Proin
227 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.
227
Total Reports
34
Deaths Reported
1500.0%
Death Rate
Active Ingredients
Proin
Administration Routes
OralUnknownTopical
Species Affected
Dog 225
Cat 2
Most Affected Breeds
Retriever - Labrador 44
Shepherd Dog - German 15
Crossbred Canine/dog 14
Shepherd Dog - Australian 11
Doberman Pinscher 8
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 8
Siberian Husky 7
Collie - Border 7
Deutsche Dogge, Great Dane 7
Spaniel (unspecified) 5
Most Reported Reactions
Vomiting 32
Urinary incontinence 32
Polydipsia 31
Death by euthanasia 26
Polyuria 26
Lethargy (see also Central nervous system depression in Neurological) 26
Ataxia 23
Not eating 22
Diarrhoea 19
Seizure NOS 18
Decreased appetite 18
Panting 14
Outcome Breakdown
Ongoing
134 (59.0%)
Recovered/Normal
39 (17.2%)
Euthanized
26 (11.5%)
Outcome Unknown
19 (8.4%)
Died
8 (3.5%)
Recovered with Sequela
1 (0.4%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.