Bordetella Oral

12 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.

Total Reports

Deaths Reported

830.0%

Death Rate

Active Ingredients

Bordetella Oral

Administration Routes

OralUnknown

Species Affected

Dog 12

Most Affected Breeds

Retriever - Labrador 3

Bichon Frise 2

Crossbred Canine/dog 1

Retriever - Golden 1

Terrier - Yorkshire 1

Terrier - Bull - American Pit 1

Siberian Husky 1

Shepherd Dog - German 1

Beagle 1

Most Reported Reactions

Facial swelling (see also Skin) 3

Lethargy (see also Central nervous system depression in Neurological) 3

Limb weakness 3

Not himself/herself 2

Involuntary defecation 2

Partial anorexia 2

Decreased drinking 2

Proprioception deficit 2

Anaemia NOS 2

Elevated blood urea nitrogen (BUN) 2

Elevated creatinine 2

Hyperphosphataemia 2

Outcome Breakdown

Ongoing

7 (58.3%)

Recovered/Normal

4 (33.3%)

Euthanized

1 (8.3%)

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