Ivermectin 0.5% Pour-On Topical Solution

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347 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.
347
Total Reports
12
Deaths Reported
350.0%
Death Rate

Active Ingredients

Ivermectin 0.5% Pour-On Topical Solution

Administration Routes

TopicalOtherUnknownOralSubcutaneousTransdermal

Species Affected

Cattle 286
Unknown 38
Dog 10
Human 7
Cat 2
Goat 2
Sheep 1
Rabbit 1

Most Affected Breeds

Aberdeen Angus 121
Cattle (unknown) 59
Unknown 49
Crossbred Bovine/Cattle 46
Cattle (other) 35
Charolais 8
Simmental 5
Hereford cattle 3
Dog (unknown) 2
European 2

Most Reported Reactions

Systemic disorder NOS 179
Lack of efficacy (ectoparasite) - lice 145
Hair loss NOS 111
Scratching 85
Rubbing 66
INEFFECTIVE, LICE BITING 61
Pruritus 33
Itching 29
General hair loss 26
SKIN SCRAPING ABNORMAL 26
Rubra 23
Lack of efficacy (ectoparasite) - NOS 21

Outcome Breakdown

Outcome Unknown
217 (69.6%)
Recovered with Sequela
48 (15.4%)
Ongoing
23 (7.4%)
Recovered/Normal
12 (3.8%)
Died
11 (3.5%)
Euthanized
1 (0.3%)

Data Summary

Metric Value
Total adverse event reports 347
Reports involving death 12
Case-fatality rate (reported events) 350.0%
Distinct species in reports 8
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 0.5% Pour-On Topical Solution Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 347 adverse event reports referencing Ivermectin 0.5% Pour-On Topical Solution, including 12 reports in which the animal died — a 350.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Ivermectin 0.5% Pour-On Topical Solution. Reported administration routes include Topical, Other, Unknown, Oral. 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 0.5% Pour-On Topical Solution reports are Cattle (286 reports), Unknown (38 reports), Dog (10 reports), with Cattle accounting for the largest share. Within those species, Aberdeen Angus (121), Cattle (unknown) (59), Unknown (49) 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 0.5% Pour-On Topical Solution are Systemic disorder NOS (179), Lack of efficacy (ectoparasite) - lice (145), Hair loss NOS (111), Scratching (85). Of the 312 reports with a coded outcome, Outcome Unknown is the leading category at 69.6%. 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 0.5% Pour-On Topical Solution.

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