Reaction profile

The FDA adverse-event record for lethargy (see also central nervous system depression in neurological)

14,207 FDA adverse-event reports reference lethargy (see also central nervous system depression in neurological) (VeDDRA 1018). See the species, breeds, and drugs most associated with it below.

14,207
reports citing this reaction
14.2%
death-coded share
Dog
most-affected species
Bedinvetmab
most-associated drug
Verify with FDA CVM →
14,207
Total Reports
2,016
Deaths
14.2%
Death Rate

Species Most Affected

Dog 10,390
Cat 3,662
Horse 70
Cattle 30
Ferret 9
Pig 8
Goat 5
Other Birds 5
Rabbit 4
Chicken 4

Breeds Most Affected

Domestic Shorthair 2,294
Retriever - Labrador 1,061
Crossbred Canine/dog 745
Retriever - Golden 619
Chihuahua 456
Shepherd Dog - German 410
Dog (unknown) 358
Shih Tzu 322
Terrier - Yorkshire 300
Domestic Longhair 297

Associated Drugs

Bedinvetmab 1,963
Pyrantel Pamoate;Sarolaner 1,265
Maropitant Citrate 988
Gabapentin 880
Carprofen 763
Afoxolaner 739
Moxidectin 738
Oclacitinib Maleate 647
Fluralaner 13.64% 12-Week Chew 613
Frunevetmab 613
Milbemycin Oxime + Praziquantel 441
Trilostane 425
Velagliflozin Proline Monohydrate 419
Eprinomectin + Esafoxolaner + Praziquantel 406
Lotilaner 397
Prednisone 390
Bexagliflozin 373
Ivermectin + Pyrantel As Pamoate Salt 354
Buprenorphine 337
Cefovecin 314

Lethargy (see also Central nervous system depression in Neurological) Reaction Insights

14,207 reports name Lethargy (see also Central nervous system depression in Neurological); 2,016 recorded a death outcome (14.2% of reported events, not a population-level mortality rate). VeDDRA code: 1018.

By species: Dog (10,390 reports), Cat (3,662 reports), Horse (70 reports). By breed: Domestic Shorthair (2,294), Retriever - Labrador (1,061), Crossbred Canine/dog (745).

Most co-reported drugs: Bedinvetmab (1,963 reports), Pyrantel Pamoate;Sarolaner (1,265 reports), Maropitant Citrate (988 reports), Gabapentin (880 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.