Drug profile

The FDA adverse-event record for Ketorolac Tromethamine

17 FDA reports name Ketorolac Tromethamine, a lower-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#1973 of 2,679
by report volume (all drugs)
17
adverse-event reports
5.9%
death-coded share
Dog
most-reported species
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Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Ketorolac Tromethamine ranks #1937 of 2679 by total reports (17). Death-coded-share rank requires at least 50 reports. 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)
#1937
This drug, reports of 2679

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. Ketorolac Tromethamine has 17 reports now versus 16 in that prior snapshot: 1 more (6.3%).

Report change
+1
Death-coded reports
+0
Death-coded share
−0.4 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 Ketorolac Tromethamine changes

Signature read: death-coded report count at 1 is the most distinctive stamp on Ketorolac Tromethamine'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.
17
Total Reports
1
Deaths Reported
5.9%
Death-coded share of reports

Active Ingredients

Ketorolac Tromethamine

Administration Routes

UnknownOphthalmicOtherOralIntraocular

Species Affected

Dog 15
Cat 1
Horse 1

Most Affected Breeds

Terrier - Boston 2
Crossbred Canine/dog 2
Domestic Shorthair 1
Corgi - Welsh Cardigan 1
Bulldog 1
Spitz - German Pomeranian 1
Unknown 1
Chihuahua 1
Japanese Chin (Spaniel) 1
Shepherd Dog - German 1

Most Reported Reactions

Weight loss 3
Corneal ulcer 3
Diarrhoea 3
Other abnormal test result NOS 3
Bloody diarrhoea 2
Not eating 2
Elevated temperature 2
Elevated blood urea nitrogen (BUN) 2
Elevated cholesterol (total) 2
Elevated creatinine 2
Urinary tract infection 2
Uveitis 2

Outcome Breakdown

Ongoing
7 (41.2%)
Outcome Unknown
6 (35.3%)
Recovered/Normal
3 (17.6%)
Euthanized
1 (5.9%)

Ketorolac Tromethamine: low 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.

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 Ketorolac Tromethamine (#1973 of 2,679 by report volume); death-coded 5.9%. PlainBreed drug row · death-coded report count stamp 1 · 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 →