Ivermectin 10 Mg/Ml Solution For Injection

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247 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.
247
Total Reports
23
Deaths Reported
930.0%
Death Rate

Active Ingredients

Ivermectin 10 Mg/Ml Solution For Injection

Administration Routes

UnknownSubcutaneousOralParenteralIntramuscularOtherOphthalmicTopicalIntravenousImmersion

Species Affected

Dog 78
Cattle 38
Unknown 36
Human 36
Cat 12
Sheep 11
Horse 10
Pig 10
Goat 9
Other Birds 4

Most Affected Breeds

Unknown 79
Cattle (unknown) 12
Sheep (unknown) 11
Dog (unknown) 9
Crossbred Canine/dog 8
Nelore 8
Retriever - Labrador 7
Pit Bull 7
Cattle (other) 6
Pig (unknown) 6

Most Reported Reactions

Labeled drug-species interaction 32
Ataxia 24
Accidental exposure 22
Mydriasis 21
Death 19
Lethargy (see also Central nervous system depression in 'Neurological') 15
Injection site pain 13
Overdose 13
Color, Abnormal 12
Skin lesion NOS 11
Vomiting 11
Cardiac disorder NOS 10

Outcome Breakdown

Outcome Unknown
129 (59.2%)
Recovered/Normal
41 (18.8%)
Died
19 (8.7%)
Ongoing
12 (5.5%)
Recovered with Sequela
11 (5.0%)
Euthanized
6 (2.8%)

Data Summary

Metric Value
Total adverse event reports 247
Reports involving death 23
Case-fatality rate (reported events) 930.0%
Distinct species in reports 10
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 10 Mg/Ml Solution For Injection Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 247 adverse event reports referencing Ivermectin 10 Mg/Ml Solution For Injection, including 23 reports in which the animal died — a 930.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Ivermectin 10 Mg/Ml Solution For Injection. Reported administration routes include Unknown, Subcutaneous, Oral, Parenteral. 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 10 Mg/Ml Solution For Injection reports are Dog (78 reports), Cattle (38 reports), Unknown (36 reports), with Dog accounting for the largest share. Within those species, Unknown (79), Cattle (unknown) (12), Sheep (unknown) (11) 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 10 Mg/Ml Solution For Injection are Labeled drug-species interaction (32), Ataxia (24), Accidental exposure (22), Mydriasis (21). Of the 218 reports with a coded outcome, Outcome Unknown is the leading category at 59.2%. 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 10 Mg/Ml Solution For Injection.

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