Drug profile

The FDA adverse-event record for Canine Parainfluenza + Bordetella Bronchiseptica Vaccine

14 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Canine Parainfluenza + Bordetella Bronchiseptica Vaccine. See the species affected, top reactions, and outcomes below.

14
adverse-event reports
21.4%
death-coded share
Dog
most-reported species
9
Vomiting - 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.
14
Total Reports
3
Deaths Reported
21.4%
Death Rate

Active Ingredients

Canine Parainfluenza + Bordetella Bronchiseptica Vaccine

Administration Routes

NasalUnknownParenteral

Species Affected

Dog 14

Most Affected Breeds

Retriever - Labrador 3
Boxer (German Boxer) 2
Corgi (unspecified) 1
Terrier - Boston 1
Bichon Frise 1
Hound - Basset 1
Retriever - Golden 1
Terrier - Bull - Miniature 1
Pit Bull 1
Mountain Dog - Bernese 1

Most Reported Reactions

Vomiting 9
Death 3
Weight gain 3
Bloody diarrhoea 2
Lethargy (see also Central nervous system depression in 'Neurological') 2
Other abnormal test result NOS 2
Diarrhoea 2
Lethargy (see also Central nervous system depression in Neurological) 2
Not eating 2
Sleepiness - neurological disorder 1
Reduced responses 1
Limpness 1

Outcome Breakdown

Recovered/Normal
5 (35.7%)
Ongoing
4 (28.6%)
Died
3 (21.4%)
Outcome Unknown
2 (14.3%)

Canine Parainfluenza + Bordetella Bronchiseptica Vaccine Adverse Event Insights

14 reports name Canine Parainfluenza + Bordetella Bronchiseptica Vaccine; 3 recorded a death outcome (21.4% of reported events, not a population-level mortality rate). Active ingredient: Canine Parainfluenza + Bordetella Bronchiseptica Vaccine. Administration routes: Nasal, Unknown, Parenteral.

By species: Dog (14 reports). By breed: Retriever - Labrador (3), Boxer (German Boxer) (2), Corgi (unspecified) (1).

Leading clinical signs: Vomiting (9), Death (3), Weight gain (3), Bloody diarrhoea (2). Outcome, 14 coded reports: Recovered/Normal leads at 35.7%.

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.