Reaction profile

The FDA adverse-event record for ineffective, loss of effect

3,644 FDA adverse-event reports reference ineffective, loss of effect (VeDDRA 99125). See the species, breeds, and drugs most associated with it below.

3,644
reports citing this reaction
2.4%
death-coded share
Dog
most-affected species
Oclacitinib Maleate
most-associated drug
Verify with FDA CVM →
3,644
Total Reports
88
Deaths
2.4%
Death Rate

Species Most Affected

Dog 3,186
Cat 433
Horse 11
Cattle 4
Other 3
Pig 2
Fish 1
Unknown 1
Other Deer 1
Sheep 1

Breeds Most Affected

Retriever - Labrador 283
Crossbred Canine/dog 256
Dog (unknown) 245
Shih Tzu 161
Domestic Shorthair 156
Terrier - Yorkshire 144
Chihuahua 125
Shepherd Dog - German 106
Retriever - Golden 101
Cat (unknown) 87

Associated Drugs

Oclacitinib Maleate 1,805
Insulin Injectable Vial 451
Trilostane 299
Fluralaner Chew Tablets 131
Anti-Il31 Mab Mcs Lot #1283563 127
Spinosad 112
Porcine Insulin 109
Prednisolone; Trimeprazine Tartrate 100
Fluralaner 13.64% 12-Week Chew 97
Fluralaner Spot-On Solution 83
Human Insulin 74
Protamine Zinc Recombinant Human Insulin 66
Carprofen 55
Prednisone 50
Cyclosporine 43
Recombinant Human Insulin 42
Selamectin 39
Cefpodoxime Proxetil 39
Nitenpyram 37
Afoxolaner 36

INEFFECTIVE, LOSS OF EFFECT Reaction Insights

3,644 reports name INEFFECTIVE, LOSS OF EFFECT; 88 recorded a death outcome (2.4% of reported events, not a population-level mortality rate). VeDDRA code: 99125.

By species: Dog (3,186 reports), Cat (433 reports), Horse (11 reports). By breed: Retriever - Labrador (283), Crossbred Canine/dog (256), Dog (unknown) (245).

Most co-reported drugs: Oclacitinib Maleate (1,805 reports), Insulin Injectable Vial (451 reports), Trilostane (299 reports), Fluralaner Chew Tablets (131 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.