Tulathromycin Inj Sol
49 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.
49
Total Reports
37
Deaths Reported
7550.0%
Death Rate
Active Ingredients
Tulathromycin Inj Sol
Administration Routes
SubcutaneousUnknownIntramuscularTopicalParenteral
Species Affected
Cattle 44
Unknown 2
Human 2
Pig 1
Most Affected Breeds
Cattle (other) 29
Unknown 4
Aberdeen Angus 4
Crossbred Bovine/Cattle 3
Mixed (Cattle) 3
Cattle (unspecified) 2
Holstein-Friesian also known as Holstein 2
Pig (unknown) 1
Simmental 1
Most Reported Reactions
Death 34
Lack of efficacy - NOS 31
Necropsy performed 4
Lack of efficacy (mycoplasma) - NOS 3
Lack of efficacy (bacteria) - Histophilus somni 3
Recumbency 3
Anaphylaxis 3
Fibrinous (broncho) pneumonia/fibrinous pleuropneumonia 2
Hypersensitivity reaction 2
Death by euthanasia 2
Laboured breathing 2
Physical label missing 1
Outcome Breakdown
Died
36 (44.4%)
Ongoing
22 (27.2%)
Outcome Unknown
16 (19.8%)
Recovered/Normal
5 (6.2%)
Euthanized
2 (2.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.