Reaction profile

The FDA adverse-event record for abrasion

171 FDA adverse-event reports reference abrasion (VeDDRA 2594). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1118 of 2,481
by report volume (all reactions)
171
reports citing this reaction
4.7%
death-coded share
Cat
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. Abrasion has 171 reports now versus 163 in that prior snapshot: 8 more (4.9%).

Report change
+8
Death-coded reports
+0
Death-coded share
−0.2 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 Abrasion changes

FDA AER · VeDDRA plate

Code 2594 VOL-LOW

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

  • VOL-LOW 171 reports
  • DEATH-LOW 4.7%
  • MID-PACK #1118/2481
  • PHOTO-FINISH Hypoxia
  • SPECIES-CAT Cat · 79
  • DRUG-LEAD Frunevetmab · 43
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hypoxia (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Report-volume neighbourhood around Abrasion

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Abrasion · this reaction171Hypoxia · near171Myositis · near171Piloerection · near171Defecation related to… · near170Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Abrasion

Abrasion: low death-coded share in the FDA AER plate

Signature read: Abrasion's 4.7% death-coded share is among the lowest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is lower-third: 8 of 171 reports (4.7% of named reports). Nearest volume peer: Hypoxia (±0 reports). Lead species Cat (79). Lead co-reported drug Frunevetmab (43).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Frunevetmab appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Cat 79
Dog 75
Human 12
Cattle 2
Horse 2
Rat 1

Breeds Most Affected

Domestic Shorthair 46
Domestic Longhair 12
Unknown 12
Retriever - Labrador 10
Domestic Mediumhair 9
Beagle 7
Crossbred Canine/dog 5
Greyhound 4
Terrier - Boston 3
Terrier - Yorkshire 3

Associated Drugs

Frunevetmab 43
Selamectin 12
Oclacitinib Maleate 12
Carprofen 11
Gabapentin 10
Milbemycin Oxime + Praziquantel 8
Selamectin;Sarolaner 8
Bedinvetmab 8
Prednisone 7
Buprenorphine 7
Afoxolaner 6
Maropitant Citrate 6
Cefovecin 5
Anti-Il31 Mab Mcs Lot #1283563 5
Butorphanol 5
Meloxicam 5
Grapiprant 5
Fluralaner Chew Tablets 4
Melarsomine Dihydrochloride 4
Fluralaner 4

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Abrasion, 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 (171 here).

Similar death-coded share

Nearest other reactions by death-coded share (4.7% 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 Abrasion (#1118 of 2,481 by report volume); death-coded 4.7%. PlainBreed reaction plate · death-coded share stamp 4.7% · 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 →