Drug profile

The FDA adverse-event record for Oral Bbpi Lb/Lv

21 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Oral Bbpi Lb/Lv. See the species affected, top reactions, and outcomes below.

21
adverse-event reports
4.8%
death-coded share
Dog
most-reported species
6
Lethargy (see also Central nervous system depression in Neurological) - 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.
21
Total Reports
1
Deaths Reported
4.8%
Death Rate

Active Ingredients

Oral Bbpi Lb/Lv

Administration Routes

Oral

Species Affected

Dog 21

Most Affected Breeds

Crossbred Canine/dog 5
Retriever - Labrador 4
Chihuahua 2
Terrier - Airedale 1
Retriever - Golden 1
Pointer - English Pointer 1
Pug 1
Poodle - Miniature 1
Siberian Husky 1
Shepherd Dog - Australian 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 6
Hypersensitivity reaction 6
Facial swelling (see also Skin) 5
Emesis (multiple) 4
Vomiting 4
Hives (see also Skin) 4
Anaphylaxis 3
Stiffness NOS 3
Breathing difficulty 3
Panting 3
Abdominal discomfort 2
Gagging 2

Outcome Breakdown

Recovered/Normal
10 (47.6%)
Ongoing
8 (38.1%)
Outcome Unknown
2 (9.5%)
Died
1 (4.8%)

Oral Bbpi Lb/Lv Adverse Event Insights

21 reports name Oral Bbpi Lb/Lv; 1 recorded a death outcome (4.8% of reported events, not a population-level mortality rate). Active ingredient: Oral Bbpi Lb/Lv. Administration route: Oral.

By species: Dog (21 reports). By breed: Crossbred Canine/dog (5), Retriever - Labrador (4), Chihuahua (2).

Leading clinical signs: Lethargy (see also Central nervous system depression in Neurological) (6), Hypersensitivity reaction (6), Facial swelling (see also Skin) (5), Emesis (multiple) (4). Outcome, 21 coded reports: Recovered/Normal leads at 47.6%.

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.