WHO Pharmaceuticals Newsletter 2002, No. 02
(2002; 18 pages) View the PDF document
Table of Contents
View the documentEDITORIAL
Open this folder and view contentsREGULATORY MATTERS
Close this folderSAFETY OF MEDICINES
View the documentALENDRONATE - Case reports of pancreastitis with alendronic acid suggest a link? (Canada)
View the documentAMIODARONE - Reports of pulmonary toxicity (Australia)
View the documentANTIRETROVIRAL THERAPY (ART) - Lipodystrophy syndrome with ART under-reported in Canada (Canada)
View the documentARISTOLOCHIA - Safety update from Oman (Sultanate of Oman)
View the documentBUPROPION - Risk of seizure (UK)
View the documentCLOZAPINE - Clear association with myocarditis; revised labelling to indicate cardiovascular toxicity (Canada)
View the documentDROPERIDOL - Warnings of cardiovascular toxicity (Canada)
View the documentEPHEDRINE/EPHEDRA - Products recalled following risk assessment (Canada)
View the documentMETHOTREXATE - Adverse reactions influence treatment and prescribing decisions (India)
View the documentOLANZAPINE - Cardiomyopathy: case report (Sweden)
View the documentROFECOXIB/WARFARIN - Clinically significant interactions possible (Australia)
View the documentROSIGLITAZONE - Reminder about restrictions in use (Singapore)
View the documentSIBUTRAMINE - Safety reviews on anti-obesity drug (Canada, Europe)
View the documentSODIUM PICOSULFATE - Reports of severe electrolyte disturbances (Australia)
View the documentSTATINS - News from India and Singapore (India)
View the documentSTAVUDINE - Safety information updated (Canada, USA)
View the documentZOLPIDEM - Neurological and psychiatric reactions reported (Australia)
Open this folder and view contentsDRUG OF CURRENT INTEREST
View the documentADVERSE DRUG REACTIONS (ADR) - ASSOCIATIONS
Open this folder and view contentsFEATURE
View the documentEVENTS & ANNOUNCEMENTS
 

ROFECOXIB/WARFARIN - Clinically significant interactions possible (Australia)

Australia. Since late 2000, the Australian Adverse Reactions Advisory Committee (ADRAC) has received 8 reports of increased International Normalised Ratio (INR) in patients simultaneously using rofecoxib and warfarin. Of these, 2 reports described bleeding events (epistaxis and rectal haemorrhage) and 1 described anaemia. The committee recommends increased monitoring of INR in patients taking warfarin and concomitant rofecoxib.

Reference:

Australian Adverse Drug Reactions Bulletin 21(1): 3, Feb 2002.

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Last updated: May 3, 2013