Recombitek C8 - 47K9.R0

206 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.

206

Total Reports

Deaths Reported

920.0%

Death Rate

Active Ingredients

Recombitek C8 - 47K9.R0

Administration Routes

SubcutaneousUnknownOral

Species Affected

Dog 206

Most Affected Breeds

Retriever - Labrador 16

Shih Tzu 15

Retriever - Golden 14

Chihuahua 10

Shepherd Dog - Australian 9

Pit Bull 9

Dachshund (unspecified) 9

Shepherd Dog - German 9

Spaniel - King Charles Cavalier 7

Terrier - Yorkshire 7

Most Reported Reactions

Vomiting 49

Injection site pain 34

Diarrhoea 23

Injection site swelling 22

Lethargy (see also Central nervous system depression in 'Neurological') 22

Lethargy (see also Central nervous system depression in Neurological) 21

Injection site lump 20

Anorexia 15

Seizure NOS 14

Pain NOS 13

Death 12

Lack of efficacy (virus) - parvovirus (including feline panleukopenia) 11

Outcome Breakdown

Outcome Unknown

88 (42.5%)

Recovered/Normal

80 (38.6%)

Ongoing

20 (9.7%)

Died

12 (5.8%)

Euthanized

7 (3.4%)

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