Flunixin + Oxytetracycline

12 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.

Total Reports

Deaths Reported

3330.0%

Death Rate

Active Ingredients

FlunixinOxytetracycline

Administration Routes

SubcutaneousUnknownParenteral

Species Affected

Cattle 8

Human 2

Sheep 1

Unknown 1

Most Affected Breeds

Unknown 4

Aberdeen Angus 3

Holstein-Friesian also known as Holstein 2

Rambouillet 1

Charolais 1

Simmental 1

Most Reported Reactions

Death 3

Injection site swelling 3

Accidental exposure 2

Anaphylaxis 2

Recumbency 2

Breathing difficulty 2

Injection site stiffness 1

Nasal discharge 1

Hypersalivation 1

Distress 1

Pulmonary oedema 1

Nasal bleeding 1

Outcome Breakdown

Ongoing

4 (36.4%)

Died

4 (36.4%)

Recovered/Normal

3 (27.3%)

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