Gentamicin, Mometasone Furoate, And Clotrimazole

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160 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.
160
Total Reports
21
Deaths Reported
1310.0%
Death Rate

Active Ingredients

Gentamicin, Mometasone Furoate, And Clotrimazole

Administration Routes

Auricular (Otic)UnknownTopical

Species Affected

Dog 156
Cat 4

Most Affected Breeds

Retriever - Labrador 30
Retriever - Golden 10
Bulldog 8
Shih Tzu 7
Terrier - Bull - American Pit 6
Chihuahua 5
Crossbred Canine/dog 5
Shepherd Dog - German 5
Maltese 4
Pug 4

Most Reported Reactions

Vomiting 45
Lethargy (see also Central nervous system depression in 'Neurological') 42
Diarrhoea 24
Other abnormal test result NOS 17
Elevated serum alkaline phosphatase (SAP) 17
Anorexia 16
Death by euthanasia 16
Elevated alanine aminotransferase (ALT) 15
Seizure NOS 13
Not eating 11
Anaemia NOS 10
Lack of efficacy - NOS 10

Outcome Breakdown

Ongoing
115 (71.9%)
Recovered/Normal
17 (10.6%)
Euthanized
15 (9.4%)
Outcome Unknown
7 (4.4%)
Died
6 (3.8%)

Data Summary

Metric Value
Total adverse event reports 160
Reports involving death 21
Case-fatality rate (reported events) 1310.0%
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.

Gentamicin, Mometasone Furoate, And Clotrimazole Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 160 adverse event reports referencing Gentamicin, Mometasone Furoate, And Clotrimazole, including 21 reports in which the animal died — a 1310.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Gentamicin, Mometasone Furoate, And Clotrimazole. Reported administration routes include Auricular (Otic), Unknown, Topical. 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 Gentamicin, Mometasone Furoate, And Clotrimazole reports are Dog (156 reports), Cat (4 reports), with Dog accounting for the largest share. Within those species, Retriever - Labrador (30), Retriever - Golden (10), Bulldog (8) 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 Gentamicin, Mometasone Furoate, And Clotrimazole are Vomiting (45), Lethargy (see also Central nervous system depression in 'Neurological') (42), Diarrhoea (24), Other abnormal test result NOS (17). Of the 160 reports with a coded outcome, Ongoing is the leading category at 71.9%. 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 Gentamicin, Mometasone Furoate, And Clotrimazole.

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