WHO Pharmaceuticals Newsletter 1999, No. 03&04
(1999; 16 pages)
Table of Contents
Open this folder and view contentsRegulatory actions
Close this folderDrug surveillance
View the documentACE inhibitors: survey of renal monitoring: UK
View the documentAcenocoumarol: alopecia: Spain
View the documentAnti-thyroid drugs: agranulocytosis: UK
View the documentCannabis: two clinical trials to start soon: UK
View the documentClozapine: gastrointestinal obstruction: UK
View the documentDonepezil: review of adverse reactions: seizure and heart block: UK
View the documentDrugs and children: ADR reporting: new rules for paediatric trials of medicines: unlicensed drug use in neonates: UK
View the documentErgotamine: interaction with HIV protease inhibitors: France, Switzerland
View the documentFexofenadine: cardiac reaction: Netherlands
View the documentInhaled corticosteroids: peri-oral dermatitis: Israel
View the documentMirtazepine: intrahepatic cholestasis: Finland
View the documentNicorandil: mouth ulcers: France
View the documentOrlistat: caution against nonprescription use: UK
View the documentSildenafil: interaction with HIV protease inhibitors: UK
View the documentSucralfate: bezoar formation: UK
View the documentTopiramate: transient hemiparesis: UK
Open this folder and view contentsNew developments
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Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary medicine
 

Fexofenadine: cardiac reaction: Netherlands

Netherlands. A case study reports a patient who suffered QTc interval lengthening and ventricular tachycardia after taking the antihistamine fexofenadine (Telfast: Hoechst Marion Roussel), which is the active metabolite of terfenadine. The effect was reversible on withdrawal of fexofenadine and recurred on rechallenge.

Although a causal relationship with fexofenadine is suggested by the effects of rechallenge, the authors point out that the patient tended to have a long QTc interval even when not taking fexofenadine, suggesting that he had a predisposition to this problem. They conclude that fexofenadine may increase QTc interval time and induce ventricular arrhythmias in susceptible patients but that further studies are needed before a more definite risk-benefit analysis can be made.

References:

1) The Pharmaceutical Journal Vol. 262, p. 423, 27 March 1999.

2) Pinto YM, van Gelder IC, Heringa M et al. QT lengthening and life-threatening arrhythmias associated with fexofenadine. Lancet 353:980 (1999).

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Last updated: May 3, 2013