Reaction profile

The FDA adverse-event record for uraemia

Name: Uraemia - FDA Animal Adverse Reaction
Creator: PlainBreed
License: https://open.fda.gov/license/

25 FDA reports name uraemia, a lower-volume reaction in the CVM extract (VeDDRA 722). Plate stamps and neighbourhood peers follow.

#2079 of 2,481
by report volume (all reactions): 25
reports citing this reaction: 76.0%
death-coded share: Dog
most-affected species

Compiled by PlainBreed

Verify with FDA CVM →

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Uraemia has 25 reports now versus 24 in that prior snapshot: 1 more (4.2%).

Report change: +1
Death-coded reports: +1
Death-coded share: +1.0 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Uraemia changes

FDA AER · VeDDRA plate

Code 722 VOL-TRACE

VOL-TRACE · DEATH-HOT · LOWER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

VOL-TRACE 25 reports
DEATH-HOT 76.0%
LOWER-Q #2079/2481
PHOTO-FINISH Abnormal behaviour NOS
SPECIES-DOG Dog · 21
DRUG-LEAD Meloxicam · 4
DESK-WIDE 20 breeds
BOOK-FULL 8/8 fields

Nearest volume peer: Abnormal behaviour NOS (±0 reports)

Upper-third death-coded share drives the outcome stamps on this plate; volume band, corpus rank, and co-report peers follow. Not a clinical diagnosis.

Lower-volume neighbourhood around Uraemia

Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.

FDA AER report volume · neighbourhood around Uraemia

Uraemia: high death-coded share in the FDA AER plate

Signature read: Uraemia's 76.0% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 25 named reports in the openFDA extract. Death-coded share is upper-third: 19 of 25 reports (76.0% of named reports). Nearest volume peer: Abnormal behaviour NOS (±0 reports). Lead species Dog (21). Lead co-reported drug Meloxicam (4).

Read these counts as reporting volume, not risk: per our methodology, A high death-coded share in FDA filings does not prove causation; co-reporting is voluntary temporal association only. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 21

Cat 4

Breeds Most Affected

Chihuahua 2

Domestic Shorthair 2

Cat (unknown) 2

Crossbred Canine/dog 1

Corgi (unspecified) 1

Terrier - Bull - Staffordshire 1

Terrier - Yorkshire 1

Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1

Dog (unknown) 1

Spaniel - Cocker American 1

Associated Drugs

Meloxicam 4

Carprofen 3

Trilostane 3

Deracoxib 2

Afoxolaner 2

Firocoxib 2

Doxycycline 2

Imidacloprid, Moxidectin 1

Firocoxib 57 Mg Chewable 1

Thyroxine 1

Denamarin 1

Milbemycin Oxime + Spinosad 1

Tramadol 1

Fish Oil 1

Glucosamine 1

Semintra Telmisartan 4 Mg/Ml 1

Cefovecin 1

Praziquantel 1

Unspecified Medications 1

Fluids 1

What to do with this reaction

Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
Browse the full reaction directory to compare report counts across reaction types. All reactions

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Uraemia (#2079 of 2,481 by report volume); death-coded 76.0%. PlainBreed reaction plate · death-coded share stamp 76.0% · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →