Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide

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22 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.
22
Total Reports
2
Deaths Reported
910.0%
Death Rate

Active Ingredients

Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide

Administration Routes

TopicalAuricular (Otic)Unknown

Species Affected

Dog 16
Cat 6

Most Affected Breeds

Domestic Shorthair 3
Retriever - Labrador 2
Bulldog 2
Poodle - Toy 1
Dachshund (unspecified) 1
Terrier - Bull - American Pit 1
Chihuahua 1
Boxer (German Boxer) 1
Spaniel - Springer English 1
Dog (unknown) 1

Most Reported Reactions

Decreased appetite 2
Vomiting 2
Application site infection 2
Underdose 2
Lethargy (see also Central nervous system depression in 'Neurological') 2
Decreased packed cell volume (PCV) 2
Emesis 1
Salivary gland disorder 1
Walking difficulty 1
Muscle spasm NOS 1
Moist dermatitis 1
Dermal mass 1

Outcome Breakdown

Ongoing
9 (40.9%)
Outcome Unknown
8 (36.4%)
Recovered/Normal
3 (13.6%)
Died
2 (9.1%)

Data Summary

Metric Value
Total adverse event reports 22
Reports involving death 2
Case-fatality rate (reported events) 910.0%
Distinct species in reports 2
Distinct breeds in reports 18
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.

Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 22 adverse event reports referencing Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide, including 2 reports in which the animal died — a 910.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide. Reported administration routes include Topical, 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 Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide reports are Dog (16 reports), Cat (6 reports), with Dog accounting for the largest share. Within those species, Domestic Shorthair (3), Retriever - Labrador (2), Bulldog (2) 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 Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide are Decreased appetite (2), Vomiting (2), Application site infection (2), Underdose (2). Of the 22 reports with a coded outcome, Ongoing is the leading category at 40.9%. 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 Nystatin, Neomycin Sulfate, Thiostrepton And Triamcinolone Acetonide.

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