Epakitin

13 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

1540.0%

Death Rate

Active Ingredients

Epakitin

Administration Routes

OralUnknownRespiratory (Inhalation)

Species Affected

Dog 7

Cat 6

Most Affected Breeds

Domestic Shorthair 5

Retriever - Labrador 2

Spaniel - Cocker English 1

Beagle 1

Ragdoll 1

Spitz - German Pomeranian 1

Pug 1

Spaniel - King Charles Cavalier 1

Most Reported Reactions

Elevated blood urea nitrogen (BUN) 4

Vomiting 3

Seizure NOS 2

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

Elevated creatinine 2

Diarrhoea 2

Not eating 2

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

Temporary blindness 1

Emesis (multiple) 1

Polydipsia 1

Elevated renal parameters 1

Outcome Breakdown

Ongoing

6 (46.2%)

Recovered/Normal

3 (23.1%)

Outcome Unknown

2 (15.4%)

Euthanized

1 (7.7%)

Died

1 (7.7%)

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