Ivermectin 68Mcg Pyrantel 57Mg

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833 adverse event reports submitted to the FDA

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
833
Total Reports
17
Deaths Reported
200.0%
Death Rate

Active Ingredients

Ivermectin 68Mcg Pyrantel 57Mg

Administration Routes

OralUnknown

Species Affected

Dog 778
Unknown 53
Human 1
Cat 1

Most Affected Breeds

Terrier - Yorkshire 83
Chihuahua 73
Unknown 54
Maltese 54
Shih Tzu 46
Poodle - Toy 38
Dachshund (unspecified) 37
Dog (unknown) 34
Crossbred Canine/dog 26
Retriever - Labrador 25

Most Reported Reactions

Vomiting 340
INEFFECTIVE, HEARTWORM LARVAE 144
Lethargy (see also Central nervous system depression in 'Neurological') 130
Diarrhoea 102
Lack of efficacy (endoparasite) - hookworm 94
Lack of efficacy - NOS 71
INEFFECTIVE, ASCARIDS NOS 47
Underfilling, Package 41
Behavioural disorder NOS 21
Underdose 20
Uncoded sign 19
Seizure NOS 19

Outcome Breakdown

Recovered/Normal
431 (55.2%)
Outcome Unknown
310 (39.7%)
Ongoing
13 (1.7%)
Recovered with Sequela
10 (1.3%)
Euthanized
9 (1.2%)
Died
8 (1.0%)

Data Summary

Metric Value
Total adverse event reports 833
Reports involving death 17
Case-fatality rate (reported events) 200.0%
Distinct species in reports 4
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 68Mcg Pyrantel 57Mg Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 833 adverse event reports referencing Ivermectin 68Mcg Pyrantel 57Mg, including 17 reports in which the animal died — a 200.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Ivermectin 68Mcg Pyrantel 57Mg. Reported administration routes include Oral, Unknown. 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 68Mcg Pyrantel 57Mg reports are Dog (778 reports), Unknown (53 reports), Human (1 reports), with Dog accounting for the largest share. Within those species, Terrier - Yorkshire (83), Chihuahua (73), Unknown (54) 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 68Mcg Pyrantel 57Mg are Vomiting (340), INEFFECTIVE, HEARTWORM LARVAE (144), Lethargy (see also Central nervous system depression in 'Neurological') (130), Diarrhoea (102). Of the 781 reports with a coded outcome, Recovered/Normal is the leading category at 55.2%. 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 68Mcg Pyrantel 57Mg.

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

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial