Tilmicosin

469 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.

469

Total Reports

144

Deaths Reported

3070.0%

Death Rate

Active Ingredients

Tilmicosin

Administration Routes

ParenteralUnknownOralSubcutaneousTopicalIntramuscularCutaneousIntraocularIntradermalOphthalmic

Species Affected

Human 188

Cattle 166

Unknown 81

Pig 30

Sheep 2

Horse 1

Dog 1

Most Affected Breeds

Unknown 270

Cattle (unknown) 61

Crossbred Bovine/Cattle 27

Aberdeen Angus 23

Holstein-Friesian also known as Holstein 18

Pig (unknown) 14

Mixed (Cattle) 13

Crossbred Porcine/Pig 10

Cattle (other) 7

Jersey 4

Most Reported Reactions

Death 129

Accidental exposure 111

Injection site bleeding 37

Injection site swelling 28

Injection site pain 25

Containers, Leaking 25

Lack of efficacy - NOS 24

Bad taste 22

Anaphylaxis 17

Unclassifiable adverse event 17

High blood pressure 16

Increased heart rate 16

Outcome Breakdown

Died

143 (32.4%)

Recovered/Normal

123 (27.8%)

Outcome Unknown

105 (23.8%)

Ongoing

57 (12.9%)

Euthanized

14 (3.2%)

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