Nutraceutical Joint Supplement
62 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.
62
Total Reports
4
Deaths Reported
650.0%
Death Rate
Active Ingredients
Nutraceutical Joint Supplement
Administration Routes
UnknownOralOther
Species Affected
Dog 54
Cat 8
Most Affected Breeds
Retriever - Labrador 18
Domestic Shorthair 5
Collie - Border 3
Spitz - German Pomeranian 3
Crossbred Canine/dog 3
Dog (unknown) 3
Retriever - Golden 2
Spaniel - Cocker English 2
Pointing Dog - German Short-haired 2
Spaniel - King Charles Cavalier 2
Most Reported Reactions
Diarrhoea 13
Vomiting 9
Anorexia 6
Abnormal radiograph finding 6
Lack of efficacy - NOS 6
Decreased appetite 5
Not eating 5
Lack of efficacy (endoparasite) - roundworm NOS 5
Nausea 4
Anaemia NOS 4
Emesis (multiple) 4
Lethargy (see also Central nervous system depression in Neurological) 4
Outcome Breakdown
Outcome Unknown
25 (40.3%)
Ongoing
23 (37.1%)
Recovered/Normal
10 (16.1%)
Died
2 (3.2%)
Euthanized
2 (3.2%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.