Patient´s awareness of a direct adverse drug reaction reporting system: an exploratory survey conducted at the Medical Center - University of Freiburg.
- Conditions
- Report of adverse drug reactions by patients.
- Registration Number
- DRKS00007917
- Lead Sponsor
- niversitätsklinikum FreiburgStudienzentrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 131
Inclusion Criteria
Patients that are treated in one of the three clinical departments.
Exclusion Criteria
Under age.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method it should be investigated whether patients are aware that they can report adverse drug reactions directly to the German competent authorities (Federal Institute for Drugs and Medical Devices (BfArM) and the Paul Ehrlich Institute (PEI)).<br><br>
- Secondary Outcome Measures
Name Time Method Additionally it should be investigated whether adverse drug reaction reporting rates differ among three clinical departments at the Medical Center – University of Freiburg.