Reaction profile

The FDA adverse-event record for localised pain nos (see other 'socs' for specific pain)

1,415 FDA adverse-event reports reference localised pain nos (see other 'socs' for specific pain) (VeDDRA 1026). See the species, breeds, and drugs most associated with it below.

1,415
reports citing this reaction
12.2%
death-coded share
Dog
most-affected species
Milbemycin Oxime + Spinosad
most-associated drug
Verify with FDA CVM →
1,415
Total Reports
172
Deaths
12.2%
Death Rate

Species Most Affected

Dog 1,166
Cat 123
Human 74
Horse 40
Cattle 10
Goat 1
Other Birds 1

Breeds Most Affected

Retriever - Labrador 102
Unknown 76
Domestic Shorthair 72
Crossbred Canine/dog 68
Shepherd Dog - German 47
Chihuahua 46
Boxer (German Boxer) 43
Retriever - Golden 42
Shih Tzu 42
Terrier - Yorkshire 40

Associated Drugs

Milbemycin Oxime + Spinosad 213
Carprofen 143
Moxidectin 106
Oclacitinib Maleate 88
Maropitant Citrate 84
Fluralaner Chew Tablets 73
Prednisone 72
Cefovecin 70
Afoxolaner 47
Spinosad 46
Tramadol 46
Gabapentin 46
Trilostane 43
Meloxicam 43
Selamectin 41
Melarsomine Dihydrochloride 41
Ivermectin + Pyrantel As Pamoate Salt 37
Buprenorphine 36
Milbemycin Oxime + Praziquantel 36
Canine Adenovirus Type 2, Strain Manhattan, 12-13-76; Canine Distemper Virus, St 32

Localised pain NOS (see other 'SOCs' for specific pain) Reaction Insights

1,415 reports name Localised pain NOS (see other 'SOCs' for specific pain); 172 recorded a death outcome (12.2% of reported events, not a population-level mortality rate). VeDDRA code: 1026.

By species: Dog (1,166 reports), Cat (123 reports), Human (74 reports). By breed: Retriever - Labrador (102), Unknown (76), Domestic Shorthair (72).

Most co-reported drugs: Milbemycin Oxime + Spinosad (213 reports), Carprofen (143 reports), Moxidectin (106 reports), Oclacitinib Maleate (88 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.