Drug profile

The FDA adverse-event record for Firocoxib 57 Mg

61 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Firocoxib 57 Mg. Species, reactions, and outcomes follow.

#1008 of 2,679
by report volume (all drugs)
61
adverse-event reports
11.5%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Firocoxib 57 Mg ranks #1004 of 2679 by total reports (61) and #480 of 1130 by death-coded share (11.5%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#1004
This drug, reports of 2679
#480
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

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. Firocoxib 57 Mg has 61 reports now versus 61 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 Firocoxib 57 Mg changes

Signature read: report volume at 61 is the most distinctive stamp on Firocoxib 57 Mg's FDA AER row.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
61
Total Reports
7
Deaths Reported
11.5%
Death-coded share of reports

Active Ingredients

Firocoxib 57 Mg

Administration Routes

OralUnknown

Species Affected

Dog 35
Unknown 23
Human 2
Horse 1

Most Affected Breeds

Unknown 25
Dog (other) 4
Spitz - German Pomeranian 4
Dog (unknown) 3
Chihuahua 3
Poodle - Miniature 3
Dachshund (unspecified) 3
Schnauzer - Miniature 2
Beagle 2
Shepherd Dog - Australian 1

Most Reported Reactions

Uncoded sign 23
Tablets, Abnormal 12
Vomiting 10
Death 5
Lethargy (see also Central nervous system depression in 'Neurological') 4
Elevated serum alkaline phosphatase (SAP) 4
Underfilling, Container 3
Underfilling, Bottles 3
Ataxia 3
Diarrhoea 3
Containers, Damaged 2
Underfilling, Package 2

Outcome Breakdown

Outcome Unknown
23 (60.5%)
Died
7 (18.4%)
Recovered/Normal
6 (15.8%)
Ongoing
2 (5.3%)

Firocoxib 57 Mg Adverse Event Insights

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Nationwide drugs with similar profiles

Two openFDA-derived peer sets for Firocoxib 57 Mg, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

What to do with this drug

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 Firocoxib 57 Mg (#1008 of 2,679 by report volume); death-coded 11.5%. PlainBreed drug row · report volume stamp 61 · 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 →