Drug profile

The FDA adverse-event record for Claro Otic

26 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Claro Otic. See the species affected, top reactions, and outcomes below.

26
adverse-event reports
7.7%
death-coded share
Dog
most-reported species
6
Lack of efficacy - NOS - 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.
26
Total Reports
2
Deaths Reported
7.7%
Death Rate

Active Ingredients

Claro Otic

Administration Routes

Auricular (Otic)Unknown

Species Affected

Dog 26

Most Affected Breeds

Terrier - Irish Soft-coated Wheaten 3
Spaniel - Boykin 3
Chihuahua 2
Collie - Border 2
Bulldog - English 2
Crossbred Canine/dog 2
Terrier - Bull 2
Coton de Tuléar 1
Bulldog 1
Terrier - Jack Russell 1

Most Reported Reactions

Lack of efficacy - NOS 6
Vomiting 4
Lethargy (see also Central nervous system depression in Neurological) 4
Deafness NOS 3
Bacterial skin infection NOS 3
Crust 3
Ear infection NOS 3
Intentional misuse 3
Grand mal seizure 3
Decreased appetite 2
Seizure NOS 2
Skin scab 2

Outcome Breakdown

Ongoing
12 (46.2%)
Outcome Unknown
6 (23.1%)
Recovered with Sequela
4 (15.4%)
Recovered/Normal
2 (7.7%)
Euthanized
2 (7.7%)

Claro Otic Adverse Event Insights

26 reports name Claro Otic; 2 recorded a death outcome (7.7% of reported events, not a population-level mortality rate). Active ingredient: Claro Otic. Administration routes: Auricular (Otic), Unknown.

By species: Dog (26 reports). By breed: Terrier - Irish Soft-coated Wheaten (3), Spaniel - Boykin (3), Chihuahua (2).

Leading clinical signs: Lack of efficacy - NOS (6), Vomiting (4), Lethargy (see also Central nervous system depression in Neurological) (4), Deafness NOS (3). Outcome, 26 coded reports: Ongoing leads at 46.2%.

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.