Drug profile

The FDA adverse-event record for Hypertension Medication (Unknown)

18 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Hypertension Medication (Unknown). See the species affected, top reactions, and outcomes below.

18
adverse-event reports
5.6%
death-coded share
Human
most-reported species
4
Accidental exposure - 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.
18
Total Reports
1
Deaths Reported
5.6%
Death Rate

Active Ingredients

Hypertension Medication (Unknown)

Administration Routes

UnknownOral

Species Affected

Human 14
Dog 3
Cat 1

Most Affected Breeds

Unknown 14
Schnauzer (unspecified) 1
Collie - Border 1
Cat (unknown) 1
Spaniel - King Charles Cavalier 1

Most Reported Reactions

Accidental exposure 4
Injection site bleeding 3
Skin irritation 2
Itching 2
Diarrhoea 2
Bad taste 2
Constipation 1
Food intolerance syndrome 1
Swallowing difficult 1
Sleepiness - neurological disorder 1
Anaphylaxis 1
Emesis (multiple) 1

Outcome Breakdown

Outcome Unknown
8 (44.4%)
Recovered/Normal
5 (27.8%)
Ongoing
3 (16.7%)
Recovered with Sequela
1 (5.6%)
Euthanized
1 (5.6%)

Hypertension Medication (Unknown) Adverse Event Insights

18 reports name Hypertension Medication (Unknown); 1 recorded a death outcome (5.6% of reported events, not a population-level mortality rate). Active ingredient: Hypertension Medication (Unknown). Administration routes: Unknown, Oral.

By species: Human (14 reports), Dog (3 reports), Cat (1 reports). By breed: Unknown (14), Schnauzer (unspecified) (1), Collie - Border (1).

Leading clinical signs: Accidental exposure (4), Injection site bleeding (3), Skin irritation (2), Itching (2). Outcome, 18 coded reports: Outcome Unknown leads at 44.4%.

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.