At Zoetis, we take suspected adverse events very seriously for all of our products, including Librela. Our team of veterinary experts work alongside both pet owners and their attending veterinarians to understand each pet’s unique situation when brought to our attention. We know that all pets have different lifestyles, health conditions, genetics etc., and understanding all of these elements is important to evaluating a pet’s full health profile.
Zoetis also has systems in place to continuously monitor the volume and trends of adverse event reporting related to all of our veterinary medicines, including Librela. We are required to share these reports of aggregated case data to regulatory agencies around the world, and if a new safety signal emerges, we partner with regulatory authorities on appropriate actions which could include amendment of our label as necessary to better inform veterinarians and pet owners of potential risks or safety concerns to mitigate risks to the pet.
We encourage all pet owners who believe their pet may have had an adverse reaction to any medication to contact their pet’s veterinarian first. Pet owners also need to contact Zoetis, and when they do, we document the conversation and make every effort to include the attending veterinarian in the conversation. This helps us fully understand each case and report a potential adverse effect to the appropriate regulatory body. We always encourage pet owners to also speak with their veterinarian for further consultation and advice after speaking with the Zoetis team.