Bordetella

474 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.

474

Total Reports

Deaths Reported

820.0%

Death Rate

Active Ingredients

Bordetella

Administration Routes

UnknownNasalOralSubcutaneousParenteralIntralesional

Species Affected

Dog 470

Cat 3

Goat 1

Most Affected Breeds

Retriever - Labrador 40

Terrier - Bull - American Pit 36

Crossbred Canine/dog 28

Chihuahua 26

Terrier - Yorkshire 22

Retriever - Golden 21

Shepherd Dog - German 18

Boxer (German Boxer) 16

Shih Tzu 15

Terrier (unspecified) 12

Most Reported Reactions

Vomiting 175

Lethargy (see also Central nervous system depression in 'Neurological') 77

Anaphylaxis 73

Facial swelling (see also 'Skin') 57

Hives (see also 'Skin') 56

Diarrhoea 53

Pale mucous membrane 40

Lethargy (see also Central nervous system depression in Neurological) 37

Seizure NOS 29

Emesis (multiple) 27

Not eating 27

Emesis 25

Outcome Breakdown

Ongoing

194 (40.9%)

Recovered/Normal

188 (39.7%)

Outcome Unknown

53 (11.2%)

Died

20 (4.2%)

Euthanized

19 (4.0%)

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