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View the documentPhenylpropanolamine withdrawn from market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
 

Bupropion update

Australia - Bupropion (Zyban SR®) was first marketed in late 2000 as a short-term aid to smoking cessation and has been used by high numbers of patients. Originally developed as an antidepressant, it is a selective inhibitor of the neuronal re-uptake of catecholamines in the brain but its mechanism to enhance the ability to quite smoking is unknown.

Assessment of reactions to bupropion is difficult because many patients experience nicotine withdrawal symptoms. Since November 2000, the Australian Adverse Drug Reactions Committee has received 780 reports of suspected adverse reactions in connection with the use of bupropion. The profile of the drug is dominated by hypersensitivity reactions and neurological and psychiatric effects. The majority of hypersensitivity reactions involve relatively minor skin reactions although cases have been described of facial oedema or angioedema and serum sickness-like reactions.

Bupropion can cause seizures and is contraindicated in patients with epilepsy. It should be used with great caution in those with a predisposition to seizures including those abusing alcohol or taking another medication that can lower the seizure threshold. This includes most antidepressant and antipsychotic drugs, insulin, oral hypoglycaemic drugs and anorectic products.

Reference: Australian Adverse Drug Reactions Bulletin, Volume 20, Number 2, 2001. Also at: http://www.health.gove.au/tga/docs/html/zyban.htm

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Last updated: May 3, 2013