Gnrh

19 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

530.0%

Death Rate

Active Ingredients

Gnrh

Administration Routes

UnknownIntramuscular

Species Affected

Cattle 19

Most Affected Breeds

Mixed (Cattle) 6

Aberdeen Angus 4

Cattle (other) 3

Cattle (unspecified) 2

Limousin 1

Simmental 1

Hereford cattle 1

Belted Galloway 1

Most Reported Reactions

Lack of efficacy - NOS 12

INEFFECTIVE, ESTRUS SYNCHRONIZ 6

Rectal prolapse 2

Infertility NOS 1

Unexplained death 1

Injection site gaseous gangrene 1

Injection site oedema 1

PR-LUNG(S), LESION(S) 1

Cutaneous emphysema 1

Application site abscess 1

Lateral recumbency 1

Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') 1

Outcome Breakdown

Outcome Unknown

15 (78.9%)

Recovered/Normal

3 (15.8%)

Died

1 (5.3%)

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