Reaction profile

The FDA adverse-event record for physical product label issues

142 FDA adverse-event reports reference physical product label issues (VeDDRA 99850). See the species, breeds, and drugs most associated with it below.

142
reports citing this reaction
0.0%
death-coded share
Unknown
most-affected species
Meloxicam
most-associated drug
Verify with FDA CVM →
142
Total Reports
0
Deaths
0.0%
Death Rate

Species Most Affected

Unknown 137
Dog 4
Cat 1

Breeds Most Affected

Unknown 137
Terrier - Yorkshire 1
Retriever - Labrador 1
Maltese 1
Poodle (unspecified) 1
Domestic Shorthair 1

Associated Drugs

Meloxicam 22
Afoxolaner 16
Milbemycin Oxime + Spinosad 8
Ivermectin + Pyrantel As Pamoate Salt 8
Velagliflozin Proline Monohydrate 8
Tiletamine + Zolazepam 6
Furosemide Tablets 5
Pimobendan 5
Ivermectin(1.55%)/Praziquantel(7.75%) Paste 4
Carprofen 4
Gamithromycin 15% 3
Cyclosporine 3
Nitenpyram 3
Cyclosporine A 2
Ivermectin 2
Firocoxib 2
Eprinomectin 2
Milbemycin Oxime + Praziquantel 2
Robenacoxib 2
Ketamine Hydrochloride 2

Physical product label issues Reaction Insights

142 reports name Physical product label issues; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 99850.

By species: Unknown (137 reports), Dog (4 reports), Cat (1 reports). By breed: Unknown (137), Terrier - Yorkshire (1), Retriever - Labrador (1).

Most co-reported drugs: Meloxicam (22 reports), Afoxolaner (16 reports), Milbemycin Oxime + Spinosad (8 reports), Ivermectin + Pyrantel As Pamoate Salt (8 reports).

Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.