Drug profile

The FDA adverse-event record for Saline Solution

13 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Saline Solution. See the species affected, top reactions, and outcomes below.

13
adverse-event reports
7.7%
death-coded share
Dog
most-reported species
5
Ataxia - 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.
13
Total Reports
1
Deaths Reported
7.7%
Death Rate

Active Ingredients

Saline Solution

Administration Routes

UnknownTopicalSubcutaneousAuricular (Otic)Intravenous

Species Affected

Dog 12
Cat 1

Most Affected Breeds

Retriever - Golden 3
Pit Bull 2
Mixed (Dog) 1
Pug 1
Spaniel - Cocker American 1
Japanese Chin (Spaniel) 1
Mastiff 1
Domestic Mediumhair 1
Schnauzer - Miniature 1
Dog (unknown) 1

Most Reported Reactions

Ataxia 5
Anorexia 4
Nystagmus 3
Head tilt - ear disorder 3
Tympanic rupture 3
Other abnormal test result NOS 2
Corneal ulcer 2
Conjunctivitis 2
Hearing decreased 2
Vestibular disorder NOS 2
Injection site swelling 2
Injection site necrosis 2

Outcome Breakdown

Outcome Unknown
7 (53.8%)
Recovered/Normal
3 (23.1%)
Ongoing
2 (15.4%)
Euthanized
1 (7.7%)

Saline Solution Adverse Event Insights

13 reports name Saline Solution; 1 recorded a death outcome (7.7% of reported events, not a population-level mortality rate). Active ingredient: Saline Solution. Administration routes: Unknown, Topical, Subcutaneous, Auricular (Otic).

By species: Dog (12 reports), Cat (1 reports). By breed: Retriever - Golden (3), Pit Bull (2), Mixed (Dog) (1).

Leading clinical signs: Ataxia (5), Anorexia (4), Nystagmus (3), Head tilt - ear disorder (3). Outcome, 13 coded reports: Outcome Unknown leads at 53.8%.

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.