Literature DB >> 8861549

Losartan potassium: a review of its pharmacology, clinical efficacy and tolerability in the management of hypertension.

K L Goa1, A J Wagstaff.   

Abstract

Losartan potassium is an orally active, nonpeptide angiotensin II (AII) receptor antagonist. It is the first of a new class of drugs to be introduced for clinical use in hypertension. This novel agent binds competitively and selectively to the AII subtype 1 (AT(1)) receptor, thereby blocking AII-induced physiological effects. An active metabolite, E3174, contributes substantially to its antihypertensive effect, which persists throughout 24 hours after once-daily administration. In patients with mild to moderate hypertension, losartan potassium 50 to 100mg once daily as monotherapy lowers blood pressure to a similar degree to enalapril, atenolol and felodipine extended release (ER). Losartan potassium combined with hydrochlorothiazide reduces blood pressure further than either drug given separately. About one-third of patients with severe hypertension have responded to the combination product. Losartan potassium appears to be effective in elderly patients. Losartan potassium is very well tolerated. In clinical trials, dizziness was the only drug-related event reported more frequently with losartan potassium monotherapy than with placebo. First-dose hypotension is uncommon. An aspect of the drug's tolerability profile which may prove to be particularly advantageous is that it is associated with a similar incidence of cough to placebo in patients with a history of ACE inhibitor-related cough. Additionally, clinically relevant adverse metabolic effects or laboratory abnormalities have not been documented during losartan potassium therapy and renal function is preserved in patients with or without renal insufficiency. The adverse effect profile of the losartan potassium-hydrochlorothiazide combination resembles those for losartan potassium monotherapy and placebo. Long term tolerability data are limited (<2 years) but support the very good tolerability profile in shorter studies. Elements of the drug's profile yet to be assessed or reported fully in the literature include long term efficacy; potential to favourably influence cardiovascular and renovascular systems (and ultimately mortality) in patients with hypertension and, lastly, cost effectiveness and influence on quality of life. In summary, losartan potassium is the first AT(1)+ receptor antagonist to become available for the management of hypertension and, as such, it is an important new antihypertensive agent. Pending long term data as outlined above, it is likely to find initial use in patients with mild to severe hypertension who are unresponsive to, or intolerant of their current therapy. However, with its novel mechanism of action, good efficacy and favourable tolerability profile, losartan potassium is well placed to claim a prominent position in the management of patients with essential hypertension in the future.

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Year:  1996        PMID: 8861549     DOI: 10.2165/00003495-199651050-00008

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


  100 in total

1.  Type-1 and type-2 angiotensin II receptors in fetal rat brain.

Authors:  K Tsutsumi; M Viswanathan; C Strömberg; J M Saavedra
Journal:  Eur J Pharmacol       Date:  1991-05-30       Impact factor: 4.432

2.  Acute renal excretory actions of losartan in spontaneously hypertensive rats: role of AT2 receptors, prostaglandins, kinins and nitric oxide.

Authors:  R Munoz-Garcia; R Maeso; E Rodrigo; J Navarro; L M Ruilope; M C Casal; V Cachofeiro; V Lahera
Journal:  J Hypertens       Date:  1995-12       Impact factor: 4.844

Review 3.  The preclinical basis of the therapeutic evaluation of losartan.

Authors:  P B Timmermans; P C Wong; A T Chiu; R D Smith
Journal:  J Hypertens Suppl       Date:  1995-07

4.  Antihypertensive and anti-albuminuric effects of losartan potassium and felodipine in Chinese elderly hypertensive patients with or without non-insulin-dependent diabetes mellitus.

Authors:  J C Chan; J A Critchley; B Tomlinson; T Y Chan; C S Cockram
Journal:  Am J Nephrol       Date:  1997       Impact factor: 3.754

5.  Effect of multiple doses of losartan on the pharmacokinetics of single doses of digoxin in healthy volunteers.

Authors:  M De Smet; D F Schoors; G De Meyer; R Verbesselt; M R Goldberg; V Fitzpatrick; G Somers
Journal:  Br J Clin Pharmacol       Date:  1995-12       Impact factor: 4.335

6.  The effects of angiotensin II receptor blockade with losartan on systemic blood pressure and renal and extrarenal prostaglandin synthesis in women with essential hypertension.

Authors:  M C Smith; S Barrows; A Meibohm; S Shahinfar; R L Simpson; K Weigel; M J Dunn
Journal:  Am J Hypertens       Date:  1995-12       Impact factor: 2.689

7.  The metabolism of DuP 753, a nonpeptide angiotensin II receptor antagonist, by rat, monkey, and human liver slices.

Authors:  R A Stearns; R R Miller; G A Doss; P K Chakravarty; A Rosegay; G J Gatto; S H Chiu
Journal:  Drug Metab Dispos       Date:  1992 Mar-Apr       Impact factor: 3.922

8.  Effects of losartan on a background of hydrochlorothiazide in patients with hypertension.

Authors:  B A Soffer; J T Wright; J H Pratt; B Wiens; A I Goldberg; C S Sweet
Journal:  Hypertension       Date:  1995-07       Impact factor: 10.190

Review 9.  Modulation of the renin-angiotensin-aldosterone system and cough.

Authors:  Y Lacourcière; J Lefebvre
Journal:  Can J Cardiol       Date:  1995-08       Impact factor: 5.223

10.  Biotransformation of losartan to its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome P4502C and 3A subfamily members.

Authors:  R A Stearns; P K Chakravarty; R Chen; S H Chiu
Journal:  Drug Metab Dispos       Date:  1995-02       Impact factor: 3.922

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  35 in total

Review 1.  [Reserpine-diuretic combinations in therapy of arterial hypertension. Current considerations].

Authors:  M Siepmann; W Kirch
Journal:  Med Klin (Munich)       Date:  1998-12-15

Review 2.  Angiotensin converting enzyme inhibitors and angiotensin II antagonists as therapy in chronic liver disease.

Authors:  J Vlachogiannakos; A K Tang; D Patch; A K Burroughs
Journal:  Gut       Date:  2001-08       Impact factor: 23.059

3.  Population pharmacokinetic-pharmacodynamic modelling of angiotensin receptor blockade in healthy volunteers.

Authors:  Chantal Csajka; Thierry Buclin; Karin Fattinger; Hans R Brunner; Jérôme Biollaz
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

4.  Role of the renin-angiotensin system in cardiac hypertrophy induced in rats by hyperthyroidism.

Authors:  H Kobori; A Ichihara; H Suzuki; T Takenaka; Y Miyashita; M Hayashi; T Saruta
Journal:  Am J Physiol       Date:  1997-08

Review 5.  Valsartan. A review of its pharmacology and therapeutic use in essential hypertension.

Authors:  A Markham; K L Goa
Journal:  Drugs       Date:  1997-08       Impact factor: 9.546

Review 6.  Losartan: a review of its use in stroke risk reduction in patients with hypertension and left ventricular hypertrophy.

Authors:  Marit D Moen; Antona J Wagstaff
Journal:  Drugs       Date:  2005       Impact factor: 9.546

7.  Encapsulation of commercially available losartan for blinding purposes does not affect its bioavailability.

Authors:  L Nyman; K Taure; M Cullberg; P O Lagerström
Journal:  Clin Drug Investig       Date:  1998       Impact factor: 2.859

Review 8.  A risk-benefit assessment of losartan potassium in the treatment of hypertension.

Authors:  L M Burrell
Journal:  Drug Saf       Date:  1997-01       Impact factor: 5.606

Review 9.  Interactions between antiretroviral drugs and drugs used for the therapy of the metabolic complications encountered during HIV infection.

Authors:  Carl J Fichtenbaum; John G Gerber
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

Review 10.  Losartan: a review of its use, with special focus on elderly patients.

Authors:  K L Simpson; K J McClellan
Journal:  Drugs Aging       Date:  2000-03       Impact factor: 3.923

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