Nystatin + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide

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29 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.
29
Total Reports
1
Deaths Reported
340.0%
Death Rate

Active Ingredients

Nystatin + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide

Administration Routes

UnknownAuricular (Otic)TopicalCutaneousSubcutaneous

Species Affected

Dog 26
Cat 3

Most Affected Breeds

Crossbred Canine/dog 4
Retriever - Golden 3
Pug 2
Terrier - West Highland White 2
Bulldog 2
Domestic Shorthair 2
Retriever - Labrador 1
Maltese 1
Hound - Basset 1
Retriever (unspecified) 1

Most Reported Reactions

Emesis 9
Elevated alanine aminotransferase (ALT) 7
Lethargy (see also Central nervous system depression in 'Neurological') 4
Lack of efficacy - NOS 4
Vomiting 4
Behavioural disorder NOS 3
Elevated creatinine 3
Leucopenia NOS 3
Other abnormal test result NOS 3
Seizure NOS 2
Diarrhoea 2
UNPALATABLE 2

Outcome Breakdown

Recovered/Normal
16 (55.2%)
Outcome Unknown
5 (17.2%)
Ongoing
5 (17.2%)
Recovered with Sequela
2 (6.9%)
Died
1 (3.4%)

Data Summary

Metric Value
Total adverse event reports 29
Reports involving death 1
Case-fatality rate (reported events) 340.0%
Distinct species in reports 2
Distinct breeds in reports 20
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 + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 29 adverse event reports referencing Nystatin + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide, including 1 reports in which the animal died — a 340.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Nystatin + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide. Reported administration routes include Unknown, Auricular (Otic), Topical, Cutaneous. 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 + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide reports are Dog (26 reports), Cat (3 reports), with Dog accounting for the largest share. Within those species, Crossbred Canine/dog (4), Retriever - Golden (3), Pug (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 + Thiostrepton + Neomycin Sulfate + Triamcinolone Acetonide are Emesis (9), Elevated alanine aminotransferase (ALT) (7), Lethargy (see also Central nervous system depression in 'Neurological') (4), Lack of efficacy - NOS (4). Of the 29 reports with a coded outcome, Recovered/Normal is the leading category at 55.2%. 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 + Thiostrepton + Neomycin Sulfate + 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