Joint Supplement

331 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.

331

Total Reports

Deaths Reported

1780.0%

Death Rate

Active Ingredients

Joint Supplement

Administration Routes

OralUnknownParenteral

Species Affected

Dog 317

Cat 13

Other 1

Most Affected Breeds

Retriever - Labrador 41

Crossbred Canine/dog 25

Retriever - Golden 20

Shepherd Dog - German 16

Terrier - Bull - American Pit 15

Chihuahua 11

Shepherd Dog - Australian 10

Collie - Border 8

Domestic Shorthair 8

Terrier - Yorkshire 7

Most Reported Reactions

Vomiting 54

Death by euthanasia 44

Lethargy (see also Central nervous system depression in Neurological) 44

Diarrhoea 40

Lack of efficacy - NOS 26

Polyuria 25

Urinary tract infection 25

Decreased appetite 25

Anorexia 22

Elevated alanine aminotransferase (ALT) 22

Not eating 22

Elevated serum alkaline phosphatase (ALP) 22

Outcome Breakdown

Ongoing

141 (42.6%)

Outcome Unknown

72 (21.8%)

Recovered/Normal

59 (17.8%)

Euthanized

44 (13.3%)

Died

15 (4.5%)

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