Reaction profile

The FDA adverse-event record for abscess nos

474 FDA reports name abscess nos, a high-volume reaction in the CVM extract (VeDDRA 2074). Plate stamps and neighbourhood peers follow.

#660 of 2,481
by report volume (all reactions)
474
reports citing this reaction
26.4%
death-coded share
Dog
most-affected species

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. Abscess NOS has 474 reports now versus 468 in that prior snapshot: 6 more (1.3%).

Report change
+6
Death-coded reports
+0
Death-coded share
−0.3 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 Abscess NOS changes

FDA AER · VeDDRA plate

Code 2074 VOL-LOW

VOL-LOW · DEATH-HOT · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-LOW 474 reports
  • DEATH-HOT 26.4%
  • MID-PACK #660/2481
  • PHOTO-FINISH Apprehension
  • SPECIES-DOG Dog · 285
  • DRUG-LEAD Carprofen · 50
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Apprehension (±1 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.

High-volume neighbourhood around Abscess NOS

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

Vomiting · highest174348Abscess NOS · this reaction474Apprehension · near473Paralysis · near473Heart failure · near472Welt · near472Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Abscess NOS

Abscess NOS: high death-coded share in the FDA AER plate

Signature read: 125 death-coded reports is a heavy tail count for Abscess NOS in the CVM extract. Report volume is upper-third scale: 474 named reports in the openFDA extract. Death-coded share is upper-third: 125 of 474 reports (26.4% of named reports). Nearest volume peer: Apprehension (±1 reports). Lead species Dog (285). Lead co-reported drug Carprofen (50).

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 285
Cat 80
Cattle 65
Horse 34
Guinea Pig 3
Rabbit 3
Pig 2
Chicken 1
Tortoise 1

Breeds Most Affected

Domestic Shorthair 48
Retriever - Labrador 32
Cattle (other) 22
Crossbred Canine/dog 17
Chihuahua 15
Holstein-Friesian also known as Holstein 13
Terrier - Yorkshire 12
Beagle 11
Cat (unknown) 11
Retriever - Golden 11

Associated Drugs

Carprofen 50
Oclacitinib Maleate 47
Maropitant Citrate 31
Milbemycin Oxime + Spinosad 30
Cefovecin 27
Enrofloxacin 25
Monensin Sodium 23
Prednisone 23
Bedinvetmab 22
Meloxicam 21
Ceftiofur Crystalline Free Acid 15
Afoxolaner 15
Gabapentin 14
Buprenorphine 14
Moxidectin 13
Tylosin Phosphate 12
Doxycycline 12
Tulathromycin 11
Rabies Vaccine 11
Firocoxib 11

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Abscess NOS, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar report volume

Nearest other reactions by FDA report count (474 here).

Similar death-coded share

Nearest other reactions by death-coded share (26.4% here), distinct from the volume row.

What to do with this reaction

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 Abscess NOS (#660 of 2,481 by report volume); death-coded 26.4%. PlainBreed reaction plate · death-coded report count stamp 125 · 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 →