Ivermectin 0.08% Oral Liquid

37 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.

Total Reports

Deaths Reported

1350.0%

Death Rate

Active Ingredients

Ivermectin 0.08% Oral Liquid

Administration Routes

UnknownOralOphthalmic

Species Affected

Unknown 18

Sheep 12

Human 3

Dog 2

Goat 2

Most Affected Breeds

Unknown 21

Sheep (unknown) 12

Goat (unknown) 2

Dog (unknown) 1

Greyhound 1

Most Reported Reactions

Containers, Damaged 9

Digestive tract disorder NOS 6

Lack of efficacy (endoparasite) - roundworm NOS 6

Vials, Leaking 4

Death 4

Containers, Leaking 4

Uncoded sign 2

Labeled drug-species interaction 2

INEFFECTIVE, WORMS NOS 2

Apathy 2

Overdose 2

Closure, Abnormal 2

Outcome Breakdown

Outcome Unknown

12 (57.1%)

Died

4 (19.0%)

Recovered/Normal

3 (14.3%)

Ongoing

1 (4.8%)

Euthanized

1 (4.8%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.