Drug profile

The FDA adverse-event record for Skin Treatment (Unknown)

32 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Skin Treatment (Unknown). See the species affected, top reactions, and outcomes below.

32
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
11
Emesis - 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.
32
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Skin Treatment (Unknown)

Administration Routes

UnknownTopicalOralCutaneous

Species Affected

Dog 32

Most Affected Breeds

Retriever - Labrador 6
Dog (unknown) 3
Boxer (German Boxer) 2
Pug 2
Terrier - Cairn 1
Dachshund - Miniature 1
Shih Tzu 1
Bichon Frise 1
Hound - Basset 1
Dachshund (unspecified) 1

Most Reported Reactions

Emesis 11
Vomiting 6
Lethargy (see also Central nervous system depression in 'Neurological') 3
Diarrhoea 3
Decreased appetite 3
Lack of efficacy (ectoparasite) - flea 2
Inflammatory bowel disorder 2
Pinnal reddening 1
Facial swelling (see also 'Skin') 1
Reddening of the skin 1
Nausea 1
Lack of efficacy - NOS 1

Outcome Breakdown

Recovered/Normal
15 (46.9%)
Outcome Unknown
11 (34.4%)
Recovered with Sequela
3 (9.4%)
Ongoing
3 (9.4%)

Skin Treatment (Unknown) Adverse Event Insights

32 reports name Skin Treatment (Unknown); 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Skin Treatment (Unknown). Administration routes: Unknown, Topical, Oral, Cutaneous.

By species: Dog (32 reports). By breed: Retriever - Labrador (6), Dog (unknown) (3), Boxer (German Boxer) (2).

Leading clinical signs: Emesis (11), Vomiting (6), Lethargy (see also Central nervous system depression in 'Neurological') (3), Diarrhoea (3). Outcome, 32 coded reports: Recovered/Normal leads at 46.9%.

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.