WHO Pharmaceuticals Newsletter 1998, No. 11&12
(1998; 10 pages)
Table of Contents
Open this folder and view contentsRegulatory actions
Open this folder and view contentsDrug surveillance
Close this folderNew developments
View the documentCarvedilol: approved for use in chronic heart failure: UK
View the documentEfavirenz: approved for use in HIV infection and AIDS: USA
View the documentEssential fatty acids and coal tar (Exorex): approved for treatment of psoriasis: UK
View the documentEtanercept: first biotechnology product approved for arthritis: USA
View the documentFentanyl citrate lozenges: approved for breakthrough cancer pain: USA
View the documentRizatriptan: approved for treatment of migraine: UK
View the documentTamoxifen: approved for reduction of breast cancer incidence: USA
View the documentTrastuzumab: new monoclonal antibody approved for advanced breast cancer: USA
View the documentNew indications
View the documentNewly approved products
Open this folder and view contentsMedical devices
Open this folder and view contentsGeneral information
Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary medicine
 

Carvedilol: approved for use in chronic heart failure: UK

United Kingdom. Carvedilol (Eucardic: SmithKline Beecham) has been licensed for use in chronic heart failure. It is the first-adrenoreceptor antagonist to be granted such a licence.

Carvedilol is indicated for patients with mild to moderate symptomatic heart failure as an adjunct to standard therapies. Treatment should be initiated at low doses (3.125 mg twice a day for two weeks) with dose titration to stabilise the patient, under the supervision of a hospital doctor. The most commonly reported adverse reaction is dizziness.

For many years, -adrenoreceptor antagonists were thought to be dangerous in heart failure, but recent studies have shown benefit with certain drugs. Carvedilol is a non-selective -adrenoreceptor antagonist with vasodilating properties. The vasodilatation is predominantly mediated through -1 antagonism.

Reference: The Pharmaceutical Journal Vol. 261, p. 150, 1 August 1998.

to previous section to next section
 

Last updated: May 3, 2013