Recombitek C7- 47M9.R0
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.
10
Total Reports
0
Deaths Reported
0.0%
Death Rate
Active Ingredients
Recombitek C7- 47M9.R0
Administration Routes
Subcutaneous
Species Affected
Dog 10
Most Affected Breeds
Retriever - Labrador 2
Poodle - Miniature 2
Spitz - American Eskimo Dog 1
Spaniel - Cocker American 1
Bulldog - French 1
Pekingese 1
Deutsche Dogge, Great Dane 1
Poodle - Standard 1
Most Reported Reactions
Vomiting 4
Diarrhoea 4
Lethargy (see also Central nervous system depression in 'Neurological') 3
Shaking 2
Hyperglycaemia 2
Not eating 2
Injection site alopecia 2
Hyperpigmentation 2
Restlessness 1
Injection site pain 1
Anorexia 1
Adipsia 1
Outcome Breakdown
Outcome Unknown
6 (60.0%)
Recovered/Normal
3 (30.0%)
Ongoing
1 (10.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.