Drug profile

The FDA adverse-event record for Glucosamine Chondroitin Msm

12 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Glucosamine Chondroitin Msm. See the species affected, top reactions, and outcomes below.

12
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
3
Cough - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
12
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Glucosamine Chondroitin Msm

Administration Routes

Oral

Species Affected

Dog 12

Most Affected Breeds

Spaniel - King Charles Cavalier 12

Most Reported Reactions

Cough 3
Congestive heart failure 3
Skin lump 2
Other abnormal test result NOS 2
Scratching 1
Ear infection NOS 1
Anxiety 1
Arrhythmia 1
Panting 1
Oral mass 1
Dermal mass 1
Difficulty going up/down stairs 1

Outcome Breakdown

Recovered/Normal
6 (50.0%)
Outcome Unknown
6 (50.0%)

Glucosamine Chondroitin Msm Adverse Event Insights

12 reports name Glucosamine Chondroitin Msm; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Glucosamine Chondroitin Msm. Administration route: Oral.

By species: Dog (12 reports). By breed: Spaniel - King Charles Cavalier (12).

Leading clinical signs: Cough (3), Congestive heart failure (3), Skin lump (2), Other abnormal test result NOS (2). Outcome, 12 coded reports: Recovered/Normal leads at 50.0%.

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.