WHO Pharmaceuticals Newsletter 1997, No. 11&12
(1997; 24 pages)
Table of Contents
Open this folder and view contentsRegulatory actions
Close this folderDrug surveillance
View the documentAlendronic acid - oesophagitis: Australia
View the documentBenzodiazepines in pregnancy and lactation - reminder: to be avoided: United Kingdom
View the documentDrug-induced gynaecomastia - review of reports: Australia
View the documentGinkgo biloba - spontaneous haemorrhage: New Zealand
View the documentHydroxyamfetamine/tropicamide (ParemydR) - adverse reactions: United States of America
View the documentMethotrexate (low-dose) - blood dyscrasias and other adverse reactions: United Kingdom
View the documentPethidine - convulsions: Australia
View the documentPyrithyldione/diphenhydramine - agranulocytosis: Spain
View the documentTherapeutic switches - evaluation of risks: call for data: United States of America
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
 

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.

.
.

to previous section to next section
 

Last updated: May 3, 2013