WHO Pharmaceuticals Newsletter 1999, No. 03&04
(1999; 16 pages)
Table of Contents
Close this folderRegulatory actions
View the documentAlatrofloxacin: revised labelling: incompatibility with certain diluents: Pfizer, USA
View the documentBeclometasone: recommended total daily dose in CFC-free inhalers: UK
View the documentCholestin reinstated as a dietary product: federal judge overrules FDA decision: USA
View the documentFluticasone: revised package insert: systemic eosinophilia: Glaxo Wellcome
View the documentFosphenytoin sodium injection (Cerebyx): overdoses due to medication errors: label changes: Parke-Davis
View the documentHeparin-induced suppression of aldosterone secretion: product information revised: UK
View the documentLaxatives containing dantron and phenolphthalein: unacceptable ingredients in OTC drug products: USA
View the documentNicotine chewing gum: available for general sale: UK
View the documentNonprescription drugs: simplified labelling: USA
View the documentRituximab (Mabthera): recommendations for safe use: UK
View the documentTroglitazone: application for re-introduction rejected: UK
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Open this folder and view contentsMedical devices
Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary medicine
 

Beclometasone: recommended total daily dose in CFC-free inhalers: UK

United Kingdom. Beclometasone (beclomethasone dipropionate) is now available in a CFC-free inhaler (Qvar) for the prophylactic management of mild, moderate or severe asthma in adults. This new formulation containing HFA-134a as the propellant results in smaller particles of beclometasone and greater lung deposition compared with inhalers using CFCs. Studies have shown that the increased lung delivery results in a 2 to 2.5-fold greater potency of Qvar compared with the old formulation. Since the use of high-dose inhaled corticosteroids has been associated with systemic adverse effects, it is important that patients being switched from the CFC-containing inhaler to Qvar are commenced on the appropriate equivalent dose.

The conversion can be done using the following table:

Total daily dose (micrograms/day)

beclometasone with
a CFC propellant

Qvar

200-250

100

300

150

400-500

250

600-700

300

800-1000

400

1100

400

1200-1500

600

1600-2000

800

If patients using budesonide inhalers are to be transferred to Qvar, the same instructions should be applied. If transferring patients using fluticasone inhalers, the same total daily dose, up to a maximum of 800 micrograms/day should be substituted.

Once patients are transferred to Qvar, the dose should be adjusted to meet the needs of the individual patient, bearing in mind that, to avoid systemic adverse effects, the minimum dose should be used at which asthma control is maintained.

In patients not previously treated with an inhaled corticosteroid, Qvar may be started at doses of between 100 micrograms/day and 800 micrograms/day in two divided doses according to the severity of the asthma.

Patients should be instructed in the proper use of their inhaler, including rinsing out their mouth with water after use. They should also be advised that Qvar may have a different taste and feel than a CFC inhaler.

Reference: Current Problems in Pharmacovigilance Vol. 25, March 1999.

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Last updated: May 3, 2013