Mineral Supplement

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

4170.0%

Death Rate

Active Ingredients

Mineral Supplement

Administration Routes

UnknownOralParenteral

Species Affected

Cattle 9

Dog 3

Most Affected Breeds

Cattle (unknown) 4

Cattle (other) 2

Pointer (unspecified) 1

Pit Bull 1

Aberdeen Angus 1

Hound (unspecified) 1

Crossbred Bovine/Cattle 1

Holstein-Friesian also known as Holstein 1

Most Reported Reactions

Death 4

Lack of efficacy - NOS 3

Vomiting 2

Diarrhoea 2

Abortion 2

Tiredness 1

Vocalisation 1

INEFFECTIVE, WORMS 1

Malaise 1

Not eating 1

Pica NOS 1

Lethargy (see also Central nervous system depression in 'Neurological') 1

Outcome Breakdown

Outcome Unknown

5 (27.8%)

Ongoing

4 (22.2%)

Recovered/Normal

4 (22.2%)

Died

4 (22.2%)

Euthanized

1 (5.6%)

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