Alpha-1 blockers (also called alpha-adrenergic blocking agents) constitute a variety of drugs that block alpha-1-adrenergic receptors in arteries, smooth muscles, and central nervous system tissues. By blocking alpha-1 receptors it causes the smooth muscles and arteries to dilate. It is mainly used to treat benign prostatic hyperplasia (BPH), hypertension and post-traumatic stress disorder.
Over the last 40 years variety of drugs has been developed from non-selective alpha-1 blocker to selective alpha-1 blocker. The first drug that was used was non-selective alpha blocker, named phenoxybenzamine and was used to treat BPH. Today tamsulosin is the first line treatment for BPH and is a selective alpha-1 blocker.
Tamsulosin, alpha-1 adrenergic blocker
|Use||Benign prostate hyperplasia, hypertension.|
|Biological target||Alpha-1 adrenergic receptor|
- 1 Medical uses
- 2 Adverse effects
- 3 Interactions and contraindication
- 4 List of alpha-1 blockers
- 5 Pharmacokinetics
- 6 Mechanism of action
- 7 Structure activity relationship (SAR)
- 8 History
- 9 References
- 10 External links
Benign prostatic hyperplasia
Benign prostatic hyperplasia (BPH) is an enlarged prostate gland. Alpha-1 blockers are the most commonly used medicine to treat BPH. Alpha-1 blockers are first line treatment for the symptoms of BPH in men. Doxazosin, terazosin, alfuzosin and tamsulosin have all been well established in treatment to reduce lower urine tract symptoms (LUTS) caused by benign prostatic hyperplasia. They are all believed to be similarly effective for this purpose. First generation alpha-1 blockers, like prazosin are not recommended to treat lower urine tract symptoms because of their blood pressure lowering effect. Second and third generations are recommended though. In some cases alpha-1 blockers have been used in combined therapy with 5-alpha reductase blockers. Dutasteride and tamsulosin are on the market as combined therapy and results have shown that they improve symptoms significantly versus monotherapy.
Alpha-1 blockers are used as second line treatment for high blood pressure. They are not thought to be good as first line treatment because there are other more selective, although they can be good for treating men with hypertension and BPH. Doxazosin have shown to improve symptoms of BPH in elderly and reduce blood pressure at the same time. BPH is very common in men over 60 years old and hypertension as well. Terazosin is also safe and effective to use against hypertension and BPH but is of first generation while doxazosin is second generation alpha-1 blockers.
Post-traumatic stress disorder (PTSD) and nightmares
Post-traumatic stress disorder is a disabling condition that can be caused by after some kind of life-threatening trauma. It is common in veteran soldiers who have experienced some kind of trauma. Prazosin which is commonly used as antihypertension but because of the alpha-1 adrenergic activity of Prazosin, that activity has been connected to fear and startle responses. Prazosin has been established as an effective and safe, brain active alpha-1 adrenergic receptor antagonist. It can be used against trauma nightmares, sleep disturbance and chronic PTSD.
As Alpha-1-a blockers affect the symptoms of BPH more specifically than the Alpha-1 blockers, the adverse effects seem to be more linked to the reproductive system while minimizing the effect on the blood-pressure system. Hypotension and its complications (such as weakness and dizziness) are a constant risk, however, even though a selective alpha-1a blocker is being used. It is therefore important when starting treatment with an alpha-1 blocker to monitor the blood pressure to minimize the risk for adverse effects connected to low blood pressure.
|Selectivity||Adverse effects||Main hepatic pathway|
|Prazosin||Alpha-1||Dizziness, headache, drowsiness, asthenia, weakness, palpitations, nausea, vomiting, diarrhea, constipation, edema, hypotension, dyspnea, vertigo, nervousness, rash, blurred vision||CYP1A1|
|Terazosin||Alpha-1||Nervousness, vertigo, palpitations, tachycardia, chest pain, hypotension, dyspnoea, nausea, constipation, diarrhoea, vomiting, pruritus, rash, back pain, impotence, dizziness, asthenia, oedema, headache, pain (extreme)||CYP3A1|
|Doxazosin||Alpha-1||Hypotension (dizziness and weakness), priapism (prolonged erection), floppy iris syndrome during cataract surgery, vertigo, palpitation/tachycardia, bronchitis, cough, dyspnea, pruritus, back pain, cystitis, asthenia, peripheral oedema, retrogade ejaculation||CYP3A4|
|Silodosin||Alpha-1-a||Problem with ejaculation/orgasm, hypotension, dizziness, nasal congestion, diarrhoea||CYP3A4|
|Alfuzosin||Alpha-1-a||Dizziness(due to hypotension), upper respiratory tract infection, headache, fatigue, impotence, pain in whole body, bronchitis, gastro-intestinal pain, swelling, rash, difficulty swallowing or breathing, chest pain, fainting, hoarsing||CYP3A4|
|Tamsulosin||Alpha-1-a||Hypotension, problem with ejaculation/orgasm, disorientation, headache, floppy iris syndrome during cataract surgery||CYP3A4 & CYP2D6|
By reducing alpha-1-adrenergic activity of the blood vessels, these drugs may cause hypotension (low blood pressure) and interrupt the baroreflex response. In doing so, they may cause dizziness, lightheadedness, or fainting when rising from a lying or sitting posture (known as orthostatic hypotension or postural hypotension). For this reason, it is generally recommended that alpha blockers should be taken at bedtime. The risk of first dose phenomenon may be reduced or eliminated by gradual-dose titration, since the adverse effects of Prazosin are dose-related. This is also the case for Tamsulosin and it may be assumed that the others alpha-1 blockers work in a similar manner, since Tamsulosin is an alpha-1-a blocker and Prazosin is an alpha-1 blocker. The risk for floppy iris syndrome during cataract surgery is elevated when the patient is using an alpha-1 blocker. This is especially the case for Tamsulosin and other alpha-1-a blockers, since alpha-1-a receptors are present also in the iris dilator muscle, which allows unopposed action of the parasympathetically innervated iris constrictor muscle and loss of iris tone. This however can be treated if the eye surgeon is experienced and has knowledge of the use of alpha-1 blocker.
Interactions and contraindication
Contraindication : Allergies or hypersensitivity to alpha-1 blockers or any of the active ingredient, that includes angiodema induced by the drug. Patients with a history of orthostatic hypotension or severe hepatic impairment.
Interactions : No interactions were recorded when administered with atenolol (beta blocker), enalapril (ACE inhibitor) and theophylline. Furosemide has drop effect on plasma level for tamsulosin, and a rise in plasma level with cimetidine. No dose adjustment needs to be done when the levels are in normal range. Drugs that inhibit CYP3A4 for example itraconazol, ketoconazol and ritonavir can increase drug exposure for tamsulosin, alfuzosin, doxazosin and silodosin. Grapefruit is also a powerful inhibitor of the CYP3A4 enzyme, so concurrent use is not recommended as it may increase the plasma levels of the Alpha-1 blockers which are metabolised by the CYP3A4 enzyme. Some drugs; such as Fluoxetine, Paroxetine and Ritonavir are strong inhibitors of the CYP2D6 enzyme and therefore it is not recommended to use at the same time as tamsulosin, as it may increase plasma levels of tamsulosin and increase the risk of adverse effects.
Since alpha-1 blockers may cause orthostatic hypotension, co-administration with antihypertensives and vasodilators must be evaluated with regards to risk-benefit as the risk for low blood pressure is greatly increased.
By reducing α1-adrenergic activity of the blood vessels, these drugs may cause hypotension (low blood pressure) and interrupt the baroreflex response. In doing so, they may cause dizziness, lightheadedness, or fainting when rising from a lying or sitting posture (known as orthostatic hypotension or postural hypotension). For this reason, it is generally recommended that alpha blockers should be taken at bedtime. Additionally, the risk of first dose phenomenon may be reduced by starting at a low dose and titrating upwards as needed.
Because these medications may cause orthostatic hypotension, as well as low blood pressure in general, these agents may interact with other medications that increase risk for low blood pressure, such as other antihypertensives and vasodilators.
As discussed above, tamsulosin may have less risk for low blood pressure and orthostatic hypotension due to its selectivity for α1a-adrenergic receptors. On the other hand, the drug (a) elevates risk for floppy iris syndrome, and (b) might show adverse drug reactions (ADRs) characteristic of the sulfa related drugs.
List of alpha-1 blockers
|Alpha-1 inhibitor||Structure||Use||Brand name||Selectivity|
||Hypertension, PTSD and nightmares||Minipress, Vasoflex, Lentopres and Hypovase.||Alpha-1|
||Hypertension and BPH||Hytrin, Zaysel and Terazosin||Alpha-1|
||Hypertension and BPH||Cardura and Carduran||Alpha-1|
||BPH||Rapaflo, Silodyx, Rapilif, Urief, Trupas, Urorec||Alpha-1a|
||BPH||Uroxatral, Xat, Xatral, Prostetrol and Alfural.||Alpha-1a|
||BPH||Alna, Flomax, Omnic||Alpha-1a|
Silodosin shows high affinity and selectivity for alpha-1a adrenergic receptors found in the prostate which ensures that it works quickly and effectively to relieve the symptoms of BPH. Silodosin's low affinity for alpha-1b receptors in the blood vessels is thought to be reflected in its low incidence of orthostatic and vasodilatory side effects.
Absorption : Bioavailability of tamsulosin and terazosin is around 90% during oral administration in fasting state. Food can have effect on absorption for tamsulosin if it has been ingested shortly before, Tmax for fasting state is 2,9-5,6 hours compared to 5,2–7 hours in fed state. Food has no effect on absorption of terazosin but can delay plasma level concentration for 1 hour, peak plasma level are around 1–2 hours. Alfuzosin bioavailability under fed state is around 49%. Tmax is 8 hours in fed state. Tamsulosin Cmax range was 13.9-18,6 ng/mL fastest and in fed state 7,2-15,6 ng/mL, Cmax for alfuzion is 13,6 mg/mL.
Distribution : Tamsulosin is 99% bound to plasma and distribution volume is low 0,2l/kg. Alfuzosin is 90% bound to plasma and distribution volume is 2,5l/kg. Terazosin is 90-94% bound to plasma.
Elimination : Elimination half-life for alfuzosin is around 8 hours, alfuzosin is metabolised mainly via liver. 75-91% is excreted in feces and 35% in unchanged form. Distribution volume and excretion increases with renal impairment do to less protein binding, but the half-life elimination rate is unchanged. therefore no dose adjustment is needed for low to moderate renal impairment. Delay in elimination half-life, peak concentration in plasma is double and bioavailability is changed in hepatic impairment patients. Alfuzosin should not be used for patients with renal impairment. Tamsulosin is excreted via urine and 9% of that is unchanged on its active form, elimination half-life for tamsulosin is between 9–13 hours for healthy volunteers. The elimination half-life for target patients is around 14–15 hours. No dose adjustment is needed for patients with renal impairment and moderate hepatic impairment. 10-20% of terazosin is excreted unchanged in urine and feces during oral administration. 40% is eliminated in urine and 60% in feces. Eliminations half-life for terazosin is between 8–13 hours. No dose adjustment is needed for patients with renal impairment. Terazosin is metabolised by the liver and is excreted by the bilary tract, so patients with moderate hepatic impairment should receive titrated doses of terazosin witch caution. Patients with severe hepatic impairment should not take terazosin do to lack of clinical data.
Mechanism of action
Alpha-1 blockers inhibit norepinephrine which inhibits the blood vessels from contraction. It happens because alpha 1 blockers inhibit the activation of post-synaptic alpha-1 receptors by releasing catecholamines and/or the circulation which are neural. Alpha-1 blockers have no effect on renin release or cardio output.
Benign prostatic hyperplasia
Alpha-1 blocker, blocks alpha receptors and it relaxes the smooth muscles in the bladder. It helps the urine to flow smoothly and it can lessen the pain. from the bladder pressing on the prostate. Selective alpha-1 blockers are better tolerated than non-selective alpha blockers in the body and therefore works better on BPH. Terazosin, tamsulosin and doxazosin are prime drug for BPH because they have a long half-life and modified release formulation. Tamsulosin is primarily used because it doesn't affect the blood pressure and the side effects of vasodilation is minimum.
Alpha-1 blocker lowers the blood pressure by blocking alpha-1 receptors so norepinephrine can't bind the receptor and it causes the blood vessels to dilate. Without the resistance in the blood vessels the blood runs more freely. Alpha-1 blockers have a good effect on lipoproteins in plasma, insulin resistance and it causes the glucose levels in blood to lower.
Structure activity relationship (SAR)
By changing the furan ring in prazosin to tetrahydrofuran ring (as in alfuzosin) the half-life is greatly increased, allowing once-a-day dosing. Silodosin is the most selective for alpha-1a receptors. The affinity and selectivity for alpha-1 receptors seems to be determined by structure between the quinazoline and the furan ring. Piperazine is present in prazosin, terazosin and doxazosin which seems to contribute to the non-selective inhibition of alpha-1 receptors.
Doxazosin 2,4-diamino-6,7-dimethoxyquinazoline variations for in vitro and in vivo performance. A key factor in these structures was the derivations from 2,4-diamino-6,7-dimethoxyquinazoline nucleus that was replaced for norepinephrine. And N-1 which protonated quinazoline was also a key factor.
Tamsulosin is most potent alpha 1 blocker and has the most selectivity for alpha 1a blockers. It doesn't do anything for beta-adrenoceptors because it lacks beta-hydroxyl group and therefor can not block beta-receptors.
The first effective treatment for benign prostatic hyperplasia (BPH) was non-selective alpha blocker phenoxybenzamine which was irreversible. Dibenzyline was the first brand name marketed. Today phenoxybenzamine is not the first choice due to many side effects like lowering blood pressure.
First selective alpha-1 blocker that was approved to treat hypertension was prazosin. Prazosin was synthesized in 1974 when Constantin and Hess were trying to discover a vasodilator which had a minimal effect on cardiac activity. Prazosin is a much better tolerated drug than phenoxybenzamine but the problem that still remained was it lowered the blood pressure to much.
Terazosin was the first long lasting alpha 1 blocker approved by FDA to treat BPH. Doxazosin and Tamsulosin was approved after. The first line treatment choice today to treat BPH is tamsulosin. It is not because it is better tolerated or had greater efficacy than the previous drugs. Only because of the minimal dose titration. Alfuzosin SR (sustained release) was the fourth alpha 1 selective blocker to be approved by FDA. It is used to treat BPH and the good thing about Alfuzosin SR is, it doesn´t need a dose titration. Over 30 years of improving alpha 1 blockers for BPH it has been primarily focused on tolerance and good use.
- Nickel, J. Curtis; Méndez-Probst, Carlos E.; Whelan, Thomas F.; Paterson, Ryan F.; Razvi, Hassan (October 2010). "2010 Update: Guidelines for the management of benign prostatic hyperplasia". Canadian Urological Association Journal. 4 (5): 310–316. doi:10.5489/cuaj.10124. ISSN 1911-6470. PMC . PMID 20944799.
- Lepor, Herbert (2007). "Alpha Blockers for the Treatment of Benign Prostatic Hyperplasia". Reviews in Urology. 9 (4): 181–190. ISSN 1523-6161. PMC . PMID 18231614.
- Stanaszek, W. F.; Kellerman, D.; Brogden, R. N.; Romankiewicz, J. A. (April 1983). "Prazosin update. A review of its pharmacological properties and therapeutic use in hypertension and congestive heart failure". Drugs. 25 (4): 339–384. doi:10.2165/00003495-198325040-00002. ISSN 0012-6667. PMID 6303744.
- Carruthers, S. G. (July 1994). "Adverse effects of alpha 1-adrenergic blocking drugs". Drug Safety. 11 (1): 12–20. doi:10.2165/00002018-199411010-00003. ISSN 0114-5916. PMID 7917078.
- Chapple, C. R. (1996). "Selective alpha 1-adrenoceptor antagonists in benign prostatic hyperplasia: rationale and clinical experience". European Urology. 29 (2): 129–144. ISSN 0302-2838. PMID 8647139.
- Lepor, H. (1990). "Role of alpha-adrenergic blockers in the treatment of benign prostatic hyperplasia". The Prostate. Supplement. 3: 75–84. ISSN 1050-5881. PMID 1689172.
- Sokhal, Ashok Kumar; Sankhwar, Satyanarayan; Goel, Apul; Singh, Kawaljit; Kumar, Manoj; Purkait, Bimalesh; Saini, Durgesh Kumar (2017-08-30). "A Prospective Study to Evaluate Sexual Dysfunction and Enlargement of Seminal Vesicles in Sexually Active Men Treated for Benign Prostatic Hyperplasia by Alpha Blockers". Urology. doi:10.1016/j.urology.2017.08.025.
- Tanguay, Simon; Awde, Murray; Brock, Gerald; Casey, Richard; Kozak, Joseph; Lee, Jay; Nickel, J. Curtis; Saad, Fred (June 2009). "Diagnosis and management of benign prostatic hyperplasia in primary care". Canadian Urological Association Journal. 3 (3 Suppl 2): S92–S100. ISSN 1911-6470. PMC . PMID 19543429.
- Roehrborn, Claus G.; Siami, Paul; Barkin, Jack; Damião, Ronaldo; Major-Walker, Kim; Morrill, Betsy; Montorsi, Francesco (2008-02-01). "The Effects of Dutasteride, Tamsulosin and Combination Therapy on Lower Urinary Tract Symptoms in Men With Benign Prostatic Hyperplasia and Prostatic Enlargement: 2-Year Results From the CombAT Study". The Journal of Urology. 179 (2): 616–621. doi:10.1016/j.juro.2007.09.084.
- Bryson CL, Chris L.; Psaty BM MD PhD, Bruce M. (2002-04-12). "A Review of the Adverse Effects of Peripheral Alpha-1 Antagonists in Hypertension Therapy". Current Controlled Trials in Cardiovascular Medicine. 3 (1): 7. doi:10.1186/1468-6708-3-7. ISSN 1468-6708. PMC . PMID 12097149.
- Weinberger, M. H.; Fawzy, A. (April 2000). "Doxazosin in elderly patients with hypertension". International Journal of Clinical Practice. 54 (3): 181–189. ISSN 1368-5031. PMID 10829361.
- Peskind, Elaine R.; Bonner, Lauren T.; Hoff, David J.; Raskind, Murray A. (September 2003). "Prazosin reduces trauma-related nightmares in older men with chronic posttraumatic stress disorder". Journal of Geriatric Psychiatry and Neurology. 16 (3): 165–171. doi:10.1177/0891988703256050. ISSN 0891-9887. PMID 12967060.
- Taylor, Fletcher; Raskind, Murray A. (February 2002). "The alpha1-adrenergic antagonist prazosin improves sleep and nightmares in civilian trauma posttraumatic stress disorder". Journal of Clinical Psychopharmacology. 22 (1): 82–85. doi:10.1097/00004714-200202000-00013. ISSN 0271-0749. PMID 11799347.
- Raskind, Murray A.; Peskind, Elaine R.; Hoff, David J.; Hart, Kimberly L.; Holmes, Hollie A.; Warren, Daniel; Shofer, Jane; O’Connell, James; Taylor, Fletcher (2007-04-15). "A Parallel Group Placebo Controlled Study of Prazosin for Trauma Nightmares and Sleep Disturbance in Combat Veterans with Post-Traumatic Stress Disorder". Biological Psychiatry. 61 (8): 928–934. doi:10.1016/j.biopsych.2006.06.032.
- Yoshida, Masaki; Kudoh, Junzo; Homma, Yukio; Kawabe, Kazuki (2011). "Safety and efficacy of silodosin for the treatment of benign prostatic hyperplasia". Clinical Interventions in Aging. 6: 161–172. doi:10.2147/CIA.S13803. ISSN 1176-9092. PMC . PMID 21753871.
- Hisasue, Shin-Ichi; Furuya, Ryoji; Itoh, Naoki; Kobayashi, Ko; Furuya, Seiji; Tsukamoto, Taiji (2006-10-01). "Ejaculatory disorder caused by alpha-1 adrenoceptor antagonists is not retrograde ejaculation but a loss of seminal emission". International Journal of Urology. 13 (10): 1311–1316. doi:10.1111/j.1442-2042.2006.01535.x. ISSN 1442-2042.
- Preissner, Saskia; Kroll, Katharina; Dunkel, Mathias; Senger, Christian; Goldsobel, Gady; Kuzman, Daniel; Guenther, Stefan; Winnenburg, Rainer; Schroeder, Michael (January 2010). "SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions". Nucleic Acids Research. 38 (Database issue): D237–243. doi:10.1093/nar/gkp970. ISSN 1362-4962. PMC . PMID 19934256.
- Oh, E Y; Bae, S K; Kwon, J W; You, M; Lee, D C; Lee, M G (May 2007). "Pharmacokinetic and pharmacodynamic consequences of inhibition of terazosin metabolism via CYP3A1 and/or 3A2 by DA-8159, an erectogenic, in rats". British Journal of Pharmacology. 151 (1): 24–34. doi:10.1038/sj.bjp.0707192. ISSN 0007-1188. PMC . PMID 17351661.
- Hammond, Kyle P.; Nielsen, Craig; Linnebur, Sunny A.; Langness, Jacob A.; Ray, Graham; Maroni, Paul; Kiser, Jennifer J. (2014-01-01). "Priapism Induced by Boceprevir-CYP3A4 Inhibition and α-Adrenergic Blockade: Case Report". Clinical Infectious Diseases. 58 (1): e35–e38. doi:10.1093/cid/cit673. ISSN 1058-4838. PMC . PMID 24092799.
- Rossi, Maxime; Roumeguère, Thierry (2010-10-27). "Silodosin in the treatment of benign prostatic hyperplasia". Drug Design, Development and Therapy. 4: 291–297. doi:10.2147/DDDT.S10428. ISSN 1177-8881. PMC . PMID 21116335.
- Doligalski, Christina Teeter; Tong Logan, Angela; Silverman, Andrew (June 2012). "Drug Interactions". Gastroenterology & Hepatology. 8 (6): 376–383. ISSN 1554-7914. PMC . PMID 22933873.
- Franco-Salinas, Gabriela; de la Rosette, Jean J. M. C. H.; Michel, Martin C. (March 2010). "Pharmacokinetics and pharmacodynamics of tamsulosin in its modified-release and oral controlled absorption system formulations". Clinical Pharmacokinetics. 49 (3): 177–188. doi:10.2165/11317580-000000000-00000. ISSN 1179-1926. PMID 20170206.
- "General effect of low-dose tamsulosin (0.2mg) as a first-line treatment for lower urinary tract symptoms associated with benign prostatic hyperplasia: A systematic review and meta-analysis (PDF Download Available)". ResearchGate. Retrieved 2017-09-26.
- Brogden, PR; Backhouse, OC; Saldana, M (2007). "Intraoperative floppy iris syndrome associated with tamsulosin". Can Fam Physician. 53: 1148. PMC . PMID 17872808.
- "Flomax (Tamsulosin Hydrochloride): Side Effects, Interactions, Warning, Dosage & Uses". RxList. Retrieved 2017-09-28.
- Roehrborn, C. G. (December 2001). "Alfuzosin: overview of pharmacokinetics, safety, and efficacy of a clinically uroselective alpha-blocker". Urology. 58 (6 Suppl 1): 55–63; discussion 63–64. ISSN 1527-9995. PMID 11750253.
- Bailey, David G; Malcolm, J; Arnold, O; David Spence, J (August 1998). "Grapefruit juice–drug interactions". British Journal of Clinical Pharmacology. 46 (2): 101–110. doi:10.1046/j.1365-2125.1998.00764.x. ISSN 0306-5251. PMC . PMID 9723817.
- "Drug Interactions Indiana University, School of Medicine, Department of Medicine". medicine.iupui.edu. Retrieved 2017-09-28.
- Nomiya, M; Yamaguchi, O (2003). "A quantitative analysis of mRNA expression of alpha 1 and beta-adrenoceptor subtypes and their functional roles in human normal and obstructed bladders". J Urol. 170 (2 Pt 1): 649–653.
- Bird, Steven T; Delaney, Joseph A C; Brophy, James M; Etminan, Mahyar; Skeldon, Sean C; Hartzema, Abraham G (2013-11-05). "Tamsulosin treatment for benign prostatic hyperplasia and risk of severe hypotension in men aged 40-85 years in the United States: risk window analyses using between and within patient methodology". The BMJ. 347: f6320. doi:10.1136/bmj.f6320. ISSN 0959-8138. PMC . PMID 24192967.
- "Terazosin 2 mg Tablets - Summary of Product Characteristics (SPC) - (eMC)". www.medicines.org.uk. Retrieved 2017-09-28.
- "Uroxatral (Alfuzosin HCl): Side Effects, Interactions, Warning, Dosage & Uses". RxList. Retrieved 2017-09-28.
- "UROXATRAL® (alfuzosin HCl) extended-release tablets Prescribing Information". products.sanofi.us. Retrieved 2017-09-28.
- Tehranchi, Ali; Rezaei, Yousef; Khalkhali, Hamidreza; Rezaei, Mahdi (November 2013). "Effects of terazosin and tolterodine on ureteral stent related symptoms: a double-blind placebo-controlled randomized clinical trial". International Braz J Urol: Official Journal of the Brazilian Society of Urology. 39 (6): 832–840. doi:10.1590/s1677-5538.ibju.2013.06.09. ISSN 1677-6119. PMID 24456787.
- Sica, Domenic A. (2005-12-01). "Alpha1-Adrenergic Blockers: Current Usage Considerations". The Journal of Clinical Hypertension. 7 (12): 757–762. doi:10.1111/j.1524-6175.2005.05300.x. ISSN 1751-7176.
- Kaplan, N. M. (1986-05-23). "Role of selective alpha 1 blockers in the therapy of hypertension". The American Journal of Medicine. 80 (5B): 100–104. ISSN 0002-9343. PMID 2872800.
- Mathur, R. P.; Nayak, Sumanlata; Sivaramakrishnan, R.; Jain, Vikas (September 2014). "Role of Alpha Blockers in Hypertension with Benign Prostatic Hyperplasia". The Journal of the Association of Physicians of India. 62 (9 Suppl): 40–44. ISSN 0004-5772. PMID 26245042.
- Sever, P. S. (1999). "Alpha 1-blockers in hypertension". Current Medical Research and Opinion. 15 (2): 95–103. doi:10.1185/03007999909113369. ISSN 0300-7995. PMID 10494492.
- Lemke, Thomas L.; Williams, David A. (2012-01-24). Foye's Principles of Medicinal Chemistry. Lippincott Williams & Wilkins. ISBN 9781609133450.
- Giardina, Dario; Gulini, Ugo; Massi, Maurizio; Piloni, Maria G.; Pompei, Pierluigi; Rafaiani, Giovanni; Melchiorre, Carlo (1993-03-01). "Structure-activity relationships in prazosin-related compounds. 2. Role of the piperazine ring on .alpha.-blocking activity". Journal of Medicinal Chemistry. 36 (6): 690–698. doi:10.1021/jm00058a005. ISSN 0022-2623.
- Campbell, Simon F.; Hardstone, J. David; Palmer, Michael J. (1988-05-01). "2,4-Diamino-6,7-dimethoxyquinoline derivatives as .alpha.1-adrenoceptor antagonists and antihypertensive agents". Journal of Medicinal Chemistry. 31 (5): 1031–1035. doi:10.1021/jm00400a025. ISSN 0022-2623.
- Ruffolo, Robert R.; Bondinell, William; Hieble, J. Paul (1995-09-01). ".alpha.- and .beta.-Adrenoceptors: From the Gene to the Clinic. 2. Structure-Activity Relationships and Therapeutic Applications". Journal of Medicinal Chemistry. 38 (19): 3681–3716. doi:10.1021/jm00019a001. ISSN 0022-2623.