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#34 Veterinary pharmacovigilance, Part I – James Mount

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Manage episode 455951951 series 2749727
Content provided by Uppsala Monitoring Centre. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Uppsala Monitoring Centre or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Human and veterinary pharmacovigilance (PV) share many goals, challenges and approaches. But there are also significant differences, such as the numerous species and breeds that veterinary PV needs to take into account. In this two-part episode of Drug Safety Matters, James Mount, Veterinary Pharmacovigilance assessor at the Swedish Medical Products Agency, and EU elected chair of the Pharmacovigilance Working Party for veterinary medicinal products, joins the show to talk about veterinary PV practice and its differences and similarities to human PV.

Tune in to find out:

  • What are the similarities and differences between veterinary and human pharmacovigilance?
  • How is animal health connected to public health?
  • What types of adverse events are reported on the veterinary side compared with the human side?
  • What can be found in the EU veterinary pharmacovigilance database?

Want to know more?

Join the conversation on social media
Follow us on X, LinkedIn, or Facebook and share your thoughts about the show with the hashtag #DrugSafetyMatters.
Got a story to share?
We’re always looking for new content and interesting people to interview. If you have a great idea for a show, get in touch!
About UMC
Read more about Uppsala Monitoring Centre and how we work to advance medicines safety.

  continue reading

Chapters

1. #34 Veterinary pharmacovigilance, Part I – James Mount (00:00:00)

2. Intro (00:00:15)

3. How similar is veterinary pharmacovigilance to human pharmacovigliance? (00:01:36)

4. The connection between animal and public health (00:06:31)

5. Side effects in animals, detection and (under-) reporting (00:10:00)

6. Proportion of ADR reports from pet owners vs professionals (00:14:20)

7. Detection and reporting of side effects in production animals (00:14:56)

8. Initiatives and innovations to stimulate more reporting on the veterinary side (00:16:31)

9. Are we tolerating more side effects from veterinary medicinal products? (00:25:23)

10. Are animal protection regulations reflected in national veterinary PV practices? (00:27:34)

11. Why, and how, are veterinarians using both human and veterinary medicinal products in their practice? (00:29:38)

12. The EU database for veterinary suspected adverse drug reactions (00:36:20)

13. Differences in ADR reporting of individuals (pets) vs masses (production animals)s (00:40:08)

14. More on veterinary pharmacovigilance databases, VeDDRA, etc. (00:42:52)

15. Thanks and goodbye (00:45:12)

52 episodes

Artwork
iconShare
 
Manage episode 455951951 series 2749727
Content provided by Uppsala Monitoring Centre. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Uppsala Monitoring Centre or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Human and veterinary pharmacovigilance (PV) share many goals, challenges and approaches. But there are also significant differences, such as the numerous species and breeds that veterinary PV needs to take into account. In this two-part episode of Drug Safety Matters, James Mount, Veterinary Pharmacovigilance assessor at the Swedish Medical Products Agency, and EU elected chair of the Pharmacovigilance Working Party for veterinary medicinal products, joins the show to talk about veterinary PV practice and its differences and similarities to human PV.

Tune in to find out:

  • What are the similarities and differences between veterinary and human pharmacovigilance?
  • How is animal health connected to public health?
  • What types of adverse events are reported on the veterinary side compared with the human side?
  • What can be found in the EU veterinary pharmacovigilance database?

Want to know more?

Join the conversation on social media
Follow us on X, LinkedIn, or Facebook and share your thoughts about the show with the hashtag #DrugSafetyMatters.
Got a story to share?
We’re always looking for new content and interesting people to interview. If you have a great idea for a show, get in touch!
About UMC
Read more about Uppsala Monitoring Centre and how we work to advance medicines safety.

  continue reading

Chapters

1. #34 Veterinary pharmacovigilance, Part I – James Mount (00:00:00)

2. Intro (00:00:15)

3. How similar is veterinary pharmacovigilance to human pharmacovigliance? (00:01:36)

4. The connection between animal and public health (00:06:31)

5. Side effects in animals, detection and (under-) reporting (00:10:00)

6. Proportion of ADR reports from pet owners vs professionals (00:14:20)

7. Detection and reporting of side effects in production animals (00:14:56)

8. Initiatives and innovations to stimulate more reporting on the veterinary side (00:16:31)

9. Are we tolerating more side effects from veterinary medicinal products? (00:25:23)

10. Are animal protection regulations reflected in national veterinary PV practices? (00:27:34)

11. Why, and how, are veterinarians using both human and veterinary medicinal products in their practice? (00:29:38)

12. The EU database for veterinary suspected adverse drug reactions (00:36:20)

13. Differences in ADR reporting of individuals (pets) vs masses (production animals)s (00:40:08)

14. More on veterinary pharmacovigilance databases, VeDDRA, etc. (00:42:52)

15. Thanks and goodbye (00:45:12)

52 episodes

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