Reaction profile

The FDA adverse-event record for lymphoma

885 FDA adverse-event reports reference lymphoma (VeDDRA 176). See the species, breeds, and drugs most associated with it below.

885
reports citing this reaction
44.0%
death-coded share
Dog
most-affected species
Oclacitinib Maleate
most-associated drug
Verify with FDA CVM →
885
Total Reports
389
Deaths
44.0%
Death Rate

Species Most Affected

Dog 766
Cat 113
Cattle 3
Ferret 1
Horse 1
Mouse 1

Breeds Most Affected

Retriever - Labrador 79
Dog (unknown) 73
Domestic Shorthair 67
Retriever - Golden 53
Crossbred Canine/dog 37
Boxer (German Boxer) 35
Terrier - Bull - American Pit 35
Shepherd Dog - German 30
Shih Tzu 20
Bulldog 18

Associated Drugs

Oclacitinib Maleate 275
Milbemycin Oxime + Spinosad 74
Bedinvetmab 58
Prednisone 48
Fluralaner Chew Tablets 45
Cyclosporine A 41
Carprofen 40
Cyclosporine 34
Maropitant Citrate 32
Anti-Il31 Mab Mcs Lot #1283563 32
Gabapentin 30
Trilostane 24
Afoxolaner 24
Frunevetmab 23
Grapiprant 22
Ketoconazole 20
Fluralaner 13.64% 12-Week Chew 20
Spinosad 19
Enrofloxacin 18
Cefovecin 17

Lymphoma Reaction Insights

885 reports name Lymphoma; 389 recorded a death outcome (44.0% of reported events, not a population-level mortality rate). VeDDRA code: 176.

By species: Dog (766 reports), Cat (113 reports), Cattle (3 reports). By breed: Retriever - Labrador (79), Dog (unknown) (73), Domestic Shorthair (67).

Most co-reported drugs: Oclacitinib Maleate (275 reports), Milbemycin Oxime + Spinosad (74 reports), Bedinvetmab (58 reports), Prednisone (48 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.