WHO Pharmaceuticals Newsletter 1997, No. 11&12
(1997; 24 pages)
Índice de contenido
Abrir esta carpeta y ver su contenidoRegulatory actions
Cerrar esta carpetaDrug surveillance
Ver el documentoAlendronic acid - oesophagitis: Australia
Ver el documentoBenzodiazepines in pregnancy and lactation - reminder: to be avoided: United Kingdom
Ver el documentoDrug-induced gynaecomastia - review of reports: Australia
Ver el documentoGinkgo biloba - spontaneous haemorrhage: New Zealand
Ver el documentoHydroxyamfetamine/tropicamide (ParemydR) - adverse reactions: United States of America
Ver el documentoMethotrexate (low-dose) - blood dyscrasias and other adverse reactions: United Kingdom
Ver el documentoPethidine - convulsions: Australia
Ver el documentoPyrithyldione/diphenhydramine - agranulocytosis: Spain
Ver el documentoTherapeutic switches - evaluation of risks: call for data: United States of America
Abrir esta carpeta y ver su contenidoNew developments
Abrir esta carpeta y ver su contenidoMedical devices
Abrir esta carpeta y ver su contenidoGeneral information
Abrir esta carpeta y ver su contenidoVeterinary medicine
 

Hydroxyamfetamine/tropicamide (ParemydR) - adverse reactions: United States of America

United States of America. The Institute for Safe Medication Practices has received 3 reports of serious adverse events following the use of hydroxyamfetamine/tropicamide (ParemydR) opthalmic solution for routine diagnostic purposes. One patient sustained a fatal myocardial infarction, another developed ventricular fibrillation and a third developed hypotension, bradycardia and syncope, which required intervention.

The manufacturer, Allergan Inc, is advising health professionals to bear in mind the drug’s sympathomimetic/parasympatholytic pharmacology, since compounds such as ParemydR have known potential effects on the cardiac system.

Reference: ISMP Medication Safety Alert! Vol. 2, Issue 14, 16 July 1997.

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Última actualización: le 3 mayo 2013