WHO Pharmaceuticals Newsletter 1997, No. 11&12
(1997; 24 pages)
Table of Contents
Close this folderRegulatory actions
View the documentAcetylsalicylic acid and paracetamol - prescription control: United Kingdom
View the documentChlormezanone - marketing authorization withdrawn: Germany
View the documentCounterfeit antimalarial detected: Kenya
View the documentDiphenhydramine - warning statements: United States of America
View the documentGeriatric use - added to labelling: United States of America
View the documentHerbal “Fen-Phen” - warning concerning “natural” anti-obesity alternatives: United States of America
View the documentHIV protease inhibitors - hyperglycaemia: United Kingdom
View the documentIrinotecan - revised data sheet: warning & precautions for use: Japan
View the documentLamotrigine - warning: severe cutaneous reactions: Australia
View the documentLaxatives containing phenolphthalein - recommendation to revoke marketing authorization: Germany
View the documentLevothyroxine sodium - new drug applications to be submitted: United States of America
View the documentLysine amidotrizoate in ionic contrast media - withdrawn: Germany
View the documentMelatonin - prescription control: New Zealand
View the documentMetamizole sodium - prohibited: Nepal
View the documentNSAIDs, including acetylsalicylic acid - proposed risk-based framework: New Zealand
View the documentPaediatric data - labelling to be required for new drugs: United States of America
View the documentParacetamol - restrictive measures: Ireland
View the documentPemoline - withdrawn: hepatotoxicity: United Kingdom
View the documentSodium hydrogen bicarbonate (paediatric) - prohibited: Nepal
View the documentSuxamethonium chloride - warnings: cardiac arrest and hyperkalaemia: United States of America
View the documentTerfenadine - restrictive measures: Ireland
View the documentTerfenadine and terfenadine/pseudoephedrine - warnings concerning interactions: United States of America
View the documentTramadol - not recommended as first choice for moderate pain: Norway
View the documentTramadol - rescheduled: Oman
View the documentTrihexyphenidyl - rescheduled: Oman
View the documentVigabatrin - visual field defects: Australia
View the documentWomen in clinical trials - proposed rule: United States of America
View the documentZafirlukast - possible association with Churg-Strauss syndrome: United States of America
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Open this folder and view contentsMedical devices
Open this folder and view contentsGeneral information
Open this folder and view contentsVeterinary medicine
 

Suxamethonium chloride - warnings: cardiac arrest and hyperkalaemia: United States of America

United States of America. The manufacturer of the neuromuscular blocking agent, suxamethonium chloride (succinylcholine, SucostrinR: Bristol-Myers Squibb), has called attention to two life-threating events that may occur with its use:

. Cardiac arrest in children and adolescents. Several reports have been received of cardiac arrest following administration of suxamethonium chloride to apparently healthy children and adolescents who were subsequently found to have undiagnosed myopathies. A non-polarizing neuromuscular blocking drug should be used for routine elective surgery in these patients.

. Hyperkalaemia. Except when used for emergency tracheal intubation or in instances where immediate securing of the airway is necessary, suxamethonium chloride is contraindicated in patients after the acute phase of injury following major burns, multiple trauma, extensive denervation of the skeletal muscle, or upper motor neuron injury because administration to such individuals may result in severe hyperkalaemia, which may lead to cardiac arrest. The risk of hyperkalaemia in these patients increases over time and usually peaks at 7 to 10 days after the injury, depending on the extent and location of the injury. The precise time of onset and the duration of the risk period are not known.

[See also Pharmaceuticals Newsletter No. 3, March 1995]

Reference: FDA Medical Bulletin Vol. 27, No.2, Summer 1997.

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Last updated: May 3, 2013