Reaction profile

The FDA adverse-event record for injection site lesion

506 FDA reports name injection site lesion, a high-volume reaction in the CVM extract (VeDDRA 86). Plate stamps and neighbourhood peers follow.

#641 of 2,481
by report volume (all reactions)
506
reports citing this reaction
4.9%
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. Injection site lesion has 506 reports now versus 497 in that prior snapshot: 9 more (1.8%).

Report change
+9
Death-coded reports
+1
Death-coded share
+0.1 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 Injection site lesion changes

FDA AER · VeDDRA plate

Code 86 VOL-MID

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

  • VOL-MID 506 reports
  • DEATH-LOW 4.9%
  • MID-PACK #641/2481
  • PHOTO-FINISH Limb non-weight beari…
  • SPECIES-DOG Dog · 258
  • DRUG-LEAD Carprofen · 74
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Limb non-weight bearing (±2 reports)

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

High-volume neighbourhood around Injection site lesion

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

Vomiting · highest174348Limb non-weight beari… · near508Injection site lesion · this…506Application site ulcer · near503Device breakage/fract… · near503Application site stic… · near502Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Injection site lesion

Injection site lesion: low death-coded share in the FDA AER plate

Signature read: Injection site lesion's 4.9% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 506 named reports in the openFDA extract. Death-coded share is lower-third: 25 of 506 reports (4.9% of named reports). Nearest volume peer: Limb non-weight bearing (±2 reports). Lead species Dog (258). Lead co-reported drug Carprofen (74).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Carprofen 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

Dog 258
Human 111
Cat 96
Cattle 15
Horse 14
Mouse 2
Goat 2
Guinea Pig 2
Pig 1
Other 1

Breeds Most Affected

Unknown 117
Domestic Shorthair 61
Retriever - Labrador 24
Dog (unknown) 19
Domestic Longhair 15
Crossbred Canine/dog 10
Shepherd Dog - German 10
Chihuahua 10
Terrier (unspecified) 9
Beagle 9

Associated Drugs

Carprofen 74
Enrofloxacin 50
Maropitant Citrate 48
Cefovecin 45
Tigilanol Tiglate 37
Praziquantel 32
Moxidectin 28
Buprenorphine 24
Eprinomectin 5% Injection 24
Meloxicam 23
Butorphanol 21
Robenacoxib 21
Dexmedetomidine 21
Gabapentin 19
Prednisone 17
Tulathromycin 16
Melarsomine Dihydrochloride 16
Anesthetic 15
Isoflurane 15
Ketamine 14

Nationwide reactions with similar profiles

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

Similar death-coded share

Nearest other reactions by death-coded share (4.9% 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 Injection site lesion (#641 of 2,481 by report volume); death-coded 4.9%. PlainBreed reaction plate · death-coded share stamp 4.9% · 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 →