Drug profile

The FDA adverse-event record for Bordetella Bronchiseptica B-C2

82 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Bordetella Bronchiseptica B-C2. See the species affected, top reactions, and outcomes below.

82
adverse-event reports
9.8%
death-coded share
Dog
most-reported species
16
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.
82
Total Reports
8
Deaths Reported
9.8%
Death Rate

Active Ingredients

Bordetella Bronchiseptica B-C2

Administration Routes

OralUnknown

Species Affected

Dog 82

Most Affected Breeds

Crossbred Canine/dog 23
Retriever - Labrador 6
Terrier (unspecified) 4
Shih Tzu 4
Pug 4
Terrier - Yorkshire 3
Doberman Pinscher 3
Spitz - German Pomeranian 3
Schnauzer - Miniature 3
Retriever - Golden 2

Most Reported Reactions

Vomiting 16
Lethargy (see also Central nervous system depression in 'Neurological') 14
Emesis (multiple) 13
Diarrhoea 10
Seizure NOS 6
Behavioural disorder NOS 5
Death 5
Ataxia 5
Decreased appetite 4
Other abnormal test result NOS 4
Restlessness 4
Abnormal radiograph finding 4

Outcome Breakdown

Ongoing
29 (35.4%)
Recovered/Normal
27 (32.9%)
Outcome Unknown
14 (17.1%)
Died
5 (6.1%)
Recovered with Sequela
4 (4.9%)
Euthanized
3 (3.7%)

Bordetella Bronchiseptica B-C2 Adverse Event Insights

82 reports name Bordetella Bronchiseptica B-C2; 8 recorded a death outcome (9.8% of reported events, not a population-level mortality rate). Active ingredient: Bordetella Bronchiseptica B-C2. Administration routes: Oral, Unknown.

By species: Dog (82 reports). By breed: Crossbred Canine/dog (23), Retriever - Labrador (6), Terrier (unspecified) (4).

Leading clinical signs: Vomiting (16), Lethargy (see also Central nervous system depression in 'Neurological') (14), Emesis (multiple) (13), Diarrhoea (10). Outcome, 82 coded reports: Ongoing leads at 35.4%.

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.