Drug profile

The FDA adverse-event record for Renal Supplement

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

11
adverse-event reports
45.5%
death-coded share
Cat
most-reported species
5
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.
11
Total Reports
5
Deaths Reported
45.5%
Death Rate

Active Ingredients

Renal Supplement

Administration Routes

OralUnknown

Species Affected

Cat 9
Dog 2

Most Affected Breeds

Domestic Shorthair 6
Domestic Longhair 2
Collie - Border 1
Cat (unknown) 1
Terrier - Bull - American Pit 1

Most Reported Reactions

Death 5
Weight loss 3
Elevated alanine aminotransferase (ALT) 2
Behavioural disorder NOS 2
Urinary incontinence 2
Hind limb ataxia 2
Elevated blood urea nitrogen (BUN) 2
Collapse (see also Cardio-vascular and Systemic disorders) 2
Respiratory arrest 2
Deafness 2
Thickened ear canal(s) 2
Limb weakness 2

Outcome Breakdown

Died
5 (38.5%)
Outcome Unknown
4 (30.8%)
Ongoing
3 (23.1%)
Recovered/Normal
1 (7.7%)

Renal Supplement Adverse Event Insights

11 reports name Renal Supplement; 5 recorded a death outcome (45.5% of reported events, not a population-level mortality rate). Active ingredient: Renal Supplement. Administration routes: Oral, Unknown.

By species: Cat (9 reports), Dog (2 reports). By breed: Domestic Shorthair (6), Domestic Longhair (2), Collie - Border (1).

Leading clinical signs: Death (5), Weight loss (3), Elevated alanine aminotransferase (ALT) (2), Behavioural disorder NOS (2). Outcome, 13 coded reports: Died leads at 38.5%.

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.