Oral Bordetella Canine - 1081.01
145 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.
145
Total Reports
16
Deaths Reported
1100.0%
Death Rate
Active Ingredients
Oral Bordetella Canine - 1081.01
Administration Routes
OralUnknownParenteral
Species Affected
Dog 145
Most Affected Breeds
Retriever - Golden 19
Retriever - Labrador 8
Poodle - Miniature 7
Chihuahua 6
Maltese 6
Bulldog - French 6
Pit Bull 5
Shih Tzu 5
Shepherd Dog - Australian 5
Poodle - Standard 4
Most Reported Reactions
Vomiting 52
Diarrhoea 27
Lethargy (see also Central nervous system depression in 'Neurological') 20
Lethargy (see also Central nervous system depression in Neurological) 17
Leucocytosis NOS 11
Neutrophilia 11
Anorexia 11
Other abnormal test result NOS 11
Cough 10
Death 10
Lack of efficacy (bacteria) - Bordetella 10
Dehydration 9
Outcome Breakdown
Recovered/Normal
54 (36.7%)
Outcome Unknown
48 (32.7%)
Ongoing
27 (18.4%)
Euthanized
9 (6.1%)
Died
9 (6.1%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.