Drug profile

The FDA adverse-event record for Cbd Supplement

15 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Cbd Supplement. See the species affected, top reactions, and outcomes below.

15
adverse-event reports
20.0%
death-coded share
Dog
most-reported species
3
Inappetence - top reaction
Verify with FDA CVM →
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
15
Total Reports
3
Deaths Reported
20.0%
Death Rate

Active Ingredients

Cbd Supplement

Administration Routes

UnknownOral

Species Affected

Dog 14
Cat 1

Most Affected Breeds

Retriever - Labrador 3
Deutsche Dogge, Great Dane 1
American Pit Bull Terrier 1
Domestic Shorthair 1
Terrier - Bull - American Pit 1
Dogue de Bordeaux 1
Pointing Dog - German Short-haired 1
Terrier (unspecified) 1
Doberman Pinscher 1
Shepherd Dog - Australian 1

Most Reported Reactions

Inappetence 3
Not himself/herself 3
Disorientation 2
Weight loss 2
Panting 2
Falling 2
Unable to walk 2
Elevated liver enzymes NOS 2
Lethargy (see also Central nervous system depression in Neurological) 2
Ataxia 2
Proprioception deficit 2
Death 2

Outcome Breakdown

Ongoing
8 (53.3%)
Outcome Unknown
3 (20.0%)
Died
3 (20.0%)
Recovered/Normal
1 (6.7%)

Cbd Supplement Adverse Event Insights

15 reports name Cbd Supplement; 3 recorded a death outcome (20.0% of reported events, not a population-level mortality rate). Active ingredient: Cbd Supplement. Administration routes: Unknown, Oral.

By species: Dog (14 reports), Cat (1 reports). By breed: Retriever - Labrador (3), Deutsche Dogge, Great Dane (1), American Pit Bull Terrier (1).

Leading clinical signs: Inappetence (3), Not himself/herself (3), Disorientation (2), Weight loss (2). Outcome, 15 coded reports: Ongoing leads at 53.3%.

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.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.