WHO Pharmaceuticals Newsletter 2005, No. 03
(2005; 17 pages) Voir le document au format PDF
Table des matières
Fermer ce répertoireRegulatory Matters
Afficher le documentAlbumin - Safety issues in critically ill patients
Afficher le documentAntiretroviral agents - Caution advised against certain combinations
Afficher le documentAtypical Antipsychotics - Risk of death in elderly patients with dementia
Afficher le documentCyclo-oxygenase-2 (COX-2) Inhibitors - To be available under strict restrictions
Afficher le documentCyproterone acetate and ethinylestradiol - Not to be used in contraception
Afficher le documentDonepezil - Warning of rhabdomyolysis
Afficher le documentDrotrecogin alfa (activated) - Only for use in high-risk patients
Afficher le documentEfavirenz - Reports of neural tube defects
Afficher le documentEfalizumab - Immune mediated haemolytic anaemia
Afficher le documentGalantamine - Death in subjects with mild cognitive impairment
Afficher le documentHydromorphone hydrochloride - To be withdrawn for safety reasons
Afficher le documentLepirudin - Information on dosage and administration
Afficher le documentMitoxantrone - Label to reflect risks of cardiotoxicity
Afficher le documentNSAIDs - Black box warning for both prescription and OTC products
Afficher le documentOxcarbazepine - Label to include serious dermatological reactions
Afficher le documentParoxetine and Pimozide - Concurrent use contraindicated
Afficher le documentPhenyl-propanolamine - Suspended while adverse reaction reports are reviewed
Afficher le documentSildenafil, Tadalafil, Vardenafil - Labels updated with NAION information
Afficher le documentValdecoxib - Sales suspended in more countries
Afficher le documentVeralipride - Suspended due to neurological and other adverse reactions
Ouvrir ce répertoire et afficher son contenuSafety of Medicines
Ouvrir ce répertoire et afficher son contenuMISCELLANY
 

Paroxetine and Pimozide - Concurrent use contraindicated

Canada. GlaxoSmithKline Inc. (GSK), following discussions with Health Canada, is advising physicians against the concurrent use of paroxetine (Paxil and Paxil CR) and pimozide, since paroxetine was found to increase plasma pimozide levels in an open-label study of healthy volunteers who were administered both drugs. Elevation of pimozide blood concentration may result in QT interval prolongation and severe arrhythmias including Torsade de Pointes.

Reference:

'Dear Health-care Professional' letter from GlaxoSmithKline Inc., 22 July 2005 (http://www.hc-sc.gc.ca).

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Dernière mise à jour: le 3 mai 2013