Multi-Vitamin
63 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.
63
Total Reports
28
Deaths Reported
4440.0%
Death Rate
Active Ingredients
Multi-Vitamin
Administration Routes
UnknownOralSubcutaneousIntramuscularTopical
Species Affected
Dog 37
Cattle 23
Cat 2
Goat 1
Most Affected Breeds
Cattle (other) 9
Mixed (Cattle) 9
Retriever - Labrador 8
Terrier - Yorkshire 3
Aberdeen Angus 2
Red Angus 2
Retriever - Golden 2
Bichon Frise 2
Cattle (unknown) 1
Bulldog 1
Most Reported Reactions
Death 16
Lack of efficacy (bacteria) - NOS 12
Lethargy (see also Central nervous system depression in 'Neurological') 10
Lack of efficacy - NOS 9
Vomiting 8
Death by euthanasia 6
Behavioural disorder NOS 5
Anorexia 5
Diarrhoea 5
Other abnormal test result NOS 4
INEFFECTIVE, LOSS OF EFFECT 4
Anaphylactic-type reaction 4
Outcome Breakdown
Died
24 (27.9%)
Outcome Unknown
24 (27.9%)
Ongoing
19 (22.1%)
Recovered/Normal
9 (10.5%)
Euthanized
7 (8.1%)
Recovered with Sequela
3 (3.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.