Proin Er

15 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

4000.0%

Death Rate

Active Ingredients

Proin Er

Administration Routes

UnknownOral

Species Affected

Dog 15

Most Affected Breeds

Retriever - Labrador 6

Crossbred Canine/dog 2

Boxer (German Boxer) 1

Shepherd Dog - German 1

Terrier (unspecified) 1

Bulldog - English 1

Mastiff (unspecified) 1

Dachshund (unspecified) 1

Mountain Cur 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 6

Urinary incontinence 4

Nystagmus 4

Collapse NOS (see also Cardio-vascular and Neurological disorders) 4

Death 3

Excessive thirst 3

Nausea 3

Hypersalivation 3

Not eating 3

Hind limb ataxia 3

Aspiration pneumonia 3

Emesis (multiple) 3

Outcome Breakdown

Ongoing

5 (33.3%)

Died

3 (20.0%)

Euthanized

3 (20.0%)

Recovered/Normal

2 (13.3%)

Outcome Unknown

2 (13.3%)

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