Session 5: Patient Reporting & PROMs
This session explores the importance of recognising and reporting treatment-related side effects and adverse drug reactions (ADRs), particularly in the context of polypharmacy. It introduces Patient-Reported Outcomes (PROs) and Patient-Reported Outcome Measures (PROMs), highlighting how patients' experiences and preferences can contribute to medication safety, informed decision-making, and more patient-centred healthcare.
Video 1
Download handout (PDF)Video 2
Download handout (PDF)These materials have been developed within the EU-funded SafePolyMed project for educational, informational and non-commercial purposes only. They do not constitute medical advice and are not intended to replace consultation with a qualified healthcare professional. The SafePolyMed project received funding from the European Union’s Horizon Europe Research and Innovation Programme under Grant Agreement No. 101057639. Views and opinions expressed are, however, those of the author(s) only and do not necessarily reflect those of the European Union or the Health and Digital Executive Agency. Neither the European Union nor the granting authority can be held responsible for them.
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