Evidence map›Paper›PMID 30104865›Full record

ArticlePatient preference and adherence2018

Consumer opinions on adverse events associated with medicines and vaccines.

Parisa Aslani, Kim Hamrosi, Vivien Tong, Timothy F Chen, Jane Cook, Romano Fois, Theresa McGarry, Carter Moore, Rodney Peters, Sarah Spagnardi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Patient preference and adherence, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Immediate side effects of Comirnaty COVID-19 vaccine: A nationwide survey of vaccinated people in Israel, December 2020 to March 2021.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 3 countries.

Parisa AslaniFaculty of Pharmacy, The University of Sydney, Camperdown, NSW, Australia, parisa.aslani@sydney.edu.au.
Kim HamrosiFaculty of Pharmacy, The University of Sydney, Camperdown, NSW, Australia, parisa.aslani@sydney.edu.au.
Vivien TongFaculty of Pharmacy, The University of Sydney, Camperdown, NSW, Australia, parisa.aslani@sydney.edu.au.
Timothy F ChenFaculty of Pharmacy, The University of Sydney, Camperdown, NSW, Australia, parisa.aslani@sydney.edu.au.
Jane CookTherapeutic Goods Administration, Canberra, ACT, Australia.
Romano FoisFaculty of Pharmacy, The University of Sydney, Camperdown, NSW, Australia, parisa.aslani@sydney.edu.au.
Theresa McGarryCelgene Pty Ltd., Southbank, VIC, Australia.
Carter MooreConsumers Health Forum of Australia, Canberra, ACT, Australia.
Rodney PetersPharmacovigilant Consultant, Sydney, NSW, Australia.
Sarah SpagnardiNPS MedicineWise, Sydney, NSW, Australia.
Karen WhitelockNovartis Pharmaceuticals Australia Pty Ltd., Sydney, NSW, Australia.
The University of Sydney · AUBristol-Myers Squibb (Switzerland) · CHNetherlands Pharmacovigilance Centre Lareb · NLTeva Pharmaceuticals (Australia) · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite the availability of an Australian consumer adverse event (AE) reporting system for over 50 years, reporting rates remain low. A comprehensive understanding of consumer perceptions and experiences regarding AEs is needed to further ascertain factors impacting their engagement in AE reporting.

aimThe aim of this study was to explore consumer opinions about AEs potentially associated with medicines and vaccines, and their experiences and understanding of managing and reporting AEs.

methodsSix focus groups were conducted across metropolitan Sydney with a total of 48 adult participants. A semi-structured focus group topic guide was developed to explore consumers' understanding, experiences, and actions taken in relation to AEs; and perspectives on managing treatment benefits and harms. Discussions were audio-recorded with participant permission and transcribed verbatim. Transcripts were thematically analyzed.

resultsConsumers acknowledged the potential for side effects (SEs), however inaccurately estimated SE risk in response to verbal descriptors such as "common." Consumer appraisal of treatment benefits and harms was influenced by factors such as medical condition(s), previous experiences, and beliefs. Although many had experienced SEs, consumers only reported them if considered severe or troublesome. Minimal awareness of consumer AE reporting systems was evident. Doctors were the primary avenue for reporting; consumers preferred doctors to act as the intermediary in reporting AEs to an independent body.

conclusionConsumers' lack of awareness of AE reporting systems was evident. With the complexities inherent in benefit/harm risk appraisal, information seeking, and AE reporting preferences, better consumer understanding of AEs and the systems available for reporting is needed.

Indexed as

drugsfocus groupspatientqualitativereportingside effectsvaccines

Identifiers

PMID30104865
PMCPMC6074778
OpenAlexW2884797241

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.