Drug profile

The FDA adverse-event record for Naloxone

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

#689 of 2,679
by report volume (all drugs)
127
adverse-event reports
39.4%
death-coded share
Cat
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Naloxone ranks #687 of 2679 by total reports (127) and #85 of 1130 by death-coded share (39.4%). 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)
#687
This drug, reports of 2679
#85
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. Naloxone has 127 reports now versus 114 in that prior snapshot: 13 more (11.4%).

Report change
+13
Death-coded reports
+4
Death-coded share
−1.0 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 Naloxone changes

Signature read: Naloxone's 39.4% 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.
127
Total Reports
50
Deaths Reported
39.4%
Death-coded share of reports

Active Ingredients

Naloxone

Administration Routes

UnknownIntravenousParenteralIntramuscularSubcutaneousNasal

Species Affected

Cat 87
Dog 39
Ferret 1

Most Affected Breeds

Domestic Shorthair 53
Domestic Longhair 10
Boxer (German Boxer) 4
Siamese 4
Crossbred Canine/dog 4
Terrier - Bull - Staffordshire 4
Cat (unknown) 4
Domestic Mediumhair 4
Retriever - Labrador 3
Pit Bull 3

Most Reported Reactions

Death 27
Behavioural disorder NOS 26
Dilated pupils 25
Not eating 23
Death by euthanasia 22
Hypothermia 18
Ataxia 17
Dysphoria 16
Other abnormal test result NOS 14
Cardiac arrest 14
Lethargy (see also Central nervous system depression in Neurological) 14
Bradycardia 13

Outcome Breakdown

Ongoing
37 (29.1%)
Recovered/Normal
30 (23.6%)
Died
27 (21.3%)
Euthanized
23 (18.1%)
Outcome Unknown
9 (7.1%)
Recovered with Sequela
1 (0.8%)

Naloxone: 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 Naloxone, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

Similar death-coded share

Nearest other drugs by death-coded share (39.4% 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 Naloxone (#689 of 2,679 by report volume); death-coded 39.4%. PlainBreed drug row · death-coded share stamp 39.4% · 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 →