1
BPH
Administer once daily at bedtime.1
Dosage
Available as terazosin hydrochloride; dosage expressed in terms of terazosin.1
Individualize dosage according to patient response and tolerance.1 3 Initiate at low dosage to minimize frequency of postural hypotension and syncope.1
Monitor BP 2–3 hours after dosing and at end of dosing interval to determine whether peak and trough responses are similar and to assess potential manifestations (e.g., dizziness, palpitations) of an excessive response.1
If therapy is interrupted for several days or longer, restart using initial dosage regimen.1
Pediatric Patients
Hypertension† [off-label]
Oral
Some experts have recommended an initial dosage of 1 mg once daily.76 Increase dosage as necessary up to a maximum of 20 mg once daily.76 (See Pediatric Use under Cautions.)
Adults
Hypertension
Oral
Initially, 1 mg daily at bedtime.1 3 May increase dosage gradually to 5 mg daily,1 3 with further titration up to 20 mg daily if BP is not controlled.1
Each increase should be delayed until BP has stabilized at a given dosage.1 3
Usual maintenance dosage: Some experts state 1–20 mg daily, administered as a single dose or in 2 divided doses daily.1200
BPH
Oral
Initially, 1 mg daily at bedtime.1 9 May increase daily dosage to 2 mg and thereafter to 5 mg and 10 mg, if necessary, to reduce symptoms and/or improve urinary flow rates.1 9
Prescribing Limits
Pediatric Patients
Hypertension† [off-label]
Oral
Maximum 20 mg daily.76
Adults
Hypertension
Oral
Maximum 40 mg daily;1 however, dosages >20 mg daily do not appear to improve BP control.1 3
BPH
Oral
Maximum 20 mg daily.1
Special Populations
Hepatic Impairment
Manufacturer makes no specific dosage recommendations; effects on the pharmacokinetics of terazosin have not been elucidated.1
Renal Impairment
Clinically important alterations in the pharmacokinetics of terazosin not observed to date;1 3 28 29 dosage adjustment not necessary.3 28 29 33
Administration of supplemental doses of the drug following hemodialysis does not appear to be necessary.1
Geriatric Patients
Use with caution; generally, increase dosage more slowly in geriatric patients than in younger adults.7 9
Cautions for Terazosin
Contraindications
-
Known hypersensitivity to terazosin, quinazolines (e.g., doxazosin, prazosin), or any ingredient in the formulation.1 33
Warnings/Precautions
Warnings
Postural Hypotension
Marked hypotension, especially in the upright position, can occur; may be accompanied by syncope, palpitations, and other postural effects (e.g., dizziness, lightheadedness, vertigo).1 2 3 4 6 9 13 30
Postural effects are most common after an initial dose, shortly after dosing (e.g., within 90 minutes), when dosage is increased, or when therapy is resumed after an interruption exceeding a few days.1
To decrease risk of excessive hypotension and syncope, initiate therapy at low dose and titrate carefully, lessen level of salt restriction, and avoid diuretics just prior to initiation of terazosin therapy.1 3 4 6 30
Priapism
Priapism reported rarely; may lead to permanent impotence if not treated promptly.1 48 49 (See Advice to Patients.)
General Precautions
Prostate Cancer
Exclude possibility of prostate cancer before initiation of therapy for BPH.1 9
Specific Populations
Pregnancy
Category C.1
Lactation
Not known whether terazosin is distributed into milk.1 Caution if used in nursing women.1
Pediatric Use
Manufacturer states that safety and efficacy not established in patients <21 years of age.1 33
Some experts suggest reserving use of centrally acting antihypertensive agents (e.g., terazosin) for children who do not respond to therapy with 2 or more preferred classes of antihypertensive agents (angiotensin-converting enzyme [ACE] inhibitors, angiotensin II receptor antagonists, long-acting calcium-channel blockers, or thiazide diuretics).1150 1230
Geriatric Use
Geriatric patients may be particularly susceptible to postural effects and other adverse effects.9 (See Geriatric Patients under Dosage and Administration.)
Common Adverse Effects
In the treatment of hypertension: dizziness, headache, asthenia (weakness, tiredness, lassitude, fatigue), nasal congestion, peripheral edema, somnolence, nausea, palpitation.1 3 4 6 13
In the treatment of BPH: dizziness, asthenia, headache, postural hypotension, somnolence.1 9
Drug Interactions
Antihypertensive Agents
Possible rapid fall in BP and exacerbation of postural effects.1 9 Use with caution; may need to reduce and/or retitrate dosage.1
Specific Drugs
Drug |
Interaction |
---|---|
Acetaminophen |
No interaction observed1 |
β-Blockers (e.g., atenolol, propranolol) |
No interaction observed1 |
Allopurinol |
No interaction observed1 |
Antacids |
No interaction observed1 |
Antihistamines (e.g., chlorpheniramine) |
No interaction observed1 |
Captopril |
Increased peak plasma concentrations of terazosin1 |
Codeine |
No interaction observed1 |
Corticosteroids |
No interaction observed1 |
Co-trimoxazole |
No interaction observed1 |
Diazepam |
No interaction observed1 |
Diuretics, thiazide (e.g., hydrochlorothiazide) |
No interaction observed1 |
Erythromycin |
No interaction observed1 |
Hypoglycemic agents |
No interaction observed1 |
NSAIAs (e.g., aspirin, ibuprofen, indomethacin) |
No interaction observed1 |
Sympathomimetic (adrenergic) agents (e.g., phenylephrine, pseudoephedrine) |
No interaction observed1 |
Verapamil |
Increased AUC of terazosin; decreased time to peak plasma terazosin concentrations1 |
Terazosin Pharmacokinetics
Absorption
Bioavailability
Rapidly and almost completely absorbed from the GI tract following oral administration.1 2 Peak plasma concentration attained in about 1 hour.1
Food
Food has minimal effect on extent of absorption; however, time to peak plasma concentration is delayed by about 40 minutes.1 28
Distribution
Extent
Not known whether terazosin is distributed into breast milk.1
Plasma Protein Binding
Elimination
Metabolism
Extensively metabolized in the liver,a with minimal first-pass metabolism.1
Elimination Route
Excreted in urine (40%) and in feces (60%).1
Half-life
Adults: approximately 12 hours.1
Geriatric patients: approximately 14 hours.1
Special Populations
In geriatric patients, plasma clearance is decreased by about 30%.1
Stability
Storage
Oral
Capsules
20–25°C.1 Protect from light and moisture.1
Actions
-
Reduces peripheral vascular resistance and BP as a result of vasodilating effects; produces both arterial and venous dilation.1 3 4 6 10
-
Binds to α1-adrenergic receptors in the prostate and the bladder trigone, resulting in decreased urinary outflow resistance in men.5 9
-
May improve to limited extent the serum lipid profile (e.g., small increases in HDL/total cholesterol ratio; small decreases in LDL, total cholesterol, and triglyceride concentrations).1 3 8 9 10 11 28 31 32
Advice to Patients
-
Possible syncopal and orthostatic symptoms, especially at initiation of therapy; importance of avoiding driving or other hazardous tasks for 12 hours after first dose, a dosage increase, or when resumed after therapy interruption.1 9
-
Importance of sitting or lying down when symptoms of lowered BP occur, and of rising carefully from a sitting or lying position.1
-
Importance of informing clinician if bothersome dizziness, lightheadedness, or palpitations occur.1
-
Possible drowsiness or somnolence; use caution when operating machinery or driving a motor vehicle until effects on individual are known.1 9
-
Importance of men seeking medical treatment if painful or sustained (for hours) erection occurs.1 48 49
-
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1
-
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as concomitant illnesses.1
-
Importance of advising patients of other important precautionary information.1 (See Cautions.)
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Oral |
Capsules |
1 mg (of terazosin)* |
Terazosin Hydrochloride Capsules |
|
2 mg (of terazosin)* |
Terazosin Hydrochloride Capsules |
|||
5 mg (of terazosin)* |
Terazosin Hydrochloride Capsules |
|||
10 mg (of terazosin)* |
Terazosin Hydrochloride Capsules |
AHFS DI Essentials™. © Copyright 2025, Selected Revisions April 10, 2024. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.
† Off-label: Use is not currently included in the labeling approved by the US Food and Drug Administration.
References
1. Abbott Laboratories. Hytrin (terazosin hydrochloride) capsules prescribing information. North Chicago, IL; 2001 Feb.
2. Babamoto KS, Hirokawa WT. Doxazosin: a new α1-adrenergic antagonist. Clin Pharm. 1992; 11:415-27. https://pubmed.ncbi.nlm.nih.gov/1349855
3. Titmarsh S, Monk JP. Terazosin: a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in essential hypertension. Drugs. 1987; 33:461-77. https://pubmed.ncbi.nlm.nih.gov/2885169
4. Khoury AF, Kaplan NM. α-Blocker therapy of hypertension. JAMA. 1991; 266:394-8. https://pubmed.ncbi.nlm.nih.gov/1676077
5. Monda JM, Oesterling JE. Medical treatment of benign prostatic hyperplasia: 5α-reductase inhibitors and α- adrenergic antagonists. Mayo Clin Proc. 1993; 68:670-9. https://pubmed.ncbi.nlm.nih.gov/7688840
6. Itskovitz HD. Alpha1 blockers: safe, effective treatment for hypertension. Postgrad Med. 1991; 89:89-112. https://pubmed.ncbi.nlm.nih.gov/1674822
7. Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. The fifth report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure (JNC V). Arch Intern Med. 1993; 153:154-83. https://pubmed.ncbi.nlm.nih.gov/8422206
8. Anon. Terazosin for hypertension. Med Lett Drugs Ther. 1987; 29:112-3. https://pubmed.ncbi.nlm.nih.gov/2891021
9. Wilde MI, Fitton A, Sorkin EM. Terazosin: a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in benign prostatic hypertrophy. Drugs Aging. 1993; 3:258-77. https://pubmed.ncbi.nlm.nih.gov/7686794
10. Kyncl JJ. Pharmacology of terazosin. Am J Med. 1986; 80(Suppl 5B):12-9. https://pubmed.ncbi.nlm.nih.gov/2872801
11. Deger G. Effect of terazosin on serum lipids. Am J Med. 1986; 80(Suppl 5B):82-5. https://pubmed.ncbi.nlm.nih.gov/2872813
12. Deger G. Comparison of the safety and efficacy of once- daily terazosin versus twice-daily prazosin for the treatment of mild to moderate hypertension. Am J Med. 1986; 80(Suppl 5B):62-7. https://pubmed.ncbi.nlm.nih.gov/2872809
13. Cohen JD. Long-term efficacy and safety of terazosin alone and in combination with other antihypertensive agents. Am Heart J. 1991; 122:919-25. https://pubmed.ncbi.nlm.nih.gov/1678923
14. Ruoff G. Comparative trials of terazosin with other antihypertensive agents. Am J Med. 1986; 80(Suppl 5B):42-8. https://pubmed.ncbi.nlm.nih.gov/2872806
15. 1988 Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. The 1988 report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. Arch Intern Med. 1988; 148:1023-38. https://pubmed.ncbi.nlm.nih.gov/3365073
16. Weber MA, Laragh JH. Hypertension: steps forward and steps backward. The Joint National Committee fifth report. Arch Intern Med. 1993; 153:149-52. https://pubmed.ncbi.nlm.nih.gov/8422205
17. Lepor H, Meretyk S, Knapp-Maloney G. The safety, efficacy and compliance of terazosin therapy for benign prostatic hyperplasia. J Urol. 1992; 147:1554-7. https://pubmed.ncbi.nlm.nih.gov/1375659
18. Lepor H. The emerging role of alpha antagonists in the therapy of benign prostatic hyperplasia. J Androl. 1991; 12:389-94. https://pubmed.ncbi.nlm.nih.gov/1722795
19. Chapple CR, Christmas TJ, Milroy EJ. A twelve-week placebo-controlled study of prazosin in the treatment of prostatic obstruction. Urol Int. 1990; 45(Suppl 1):47-55. https://pubmed.ncbi.nlm.nih.gov/1690482
20. Kirby RS, Coppinger SW, Corcoran MO et al. Prazosin in the treatment of prostatic obstruction. A placebo-controlled study. Br J Urol. 1987; 60:136-42. https://pubmed.ncbi.nlm.nih.gov/2444306
21. Chapple C. Medical treatment for benign prostatic hyperplasia. BMJ. 1992; 304:1198-9. https://pubmed.ncbi.nlm.nih.gov/1381250 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1881763/
22. Andersson KE. Current concepts in the treatment of disorders of micturition. Drugs. 1988; 35:477-94. https://pubmed.ncbi.nlm.nih.gov/3292211
23. Lepor H. Role of long-acting selective alpha-1 blockers in the treatment of benign prostatic hyperplasia. Urol Clin North Am. 1990; 17:651-9. https://pubmed.ncbi.nlm.nih.gov/1695785
24. Kirby RS. Alpha-adrenoceptor inhibitors in the treatment of benign prostatic hyperplasia. Am J Med. 1989; 87(Suppl 2A):26-30S.
25. Chisholm GD. Benign prostatic hyperplasia: the best treatment. BMJ. 1989; 299:215-6. https://pubmed.ncbi.nlm.nih.gov/2475197 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1836932/
26. Geller J. Nonsurgical treatment of prostatic hyperplasia. Cancer. 1992; 70(Suppl 1):339-45. https://pubmed.ncbi.nlm.nih.gov/1376202
27. Garraway WM, Collins GN, Lee RJ. High prevalence of benign prostatic hypertrophy in the community. Lancet. 1991; 338:469-71. https://pubmed.ncbi.nlm.nih.gov/1714529
28. Somberg JC. Terazosin: pharmacokinetics and the effect of age and dose on the incidence of adverse events. Am Heart J. 1991; 122:901-5. https://pubmed.ncbi.nlm.nih.gov/1678920
29. Jungers P, Ganeval D, Pertuiset N et al. Influence of renal insufficiency on the pharmacokinetics and pharmacodynamics of terazosin. Am J Med. 1986; 80(Suppl 5B):94-9. https://pubmed.ncbi.nlm.nih.gov/2872815
30. Sperzel WD, Glassman HN, Jordan DC et al. Overall safety of terazosin as an antihypertensive agent. Am J Med. 1986; 80(Suppl 5B):77-81. https://pubmed.ncbi.nlm.nih.gov/2872812
31. Luther RR, Glassman HN, Estep CB et al. The effects of terazosin and methyclothiazide on blood pressure and serum lipids. Am Heart J. 1989; 117:842-7. https://pubmed.ncbi.nlm.nih.gov/2564723
32. Holtzman JL, Kaihlanen PM, Rider A et al. Concomitant administration of the terazosin and atenolol for the treatment of essential hypertension. Arch Intern Med. 1988; 148:1539-43. https://pubmed.ncbi.nlm.nih.gov/3382300
33. Abbott Laboratories, Abbott Park, IL: Personal communication.
34. National Heart, Lung, and Blood Institute. NHLBI panel reviews safety of calcium channel blockers. Rockville, MD; 1995 Aug 31. Press release.
35. National Heart, Lung, and Blood Institute. New analysis regarding the safety of calcium-channel blockers: a statement for health professionals from the National Heart, Lung, and Blood Institute. Rockville, MD; 1995 Sep 1.
36. Psaty BM, Heckbert SR, Koepsell TD et al. The risk of myocardial infarction associated with antihypertensive drug therapies. JAMA. 1995; 274:620-5. https://pubmed.ncbi.nlm.nih.gov/7637142
37. Yusuf S. Calcium antagonists in coronary artery disease and hypertension: time for reevaluation? Circulation. 1995; 92:1079-82. Editorial.
38. Pfizer Roerig. Cardura (doxazosin mesylate) tablets prescribing information. New York, NY; 1994 Dec.
39. Bruskewitz RC. Benign prostatic hyperplasia: drug and nondrug therapies. Geriatrics. 1992; 47:39-45. https://pubmed.ncbi.nlm.nih.gov/1280242
40. Oesterling JE. Benign prostatic hyperplasia: medical and minimally invasive treatment options. N Engl J Med. 1995; 332:99-109. https://pubmed.ncbi.nlm.nih.gov/7527494
41. Hill SJ, Lawrence SL, Lepor H. New use for alpha blockers: benign prostatic hyperplasia. Am Fam Physician. 1994; 49:1885-8. https://pubmed.ncbi.nlm.nih.gov/7515555
42. Roberts RG. Novel idea in BPH guideline: the patient as decision maker. Am Fam Physician. 1994; 49:1044-51. https://pubmed.ncbi.nlm.nih.gov/7512307
43. Bostwick DG, Cooner WH, Denis L et al. The association of benign prostatic hyperplasia and cancer of the prostate. Cancer. 1992; 70(Suppl 1):291-301. https://pubmed.ncbi.nlm.nih.gov/1376199
44. National Heart, Lung, and Blood Institute National High Blood Pressure Education Program. The sixth report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC VI). Bethesda, MD: National Institutes of Health; 1997 Nov. (NIH publication No. 98-4080.)
45. Kaplan NM. Choice of initail therapy for hypertension. JAMA. 1996; 275:1577-80. https://pubmed.ncbi.nlm.nih.gov/8622249
46. Psaty BM, Smith NL, Siscovich DS et al. Health outcomes associated with antihypertensive therapies used as first-line agents: a systematic review and meta-analysis. JAMA. 1997; 277:739-45. https://pubmed.ncbi.nlm.nih.gov/9042847
47. Whelton PK, Appel LJ, Espeland MA et al. for the TONE Collaborative Research Group. Sodium reduction and weight loss in the treatment of hypertension in older persons: a randomized controlled trial of nonpharmacologic interventions in the elderly (TONE). JAMA. 1998; 279:839-46. https://pubmed.ncbi.nlm.nih.gov/9515998
48. Upjohn Company. Caverject (alprostadil) injection for intracavernosal use prescribing information. Kalamazoo, MI; 1995 Jul.
49. Krane RJ, Goldstein I, Saenz de Tejada I. Impotence. N Engl J Med. 1989; 321:1648-59. https://pubmed.ncbi.nlm.nih.gov/2685600
50. The ALLHAT collaborative research group. Major cardiovascular events in hypertensive patients randomized to doxazosin vs chlorthalidone: the Antihypertensive and Lipid-Lowering treatment to prevent Heart Attack Trial (ALLHAT). JAMA. 2000; 283:1967-75. https://pubmed.ncbi.nlm.nih.gov/10789664
51. Lasagna L. Diuretics vs α-blockers for treatment of hypertension: lessons from ALLHAT. JAMA. 2000; 283:2013-4. https://pubmed.ncbi.nlm.nih.gov/10789671
52. Izzo JL, Levy D, Black HR. Importance of systolic blood pressure in older Americans. Hypertension. 2000; 35:1021-4. https://pubmed.ncbi.nlm.nih.gov/10818056
53. Frohlich ED. Recognition of systolic hypertension for hypertension. Hypertension. 2000; 35:1019-20. https://pubmed.ncbi.nlm.nih.gov/10818055
54. Bakris GL, Williams M, Dworkin L et al. Preserving renal function in adults with hypertension and diabetes: a consensus approach. Am J Kidney Dis. 2000; 36:646-61. https://pubmed.ncbi.nlm.nih.gov/10977801
55. Associated Press (American Diabetes Association). Diabetics urged: drop blood pressure. Chicago, IL; 2000 Aug 29. Press Release from web site. http://www.diabetes.org/newsroom/
56. Appel LJ. The verdict from ALLHAT—thiazide diuretics are the preferred initial therapy for hypertension. JAMA. 2002; 288:3039-60. https://pubmed.ncbi.nlm.nih.gov/12479770
57. The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. 2002; 288:2981-97. https://pubmed.ncbi.nlm.nih.gov/12479763
58. The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. Major outcomes in moderately hypercholesterolemic, hypertensive patients randomized to pravastatin vs usual care: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT). JAMA. 2002; 288:2998-3007. https://pubmed.ncbi.nlm.nih.gov/12479764
59. American Urological Association Practice Guideline Committee. AUA guidelines on management of benign prostatic hyperplasia (2003). Chapter 1: Diagnosis and treatment recommendations. J Urol. 2003; 170:530-47. https://pubmed.ncbi.nlm.nih.gov/12853821
60. Kaplan NM. Initial treatment of adult patients with essential hypertension. Part 2: alternating monotherapy is the preferred treatment. Pharmacotherapy. 1985; 5:195-200. https://pubmed.ncbi.nlm.nih.gov/4034407
61. Bauer JH. Stepped-care approach to the treatment of hypertension: is it obsolete? (unpublished observations)
63. Neal B, MacMahon S, Chapman N. Effects of ACE inhibitors, calcium antagonists, and other blood-pressure-lowering drugs. Lancet. 2000;356:1955-64.
64. Cushman WC, Ford CE, Cutler JA, et al. Success and predictors of blood pressure control in diverse North American settings: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). J Clin Hypertens (Greenwich). 2002;4:393-404.
65. Black HR, Elliott WJ, Neaton JD et al. Baseline characteristics and elderly blood pressure control in the CONVINCE trial. Hypertension. 2001; 37:12-18. https://pubmed.ncbi.nlm.nih.gov/11208750
66. Black HR, Elliott WJ, Grandits G, et al. Principal results of the Controlled Onset Verapamil Investigation of Cardiovascular End Points (CONVINCE) trial. JAMA. 2003;289:2073-2082.
67. Dahlof B, Devereux RB, Kjeldsen SE, et al. Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint Reduction in Hypertension Study (LIFE). Lancet. 2002;359:995-1003.
68. The Heart Outcomes Prevention Evaluation Study Investigators. Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients. N Engl J Med. 2000;342:145-153.
69. PROGRESS Collaborative Group. Randomised trial of a perindopril-based blood-pressure-lowering regimen among 6105 individuals with previous stroke or transient ischaemic attack. Lancet. 2001;358:1033-41.
70. Wing LMH, Reid CM, Ryan P, et al, for Second Australian National Blood Pressure Study Group. A comparison of outcomes with angiotensin-converting-enzyme inhibitors and diuretics for hypertension in the elderly. N Engl J Med. 2003;348:583-92.
72. Hunt SA, Baker DW, Chin MH, et al. ACC/AHA guidelines for the evaluation and management of chronic heart failure in the adult. J Am Coll Cardiol. 2001;38:2101-2113.
74. The Guidelines Subcommittee of the WHO/ISH Mild Hypertension Liaison Committee. 1999 guidelines for the management of hypertension. J Hypertension. 1999; 17:392-403.
76. National High Blood Pressure Education Program Working Group on Hypertension Control in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics. 2004; 114(Suppl 2):555-76. https://pubmed.ncbi.nlm.nih.gov/15286277
230. American Urological Association Panel Members. American Urological Association guideline: Management of benign prostatic hyperplasia (BPH). Linthicum, MD. 2010. From AUA website. http://www.auanet.org
501. James PA, Oparil S, Carter BL et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA. 2014; 311:507-20. https://pubmed.ncbi.nlm.nih.gov/24352797
502. Mancia G, Fagard R, Narkiewicz K et al. 2013 ESH/ESC Guidelines for the management of arterial hypertension: the Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens. 2013; 31:1281-357. https://pubmed.ncbi.nlm.nih.gov/23817082
503. Go AS, Bauman MA, Coleman King SM et al. An effective approach to high blood pressure control: a science advisory from the American Heart Association, the American College of Cardiology, and the Centers for Disease Control and Prevention. Hypertension. 2014; 63:878-85. https://pubmed.ncbi.nlm.nih.gov/24243703
504. Weber MA, Schiffrin EL, White WB et al. Clinical practice guidelines for the management of hypertension in the community: a statement by the American Society of Hypertension and the International Society of Hypertension. J Clin Hypertens (Greenwich). 2014; 16:14-26. https://pubmed.ncbi.nlm.nih.gov/24341872
505. Wright JT, Fine LJ, Lackland DT et al. Evidence supporting a systolic blood pressure goal of less than 150 mm Hg in patients aged 60 years or older: the minority view. Ann Intern Med. 2014; 160:499-503. https://pubmed.ncbi.nlm.nih.gov/24424788
506. Mitka M. Groups spar over new hypertension guidelines. JAMA. 2014; 311:663-4. https://pubmed.ncbi.nlm.nih.gov/24549531
507. Peterson ED, Gaziano JM, Greenland P. Recommendations for treating hypertension: what are the right goals and purposes?. JAMA. 2014; 311:474-6. https://pubmed.ncbi.nlm.nih.gov/24352710
508. Bauchner H, Fontanarosa PB, Golub RM. Updated guidelines for management of high blood pressure: recommendations, review, and responsibility. JAMA. 2014; 311:477-8. https://pubmed.ncbi.nlm.nih.gov/24352759
515. Thomas G, Shishehbor M, Brill D et al. New hypertension guidelines: one size fits most?. Cleve Clin J Med. 2014; 81:178-88. https://pubmed.ncbi.nlm.nih.gov/24591473
523. Fihn SD, Gardin JM, Abrams J et al. 2012 ACCF/AHA/ACP/AATS/PCNA/SCAI/STS guideline for the diagnosis and management of patients with stable ischemic heart disease: a report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines, and the American College of Physicians, American Association for Thoracic Surgery, Preventive Cardiovascular Nurses Association, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons. Circulation. 2012; 126:e354-471.
526. Kernan WN, Ovbiagele B, Black HR et al. Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association. Stroke. 2014; :. https://pubmed.ncbi.nlm.nih.gov/24788967
530. Myers MG, Tobe SW. A Canadian perspective on the Eighth Joint National Committee (JNC 8) hypertension guidelines. J Clin Hypertens (Greenwich). 2014; 16:246-8. https://pubmed.ncbi.nlm.nih.gov/24641124
536. Kidney Disease: Improving Global Outcomes (KDIGO) Blood Pressure Work Group. KDIGO clinical practice guideline for the management of blood pressure in chronic kidney disease. Kidney Int Suppl. 2012: 2: 337-414.
1150. Flynn JT, Kaelber DC, Baker-Smith CM et al. Clinical practice guideline for screening and management of high blood pressure in children and adolescents. Pediatrics. 2017; 140 https://pubmed.ncbi.nlm.nih.gov/28827377
1200. Whelton PK, Carey RM, Aronow WS et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Hypertension. 2018; 71:el13-e115. https://pubmed.ncbi.nlm.nih.gov/29133356
1201. Bakris G, Sorrentino M. Redefining hypertension - assessing the new blood-pressure guidelines. N Engl J Med. 2018; 378:497-499. https://pubmed.ncbi.nlm.nih.gov/29341841
1202. Carey RM, Whelton PK, 2017 ACC/AHA Hypertension Guideline Writing Committee. Prevention, detection, evaluation, and management of high blood pressure in adults: synopsis of the 2017 American College of Cardiology/American Heart Association hypertension guideline. Ann Intern Med. 2018; 168:351-358. https://pubmed.ncbi.nlm.nih.gov/29357392
1207. Burnier M, Oparil S, Narkiewicz K et al. New 2017 American Heart Association and American College of Cardiology guideline for hypertension in the adults: major paradigm shifts, but will they help to fight against the hypertension disease burden?. Blood Press. 2018; 27:62-65. https://pubmed.ncbi.nlm.nih.gov/29447001
1209. Qaseem A, Wilt TJ, Rich R et al. Pharmacologic treatment of hypertension in adults aged 60 years or older to higher versus lower blood pressure targets: a clinical practice guideline from the American College of Physicians and the American Academy of Family Physicians. Ann Intern Med. 2017; 166:430-437. https://pubmed.ncbi.nlm.nih.gov/28135725
1210. SPRINT Research Group, Wright JT, Williamson JD et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med. 2015; 373:2103-16. https://pubmed.ncbi.nlm.nih.gov/26551272
1216. Taler SJ. Initial treatment of hypertension. N Engl J Med. 2018; 378:636-644. https://pubmed.ncbi.nlm.nih.gov/29443671
1220. Cifu AS, Davis AM. Prevention, detection, evaluation, and management of high blood pressure in adults. JAMA. 2017; 318:2132-2134. https://pubmed.ncbi.nlm.nih.gov/29159416
1222. Bell KJL, Doust J, Glasziou P. Incremental benefits and harms of the 2017 American College of Cardiology/American Heart Association high blood pressure guideline. JAMA Intern Med. 2018; 178:755-7. https://pubmed.ncbi.nlm.nih.gov/29710197
1223. LeFevre M. ACC/AHA hypertension guideline: what is new? what do we do?. Am Fam Physician. 2018; 97(6):372-3. https://pubmed.ncbi.nlm.nih.gov/29671534
1224. Brett AS. New hypertension guideline is released. From NEJM Journal Watch website. Accessed 2018 Jun 18. https://www.jwatch.org/na45778/2017/12/28/nejm-journal-watch-general-medicine-year-review-2017
1229. Ioannidis JPA. Diagnosis and treatment of hypertension in the 2017 ACC/AHA guidelines and in the real world. JAMA. 2018; 319(2):115-6. https://pubmed.ncbi.nlm.nih.gov/29242891
1230. Flynn J (American Academy of Pediatrics, Seattle, WA): Personal communication; 2019 Mar 6.
a. Sonders RC. Pharmacokinetics of terazosin. Am J Med. 1986; 80:20-24. https://pubmed.ncbi.nlm.nih.gov/2872802
More about terazosin
- Check interactions
- Compare alternatives
- Pricing & coupons
- Reviews (54)
- Drug images
- Side effects
- Dosage information
- During pregnancy
- Drug class: alpha blockers
- Breastfeeding
- En español