Drug profile

The FDA adverse-event record for Beta-Mannanase

12 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Beta-Mannanase. See the species affected, top reactions, and outcomes below.

12
adverse-event reports
100.0%
death-coded share
Pig
most-reported species
12
Death - 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.
12
Total Reports
12
Deaths Reported
100.0%
Death Rate

Active Ingredients

Beta-Mannanase

Administration Routes

Oral

Species Affected

Pig 6
Chicken 5
Turkey 1

Most Affected Breeds

Mixed (Pig) 3
Chicken (other) 3
Mixed (Chicken) 2
PIC International Commercial Swine Lines 2
Crossbred Porcine/Pig 1
Turkey (other) 1

Most Reported Reactions

Death 12
Lameness 5
Digestive tract disorder NOS 4
Respiratory tract disorder NOS 4
Musculoskeletal disorder NOS 4
Unthrifty 3
Trauma NOS 3
Systemic disorder NOS 3
Ulceration NOS 2
Hernia NOS 2
Dehydration 2
Death by euthanasia 2

Outcome Breakdown

Died
12 (60.0%)
Euthanized
5 (25.0%)
Outcome Unknown
3 (15.0%)

Beta-Mannanase Adverse Event Insights

12 reports name Beta-Mannanase; 12 recorded a death outcome (100.0% of reported events, not a population-level mortality rate). Active ingredient: Beta-Mannanase. Administration route: Oral.

By species: Pig (6 reports), Chicken (5 reports), Turkey (1 reports). By breed: Mixed (Pig) (3), Chicken (other) (3), Mixed (Chicken) (2).

Leading clinical signs: Death (12), Lameness (5), Digestive tract disorder NOS (4), Respiratory tract disorder NOS (4). Outcome, 20 coded reports: Died leads at 60.0%.

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.