Thiabendazole/Neomycin/Dexamethason

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49 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.
49
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Thiabendazole/Neomycin/Dexamethason

Administration Routes

UnknownAuricular (Otic)OphthalmicOral

Species Affected

Dog 20
Unknown 14
Human 8
Cat 7

Most Affected Breeds

Unknown 22
Domestic Shorthair 6
Terrier - West Highland White 1
Crossbred Canine/dog 1
Retriever - Labrador 1
Sheepdog - Old English 1
Shih Tzu 1
Poodle - Miniature 1
Bulldog - French 1
Dog (other) 1

Most Reported Reactions

Uncoded sign 14
Dropper, Abnormal 5
Eye irritation 5
Caps, Abnormal 4
Vials, Leaking 4
Lethargy (see also Central nervous system depression in 'Neurological') 3
Eye redness 3
Accidental exposure 3
Deafness NOS 3
External ear disorder NOS 3
Vomiting 2
Elevated liver enzymes 2

Outcome Breakdown

Outcome Unknown
25 (71.4%)
Recovered/Normal
9 (25.7%)
Recovered with Sequela
1 (2.9%)

Data Summary

Metric Value
Total adverse event reports 49
Reports involving death 0
Case-fatality rate (reported events) 0.0%
Distinct species in reports 4
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.

Thiabendazole/Neomycin/Dexamethason Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 49 adverse event reports referencing Thiabendazole/Neomycin/Dexamethason, 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: Thiabendazole/Neomycin/Dexamethason. Reported administration routes include Unknown, Auricular (Otic), Ophthalmic, Oral. 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 Thiabendazole/Neomycin/Dexamethason reports are Dog (20 reports), Unknown (14 reports), Human (8 reports), with Dog accounting for the largest share. Within those species, Unknown (22), Domestic Shorthair (6), Terrier - West Highland White (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 Thiabendazole/Neomycin/Dexamethason are Uncoded sign (14), Dropper, Abnormal (5), Eye irritation (5), Caps, Abnormal (4). Of the 35 reports with a coded outcome, Outcome Unknown is the leading category at 71.4%. 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 Thiabendazole/Neomycin/Dexamethason.

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