Unspecified Joint Supplements

15 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

670.0%

Death Rate

Active Ingredients

Unspecified Joint Supplements

Administration Routes

UnknownOral

Species Affected

Dog 14

Horse 1

Most Affected Breeds

Deutsche Dogge, Great Dane 3

Retriever - Labrador 2

Rottweiler 2

Shepherd Dog - German 1

Pit Bull 1

Shepherd Dog - Australian 1

Warmblood - Dutch 1

Poodle (unspecified) 1

Catahoula Leopard Dog 1

Weimaraner 1

Most Reported Reactions

Vomiting 3

Diarrhoea 3

Emesis (multiple) 3

Seizure NOS 2

Urinary incontinence 2

Weight loss 2

Anorexia 2

Lethargy (see also Central nervous system depression in Neurological) 2

Not eating 2

Inappropriate defecation 2

Lack of efficacy (endoparasite) - hookworm 2

Vocalisation 1

Outcome Breakdown

Ongoing

7 (46.7%)

Recovered/Normal

4 (26.7%)

Outcome Unknown

3 (20.0%)

Euthanized

1 (6.7%)

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