Oral Bordetella

16 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

0.0%

Death Rate

Active Ingredients

Oral Bordetella

Administration Routes

OralUnknown

Species Affected

Dog 16

Most Affected Breeds

Retriever - Labrador 3

Setter - Irish Red 2

Crossbred Canine/dog 1

Pointing Dog - German Short-haired 1

Catahoula Leopard Dog 1

Terrier - Yorkshire 1

Maltese 1

Boxer (German Boxer) 1

Collie - Border 1

Rottweiler 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 6

Not eating 6

Diarrhoea 4

Decreased appetite 3

Lethargy (see also Central nervous system depression in 'Neurological') 2

Emesis 2

Vomiting 2

Hives (see also 'Skin') 2

Anorexia 2

Injection site bruising 2

Thrombocytopenia 2

Injection site swelling 2

Outcome Breakdown

Outcome Unknown

6 (37.5%)

Ongoing

5 (31.3%)

Recovered/Normal

5 (31.3%)

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