Drug profile

The FDA adverse-event record for Florfenicol + Terbinafine + Mometasone Furoate

25 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Florfenicol + Terbinafine + Mometasone Furoate. Species, reactions, and outcomes follow.

#1593 of 2,679
by report volume (all drugs)
25
adverse-event reports
12.0%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Florfenicol + Terbinafine + Mometasone Furoate ranks #1577 of 2679 by total reports (25). Death-coded-share rank requires at least 50 reports. National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#1577
This drug, reports of 2679

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Florfenicol + Terbinafine + Mometasone Furoate has 25 reports now versus 22 in that prior snapshot: 3 more (13.6%).

Report change
+3
Death-coded reports
+0
Death-coded share
−1.6 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Florfenicol + Terbinafine + Mometasone Furoate changes

Signature read: report volume at 25 is the most distinctive stamp on Florfenicol + Terbinafine + Mometasone Furoate's FDA AER row.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
25
Total Reports
3
Deaths Reported
12.0%
Death-coded share of reports

Active Ingredients

Florfenicol + Terbinafine + Mometasone Furoate

Administration Routes

Auricular (Otic)Unknown

Species Affected

Dog 24
Cat 1

Most Affected Breeds

Retriever - Labrador 3
Spaniel - Cocker American 2
Retriever - Golden 2
Pit Bull 2
Bulldog - French 2
Shiba Inu 1
Terrier (unspecified) 1
Schnauzer (unspecified) 1
Terrier - Yorkshire 1
Bulldog 1

Most Reported Reactions

Vomiting 8
Death 3
Lack of efficacy - NOS 3
Lethargy (see also Central nervous system depression in Neurological) 3
Diarrhoea 3
Haematuria 2
Decreased urine concentration 2
Ear infection NOS 2
Ataxia 2
Abnormal ultrasound finding 2
Not eating 2
Dry mucous membrane 2

Outcome Breakdown

Recovered/Normal
8 (32.0%)
Outcome Unknown
8 (32.0%)
Ongoing
6 (24.0%)
Died
3 (12.0%)

Florfenicol + Terbinafine + Mometasone Furoate Adverse Event Insights

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.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

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

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Florfenicol + Terbinafine + Mometasone Furoate (#1593 of 2,679 by report volume); death-coded 12.0%. PlainBreed drug row · report volume stamp 25 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →