Reaction profile

The FDA adverse-event record for ascites

832 FDA adverse-event reports reference ascites (VeDDRA 1030). See the species, breeds, and drugs most associated with it below.

832
reports citing this reaction
51.9%
death-coded share
Dog
most-affected species
Carprofen
most-associated drug
Verify with FDA CVM →
832
Total Reports
432
Deaths
51.9%
Death Rate

Species Most Affected

Dog 724
Cat 94
Cattle 8
Chicken 2
Turkey 1
Other Birds 1
Pig 1
Goat 1

Breeds Most Affected

Retriever - Labrador 140
Crossbred Canine/dog 73
Domestic Shorthair 46
Retriever - Golden 35
Rottweiler 32
Dog (unknown) 20
Shepherd Dog - German 19
Domestic (unspecified) 17
Spaniel - Cocker American 17
Shepherd Dog - Australian 16

Associated Drugs

Carprofen 126
Deracoxib 94
Maropitant Citrate 66
Oclacitinib Maleate 49
Meloxicam 44
Milbemycin Oxime + Spinosad 43
Firocoxib 36
Fluralaner Chew Tablets 31
Spinosad 30
Moxidectin 29
Tramadol 29
Bedinvetmab 28
Prednisone 26
Maropitant 25
Firocoxib 227 Mg Chewable 23
Cefovecin 23
Ivermectin + Pyrantel As Pamoate Salt 23
Famotidine 22
Doxycycline 21
Pimobendan 19

Ascites Reaction Insights

832 reports name Ascites; 432 recorded a death outcome (51.9% of reported events, not a population-level mortality rate). VeDDRA code: 1030.

By species: Dog (724 reports), Cat (94 reports), Cattle (8 reports). By breed: Retriever - Labrador (140), Crossbred Canine/dog (73), Domestic Shorthair (46).

Most co-reported drugs: Carprofen (126 reports), Deracoxib (94 reports), Maropitant Citrate (66 reports), Oclacitinib Maleate (49 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.