drug therapy safety medication error adverse drug events
Conditions
Interventions
Group 1: part of the study:
Non-High-risk-patients
No additional investigations are planned.
Data collection after patients' consent (patient data, diagnoses, medication and medication-related proble
Sponsors
Lehrstuhl für Klinische Pharmakologie und Klinische Toxikologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - in-patient stay for at least 72h - ability to give consent - treatment in a ward of Fürth hospital which is part of the AMTS-Stewardship-Project
Exclusion criteria
Exclusion criteria: - incapable to give consent - age under 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - improvement of detection and documentation of drug-related problems (i.e. adverse drug reaction and contraindicated prescriptions) | — |
Secondary
| Measure | Time frame |
|---|---|
| - improvement of the identification of medication-therapy-safety-high-risk-patients - investigation of usage and acceptance of measurements to improve medication-therapy-safety | — |
Countries
Germany
Contacts
Public ContactRenke Maas
Lehrstuhl für Klinische Pharmakologie und Klinische Toxikologie
Outcome results
None listed