Drug profile

The FDA adverse-event record for Proviable

143 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Proviable. See the species affected, top reactions, and outcomes below.

143
adverse-event reports
13.3%
death-coded share
Dog
most-reported species
40
Diarrhoea - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
143
Total Reports
19
Deaths Reported
13.3%
Death Rate

Active Ingredients

Proviable

Administration Routes

UnknownOral

Species Affected

Dog 127
Cat 16

Most Affected Breeds

Retriever - Labrador 13
Retriever - Golden 9
Domestic Shorthair 8
Shepherd Dog - German 8
Crossbred Canine/dog 6
Shepherd Dog - Australian 6
Shih Tzu 5
Bichon Frise 4
Beagle 4
Whippet 4

Most Reported Reactions

Diarrhoea 40
Vomiting 30
Lethargy (see also Central nervous system depression in Neurological) 30
Decreased appetite 15
Not eating 14
Ataxia 13
Seizure NOS 13
Anorexia 12
Polydipsia 12
Bloody diarrhoea 11
Death by euthanasia 11
Urine abnormalities NOS 10

Outcome Breakdown

Ongoing
91 (63.6%)
Recovered/Normal
17 (11.9%)
Outcome Unknown
16 (11.2%)
Euthanized
11 (7.7%)
Died
8 (5.6%)

Proviable Adverse Event Insights

143 reports name Proviable; 19 recorded a death outcome (13.3% of reported events, not a population-level mortality rate). Active ingredient: Proviable. Administration routes: Unknown, Oral.

By species: Dog (127 reports), Cat (16 reports). By breed: Retriever - Labrador (13), Retriever - Golden (9), Domestic Shorthair (8).

Leading clinical signs: Diarrhoea (40), Vomiting (30), Lethargy (see also Central nervous system depression in Neurological) (30), Decreased appetite (15). Outcome, 143 coded reports: Ongoing leads at 63.6%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.