Florfenicol Inj Sol 30% W Pg

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229 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.
229
Total Reports
102
Deaths Reported
4450.0%
Death Rate

Active Ingredients

Florfenicol Inj Sol 30% W Pg

Administration Routes

UnknownSubcutaneousIntramuscularParenteralIntravenousTopicalOral

Species Affected

Cattle 122
Unknown 68
Human 18
Goat 11
Sheep 3
Fish 1
Other Mammals 1
Dog 1
Cat 1
Alpaca 1

Most Affected Breeds

Unknown 87
Cattle (other) 39
Crossbred Bovine/Cattle 22
Aberdeen Angus 18
Holstein-Friesian also known as Holstein 16
Cattle (unspecified) 10
Mixed (Cattle) 7
Goat (unknown) 5
Brangus 3
Pygmy 3

Most Reported Reactions

Death 83
Lack of efficacy - NOS 64
Lack of efficacy (bacteria) - NOS 37
Containers, Damaged 26
Respiratory signs 10
Injection site pain 9
Death by euthanasia 9
Closure, Abnormal 9
Physical label missing 8
Containers, Leaking 8
Uncoded sign 7
Stopper, abnormal 7

Outcome Breakdown

Died
95 (38.6%)
Ongoing
55 (22.4%)
Recovered/Normal
43 (17.5%)
Outcome Unknown
42 (17.1%)
Euthanized
10 (4.1%)
Recovered with Sequela
1 (0.4%)

Data Summary

Metric Value
Total adverse event reports 229
Reports involving death 102
Case-fatality rate (reported events) 4450.0%
Distinct species in reports 10
Distinct breeds in reports 20
Distinct reactions reported 20
Active ingredients on file 1

Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.

Florfenicol Inj Sol 30% W Pg Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 229 adverse event reports referencing Florfenicol Inj Sol 30% W Pg, including 102 reports in which the animal died — a 4450.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Florfenicol Inj Sol 30% W Pg. Reported administration routes include Unknown, Subcutaneous, Intramuscular, Parenteral. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.

The species most frequently named in Florfenicol Inj Sol 30% W Pg reports are Cattle (122 reports), Unknown (68 reports), Human (18 reports), with Cattle accounting for the largest share. Within those species, Unknown (87), Cattle (other) (39), Crossbred Bovine/Cattle (22) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.

The most commonly reported clinical signs associated with Florfenicol Inj Sol 30% W Pg are Death (83), Lack of efficacy - NOS (64), Lack of efficacy (bacteria) - NOS (37), Containers, Damaged (26). Of the 246 reports with a coded outcome, Died is the leading category at 38.6%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Florfenicol Inj Sol 30% W Pg.

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

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial