Drug profile

The FDA adverse-event record for Dexamethasone + Neomycin + Thiabendazole

24 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Dexamethasone + Neomycin + Thiabendazole. See the species affected, top reactions, and outcomes below.

24
adverse-event reports
0.0%
death-coded share
Unknown
most-reported species
5
Product dropper missing - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
24
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

DexamethasoneNeomycinThiabendazole

Administration Routes

UnknownAuricular (Otic)TopicalOphthalmic

Species Affected

Unknown 16
Dog 6
Cat 1
Human 1

Most Affected Breeds

Unknown 17
Bichon Frise 2
Domestic Shorthair 1
Pug 1
Crossbred Canine/dog 1
Terrier - Bull - Staffordshire 1
Chihuahua 1

Most Reported Reactions

Product dropper missing 5
Containers, Leaking 4
Underfilling, Bottles 2
Erythema (for urticaria see Immune SOC) 2
Burn 2
Lethargy (see also Central nervous system depression in Neurological) 2
Closure, Missing 2
Contamination, Foreign Object 1
Appearance, Abnormal 1
Warm feeling to the touch 1
Physical product label issues 1
Containers, Damaged 1

Outcome Breakdown

Outcome Unknown
4 (50.0%)
Recovered/Normal
3 (37.5%)
Ongoing
1 (12.5%)

Dexamethasone + Neomycin + Thiabendazole Adverse Event Insights

24 reports name Dexamethasone + Neomycin + Thiabendazole; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredients: Dexamethasone, Neomycin, Thiabendazole. Administration routes: Unknown, Auricular (Otic), Topical, Ophthalmic.

By species: Unknown (16 reports), Dog (6 reports), Cat (1 reports). By breed: Unknown (17), Bichon Frise (2), Domestic Shorthair (1).

Leading clinical signs: Product dropper missing (5), Containers, Leaking (4), Underfilling, Bottles (2), Erythema (for urticaria see Immune SOC) (2). Outcome, 8 coded reports: Outcome Unknown leads at 50.0%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.