Reaction profile

The FDA adverse-event record for collapse nos (see also 'cardio-vascular' and 'neurological disorders')

2,689 FDA adverse-event reports reference collapse nos (see also 'cardio-vascular' and 'neurological disorders') (VeDDRA 1001). See the species, breeds, and drugs most associated with it below.

2,689
reports citing this reaction
29.2%
death-coded share
Dog
most-affected species
Moxidectin
most-associated drug
Verify with FDA CVM →
2,689
Total Reports
784
Deaths
29.2%
Death Rate

Species Most Affected

Dog 2,375
Cat 179
Horse 70
Cattle 46
Pig 5
Sheep 3
Donkey 2
Human 2
Other Equids 2
Chicken 1

Breeds Most Affected

Retriever - Labrador 239
Boxer (German Boxer) 131
Domestic Shorthair 121
Crossbred Canine/dog 120
Retriever - Golden 110
Terrier - Bull - American Pit 100
Chihuahua 97
Shih Tzu 90
Terrier - Yorkshire 80
Shepherd Dog - German 80

Associated Drugs

Moxidectin 605
Maropitant Citrate 198
Milbemycin Oxime + Spinosad 186
Afoxolaner 179
Carprofen 145
Trilostane 131
Melarsomine Dihydrochloride 111
Diphenhydramine Hcl 102
Oclacitinib Maleate 100
Rabies Virus, 98
Cefovecin 97
Prednisone 95
Dexamethasone 89
Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str 89
Ivermectin + Pyrantel As Pamoate Salt 81
Fluralaner Chew Tablets 80
Sarolaner 67
Gabapentin 66
Pyrantel Pamoate;Sarolaner 62
Melarsomine Dihydrochloride Injection 60

Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') Reaction Insights

2,689 reports name Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders'); 784 recorded a death outcome (29.2% of reported events, not a population-level mortality rate). VeDDRA code: 1001.

By species: Dog (2,375 reports), Cat (179 reports), Horse (70 reports). By breed: Retriever - Labrador (239), Boxer (German Boxer) (131), Domestic Shorthair (121).

Most co-reported drugs: Moxidectin (605 reports), Maropitant Citrate (198 reports), Milbemycin Oxime + Spinosad (186 reports), Afoxolaner (179 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.