Docp
138 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.
138
Total Reports
9
Deaths Reported
650.0%
Death Rate
Active Ingredients
Docp
Administration Routes
UnknownIntramuscularSubcutaneousIntravenousOtherParenteral
Species Affected
Dog 136
Cat 1
Goat 1
Most Affected Breeds
Retriever - Labrador 15
Poodle - Standard 9
Retriever - Golden 7
Crossbred Canine/dog 6
Chihuahua 5
Dog (unknown) 5
Pointing Dog - German Short-haired 5
Maltese 5
Shepherd Dog - German 5
Terrier (unspecified) 4
Most Reported Reactions
Immediate pain upon injection 41
High sodium-potassium ratio (Na:K ratio) 29
Vomiting 23
Diarrhoea 19
Lethargy (see also Central nervous system depression in 'Neurological') 17
Polyuria 15
Weight loss 11
Polydipsia 11
Elevated blood urea nitrogen (BUN) 10
Hyponatremia 8
Decreased appetite 8
Hypochloraemia 8
Outcome Breakdown
Recovered/Normal
63 (45.7%)
Outcome Unknown
51 (37.0%)
Ongoing
14 (10.1%)
Died
5 (3.6%)
Euthanized
4 (2.9%)
Recovered with Sequela
1 (0.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.