Tiletamine

32 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.
32
Total Reports
3
Deaths Reported
940.0%
Death Rate

Active Ingredients

Tiletamine

Administration Routes

UnknownParenteralIntravenousIntramuscularSubcutaneous

Species Affected

Cat 21
Dog 11

Most Affected Breeds

Domestic Shorthair 15
Retriever - Labrador 3
Domestic Longhair 3
Cat (unknown) 2
Shih Tzu 1
Rottweiler 1
Shepherd Dog - German 1
Mixed (Dog) 1
Shepherd Dog - Australian 1
Terrier - Boston 1

Most Reported Reactions

Decreased appetite 5
Behavioural disorder NOS 5
Vomiting 4
Hypothermia 3
Death 3
Walking difficulty 3
Not eating 3
Seizure NOS 3
Hyperactivity 3
Elevated temperature 3
Dehydration 2
Sedation prolonged 2

Outcome Breakdown

Recovered/Normal
11 (34.4%)
Ongoing
9 (28.1%)
Outcome Unknown
9 (28.1%)
Died
3 (9.4%)

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