Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta

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20 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.
20
Total Reports
2
Deaths Reported
1000.0%
Death Rate

Active Ingredients

Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta

Administration Routes

TopicalUnknownCutaneousAuricular (Otic)

Species Affected

Dog 16
Cat 4

Most Affected Breeds

Domestic Shorthair 4
Retriever - Golden 2
Sheepdog - Shetland 2
Collie - Border 2
Retriever - Labrador 2
Shepherd Dog - German 1
Spaniel - Cocker American 1
Dog (unknown) 1
Cattle Dog (unspecified) 1
Boxer (German Boxer) 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 5
Vomiting 3
Neutropenia 3
Lack of efficacy - NOS 2
Diarrhoea 2
Liver disorder NOS 2
Arthritis 2
Ringworm 2
Lack of efficacy (flea) 2
Decreased appetite 2
Hypersalivation 2
Elevated cholesterol (total) 2

Outcome Breakdown

Ongoing
8 (40.0%)
Outcome Unknown
6 (30.0%)
Recovered/Normal
4 (20.0%)
Euthanized
2 (10.0%)

Data Summary

Metric Value
Total adverse event reports 20
Reports involving death 2
Case-fatality rate (reported events) 1000.0%
Distinct species in reports 2
Distinct breeds in reports 13
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.

Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 20 adverse event reports referencing Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta, including 2 reports in which the animal died — a 1000.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta. Reported administration routes include Topical, Unknown, Cutaneous, Auricular (Otic). 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 Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta reports are Dog (16 reports), Cat (4 reports), with Dog accounting for the largest share. Within those species, Domestic Shorthair (4), Retriever - Golden (2), Sheepdog - Shetland (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 Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta are Lethargy (see also Central nervous system depression in Neurological) (5), Vomiting (3), Neutropenia (3), Lack of efficacy - NOS (2). Of the 20 reports with a coded outcome, Ongoing is the leading category at 40.0%. 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 Miconazole Nitrate + Chlorhexidine Gluconate + Trizedta.

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