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Consumers' experiences and perspectives on reporting adverse drug reactions using digital tools: a qualitative study
Mohammed Gebre Dedefo1, Gizat M Kassie2,3,4, Eyob Alemayehu Gebreyohannes2,5
1Quality Use of Medicines and Pharmacy Research Centre, College of Health, Adelaide University, Adelaide, Australia. mohammed.dedefo@adelaide.edu.au.
Consumers are willing to report adverse drug reactions (ADRs) using digital tools, but awareness and usability barriers hinder use. Improving design and accessibility can increase consumer engagement in ADR reporting.
Area of Science:
- Pharmacovigilance
- Digital Health
- Consumer Health Informatics
Background:
- Spontaneous adverse drug reactions (ADRs) are significantly underreported.
- Digital reporting systems offer a potential solution, but consumer adoption barriers are not well understood.
Purpose of the Study:
- To identify facilitators and barriers influencing consumer use of digital tools for ADR reporting.
- To understand consumer expectations and preferences for digital ADR reporting engagement.
Main Methods:
- Qualitative descriptive study using semi-structured interviews with Australian adults who experienced ADRs.
- Inductive thematic analysis of interview data, mapped to the Combined Technology Acceptance Model and Theory of Planned Behaviour (C-TAM-TPB) framework.
Main Results:
- Consumers showed positive intentions for online ADR reporting.
- Facilitators include user-friendly design, layperson language, image use, health record integration, and dual reporting to professionals/regulators.
- Barriers include lack of awareness, registration needs, complex terminology, mandatory fields, and no feedback.
Conclusions:
- Consumers are willing to use digital ADR reporting tools but lack awareness.
- Enhancing usability, user-friendliness, and consumer-specific design can boost engagement.
- Addressing barriers like awareness, registration, jargon, and feedback is crucial for improving pharmacovigilance.
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