Drug profile

The FDA adverse-event record for Unspecified Allergy Injection

13 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Unspecified Allergy Injection. See the species affected, top reactions, and outcomes below.

13
adverse-event reports
7.7%
death-coded share
Dog
most-reported species
2
Vomiting - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
13
Total Reports
1
Deaths Reported
7.7%
Death Rate

Active Ingredients

Unspecified Allergy Injection

Administration Routes

UnknownSubcutaneous

Species Affected

Dog 13

Most Affected Breeds

Dachshund (unspecified) 2
Crossbred Canine/dog 1
Corgi - Welsh Pembroke 1
Shiba Inu 1
Mixed (Dog) 1
Pit Bull 1
Maltese 1
Spitz - German Pomeranian 1
Terrier - Yorkshire 1
Chihuahua 1

Most Reported Reactions

Vomiting 2
Anorexia 2
Emesis (multiple) 2
Digestive tract disorder NOS 1
Head tilt - ear disorder 1
Nystagmus 1
Reluctant to move 1
Facial paralysis 1
Droopy ear 1
Adipsia 1
Abnormal menace reflex test 1
Otitis NOS 1

Outcome Breakdown

Recovered/Normal
7 (53.8%)
Outcome Unknown
4 (30.8%)
Died
1 (7.7%)
Ongoing
1 (7.7%)

Unspecified Allergy Injection Adverse Event Insights

13 reports name Unspecified Allergy Injection; 1 recorded a death outcome (7.7% of reported events, not a population-level mortality rate). Active ingredient: Unspecified Allergy Injection. Administration routes: Unknown, Subcutaneous.

By species: Dog (13 reports). By breed: Dachshund (unspecified) (2), Crossbred Canine/dog (1), Corgi - Welsh Pembroke (1).

Leading clinical signs: Vomiting (2), Anorexia (2), Emesis (multiple) (2), Digestive tract disorder NOS (1). Outcome, 13 coded reports: Recovered/Normal leads at 53.8%.

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.