Epinephrine

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This page reprints a manufacturer label. Everything below in quotation marks is copied from EPINEPHRINE INJECTION, published by FDA and retrieved on 2026-09-16. Nothing has been added, reworded or left out of the sections shown. It is the manufacturer’s label, reproduced as published.

This page reprints the FDA label for EPINEPHRINE INJECTION by Sparhawk Laboratories, Inc, a epinephrine product labelled for dogs and cats. The sections below are copied from that label without change, with the set id and the date it was retrieved from DailyMed. 3 other stored labels carry the same active ingredient and are listed at the end.

The label

Product: EPINEPHRINE INJECTION. Manufacturer: Sparhawk Laboratories, Inc. FDA Structured Product Label set id 54a9cdee-791c-4eee-8d99-71a11213e9dc. Label effective 2022-05-25. Retrieved 2026-09-16 from the DailyMed animal label release, and readable on DailyMed.

Indications

For emergency use only in treating anaphylactoid shock in sheep, swine, cattle, horses, dogs and cats.

Dosage and Administration

Dogs and Cats : 0.1 to 0.5 mL injected Intramuscularly or Subcutaneously. Cattle , Horses , Sheep and Swine : 1 mL per 100 lbs of body weight injected Intramuscularly or Subcutaneously.

Warnings

Do not use this product if it's color is pinkish or darker than slightly yellow or if it contains a precipitate. COMPOSITION Each mL of sterile aqueous solution contains: Epinephrine ....................... 1 mg Sodium Chloride ................ 0.1% Benzyl Alcohol .................. 1.5% Disodium Edetate, Sodium Metabisulfite, Hydrochloric Acid, and Water for Injection. Store at controlled room temperature between 15° and 30°C (59° - 86°F) . Protect from light . TAKE TIME OBSERVE LABEL DIRECTIONS SLI Epinephrine

Other labels for this ingredient

These labels are also stored for the same active ingredient. They are not identical to the one reprinted above, and each is listed by product and set id rather than merged with it.

FDA adverse event reports

The FDA Center for Veterinary Medicine publishes the adverse event reports it receives through openFDA. The counts below are the reports naming epinephrine as an active ingredient for each species this label names, as returned on 2026-09-16, coded by the VeDDRA reaction term the reporter chose. Reactions are counted per report, so one report can appear under several terms.

These are counts, not rates. Reporting is voluntary, the number of animals treated is not known, and a widely used product accumulates reports for that reason alone. A report records that an event followed a dose; it does not establish that the product caused it. The counts say nothing about how one product compares with another.

Dogs: 320 reports

Reactions most often coded in dogs, 320 reports
VeDDRA reaction termReports
Anaphylaxis137
Vomiting119
Death99
Pale mucous membrane82
Cardiac arrest63
Lethargy (see also Central nervous system depression in 'Neurological')62
Diarrhoea47
Bradycardia44
Hypotension43
Fever41
Death by euthanasia36
Tachycardia36
Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders')35
Lateral recumbency35
Other abnormal test result NOS32

Outcome as recorded by the reporter: Died 101; Ongoing 95; Recovered/Normal 72; Euthanized 36; Outcome Unknown 15; Recovered with Sequela 1.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Cats: 84 reports

Reactions most often coded in cats, 84 reports
VeDDRA reaction termReports
Death48
Cardiac arrest33
Anaphylaxis19
Respiratory arrest18
Bradycardia17
Hypothermia16
Pale mucous membrane16
Vomiting16
Cyanosis15
Death by euthanasia13
Lethargy (see also Central nervous system depression in 'Neurological')13
Other abnormal test result NOS13
Not eating12
Diarrhoea10
Lateral recumbency9

Outcome as recorded by the reporter: Died 48; Ongoing 14; Euthanized 13; Recovered/Normal 6; Outcome Unknown 3.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Sources

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