Reaction profile

The FDA adverse-event record for cloudy eye (for miosis, mydriasis, anisocoria, nystagmus - see neurological)

66 FDA adverse-event reports reference cloudy eye (for miosis, mydriasis, anisocoria, nystagmus - see neurological) (VeDDRA 445). See the species, breeds, and drugs most associated with it below.

66
reports citing this reaction
9.1%
death-coded share
Dog
most-affected species
Prednisone
most-associated drug
Verify with FDA CVM →
66
Total Reports
6
Deaths
9.1%
Death Rate

Species Most Affected

Dog 46
Cat 15
Cattle 3
Mouse 1
Human 1

Breeds Most Affected

Domestic Shorthair 9
Crossbred Canine/dog 8
Chihuahua 4
Domestic Longhair 3
Pekingese 3
Pit Bull 2
Terrier - Yorkshire 2
Retriever - Labrador 2
Deutsche Dogge, Great Dane 2
Bulldog - French 2

Associated Drugs

Prednisone 8
Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 7
Bacitracin + Neomycin + Polymyxin B 7
Maropitant Citrate 6
Gabapentin 5
Florfenicol, Terbinafine, Betamethasone Acetate 4
Meloxicam 4
Bedinvetmab 4
Cyclosporine 4
Grapiprant 4
Florfenicol,Mometasone Furoate,Terbinafine Hydrochloride 4
Leptospirosis Vaccine 3
Bordetella Vaccine 3
Ofloxacin 3
Cyclosporine (Ophthalmic) 3
Pilocarpine Ophthalmic 3
Tobramycin 3
Lotilaner 3
Midazolam 3
Neomycin + Polymyxin + Bacitracin + Hydrocortisone Ophthalmic 3

Cloudy eye (for Miosis, Mydriasis, Anisocoria, Nystagmus - see Neurological) Reaction Insights

66 reports name Cloudy eye (for Miosis, Mydriasis, Anisocoria, Nystagmus - see Neurological); 6 recorded a death outcome (9.1% of reported events, not a population-level mortality rate). VeDDRA code: 445.

By species: Dog (46 reports), Cat (15 reports), Cattle (3 reports). By breed: Domestic Shorthair (9), Crossbred Canine/dog (8), Chihuahua (4).

Most co-reported drugs: Prednisone (8 reports), Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride (7 reports), Bacitracin + Neomycin + Polymyxin B (7 reports), Maropitant Citrate (6 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.