Unspecified Bordetella

10 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

Unspecified Bordetella

Administration Routes

UnknownNasal

Species Affected

Dog 10

Most Affected Breeds

Maltese 1

Retriever - Flat-coated 1

Terrier - Jack Russell 1

Pug 1

Terrier (unspecified) 1

Cattle Dog (unspecified) 1

Crossbred Canine/dog 1

Greyhound 1

Poodle - Toy 1

Terrier - Yorkshire 1

Most Reported Reactions

Diarrhoea 5

Lethargy (see also Central nervous system depression in Neurological) 5

Emesis (multiple) 3

Decreased appetite 2

Limb weakness 2

Restlessness 2

Eye irritation 1

Keratoconjunctivitis sicca 1

Nasal discharge 1

Schirmer tear test 1

Eye redness 1

Ocular discharge 1

Outcome Breakdown

Ongoing

7 (70.0%)

Recovered/Normal

3 (30.0%)

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