Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg
541 adverse event reports submitted to the FDA
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Data Summary
| Metric | Value |
|---|---|
| Total adverse event reports | 541 |
| Reports involving death | 2 |
| Case-fatality rate (reported events) | 40.0% |
| Distinct species in reports | 3 |
| Distinct breeds in reports | 20 |
| Distinct reactions reported | 20 |
| Active ingredients on file | 1 |
Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.
Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg Adverse Event Insights
The FDA Center for Veterinary Medicine database currently holds 541 adverse event reports referencing Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg, including 2 reports in which the animal died — a 40.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg. Reported administration routes include Oral, Unknown, Subcutaneous. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.
The species most frequently named in Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg reports are Dog (477 reports), Unknown (63 reports), Human (1 reports), with Dog accounting for the largest share. Within those species, Crossbred Canine/dog (101), Unknown (64), Beagle (53) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.
The most commonly reported clinical signs associated with Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg are Digestive tract disorder NOS (265), INEFFECTIVE, HEARTWORM LARVAE (199), Cardiac disorder NOS (133), Lack of efficacy (endoparasite) - hookworm (128). Of the 481 reports with a coded outcome, Outcome Unknown is the leading category at 64.9%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Ivermectin/Pyrantel Chew. Dog 136Mcg/114Mg.
Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates
Read our methodology — how this data is sourced, computed, and verified.