Ketoprofen;Tulathromycin
213 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.
213
Total Reports
128
Deaths Reported
6010.0%
Death Rate
Active Ingredients
Ketoprofen;Tulathromycin
Administration Routes
SubcutaneousUnknownTopicalOtherOphthalmicIntramuscularIntravenousIntraocularIntradermal
Species Affected
Cattle 163
Unknown 27
Human 18
Sheep 5
Most Affected Breeds
Mixed (Cattle) 115
Unknown 46
Aberdeen Angus 15
Cattle (other) 9
Holstein-Friesian also known as Holstein 6
Jersey 5
Crossbred Bovine/Cattle 3
Sheep (unknown) 2
Cattle (unknown) 2
Guernsey 2
Most Reported Reactions
Death 118
Lack of efficacy - NOS 111
Necropsy performed 19
Intentional misuse 13
Containers, Damaged 10
Inappropriate packaging or design 8
Anaphylaxis 8
Injection site swelling 7
Puncture wound 7
Lying down 6
Lack of efficacy (bacteria) - NOS 6
Lateral recumbency 5
Outcome Breakdown
Died
126 (42.9%)
Outcome Unknown
101 (34.4%)
Ongoing
28 (9.5%)
Recovered/Normal
24 (8.2%)
Recovered with Sequela
10 (3.4%)
Euthanized
5 (1.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.