Drug profile

The FDA adverse-event record for Ivermectin 10 Mg/Ml Solution For Injection

247 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Ivermectin 10 Mg/Ml Solution For Injection. See the species affected, top reactions, and outcomes below.

247
adverse-event reports
9.3%
death-coded share
Dog
most-reported species
32
Labeled drug-species interaction - top reaction
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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
9.3%
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%)

Ivermectin 10 Mg/Ml Solution For Injection Adverse Event Insights

247 reports name Ivermectin 10 Mg/Ml Solution For Injection; 23 recorded a death outcome (9.3% of reported events, not a population-level mortality rate). Active ingredient: Ivermectin 10 Mg/Ml Solution For Injection. Administration routes: Unknown, Subcutaneous, Oral, Parenteral.

By species: Dog (78 reports), Cattle (38 reports), Unknown (36 reports). By breed: Unknown (79), Cattle (unknown) (12), Sheep (unknown) (11).

Leading clinical signs: Labeled drug-species interaction (32), Ataxia (24), Accidental exposure (22), Mydriasis (21). Outcome, 218 coded reports: Outcome Unknown leads at 59.2%.

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.

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

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.