Literature DB >> 16162024

Doxazosin gastrointestinal therapeutic system: a review of its use in benign prostatic hyperplasia.

David R Goldsmith1, Greg L Plosker.   

Abstract

Doxazosin, a well established treatment in patients with bothersome lower urinary tract symptoms from benign prostatic hyperplasia (BPH), is available in a new controlled-release formulation, doxazosin gastrointestinal therapeutic system (GITS). Doxazosin GITS (Cardura XL, Cardular PP Uro, Diblocin PP Uro) has an altered pharmacokinetic profile, which allows a higher initial dosage to be used than with the standard formulation and less titration steps to reach a clinically effective dosage. In two large, double-blind, randomised studies (one was placebo-controlled) in patients with BPH, doxazosin GITS (4-8 mg once daily) was as effective as the standard formulation (2-8 mg once daily), and both were more effective than placebo, after 13 weeks' treatment in improving symptom scores, health-related quality of life (HR-QOL), and maximum urinary flow rate (Qmax). Doxazosin GITS was at least as well tolerated as the standard formulation of doxazosin in clinical studies in patients with BPH.

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Year:  2005        PMID: 16162024     DOI: 10.2165/00003495-200565140-00008

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  17 in total

1.  Diuretics vs alpha-blockers for treatment of hypertension: lessons from ALLHAT. Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial.

Authors:  L Lasagna
Journal:  JAMA       Date:  2000-04-19       Impact factor: 56.272

2.  Double-blind trial of the efficacy and tolerability of doxazosin in the gastrointestinal therapeutic system, doxazosin standard, and placebo in patients with benign prostatic hyperplasia.

Authors:  M Andersen; C Dahlstrand; K Høye
Journal:  Eur Urol       Date:  2000-10       Impact factor: 20.096

3.  Clinical pharmacokinetics of doxazosin in a controlled-release gastrointestinal therapeutic system (GITS) formulation.

Authors:  M Chung; V Vashi; J Puente; M Sweeney; P Meredith
Journal:  Br J Clin Pharmacol       Date:  1999-11       Impact factor: 4.335

Review 4.  Terazosin, doxazosin, and prazosin: current clinical experience.

Authors:  B Akduman; E D Crawford
Journal:  Urology       Date:  2001-12       Impact factor: 2.649

5.  Major cardiovascular events in hypertensive patients randomized to doxazosin vs chlorthalidone: the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). ALLHAT Collaborative Research Group.

Authors: 
Journal:  JAMA       Date:  2000-04-19       Impact factor: 56.272

6.  Doxazosin in a gastrointestinal therapeutic system formulation.

Authors:  A Cases
Journal:  Drugs Today (Barc)       Date:  2000-10       Impact factor: 2.245

7.  A combined analysis of double-blind trials of the efficacy and tolerability of doxazosin-gastrointestinal therapeutic system, doxazosin standard and placebo in patients with benign prostatic hyperplasia.

Authors:  R S Kirby; M Andersen; P Gratzke; C Dahlstrand; K Høye
Journal:  BJU Int       Date:  2001-02       Impact factor: 5.588

8.  EAU 2004 guidelines on assessment, therapy and follow-up of men with lower urinary tract symptoms suggestive of benign prostatic obstruction (BPH guidelines).

Authors:  Stephan Madersbacher; Gerasimos Alivizatos; Jorgen Nordling; Carlos Rioja Sanz; Mark Emberton; Jean J M C H de la Rosette
Journal:  Eur Urol       Date:  2004-11       Impact factor: 20.096

9.  The metabolism and kinetics of doxazosin in man, mouse, rat and dog.

Authors:  B Kaye; N J Cussans; J K Faulkner; D A Stopher; J L Reid
Journal:  Br J Clin Pharmacol       Date:  1986       Impact factor: 4.335

Review 10.  Doxazosin. An update of its clinical pharmacology and therapeutic applications in hypertension and benign prostatic hyperplasia.

Authors:  B Fulton; A J Wagstaff; E M Sorkin
Journal:  Drugs       Date:  1995-02       Impact factor: 9.546

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  1 in total

Review 1.  The diagnosis and treatment of lower urinary tract symptoms due to benign prostatic hyperplasia with α-blockers: focus on silodosin.

Authors:  Júlio Fonseca; Carlos Martins da Silva
Journal:  Clin Drug Investig       Date:  2015-02       Impact factor: 2.859

  1 in total

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