Drug profile

The FDA adverse-event record for Canine Vaccine

389 FDA reports name Canine Vaccine, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#359 of 2,679
by report volume (all drugs)
389
adverse-event reports
8.0%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Canine Vaccine ranks #358 of 2679 by total reports (389) and #641 of 1130 by death-coded share (8.0%). 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)
#358
This drug, reports of 2679
#641
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. Canine Vaccine has 389 reports now versus 389 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 Canine Vaccine changes

Signature read: 389 reports place Canine Vaccine in the upper third of FDA AER volume (#359 of 2,679).

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
389
Total Reports
31
Deaths Reported
8.0%
Death-coded share of reports

Active Ingredients

Canine Vaccine

Administration Routes

UnknownSubcutaneousNasal

Species Affected

Dog 389

Most Affected Breeds

Retriever - Labrador 40
Terrier - Bull - American Pit 25
Chihuahua 20
Terrier - Yorkshire 16
Boxer (German Boxer) 13
Siberian Husky 12
Retriever - Golden 12
Shepherd Dog - Australian 11
Maltese 11
Crossbred Canine/dog 10

Most Reported Reactions

Vomiting 147
Facial swelling (see also 'Skin') 92
Lethargy (see also Central nervous system depression in 'Neurological') 91
Anaphylaxis 61
Hives (see also 'Skin') 60
Diarrhoea 36
Pale mucous membrane 36
Fever 30
Seizure NOS 23
Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') 22
Erythema (for urticaria see Immune SOC) 20
Pruritus 20

Outcome Breakdown

Ongoing
191 (49.1%)
Recovered/Normal
151 (38.8%)
Died
17 (4.4%)
Outcome Unknown
16 (4.1%)
Euthanized
14 (3.6%)

Canine Vaccine: high report volume 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 Canine Vaccine, 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 Canine Vaccine (#359 of 2,679 by report volume); death-coded 8.0%. PlainBreed drug row · report volume stamp 389 · 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 →