Tris-Edta
82 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.
82
Total Reports
7
Deaths Reported
850.0%
Death Rate
Active Ingredients
Tris-Edta
Administration Routes
Auricular (Otic)UnknownOtherTopicalOral
Species Affected
Dog 73
Cat 9
Most Affected Breeds
Retriever - Golden 9
Retriever - Labrador 8
Shih Tzu 7
Domestic Shorthair 7
Pit Bull 5
Shepherd Dog - German 4
Bulldog 2
Maltese 2
Poodle (unspecified) 2
Schnauzer - Miniature 2
Most Reported Reactions
Lack of efficacy - NOS 24
Not eating 10
Head tilt - ear disorder 10
Ear discharge 9
Decreased appetite 9
Vomiting 8
Nystagmus 8
Behavioural disorder NOS 7
Loss of hearing 7
Death by euthanasia 7
Lethargy (see also Central nervous system depression in Neurological) 7
Head shake - ear disorder 6
Outcome Breakdown
Outcome Unknown
35 (42.7%)
Ongoing
29 (35.4%)
Euthanized
7 (8.5%)
Recovered/Normal
6 (7.3%)
Recovered with Sequela
5 (6.1%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.