Drug profile

The FDA adverse-event record for Bedinvetmab Injection

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

13
adverse-event reports
7.7%
death-coded share
Dog
most-reported species
3
Hypocortisolaemia - 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

Bedinvetmab Injection

Administration Routes

UnknownSubcutaneous

Species Affected

Dog 13

Most Affected Breeds

Retriever - Labrador 5
Dog (other) 2
Shiba Inu 1
Terrier - Boston 1
Collie - Border 1
Dachshund (unspecified) 1
Shepherd Dog - Australian 1
Poodle - Toy 1

Most Reported Reactions

Hypocortisolaemia 3
Abnormal adrenocorticotropic hormone (ACTH) stimulation test 3
Vomiting 3
Not eating 3
Panting 3
Weight loss 2
Limb weakness 2
Elevated blood urea nitrogen (BUN) 2
Behavioural disorder NOS 2
Polyuria 2
Polydipsia 2
Decreased activity 2

Outcome Breakdown

Outcome Unknown
10 (76.9%)
Recovered/Normal
1 (7.7%)
Euthanized
1 (7.7%)
Ongoing
1 (7.7%)

Bedinvetmab Injection Adverse Event Insights

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

By species: Dog (13 reports). By breed: Retriever - Labrador (5), Dog (other) (2), Shiba Inu (1).

Leading clinical signs: Hypocortisolaemia (3), Abnormal adrenocorticotropic hormone (ACTH) stimulation test (3), Vomiting (3), Not eating (3). Outcome, 13 coded reports: Outcome Unknown leads at 76.9%.

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.