Pyrantel Pamoate ( Pyrantel Embonate)

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155 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.
155
Total Reports
18
Deaths Reported
1160.0%
Death Rate

Active Ingredients

Pyrantel Pamoate ( Pyrantel Embonate)

Administration Routes

OralUnknownSubcutaneousTopical

Species Affected

Dog 110
Cat 19
Unknown 15
Horse 9
Sheep 1
Cattle 1

Most Affected Breeds

Unknown 15
Domestic Shorthair 14
Retriever - Labrador 9
Shih Tzu 8
Retriever - Golden 6
Dog (unknown) 6
Chihuahua 6
Shepherd Dog - German 5
Crossbred Canine/dog 5
Terrier (unspecified) 5

Most Reported Reactions

Lack of efficacy (endoparasite) - hookworm 29
Lethargy (see also Central nervous system depression in 'Neurological') 27
INEFFECTIVE, ASCARIDS NOS 22
Death 16
Vomiting 16
Anorexia 15
Anaphylactoid reaction 14
Diarrhoea 12
Emesis 10
Lack of efficacy - NOS 9
Suspension, Abnormal 8
Drug administration error 8

Outcome Breakdown

Ongoing
73 (49.0%)
Outcome Unknown
33 (22.1%)
Recovered/Normal
25 (16.8%)
Died
16 (10.7%)
Euthanized
2 (1.3%)

Data Summary

Metric Value
Total adverse event reports 155
Reports involving death 18
Case-fatality rate (reported events) 1160.0%
Distinct species in reports 6
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.

Pyrantel Pamoate ( Pyrantel Embonate) Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 155 adverse event reports referencing Pyrantel Pamoate ( Pyrantel Embonate), including 18 reports in which the animal died — a 1160.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Pyrantel Pamoate ( Pyrantel Embonate). Reported administration routes include Oral, Unknown, Subcutaneous, Topical. 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 Pyrantel Pamoate ( Pyrantel Embonate) reports are Dog (110 reports), Cat (19 reports), Unknown (15 reports), with Dog accounting for the largest share. Within those species, Unknown (15), Domestic Shorthair (14), Retriever - Labrador (9) 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 Pyrantel Pamoate ( Pyrantel Embonate) are Lack of efficacy (endoparasite) - hookworm (29), Lethargy (see also Central nervous system depression in 'Neurological') (27), INEFFECTIVE, ASCARIDS NOS (22), Death (16). Of the 149 reports with a coded outcome, Ongoing is the leading category at 49.0%. 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 Pyrantel Pamoate ( Pyrantel Embonate).

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