Drug profile

The FDA adverse-event record for Booster Vaccine (Unknown)

15 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Booster Vaccine (Unknown). See the species affected, top reactions, and outcomes below.

15
adverse-event reports
6.7%
death-coded share
Dog
most-reported species
5
Vomiting - top reaction
Verify with FDA CVM →
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
15
Total Reports
1
Deaths Reported
6.7%
Death Rate

Active Ingredients

Booster Vaccine (Unknown)

Administration Routes

UnknownParenteralOral

Species Affected

Dog 14
Cat 1

Most Affected Breeds

Retriever - Golden 3
Retriever - Labrador 2
Shepherd Dog - German 2
Maltese 1
Chihuahua 1
Terrier - Bull - Staffordshire 1
Shepherd (unspecified) 1
Terrier - Boston 1
Terrier (unspecified) 1
Domestic Shorthair 1

Most Reported Reactions

Vomiting 5
Lethargy (see also Central nervous system depression in 'Neurological') 2
Pyoderma 2
Diarrhoea 2
Skin disorders NOS 2
Death 1
Not eating 1
Retching 1
Loose stool 1
Decreased appetite 1
Pruritus 1
Lack of efficacy (ectoparasite) - flea 1

Outcome Breakdown

Ongoing
5 (33.3%)
Outcome Unknown
5 (33.3%)
Recovered/Normal
4 (26.7%)
Died
1 (6.7%)

Booster Vaccine (Unknown) Adverse Event Insights

15 reports name Booster Vaccine (Unknown); 1 recorded a death outcome (6.7% of reported events, not a population-level mortality rate). Active ingredient: Booster Vaccine (Unknown). Administration routes: Unknown, Parenteral, Oral.

By species: Dog (14 reports), Cat (1 reports). By breed: Retriever - Golden (3), Retriever - Labrador (2), Shepherd Dog - German (2).

Leading clinical signs: Vomiting (5), Lethargy (see also Central nervous system depression in 'Neurological') (2), Pyoderma (2), Diarrhoea (2). Outcome, 15 coded reports: Ongoing leads at 33.3%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.