VetSheet

Ephedrine

Ephedrine sulfate

Sympathomimetic Bronchodilator / VasopressorPOIVIMSCIntranasalDogsCats

Also known as: Enurace · Ephedrine sulphate · Ephedrine hydrochloride · Ephedrini hydrochloridum

Reviewed by the VetSheet Veterinary TeamUpdated Apr 5, 2026Evidence-based veterinary reference

1-2 mg/kg PO q8-12hPO· q8-12h
🐕

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

Dosing by species

🌎 NA — North America🌍 EU — Europe

Dogs

IndicationDoseRouteFrequencyDurationRegion
Treatment of bronchospasm (maintenance therapy)1-2 mg/kg PO q8-12hPOq8-12h🌎 NA
Treatment of bronchospasm2 mg/kg PO q8-12hPOq8-12h🌎 NA
Treatment of urinary incontinence5-15 mg (total dose) PO q8hPOq8h🌎 NA
Treatment of urinary incontinence1.2 mg/kg PO q8h or 5-15 mg (total dose) PO q8hPOq8h🌎 NA
Treatment of hypotension associated with anesthesia0.03-0.1 mg/kg IV bolusIVOnce, may repeat in 5 minutes🌎 NA
Treatment of hypotension associated with anesthesia0.1-0.25 mg/kg IV bolusIVOnce🌎 NA
Treatment of hypotension associated with anesthesia0.1-0.2 mg/kg IV bolusIVOnce15-60 minutes🌎 NA
Treatment of hypotension associated with anesthesia0.15-0.25 mg/kg IV boluses OR CRI at 5-10 micrograms/kg/minuteIVTo effect or CRI🌎 NA
Hypotension during anaesthesiaDose not specified in monographIV/IMAs needed (effects wane after 2-3 doses)Perioperative🌍 EU
Urinary incontinenceDose not specified in monographPONot specifiedLong-term🌍 EU
  • Treatment of hypotension associated with anesthesia: Dilute 5 mg in 10 mL of saline and give the lower dosage first as sinus tachycardia may accompany the higher dose.
  • Treatment of hypotension associated with anesthesia: For relatively short procedures in ASA I or II patients when hypotension is not responsive to 1 or 2 crystalloid boluses.
  • Treatment of hypotension associated with anesthesia: Dilute into 5 mL of a balanced electrolyte solution or saline and give small increment IV boluses until desirable blood pressure achieved.
  • Hypotension during anaesthesia: Assists in bradycardia. Tachyphylaxis occurs rapidly.
  • Urinary incontinence: Exclude polyuria before treatment. Can be used with phenylpropanolamine.

Cats

IndicationDoseRouteFrequencyDurationRegion
Treatment of bronchospasm (emergency treatment)2-5 mg POPOOnce🌎 NA
Treatment of urinary incontinence2-4 mg (total dose) PO q8hPOq8h🌎 NA
Treatment of urinary incontinence2-4 mg/kg PO q6-12h or 2-4 mg (total dose) PO q8hPOq6-12h or q8h🌎 NA
Treatment of urinary incontinence2-4 mg per cat PO q8-12hPOq8-12h🌎 NA
Treatment of hypotension associated with anesthesia0.15-0.25 mg/kg IV boluses OR CRI at 5-10 micrograms/kg/minuteIVTo effect or CRI🌎 NA
Hypotension during anaesthesiaDose not specified in monographIV/IMAs neededPerioperative🌍 EU
Nasal congestion (cat 'flu')Dose not specified in monographtopicalNot specifiedShort-term🌍 EU
  • Treatment of hypotension associated with anesthesia: Dilute into 5 mL of a balanced electrolyte solution or saline and give small increment IV boluses until desirable blood pressure achieved.
  • Hypotension during anaesthesia: Use with caution.
  • Nasal congestion (cat 'flu'): Proposed for treatment of nasal congestion; may be of some benefit.

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

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Overview

Ephedrine is a non-catecholamine sympathomimetic amine. In veterinary medicine, it is primarily utilized for the management of ​urethral sphincter mechanism incompetence (USMI)​ in dogs and cats, though phenylpropanolamine (PPA) is often preferred due to a lower incidence of CNS side effects.

Additionally, it serves as an injectable vasopressor to combat anesthesia-induced hypotension and as a bronchodilator for respiratory conditions.

​Clinical Pearl:​ Because ephedrine crosses the blood-brain barrier more readily than many other sympathomimetics, it can cause mild to moderate CNS stimulation, which manifests as restlessness or agitation in some patients.

Mechanism of action

Ephedrine is a mixed-acting sympathomimetic.

  • ​Indirect Action (Primary):​ It enters the sympathetic nerve terminal and promotes the release of stored norepinephrine into the synaptic cleft.
  • ​Direct Action (Secondary):​ It directly stimulates ​α- and β-adrenergic receptors​.

​Key Pathways:​

  • ​α1-receptors​ → Smooth muscle contraction → Increased internal urethral sphincter tone (improving continence) and peripheral vasoconstriction (increasing blood pressure).
  • ​β1-receptors​ → Positive inotropic and chronotropic effects on the heart → Increased cardiac output.
  • ​β2-receptors​ → Smooth muscle relaxation → Bronchodilation.

​Note:​ Because it relies heavily on endogenous norepinephrine stores, repeated frequent dosing can deplete these stores, leading to tachyphylaxis (diminished response over time).

Safety & warnings

Contraindications

  • Severe cardiovascular disease
  • Cardiac arrhythmias
  • Pregnancy
  • Lactation
  • Glaucoma

Adverse effects

  • Irritability
  • Tachycardia
  • Hypertension
  • Anorexia
  • Tachyphylaxis (decreased response to subsequent doses)
  • Panting
  • Mydriasis (dilated pupils)
  • CNS stimulation (restlessness, agitation)
  • Atrial fibrillation
  • Vasoconstriction
  • Reduction of intestinal wall motility and tone

Precautions

Use with caution in patients with glaucoma, prostatic hypertrophy, hyperthyroidism, diabetes mellitus, cardiovascular disorders, or hypertension.

When administered IV, the administration rate should be carefully controlled (in humans, not to exceed 10 mg/minute; scale appropriately for veterinary patients).

​Pregnancy/Nursing:​ FDA Category C. Excreted in milk and may have deleterious effects on nursing animals. Consider milk replacer if use is absolutely necessary in a nursing dam.

Drug interactions

Acepromazine (and other phenothiazines)

Phenothiazines block alpha-adrenergic receptors; concomitant use can lead to unopposed beta-activity causing vasodilation and increased cardiac rate.

Alpha-blockers (e.g., phentolamine, prazosin)

May negate the therapeutic effects of ephedrine.

General Anesthetics (cyclopropane, halogenated hydrocarbons)

Increased risk of arrhythmias. Propranolol may be administered should these occur.

Beta-blockers

Concomitant use may diminish the effects of both drugs.

DigoxinMajor

Increased risk of arrhythmias if used concurrently.

Monoamine Oxidase Inhibitors (including amitraz)

Should not be given within two weeks of receiving MAOIs; severe hypertension and hyperpyrexia are possible.

Other Sympathomimetic Agents (e.g., phenylpropanolamine)

Should not be administered together as increased toxicity may result.

Reserpine

May reverse the pressor effects of ephedrine.

TheophyllineModerate

May increase the risk for theophylline toxicity.

Tricyclic Antidepressants

May decrease the pressor effects of ephedrine.

Urinary Alkalinizers (e.g., sodium bicarbonate, citrates, carbonic anhydrase inhibitors)

May reduce urinary excretion of ephedrine and prolong its duration of activity, potentially requiring dosage adjustments.

Other sympathomimeticsModerate

Synergistic effects, increasing the risk of adverse cardiovascular and CNS stimulation.

Volatile anaestheticsMajor

Enhances the sensitivity of the myocardium to the arrhythmogenic effects of ephedrine.

Cardiac glycosides (e.g., digoxin)Major

Concomitant use can cause severe cardiac arrhythmias.

Tricyclic antidepressants (e.g., amitriptyline)Major

Concomitant use can cause severe cardiac arrhythmias.

MAO inhibitors (e.g., selegiline)Major

May cause severe hypertension when given concurrently.

AmitriptylineMajor

Concomitant use with tricyclic antidepressants can cause arrhythmias.

SelegilineMajor

Concomitant use with MAO inhibitors may cause severe hypertension.

PhenylpropanolamineModerate

Can be used in conjunction for urinary incontinence, but increases sympathetic load.

Monitoring

  • Clinical effectiveness (resolution of incontinence, improved blood pressure, or bronchodilation)
  • Behavioral changes (restlessness, irritability)
  • Heart rate and rhythm (ECG during anaesthesia)
  • Resolution of urinary incontinence
  • Signs of CNS stimulation or excessive panting

Pharmacokinetics

Absorption

Rapidly absorbed after oral or parenteral administration.

Distribution

Thought to cross both the blood-brain barrier and the placenta.

Metabolism

Metabolized in the liver.

Elimination

Excreted unchanged in the urine. Urine pH may significantly alter excretion characteristics.

Overdose

Clinical signs of overdosage may consist of an exacerbation of adverse effects (restlessness, tachycardia).

In a very large overdose, severe cardiovascular signs (hypertension leading to rebound hypotension, bradycardias to tachycardias, and cardiovascular collapse) or CNS effects (ranging from severe stimulation to coma) can be seen.

​Treatment:​

  • If the overdose was recent, empty the stomach using usual precautions.
  • Administer activated charcoal and a cathartic.
  • Treat clinical signs supportively as they occur.

Available products

Formulations

  • Capsules
  • 10 mg tablet
  • 15 mg tablet
  • 30 mg tablet
  • 50 mg tablet
  • 3 mg/ml solution for injection
  • 30 mg/ml solution for injection
  • 0.5% nasal drops
  • 1% nasal drops

Veterinary

  • Enurace 10 mg, 15 mg, 30 mg, 50 mg tablets

Human-labeled

  • Ephedrine Sulfate Capsules: 25 mg
  • Ephedrine Sulfate Injection: 50 mg/mL in 1 mL single-dose vials & preservative free in 1 mL single-dose amps
  • Ephedrine hydrochloride 3 mg/ml, 30 mg/ml solutions for injection
  • Ephedrine 0.5%, 1% nasal drops

Regulatory status

European Union✓ ApprovedPrescription onlyEMA
🐕 Dogs

POM-V classification in the UK/EU.

United Kingdom✓ ApprovedPrescription onlyVMD
🐕 Dogs

POM-V, POM.

No regulatory data for: 🇺🇸 US · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Storage & stability

Store ephedrine sulfate products in tight, light-resistant containers at room temperature unless otherwise directed. When used parenterally, ephedrine sulfate is usually administered directly and not diluted.

Client information

  • ​Consistency is Key:​ In order for this drug to be effective for urinary incontinence, it must be administered exactly as directed by your veterinarian. Missed doses will negate its effect and leaking may return.
  • ​Patience:​ It may take several days for the full benefit of the drug to take place.
  • ​Side Effects:​ Because this medication acts like a stimulant, it can cause your pet to feel "jittery". Contact your veterinarian if your pet demonstrates ongoing changes in behavior (restlessness, irritability, pacing) or if incontinence persists or increases.
  • ​Timing:​ To prevent sleep disturbances, try not to give the final dose of the day right before bedtime unless instructed otherwise.
  • ​Appetite:​ You may notice a temporary decrease in your pet's appetite.

VetSheet drug reference is intended for licensed veterinary professionals as a clinical decision-support aid, not a substitute for professional judgement or the manufacturer’s current label.