Table 1.
Inclusion criteria | Exclusion criteria | |
---|---|---|
Study design | Regardless of methodology, qualifying studies that answered the question ‘what factors influence the reporting of ADRs by the public?’ were included | Letters, editorials and narrative reviews were excluded |
Participants | All studies addressing patients' perceptions of ADR reporting were included | Studies addressing patient and HCP roles in pharmacovigilance; perception of HCPs on ADR reporting; studies comparing frequencies of reported ADRs by patients vs. HCPs; frequencies of ADRs reported by patients; and studies addressing the role of regulators on pharmacovigilance |
Language | Studies reported in all languages, if we were able to translate them | Studies unable to translate |
ADR, adverse drug reaction; HCP, healthcare professional