Drug profile

The FDA adverse-event record for Distemper/Parvo Vaccine

Name: Distemper/Parvo Vaccine - FDA Animal Adverse Event Reports
Creator: PlainBreed
License: https://creativecommons.org/publicdomain/zero/1.0/

11 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Distemper/Parvo Vaccine. See the species affected, top reactions, and outcomes below.

11
adverse-event reports: 0.0%
death-coded share: Dog
most-reported species: 4
Diarrhoea - top reaction

Compiled by PlainBreed Editorial, Pet Health Editorial Team

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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.

Total Reports

Deaths Reported

0.0%

Death Rate

Active Ingredients

Distemper/Parvo Vaccine

Administration Routes

UnknownSubcutaneous

Species Affected

Dog 11

Most Affected Breeds

Chihuahua 2

Terrier - Boston 2

Dog (unknown) 1

Pug 1

Spaniel - Cocker American 1

Boxer (German Boxer) 1

Shepherd Dog - German 1

Pointing Dog - German Short-haired 1

Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1

Most Reported Reactions

Diarrhoea 4

Vomiting 4

Other abnormal test result NOS 2

Emesis (multiple) 2

Anorexia 2

Behavioural disorder NOS 1

Adipsia 1

Not eating 1

Dehydration 1

Lethargy (see also Central nervous system depression in 'Neurological') 1

Reduced responses 1

Reluctant to move 1

Outcome Breakdown

Recovered/Normal

5 (45.5%)

Outcome Unknown

4 (36.4%)

Ongoing

2 (18.2%)

Distemper/Parvo Vaccine Adverse Event Insights

11 reports name Distemper/Parvo Vaccine; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Distemper/Parvo Vaccine. Administration routes: Unknown, Subcutaneous.

By species: Dog (11 reports). By breed: Chihuahua (2), Terrier - Boston (2), Dog (unknown) (1).

Leading clinical signs: Diarrhoea (4), Vomiting (4), Other abnormal test result NOS (2), Emesis (multiple) (2). Outcome, 11 coded reports: Recovered/Normal leads at 45.5%.

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.