WHO Drug Information Vol. 15, No. 2, 2001
(2001; 91 pages) Ver el documento en el formato PDF
Índice de contenido
Abrir esta carpeta y ver su contenidoPersonal Perspectives
Abrir esta carpeta y ver su contenidoReports on Individual Drugs
Abrir esta carpeta y ver su contenidoVaccines and Biomedicines
Abrir esta carpeta y ver su contenidoCurrent Topics
Abrir esta carpeta y ver su contenidoGeneral Information
Cerrar esta carpetaRegulatory and Safety Matters
Ver el documentoNew Zealand and Australia: joint medicines regulatory body
Ver el documentoBupropion safety information
Ver el documentoBupropion update
Ver el documentoItraconazole and congestive heart failure
Ver el documentoTerbinafine and hepatic failure
Ver el documentoPaediatric amiodarone labelling changes
Ver el documentoCerivastatin: marketing discontinued
Ver el documentoPhenylpropanolamine withdrawn from market
Ver el documentoCounterfeit filgrastim
Ver el documentoOxycodone: strengthened warning
Ver el documentoNesiritide for heart failure
Ver el documentoOprelvekin: paediatric safety information
Ver el documentoPeginterferon alfa-2b combined use: new labelling
Ver el documentoRibavirin for combined use
Ver el documentoSleep attacks with pramipexole and ropinirole
Ver el documentoRosiglitazone-associated hepatic and cardiovascular events
Ver el documentoClarithromycin: labelling change
Ver el documentoHerbal OTC remedy and hepatic dysfunction
Ver el documentoAntipsychotics and high prolactin
Ver el documentoSildenafil: not for use with nitrates
Ver el documentoPropofol, heart failure and high dosages
Ver el documentoBupropion and seizures
Ver el documentoNeurotoxicity with aciclovir and valaciclovir
Ver el documentoRevised labelling for levocarnitine
Ver el documentoAvoid trastuzumab and anthracyclines
Abrir esta carpeta y ver su contenidoATC/DDD Classification
Abrir esta carpeta y ver su contenidoEssential Drugs
Abrir esta carpeta y ver su contenidoRecent Publications and Sources of Information
Ver el documentoInternational Nonproprietary Names for Pharmaceutical Substances (INN)
Ver el documentoDénominations communes internationales des Substances pharmaceutiques (DCI)
Ver el documentoDenominaciones Comunes Internacionales para las Sustancias Farmacéuticas (DCI)
Ver el documentoAmendments to previous lists/Modifications apportées aux listes antérieures/Modificaciones a las listas anteriores
Ver el documentoAnnexes
 

Phenylpropanolamine withdrawn from market

Canada - Following a safety assessment, Health Canada has advised that drug products containing phenylpropanolamine are being withdrawn from the market. Following a review of information, it was concluded that use of this ingredient in prescription and nonprescription medicines cannot be justified, no matter how rare the event of a possible haemorrhagic stroke.

A regulatory process to remove all products containing PPA from the Canadian market has been initiated. A number of manufacturers have indicated that they are reformulating their cough and cold, sinus and allergy medications with safe and effective alternatives.

Reference: Health Canada Advisory, 2001-61, 30 May 2001.

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Última actualización: le 24 abril 2012