Unspecified Liver Supplement

12 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

2500.0%

Death Rate

Active Ingredients

Unspecified Liver Supplement

Administration Routes

OralUnknown

Species Affected

Dog 12

Most Affected Breeds

Maltese 2

Terrier - Bull - American Pit 2

Spaniel - Springer (unspecified) 1

Bulldog 1

Terrier - Boston 1

American Pit Bull Terrier 1

Terrier - Yorkshire 1

Boxer (German Boxer) 1

Siberian Husky 1

Retriever - Golden 1

Most Reported Reactions

Vomiting 4

Not himself/herself 3

Weakness 2

Falling 2

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

Not eating 2

Unable to walk 2

Disorientation 2

Stumbling gait 2

Decreased appetite 2

Death 2

Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') 1

Outcome Breakdown

Recovered/Normal

4 (33.3%)

Outcome Unknown

4 (33.3%)

Died

2 (16.7%)

Euthanized

1 (8.3%)

Ongoing

1 (8.3%)

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