Gonadorelin Injectable

29 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

340.0%

Death Rate

Active Ingredients

Gonadorelin Injectable

Administration Routes

UnknownIntramuscularTopicalSubcutaneousParenteral

Species Affected

Unknown 15

Cattle 10

Human 4

Most Affected Breeds

Unknown 19

Holstein-Friesian also known as Holstein 3

Aberdeen Angus 2

Crossbred Bovine/Cattle 2

Cattle (other) 1

Cattle (unspecified) 1

Hereford cattle 1

Most Reported Reactions

Underfilling, Container 7

INEFFECTIVE, ESTRUS SYNCHRONIZ 4

Lack of efficacy - NOS 4

Physical label missing 3

Uncoded sign 2

Injection site irritation 2

Accidental exposure 2

Appearance, Abnormal 2

Stopper, abnormal 1

Vials, Leaking 1

Underfilling, Vials 1

Burning sensation of eye 1

Outcome Breakdown

Outcome Unknown

9 (60.0%)

Recovered/Normal

4 (26.7%)

Ongoing

1 (6.7%)

Died

1 (6.7%)

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