Fenofibrate

14 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

2860.0%

Death Rate

Active Ingredients

Fenofibrate

Administration Routes

UnknownOral

Species Affected

Dog 9

Human 5

Most Affected Breeds

Unknown 5

Terrier (unspecified) 2

Pinscher - Miniature 2

Terrier - Yorkshire 1

Schnauzer - Miniature 1

Poodle - Standard 1

Sheepdog - Shetland 1

Retriever - Golden 1

Most Reported Reactions

Accidental exposure 4

Death 4

Diarrhoea 3

Nausea 3

Proteinuria 3

Seizure NOS 2

Not eating 2

Elevated protein:creatinine ratio 2

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

Lack of efficacy (bacteria) - Leptospira 2

Alkaline urine 2

Injection site oedema 1

Outcome Breakdown

Recovered/Normal

6 (42.9%)

Died

4 (28.6%)

Outcome Unknown

2 (14.3%)

Ongoing

2 (14.3%)

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