Reaction profile

The FDA adverse-event record for fasciitis

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

16 FDA reports name fasciitis, a lower-volume reaction in the CVM extract (VeDDRA 2467). Plate stamps and neighbourhood peers follow.

#2271 of 2,481
by report volume (all reactions): 16
reports citing this reaction: 50.0%
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. Fasciitis has 16 reports now versus 16 in that prior snapshot: 0 the same number of (0.0%).

Report change: +0
Death-coded reports: +0
Death-coded share: +0.0 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 Fasciitis changes

FDA AER · VeDDRA plate

Code 2467 VOL-TRACE

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

VOL-TRACE 16 reports
DEATH-HOT 50.0%
BOTTOM-DECILE #2271/2481
PHOTO-FINISH Abdominal transudate
SPECIES-DOG Dog · 13
DRUG-LEAD Tramadol · 4
DESK-WIDE 13 breeds
BOOK-FULL 8/8 fields

Nearest volume peer: Abdominal transudate (±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 Fasciitis

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

FDA AER report volume · neighbourhood around Fasciitis

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

Signature read: 16 reports place Fasciitis in the lower third of FDA AER volume (#2271 of 2,481). Report volume is lower-third scale: 16 named reports in the openFDA extract. Death-coded share is upper-third: 8 of 16 reports (50.0% of named reports). Nearest volume peer: Abdominal transudate (±0 reports). Lead species Dog (13). Lead co-reported drug Tramadol (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 13

Horse 3

Breeds Most Affected

Shih Tzu 3

Retriever - Labrador 2

Quarter Horse 1

Dog (unknown) 1

Spaniel - Cocker American 1

Shepherd Dog - Belgian Malinois 1

Boxer (German Boxer) 1

Thoroughbred 1

Percheron 1

Bulldog 1

Associated Drugs

Tramadol 4

Maropitant Citrate 4

Carprofen 3

Gabapentin 3

Anesthetic 2

Polysulfated Glycosaminoglycan 2

Tigilanol Tiglate 2

Prednisolone 2

Famotidine 2

Clodronate Disodium 1

Oclacitinib Maleate 1

Afoxolaner 1

Melarsomine Dihydrochloride 1

Antibiotic 1

Maropitant 1

Hepato Trubenefits Liver Supplement 1

Cefovecin 1

Buprenorphine 1

Subcutaneous Fluids 1

Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str 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 Fasciitis (#2271 of 2,481 by report volume); death-coded 50.0%. PlainBreed reaction plate · report volume stamp 16 · 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 →