Drug profile

The FDA adverse-event record for Pancreatic Supplement

20 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Pancreatic Supplement. See the species affected, top reactions, and outcomes below.

20
adverse-event reports
10.0%
death-coded share
Dog
most-reported species
5
Emesis - 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.
20
Total Reports
2
Deaths Reported
10.0%
Death Rate

Active Ingredients

Pancreatic Supplement

Administration Routes

UnknownOralOther

Species Affected

Dog 20

Most Affected Breeds

Shepherd Dog - German 8
Pekingese 2
Terrier - West Highland White 1
Dog (unknown) 1
Setter - Gordon 1
Retriever - Labrador 1
Spaniel - Cocker American 1
Collie (unspecified) 1
Dachshund - Miniature 1
Collie - Border 1

Most Reported Reactions

Emesis 5
Lack of efficacy - NOS 4
Vomiting 3
Not drinking 3
Elevated blood urea nitrogen (BUN) 3
Elevated alanine aminotransferase (ALT) 3
Tachycardia 3
Weakness 3
Dry mucous membrane 3
Enophthalmos (see also Sunken eyes in Systemic disorders) 3
Itching 2
Lethargy (see also Central nervous system depression in 'Neurological') 2

Outcome Breakdown

Outcome Unknown
7 (35.0%)
Recovered/Normal
5 (25.0%)
Recovered with Sequela
3 (15.0%)
Ongoing
3 (15.0%)
Died
2 (10.0%)

Pancreatic Supplement Adverse Event Insights

20 reports name Pancreatic Supplement; 2 recorded a death outcome (10.0% of reported events, not a population-level mortality rate). Active ingredient: Pancreatic Supplement. Administration routes: Unknown, Oral, Other.

By species: Dog (20 reports). By breed: Shepherd Dog - German (8), Pekingese (2), Terrier - West Highland White (1).

Leading clinical signs: Emesis (5), Lack of efficacy - NOS (4), Vomiting (3), Not drinking (3). Outcome, 20 coded reports: Outcome Unknown leads at 35.0%.

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.