Reaction profile

The FDA adverse-event record for eyelid ptosis - neurologic (see also drooping eyelid nos)

19 FDA adverse-event reports reference eyelid ptosis - neurologic (see also drooping eyelid nos) (VeDDRA 2392). See the species, breeds, and drugs most associated with it below.

19
reports citing this reaction
10.5%
death-coded share
Dog
most-affected species
Bedinvetmab
most-associated drug
Verify with FDA CVM →
19
Total Reports
2
Deaths
10.5%
Death Rate

Species Most Affected

Dog 16
Cat 2
Other 1

Breeds Most Affected

Retriever - Golden 3
Terrier - Bull - Staffordshire 2
Retriever - Labrador 2
Domestic Shorthair 2
Boxer (German Boxer) 1
Shiba Inu 1
Maltese 1
Pit Bull 1
Bulldog - French 1
Siberian Husky 1

Associated Drugs

Bedinvetmab 6
Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 3
Oclacitinib Maleate 3
Ear Cleaner (Unknown) 3
Florfenicol + Mometasone Furoate + Terbinafine 3
Imepitoin 2
Carprofen 2
Dexamethasone + Neomycin Sulfate + Polymyxin B Sulfate 1
Artificial Tears 1
Cyclosporine 1
Marbofloxacin 1
Eye Medication (Unknown) 1
Eye Ointment (Unknown) 1
Prescription Diet 1
Sarolaner,Moxidectin,Pyrantel 1
Fluconazole 1
Leptospirosis Vaccine 1
Tromethamine (Tris) Usp + Edetate Disodium Dihydrate (Edta) Usp 1
Moxidectin 1
Unspecified Rabies Vaccine 1

Eyelid ptosis - neurologic (see also Drooping eyelid NOS) Reaction Insights

19 reports name Eyelid ptosis - neurologic (see also Drooping eyelid NOS); 2 recorded a death outcome (10.5% of reported events, not a population-level mortality rate). VeDDRA code: 2392.

By species: Dog (16 reports), Cat (2 reports), Other (1 reports). By breed: Retriever - Golden (3), Terrier - Bull - Staffordshire (2), Retriever - Labrador (2).

Most co-reported drugs: Bedinvetmab (6 reports), Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride (3 reports), Oclacitinib Maleate (3 reports), Ear Cleaner (Unknown) (3 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.