Cattle, Mixed (Cattle), Tulathromycin

FDA Veterinary Adverse Event Report #N141244, March 3, 2025, Serious Event

Animal Information

Species Cattle
Breed Mixed (Cattle)
Gender Mixed
Age 30.00 Day
Weight 68.039 Kilogram

Event Summary

Report ID N141244
Date March 3, 2025
Serious Yes
Outcome Died

Drug Information

Active Ingredients Tulathromycin
Manufacturer MSK

Reported Reactions

Lack of efficacy - NOS; Death; Medication error NOS

Related Cattle Reports

Report ID Breed Reactions Outcome Date
N141209 Holstein-Friesian also... Staggering; Cloudy eye (for Miosis, Mydriasis, ... Outcome Unknown Jun 24, 2026
N141553 Mixed (Cattle) Localised pain NOS (see other SOCs for specific... Outcome Unknown Jun 24, 2026
N141442 Mixed (Cattle) Lack of efficacy - NOS Outcome Unknown Jun 22, 2026
N141508 Mixed (Cattle) Unrelated death Died Jun 17, 2026
N141553 Mixed (Cattle) Injection site swelling Outcome Unknown Jun 11, 2026

Frequently Asked Questions

Yes, cats have unique metabolic differences that make them significantly more sensitive to many drugs. Cats lack certain liver enzymes (particularly glucuronyl transferase) that are needed to process many compounds. This is why drugs like acetaminophen, aspirin at dog doses, and many essential oils are toxic to cats but safe for other species. Even some FDA-approved canine drugs are not safe for cats. Always use medications specifically approved or prescribed for cats, and never assume that a dog dose or human medication is safe.

Not necessarily. Adverse event reports document that a drug was given and that the animal later died, but they do not establish causation. The animal may have died from its underlying condition, from concurrent medications, or from unrelated causes. The FDA applies a structured causality assessment to each report to determine whether the drug was likely, possibly, or unlikely responsible. Still, all death reports are reviewed and tracked because they contribute to safety signal detection, even when individual causality is uncertain.

You can report a suspected adverse drug reaction to the FDA Center for Veterinary Medicine through the FDA Safety Reporting Portal at SafetyReporting.hhs.gov or by calling 1-888-FDA-VETS (1-888-332-8387). You can also contact the drug manufacturer directly, they are required to forward serious adverse event reports to the FDA. Include the drug name and dose, the animal's species, breed, age, and weight, the duration of treatment, and a detailed description of the symptoms observed and their timeline.

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