Sulfadimethoxine/Ormetoprim
15 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.
15
Total Reports
1
Deaths Reported
670.0%
Death Rate
Active Ingredients
Sulfadimethoxine/Ormetoprim
Administration Routes
OralUnknown
Species Affected
Dog 14
Cat 1
Most Affected Breeds
Terrier - Yorkshire 3
Spaniel - Cocker American 1
Crossbred Canine/dog 1
Retriever - Golden 1
Bulldog 1
Great Pyrenees 1
Dachshund (unspecified) 1
Mastiff 1
Maltese 1
Terrier (unspecified) 1
Most Reported Reactions
Emesis 6
Restlessness 2
Anxiety 1
Tachycardia 1
Facial swelling (see also 'Skin') 1
Panting 1
Congested mucous membrane 1
Pyrexia 1
Generalised allergic reaction NOS 1
Retinal degeneration 1
Diarrhoea 1
Hyperactivity 1
Outcome Breakdown
Recovered/Normal
9 (60.0%)
Outcome Unknown
3 (20.0%)
Ongoing
2 (13.3%)
Euthanized
1 (6.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.