Reaction profile

The FDA adverse-event record for nt - abnormal necropsy finding nos

1,268 FDA adverse-event reports reference nt - abnormal necropsy finding nos (VeDDRA 2142). See the species, breeds, and drugs most associated with it below.

1,268
reports citing this reaction
99.4%
death-coded share
Dog
most-affected species
Milbemycin Oxime + Spinosad
most-associated drug
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1,268
Total Reports
1,260
Deaths
99.4%
Death Rate

Species Most Affected

Dog 674
Cattle 307
Cat 148
Chicken 33
Pig 31
Horse 25
Turkey 13
Sheep 10
Goat 8
Other Birds 3

Breeds Most Affected

Domestic Shorthair 99
Retriever - Labrador 84
Holstein-Friesian also known as Holstein 77
Cattle (other) 71
Cattle (unknown) 54
Shepherd Dog - German 43
Crossbred Canine/dog 40
Aberdeen Angus 27
Mixed (Cattle) 27
Pig (unknown) 26

Associated Drugs

Milbemycin Oxime + Spinosad 236
Monensin Sodium 155
Spinosad 132
Fluralaner Chew Tablets 105
Deracoxib 54
Tulathromycin 45
Afoxolaner 45
Rabies Vaccine 35
Robenacoxib 34
Ceftiofur Crystalline Free Acid 33
Carprofen 32
Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia 26
Ivermectin + Pyrantel As Pamoate Salt 25
Moxidectin 24
Isoflurane 24
Milbemycin Oxime + Praziquantel 24
Ivermectin 23
Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn 23
Tramadol 23
Grapiprant 23

NT - Abnormal necropsy finding NOS Reaction Insights

1,268 reports name NT - Abnormal necropsy finding NOS; 1,260 recorded a death outcome (99.4% of reported events, not a population-level mortality rate). VeDDRA code: 2142.

By species: Dog (674 reports), Cattle (307 reports), Cat (148 reports). By breed: Domestic Shorthair (99), Retriever - Labrador (84), Holstein-Friesian also known as Holstein (77).

Most co-reported drugs: Milbemycin Oxime + Spinosad (236 reports), Monensin Sodium (155 reports), Spinosad (132 reports), Fluralaner Chew Tablets (105 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.