Preventable Adverse Drug Events (ADEs)
Conditions
Interventions
The intervention was an on-ward participation program for a hospital pharmacist consisting of the following activities: The hospital pharmacist assigned for this study evaluated each new medication or
Sponsors
Netherlands Organisation for Health Research and Development (ZonMw) (Netherlands)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients admitted to the ICU between October 3, 2005 and June 30, 2006
Exclusion criteria
Exclusion criteria: Does not match inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of prescribing errors per 1000 monitored patient-days. | — |
Secondary
| Measure | Time frame |
|---|---|
| The number of prescribing errors per 1000 monitored patient days that resulted in patient harm (preventable Adverse Drug Events). | — |
Countries
Netherlands
Outcome results
None listed