Chondroitin

16 adverse event reports submitted to the FDA

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.

Total Reports

Deaths Reported

620.0%

Death Rate

Active Ingredients

Chondroitin

Administration Routes

UnknownOral

Species Affected

Dog 16

Most Affected Breeds

Shepherd Dog - Australian 2

Shepherd Dog - German 2

Mastiff 1

Chihuahua 1

Terrier - Airedale 1

Retriever - Labrador 1

Catahoula Leopard Dog 1

Dachshund (unspecified) 1

Spaniel - King Charles Cavalier 1

Crossbred Canine/dog 1

Most Reported Reactions

Vomiting 3

Lack of efficacy - NOS 3

Elevated liver enzymes 2

Loose stool 2

Inappetence 1

Elevated alanine aminotransferase (ALT) 1

Elevated serum alkaline phosphatase (SAP) 1

Elevated total bilirubin 1

Lameness 1

Localised pain NOS (see other 'SOCs' for specific pain) 1

Lack of efficacy (flea) 1

UNPALATABLE 1

Outcome Breakdown

Outcome Unknown

8 (50.0%)

Ongoing

5 (31.3%)

Recovered/Normal

2 (12.5%)

Died

1 (6.3%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.