Drug profile

The FDA adverse-event record for Flea Control Product

10 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Flea Control Product. See the species affected, top reactions, and outcomes below.

10
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
4
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.
10
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Flea Control Product

Administration Routes

Unknown

Species Affected

Dog 10

Most Affected Breeds

Retriever - Golden 3
Bichon Frise 1
Terrier - Jack Russell 1
Beagle 1
Boxer (German Boxer) 1
Terrier - Bull 1
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1
Shepherd Dog - Australian 1

Most Reported Reactions

Lack of efficacy - NOS 4
INEFFECTIVE, LOSS OF EFFECT 4
Alopecia local 1
Restlessness 1
Abnormal breathing 1
Tremor 1
Other abnormal test result NOS 1
Skin and tissue infection NOS 1
Otitis NOS 1
PR-EAR(S), LESION(S) 1
Fungal skin infection NOS 1
PR-SKIN, LESION(S) 1

Outcome Breakdown

Ongoing
7 (70.0%)
Outcome Unknown
2 (20.0%)
Recovered/Normal
1 (10.0%)

Flea Control Product Adverse Event Insights

10 reports name Flea Control Product; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Flea Control Product. Administration route: Unknown.

By species: Dog (10 reports). By breed: Retriever - Golden (3), Bichon Frise (1), Terrier - Jack Russell (1).

Leading clinical signs: Lack of efficacy - NOS (4), INEFFECTIVE, LOSS OF EFFECT (4), Alopecia local (1), Restlessness (1). Outcome, 10 coded reports: Ongoing leads at 70.0%.

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.