Unspecified Joint Supplement
77 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.
77
Total Reports
12
Deaths Reported
1560.0%
Death Rate
Active Ingredients
Unspecified Joint Supplement
Administration Routes
OralUnknown
Species Affected
Dog 75
Cat 2
Most Affected Breeds
Retriever - Labrador 21
Retriever - Golden 8
Shepherd Dog - German 6
Terrier (unspecified) 4
Dachshund (unspecified) 4
Boxer (German Boxer) 3
Bulldog 2
Dachshund - Miniature 2
Crossbred Canine/dog 2
Terrier - Bull - American Pit 2
Most Reported Reactions
Vomiting 16
Diarrhoea 14
Lethargy (see also Central nervous system depression in Neurological) 11
Lethargy (see also Central nervous system depression in 'Neurological') 7
Panting 7
Death by euthanasia 6
Lack of efficacy - NOS 6
Proprioception deficit 6
Death 6
Not eating 5
Limb weakness 5
Hind limb paresis 5
Outcome Breakdown
Ongoing
26 (33.8%)
Outcome Unknown
21 (27.3%)
Recovered/Normal
18 (23.4%)
Euthanized
6 (7.8%)
Died
6 (7.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.