UK veterinary professionals’ perceptions and experiences of adverse drug reaction reporting
UK veterinary professionals’ perceptions and experiences of adverse drug reaction reporting
Davies, H, et al. (2022) UK veterinary professionals’ perceptions and experiences of adverse drug reaction reporting. Veterinary Record. p. e1796. https://doi.org/10.1002/vetr.1796
[Open Access]
Summary
This paper reports on the findings of a survey asking questions about the barriers, perceptions, attitudes, and experiences of UK veterinary professionals towards adverse drug reaction (ADR) reporting.
The August 2022 edition of inFOCUS contains a summary of this paper.
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Additional resources
Reporting adverse reactions
- RCVS Code of Professional Conduct for Veterinary Surgeons: Supporting guidance 4. Veterinary medicines. [Royal College of Veterinary Surgeons] [online] Available from: https://www.rcvs.org.uk/setting-standards/advice-and-guidance/code-of-professional-conduct-for-veterinary-surgeons/supporting-guidance/veterinary-medicines/ [Accessed 14 September 2022]
- Report a suspected problem with an animal medicine or microchip [Veterinary Medicines Directorate] [online] Available from: https://www.gov.uk/report-veterinary-medicine-problem/animal-reacts-medicine [Accessed 14 September 2022]
- Veterinary Pharmacovigilance responsibilities for authorisation holders. [Veterinary Medicines Directorate] [online] Available from: https://www.gov.uk/guidance/veterinary-pharmacovigilance-your-responsibilities [Accessed 14 September 2022] .
Although primarily written for Marketing Authorisation Holders this includes useful definitions on the different types of adverse events that should be reported. - Pharmacovigilance of veterinary medicines in Great Britain: Guidance – Adverse event reporting. [Veterinary Medicines Directorate] [online] Available from: https://www.gov.uk/government/publications/pharmacovigilance-of-veterinary-medicines-in-great-britain/adverse-event-reporting [Accessed 14 September 2022]
Section 5 provides useful information on the information that is required in an adverse reaction report - Pharmacovigilance: Monitoring the safety & efficacy of animal medicines [National Office of Animal Health] [online] Available from: https://www.noah.co.uk/briefingdocument/pharmacovigilance-monitoring-safety-efficacy-animal-medicines/ [Accessed 14 September 2022]
- Pharmacovigilance guidance [European Medicines Agency] [online] Available from: https://www.ema.europa.eu/en/veterinary-regulatory/post-authorisation/pharmacovigilance/pharmacovigilance-guidance [Accessed 14 September 2022]
Pharmacovigilance reports
- Veterinary medicines pharmacovigilance annual review reports [Veterinary Medicines Directorate] [online] Available from: https://www.gov.uk/government/collections/veterinary-medicines-pharmacovigilance-annual-review-reports [Accessed 14 September 2022]
- European Medicines Agency (2020)Veterinary pharmacovigilance 2019: annual bulletin. Amsterdam: EMA. Available from: https://www.ema.europa.eu/en/documents/newsletter/public-bulletin-veterinary-pharmacovigilance-2019_en.pdf [Accessed 14 September 2022]
- EudraVigilance – European database of suspected adverse drug reaction reports. [European Medicines Agency] [online] Available from: https://www.adrreports.eu/ [Accessed 14 September 2022]
Medicines updates are published regularly in the Veterinary Record and the Vet Times.
Lists of updates are also available from
- Product Information Database: Currently authorised products – recently updated. [Veterinary Medicines Directorate] [online] Available from: https://www.vmd.defra.gov.uk/ProductInformationDatabase/current/recently-updated [Accessed 14 September 2022]
- NOAH compendium: new and updated datasheets. [National Office of Animal Health] [online] Available from: https://www.noahcompendium.co.uk/?id=-312948&cid=-312948 [Accessed 14 September 2022]
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