Watch the trailer below for “Librela clinical update: 4 years of clinical experience” by George Matthews BVMedSci (Hons) BVM BVS (Hons) PGDipVCP MRCVS

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This webinar is kindly sponsored by:

Lecture Synopsis:

Pharmacovigilance is based on continuous product monitoring post approval to build on the knowledge gained during clinical studies and understanding of a product’s safety and efficacy profile. This lecture will include an overview of the processes of pharmacovigilance including its benefits and limitations as well as an overview of the global pharmacovigilance data available for Librela1, the first anti-Nerve Growth Factor monoclonal antibody for management of osteoarthritis pain.

1. Monteiro, B.P., Simon, A., Knesl, O., Mandello, K., Nederveld, S., Olby, N.J., Innes, J.F., Lascelles, B.D.X. (2025) Global pharmacovigilance reporting of the first monoclonal antibody for canine osteoarthritis: a case study with bedinvetmab (Librela™). Frontiers Vet Sci. 2025;12

IMPORTANT NOTE: Please be advised that the Librela GB SPC has been updated since this presentation was written and recorded, so the SPC slide within this presentation is now out of date. The link to the most recent Librela SPC can be found on the VMD website (https://www.vmd.defra.gov.uk/ProductInformationDatabase/product/A010534).

Learning Points:

  1. Understand how a product safety profile is established and the process of pharmacovigilance
  2. Understand how to report a suspected adverse reaction to a veterinary medication
  3. To gain insight into the global pharmacovigilance and safety data for Librela

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