Drug profile

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

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

40
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.
40
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Tick Treatment (Unknown)

Administration Routes

UnknownTopicalOral

Species Affected

Dog 40

Most Affected Breeds

Retriever - Golden 5
Maltese 4
Retriever - Labrador 4
Terrier - Yorkshire 3
Beagle 3
Dog (other) 2
Schnauzer (unspecified) 2
Crossbred Canine/dog 2
Shepherd Dog - German 2
Shih Tzu 2

Most Reported Reactions

Emesis 11
Vomiting 10
Lethargy (see also Central nervous system depression in 'Neurological') 4
Other abnormal test result NOS 4
Not eating 3
Diarrhoea 3
Lack of efficacy - NOS 3
Lack of efficacy (endoparasite) - hookworm 3
INEFFECTIVE, HOOKS 3
Disorientation 2
Behavioural disorder NOS 2
Decreased appetite 2

Outcome Breakdown

Recovered/Normal
26 (65.0%)
Outcome Unknown
9 (22.5%)
Recovered with Sequela
4 (10.0%)
Ongoing
1 (2.5%)

Tick Treatment (Unknown) Adverse Event Insights

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

By species: Dog (40 reports). By breed: Retriever - Golden (5), Maltese (4), Retriever - Labrador (4).

Leading clinical signs: Emesis (11), Vomiting (10), Lethargy (see also Central nervous system depression in 'Neurological') (4), Other abnormal test result NOS (4). Outcome, 40 coded reports: Recovered/Normal leads at 65.0%.

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.