Drug profile

The FDA adverse-event record for E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk

25 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk. See the species affected, top reactions, and outcomes below.

25
adverse-event reports
44.0%
death-coded share
Dog
most-reported species
8
Vomiting - 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.
25
Total Reports
11
Deaths Reported
44.0%
Death Rate

Active Ingredients

E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk

Administration Routes

UnknownOral

Species Affected

Dog 16
Cat 9

Most Affected Breeds

Domestic Shorthair 5
Chihuahua 4
Shih Tzu 3
Persian 1
Mixed (Dog) 1
Terrier - Bull - American Pit 1
Retriever - Labrador 1
Retriever - Golden 1
Dachshund - Miniature 1
Terrier - Yorkshire 1

Most Reported Reactions

Vomiting 8
Death by euthanasia 7
Anorexia 7
Elevated renal parameters 6
Seizure NOS 5
Lethargy (see also Central nervous system depression in 'Neurological') 5
Elevated creatinine 4
Elevated blood urea nitrogen (BUN) 4
Other abnormal test result NOS 4
Death 4
Anaemia NOS 3
Weight loss 3

Outcome Breakdown

Euthanized
7 (28.0%)
Ongoing
6 (24.0%)
Recovered/Normal
5 (20.0%)
Died
4 (16.0%)
Outcome Unknown
3 (12.0%)

E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk Adverse Event Insights

25 reports name E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk; 11 recorded a death outcome (44.0% of reported events, not a population-level mortality rate). Active ingredient: E. Thermophilus, L. Acidophilus, B. Longum, Psyllium Husk. Administration routes: Unknown, Oral.

By species: Dog (16 reports), Cat (9 reports). By breed: Domestic Shorthair (5), Chihuahua (4), Shih Tzu (3).

Leading clinical signs: Vomiting (8), Death by euthanasia (7), Anorexia (7), Elevated renal parameters (6). Outcome, 25 coded reports: Euthanized leads at 28.0%.

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.