Florfenicol, Flunixin

147 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.

147

Total Reports

105

Deaths Reported

7140.0%

Death Rate

Active Ingredients

Florfenicol, Flunixin

Administration Routes

SubcutaneousUnknownTopicalOphthalmicIntramuscular

Species Affected

Cattle 116

Human 15

Unknown 12

Goat 2

Sheep 2

Most Affected Breeds

Holstein-Friesian also known as Holstein 62

Unknown 27

Crossbred Bovine/Cattle 24

Cattle (unknown) 19

Aberdeen Angus 7

Sheep (unknown) 2

Pygmy 1

Jersey 1

Goat (unknown) 1

Mixed (Cattle) 1

Most Reported Reactions

Lack of efficacy (bacteria) - NOS 66

Death 59

DEATH-TREATMENT FAILURE 42

CULTURE/TITER DATA ABNORMAL 39

PR-LUNG(S), LESION(S) 31

Unclassifiable adverse event 23

PR-GI, LESION(S) 16

Accidental exposure 14

PR-LIVER, LESION(S) 14

PR-SPLEEN, LESION(S) 14

PR-THYMUS, LESION(S) 8

PR-KIDNEY(S), LESION(S) 8

Outcome Breakdown

Died

105 (97.2%)

Outcome Unknown

1 (0.9%)

Ongoing

1 (0.9%)

Recovered/Normal

1 (0.9%)

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