Drug profile

The FDA adverse-event record for Milk Protein Concentrate

29 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Milk Protein Concentrate. See the species affected, top reactions, and outcomes below.

29
adverse-event reports
13.8%
death-coded share
Dog
most-reported species
8
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.
29
Total Reports
4
Deaths Reported
13.8%
Death Rate

Active Ingredients

Milk Protein Concentrate

Administration Routes

OralUnknown

Species Affected

Dog 25
Cat 4

Most Affected Breeds

Pug 3
Retriever - Labrador 3
Cat (unknown) 3
Crossbred Canine/dog 2
Pit Bull 2
Shepherd Dog - German 2
Spaniel - King Charles Cavalier 1
Corgi (unspecified) 1
Shiba Inu 1
Terrier - Yorkshire 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in 'Neurological') 8
Vomiting 6
Emesis 3
Lack of efficacy - NOS 3
Rash 2
Elevated serum alkaline phosphatase (SAP) 2
Panting 2
Elevated alanine aminotransferase (ALT) 2
Diarrhoea 2
Low platelet count 2
Death by euthanasia 2
Death 2

Outcome Breakdown

Recovered/Normal
10 (34.5%)
Ongoing
6 (20.7%)
Outcome Unknown
6 (20.7%)
Recovered with Sequela
3 (10.3%)
Euthanized
2 (6.9%)
Died
2 (6.9%)

Milk Protein Concentrate Adverse Event Insights

29 reports name Milk Protein Concentrate; 4 recorded a death outcome (13.8% of reported events, not a population-level mortality rate). Active ingredient: Milk Protein Concentrate. Administration routes: Oral, Unknown.

By species: Dog (25 reports), Cat (4 reports). By breed: Pug (3), Retriever - Labrador (3), Cat (unknown) (3).

Leading clinical signs: Lethargy (see also Central nervous system depression in 'Neurological') (8), Vomiting (6), Emesis (3), Lack of efficacy - NOS (3). Outcome, 29 coded reports: Recovered/Normal leads at 34.5%.

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.