Librela Petition Comments Guide
Use this guide to submit a public comment on the FDA docket for the Librela citizen petition.
You can submit a public comment on the official FDA docket for the Librela citizen petition.
Public comments help FDA reviewers understand owner experiences, prescribing practices, timelines, documentation, and concerns related to Librela / bedinvetmab.
How to submit a comment
Click the official FDA docket link.
On the regulations.gov page, select Comment.
In the “Select a comment category” dropdown, choose:
Individual Consumer
Write your comment.
Upload supporting documents if you have them.
Examples may include veterinary records, invoices, receipts, medication timelines, lab results, imaging records, discharge summaries, or written timelines of what happened.
Review your comment before submitting.
What to include in your comment
Your comment does not need to be long. It should be truthful, clear, and based on your own experience or evidence.
Helpful details may include:
Your dog’s age, breed, and general health before Librela
Date of Librela injection or approximate timing
Whether imaging was done before Librela
Whether your dog was taking NSAIDs, steroids, or other medications
Whether any washout period was used before the first injection
What happened after Librela
How soon signs appeared after the injection
Whether the veterinarian was contacted
Whether records, receipts, or other documents support the timeline
Simple comment structure
You can use this format:
1. I support the petition.
Briefly say whether you support the petition and why.
2. My dog’s experience.
Explain what happened in chronological order.
3. Supporting details.
Mention any records, receipts, medication history, imaging, lab work, or timeline information.
4. What I want FDA to consider.
Explain why you believe stronger Librela prescribing protocols, screening, warnings, monitoring, or owner documentation are needed.
Important note
Public comments should be accurate and based on your own experience or evidence.
These adverse-event reports and owner comments do not prove incidence or causation by themselves. However, detailed comments can help FDA reviewers evaluate real-world prescribing practices, timelines, documentation, and safety concerns.
Click below to open the official FDA docket and submit your public comment.