WHO Pharmaceuticals Newsletter 2004, No. 06
(2004; 13 pages) View the PDF document
Table of Contents
Close this folderREGULATORY MATTERS
View the documentACTRA-RX AND YILISHEN - Presence of undeclared sildenafil
View the documentADALIMUMAB - Serious infections if used together with anakinra
View the documentANTIDEPRESSANTS Label to warn of increased suicidality in children; Patient Medication Guide to advise on risks and precautions to be taken
View the documentATORVASTATIN - Interaction with grapefruit juice
View the documentBLACK COHOSH COMBINATION #2; YELLOW DOCK COMBINATION #3 - Presence of aristolochic acid
View the documentCELECOXIB - Withdrawn in Turkey
View the documentEPOETIN ALFA - Label change to reflect thrombosis risk
View the documentETANERCEPT, INFLIXIMAB - Reports of serious infections
View the documentINFLIXIMAB - Lymphoma warning added to US Remicade label
View the documentISOTRETINOIN - Enhancement to risk management programme
View the documentLEVOTHYROXINE SODIUM - Dysphagia and risk of choking
View the documentMIFEPRISTONE - Important labelling changes proposed
View the documentPERGOLIDE MESYLATE - Label change: risk of cardiac valvulopathy
View the documentREMINYL AND AMARYL - Reports of medication errors
View the documentVALDECOXIB - Label updated to warn about skin reactions
Open this folder and view contentsSAFETY OF MEDICINES
View the documentFEATURE
 

PERGOLIDE MESYLATE - Label change: risk of cardiac valvulopathy

Canada. Shire BioChem Inc, following discussions with Health Canada, has issued a 'Dear Health-care Professional' letter and a Public Advisory concerning new safety information on pergolide (Permax) and the risk of cardiac valvulopathy. The letter highlights two recent studies that have shown an increased frequency of cardiac valvulopathy associated with pergolide (Permax), compared with non-ergot dopamine agonists. Given the potentially serious nature of these events, the Warnings, Dosage and Administration, Adverse Events, Post-Marketing and Consumer Information sections of the pergolide (Permax) product monograph are to be revised. The new labelling information notes that pergolide (Permax) is not recommended in patients with a history of serious inflammation, fibrosis or cardiac valvulopathy, and physicians are advised to reassess the risks and benefits of pergolide (Permax) compared with nonergot dopamine agonists. Physicians are also advised to inform patients of the risk of cardiac valvulopathy and other serious fibrotic reactions. Additionally, pretreatment cardiovascular evaluation and periodic monitoring for the development of valvular disease or fibrosis are recommended.

Reference:

'Dear Health-care Professional' letter from Shire Biochem Inc, 12 October 2004. Available on the Internet at www.hc-sc.gc.ca

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Last updated: May 3, 2013