Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B

Verify with FDA CVM →

14 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.
14
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B

Administration Routes

Auricular (Otic)Unknown

Species Affected

Dog 13
Cat 1

Most Affected Breeds

Retriever - Labrador 3
Spaniel - Cocker American 2
Retriever - Golden 1
Rottweiler 1
Schnauzer (unspecified) 1
Spitz - German Pomeranian 1
Chihuahua 1
Domestic Shorthair 1
Bulldog 1
Hound - Basset 1

Most Reported Reactions

Lack of efficacy - NOS 4
Emesis 3
Weight loss 3
Vomiting 3
INEFFECTIVE, HEARTWORM LARVAE 2
Leucocytosis NOS 2
Not eating 2
Immune mediated haemolytic anaemia 2
Splenomegaly 2
Elevated serum alkaline phosphatase (SAP) 2
Decreased activity 2
Otitis externa 2

Outcome Breakdown

Outcome Unknown
6 (42.9%)
Ongoing
5 (35.7%)
Recovered/Normal
3 (21.4%)

Data Summary

Metric Value
Total adverse event reports 14
Reports involving death 0
Case-fatality rate (reported events) 0.0%
Distinct species in reports 2
Distinct breeds in reports 11
Distinct reactions reported 20
Active ingredients on file 1

Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.

Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 14 adverse event reports referencing Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B, including 0 reports in which the animal died — a 0.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B. Reported administration routes include Auricular (Otic), Unknown. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.

The species most frequently named in Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B reports are Dog (13 reports), Cat (1 reports), with Dog accounting for the largest share. Within those species, Retriever - Labrador (3), Spaniel - Cocker American (2), Retriever - Golden (1) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.

The most commonly reported clinical signs associated with Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B are Lack of efficacy - NOS (4), Emesis (3), Weight loss (3), Vomiting (3). Of the 14 reports with a coded outcome, Outcome Unknown is the leading category at 42.9%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Enrofloxacin + Ketoconazole + Triamcinolone + Silver Sulfadazine + Tobramycin + Polymixin B.

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

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial