Drug profile

The FDA adverse-event record for Pyrantel

817 FDA reports name Pyrantel, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#213 of 2,679
by report volume (all drugs)
817
adverse-event reports
10.2%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Pyrantel ranks #212 of 2679 by total reports (817) and #539 of 1130 by death-coded share (10.2%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#212
This drug, reports of 2679
#539
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Pyrantel has 817 reports now versus 789 in that prior snapshot: 28 more (3.5%).

Report change
+28
Death-coded reports
+3
Death-coded share
+0.0 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Pyrantel changes

Signature read: 817 reports place Pyrantel in the upper third of FDA AER volume (#213 of 2,679).

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
817
Total Reports
83
Deaths Reported
10.2%
Death-coded share of reports

Active Ingredients

Pyrantel

Administration Routes

OralUnknownOphthalmicNasalSubcutaneousRespiratory (Inhalation)Topical

Species Affected

Dog 697
Cat 96
Unknown 13
Horse 6
Human 3
Pig 1
Other Reptiles 1

Most Affected Breeds

Crossbred Canine/dog 69
Domestic Shorthair 59
Retriever - Labrador 55
Pit Bull 50
Dog (unknown) 45
Greyhound 35
Chihuahua 32
Unknown 30
Retriever - Golden 27
Shepherd Dog - Australian 26

Most Reported Reactions

Vomiting 154
Lack of efficacy (endoparasite) - hookworm 100
Lethargy (see also Central nervous system depression in 'Neurological') 96
Diarrhoea 85
Death 61
Lack of efficacy (endoparasite) - roundworm NOS 60
Overdose 57
Underdose 54
Lethargy (see also Central nervous system depression in Neurological) 53
Emesis (multiple) 46
Not eating 43
Anorexia 33

Outcome Breakdown

Outcome Unknown
349 (42.8%)
Recovered/Normal
191 (23.4%)
Ongoing
184 (22.6%)
Died
70 (8.6%)
Euthanized
13 (1.6%)
Recovered with Sequela
8 (1.0%)

Pyrantel: high report volume in the FDA AER row

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.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Pyrantel, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Pyrantel (#213 of 2,679 by report volume); death-coded 10.2%. PlainBreed drug row · report volume stamp 817 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →