WHO Drug Information Vol. 15, No. 2, 2001
(2001; 91 pages) View the PDF document
Table of Contents
Open this folder and view contentsPersonal Perspectives
Open this folder and view contentsReports on Individual Drugs
Open this folder and view contentsVaccines and Biomedicines
Open this folder and view contentsCurrent Topics
Open this folder and view contentsGeneral Information
Close this folderRegulatory and Safety Matters
View the documentNew Zealand and Australia: joint medicines regulatory body
View the documentBupropion safety information
View the documentBupropion update
View the documentItraconazole and congestive heart failure
View the documentTerbinafine and hepatic failure
View the documentPaediatric amiodarone labelling changes
View the documentCerivastatin: marketing discontinued
View the documentPhenylpropanolamine withdrawn from market
View the documentCounterfeit filgrastim
View the documentOxycodone: strengthened warning
View the documentNesiritide for heart failure
View the documentOprelvekin: paediatric safety information
View the documentPeginterferon alfa-2b combined use: new labelling
View the documentRibavirin for combined use
View the documentSleep attacks with pramipexole and ropinirole
View the documentRosiglitazone-associated hepatic and cardiovascular events
View the documentClarithromycin: labelling change
View the documentHerbal OTC remedy and hepatic dysfunction
View the documentAntipsychotics and high prolactin
View the documentSildenafil: not for use with nitrates
View the documentPropofol, heart failure and high dosages
View the documentBupropion and seizures
View the documentNeurotoxicity with aciclovir and valaciclovir
View the documentRevised labelling for levocarnitine
View the documentAvoid trastuzumab and anthracyclines
Open this folder and view contentsATC/DDD Classification
Open this folder and view contentsEssential Drugs
Open this folder and view contentsRecent Publications and Sources of Information
View the documentInternational Nonproprietary Names for Pharmaceutical Substances (INN)
View the documentDénominations communes internationales des Substances pharmaceutiques (DCI)
View the documentDenominaciones Comunes Internacionales para las Sustancias Farmacéuticas (DCI)
View the documentAmendments to previous lists/Modifications apportées aux listes antérieures/Modificaciones a las listas anteriores
View the documentAnnexes
 

Sleep attacks with pramipexole and ropinirole

Canada - Recent adverse drug reaction reports associated with pramipexole (Mirapex®) and ropinirole (Requip®) have included a higher proportion of sleep disorder cases. Sleep-related disorders constituted 26 of 57 reports and 16 out of 17 of the reports of adverse reactions associated with ropinirole and pramipexole, reported to the Canadian Adverse Drug Reaction Monitoring Program (CADRMP) as of 10 October 2000. Nineteen of those associated with ropinirole and all 16 of those associated with pramipexole, were of sudden onset of sleep, or variant. In some of these cases, the patient was driving when the event occurred. The episodes typically only last for a few seconds and are often not preceded by warning symptoms such as unusual fatigue.

Warnings have previously been issued not to drive or engage in other activities in which impaired alertness may impose increased risk and the Canadian Medical Association has published guidelines to assist physicians in evaluating a patient’s ability to drive.

Reference: Canadian Adverse Drug Reaction Newsletter, 11: 1 - 2, April 2001.

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Last updated: May 3, 2013