Bordetella Bronchiseptica, Strain 78-9159

Verify with FDA CVM →

675 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.
675
Total Reports
79
Deaths Reported
1170.0%
Death Rate

Active Ingredients

Bordetella Bronchiseptica, Strain 78-9159

Administration Routes

SubcutaneousUnknownNasalOralIntravenous

Species Affected

Dog 675

Most Affected Breeds

Terrier - Bull - American Pit 50
Retriever - Labrador 46
Retriever - Golden 34
Boxer (German Boxer) 34
Terrier - Yorkshire 27
Chihuahua 27
Crossbred Canine/dog 26
Shih Tzu 23
Shepherd Dog - Australian 20
Terrier (unspecified) 19

Most Reported Reactions

Vomiting 279
Lethargy (see also Central nervous system depression in 'Neurological') 143
Facial swelling (see also 'Skin') 119
Anaphylaxis 105
Hives (see also 'Skin') 94
Diarrhoea 83
Pale mucous membrane 64
Fever 54
Lethargy (see also Central nervous system depression in Neurological) 44
Panting 42
Anorexia 40
Death 39

Outcome Breakdown

Ongoing
340 (50.2%)
Recovered/Normal
223 (32.9%)
Died
44 (6.5%)
Euthanized
35 (5.2%)
Outcome Unknown
34 (5.0%)
Recovered with Sequela
1 (0.1%)

Data Summary

Metric Value
Total adverse event reports 675
Reports involving death 79
Case-fatality rate (reported events) 1170.0%
Distinct species in reports 1
Distinct breeds in reports 20
Distinct reactions reported 20
Active ingredients on file 1

Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.

Bordetella Bronchiseptica, Strain 78-9159 Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 675 adverse event reports referencing Bordetella Bronchiseptica, Strain 78-9159, including 79 reports in which the animal died — a 1170.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Bordetella Bronchiseptica, Strain 78-9159. Reported administration routes include Subcutaneous, Unknown, Nasal, Oral. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.

The species most frequently named in Bordetella Bronchiseptica, Strain 78-9159 reports are Dog (675 reports), with Dog accounting for the largest share. Within those species, Terrier - Bull - American Pit (50), Retriever - Labrador (46), Retriever - Golden (34) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.

The most commonly reported clinical signs associated with Bordetella Bronchiseptica, Strain 78-9159 are Vomiting (279), Lethargy (see also Central nervous system depression in 'Neurological') (143), Facial swelling (see also 'Skin') (119), Anaphylaxis (105). Of the 677 reports with a coded outcome, Ongoing is the leading category at 50.2%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Bordetella Bronchiseptica, Strain 78-9159.

Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial