A Prescription-Event Monitoring (PEM) Study of Tiotropium
Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
This prescription-event monitoring study was based upon 'event' monitoring and so capable of
identifying signals of events that might be associated with the use of tiotropium, which none
of the participating general practitioners (GPs) suspected to be an adverse drug reaction.
The methodology of this study readily permits follow up of specific events and the obtaining
of additional data as appropriate.