Drug profile

The FDA adverse-event record for Piroxicam

86 FDA reports name Piroxicam, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#848 of 2,679
by report volume (all drugs)
86
adverse-event reports
24.4%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Piroxicam ranks #843 of 2679 by total reports (86) and #179 of 1130 by death-coded share (24.4%). 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)
#843
This drug, reports of 2679
#179
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. Piroxicam has 86 reports now versus 85 in that prior snapshot: 1 more (1.2%).

Report change
+1
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 Piroxicam changes

Signature read: Piroxicam's 24.4% death-coded share is among the highest in the openFDA drug corpus.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
86
Total Reports
21
Deaths Reported
24.4%
Death-coded share of reports

Active Ingredients

Piroxicam

Administration Routes

OralUnknownTopical

Species Affected

Dog 81
Cat 5

Most Affected Breeds

Retriever - Labrador 10
Domestic Shorthair 4
Beagle 4
Dog (unknown) 4
Chihuahua 3
Spitz - German Pomeranian 3
Dachshund (unspecified) 3
Spaniel (unspecified) 3
Terrier - Bull - American Pit 3
Shih Tzu 3

Most Reported Reactions

Death by euthanasia 19
Lethargy (see also Central nervous system depression in 'Neurological') 14
Vomiting 12
Diarrhoea 9
Anorexia 7
Anaemia NOS 7
Abnormal radiograph finding 7
Other abnormal test result NOS 6
Neoplasia NOS 6
Decreased appetite 5
Elevated blood urea nitrogen (BUN) 5
Haematuria 5

Outcome Breakdown

Ongoing
40 (47.1%)
Euthanized
19 (22.4%)
Outcome Unknown
12 (14.1%)
Recovered/Normal
12 (14.1%)
Died
2 (2.4%)

Piroxicam: high death-coded share in the FDA AER row

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.

High-volume nationwide drug peers

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

Similar report volume

Nearest other drugs by FDA report count (86 here).

Similar death-coded share

Nearest other drugs by death-coded share (24.4% here), distinct from the volume row.

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 Piroxicam (#848 of 2,679 by report volume); death-coded 24.4%. PlainBreed drug row · death-coded share stamp 24.4% · 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 →