Dopamine (intravenous)

Pronunciation: DOH-pa-meen.

Generic name
dopamine hydrochloride
Brand names
Intropin (historical US brand), Dopamine Juno, Dopamine Hydrochloride Sterile (DBL), Sterile Dopamine Concentrate BP (Max Health, New Zealand), Dopamine Hydrochloride and 5% Dextrose Injection (Hospira/Baxter, Canada)
Drug class
Catecholamine vasopressor/inotrope (natural precursor of noradrenaline and adrenaline); dose-dependent dopaminergic, beta-adrenergic, and alpha-adrenergic effects
Form
Concentrate for solution for infusion (ampoule) or pre-mixed infusion bag
Route
Intravenous infusion (after dilution) via a large vein, using an infusion pump
Legal status
Prescription-only, hospital/critical-care administration only

Supply Rules Vary

Trade names by country: United States · United Kingdom · Canada · Australia · New Zealand

Australia: Dopamine Hydrochloride Sterile (DBL) (4), Dopamine (Juno) (5) (4) · Full directory

What dopamine hydrochloride is and how it works

Dopamine (given intravenously) is a catecholamine used to correct dangerously low blood pressure and poor blood flow in shock and other critical-care emergencies. Its effect depends on the dose: low doses widen blood vessels in the kidneys and gut, medium doses strengthen and speed up the heartbeat, and higher doses constrict blood vessels to raise blood pressure. It is administered only in hospital critical-care settings. (1) (2) (3)

Dopamine is given exclusively by healthcare professionals in an intensive care unit, emergency department, or operating theatre. It is not a medicine you can take yourself, and it is not available for home use or through a pharmacy.

Mechanism of action: how dopamine hydrochloride works

Dopamine is a direct-acting catecholamine and natural precursor of noradrenaline and adrenaline, with dose-dependent effects: at low doses (about 0.5-2 mcg/kg/min) it acts on dopaminergic receptors causing renal/mesenteric vasodilation; at moderate doses (about 2-10 mcg/kg/min) it activates beta-1 receptors, increasing cardiac output and heart rate; at higher doses it activates alpha-adrenergic receptors, causing vasoconstriction and raising blood pressure. It is metabolised in tissues and blood by MAO and COMT. (1) (2) (3)

What dopamine hydrochloride is used for

Acute hypotension and shock

Dopamine is used to correct haemodynamic imbalance (poor blood flow and low blood pressure) in acute hypotension or shock caused by conditions such as heart attack, severe infection (endotoxic septicaemia), trauma, or kidney failure. (1) (2) (3) (4)

After open-heart surgery

It is used as an adjunct after open-heart surgery when low blood pressure persists after blood volume has been corrected. (2) (3) (4)

Chronic cardiac decompensation (congestive heart failure)

In severe, refractory congestive heart failure, dopamine may be used for a short period under close monitoring to improve heart pumping and urine output. (2) (3)

Before taking dopamine hydrochloride

Do not take / not appropriate for

  • Do not use dopamine in patients with phaeochromocytoma (a tumour that can already raise catecholamine levels), as it can cause a dangerous additive rise in blood pressure. (all indications) (1) (2) (3)
  • Do not use in patients with uncorrected atrial or ventricular tachyarrhythmias, or ventricular fibrillation. (all indications) (2) (3)
  • Do not use together with cyclopropane or halogenated hydrocarbon anaesthetics, because of the risk of serious ventricular arrhythmias or severe hypertension. (perioperative) (2) (3)
  • Do not use together with ergotamine or other ergot alkaloids, because of the risk of excessive vasoconstriction, severe hypertension, and rupture of cerebral blood vessels. (all indications) (3)
  • Do not use in patients with hyperthyroidism without specialist caution. (all indications) (2) (3)

Tell your clinician about

  • Clinicians must ensure hypovolaemia (low blood volume) is corrected first, with a plasma expander, whole blood, or plasma as appropriate.
  • Assess for peripheral vascular disease (atherosclerosis, Buerger's disease, Raynaud's disease, diabetic endarteritis) or cold injury/frostbite, which increase the risk of ischaemia and gangrene.
  • Check for concomitant monoamine oxidase inhibitors (MAOIs, or use within the previous 2-3 weeks), which require a substantially reduced starting dose (about 1/10th usual).
  • Check for concurrent IV phenytoin, which can cause sudden, dose-dependent hypotension, bradycardia, and possibly cardiac arrest.
  • Check for tricyclic antidepressants and digitalis glycosides, which can increase cardiovascular risk (arrhythmias, severe hypertension, hyperpyrexia).
  • Pregnancy: life-sustaining therapy for shock should not be withheld; limited data exist on effects on the fetus.
  • Pediatric use differs by country: the US label describes use from birth through adolescence, while the UK and New Zealand labels state that pediatric safety and effectiveness have not been established.
(1) (2) (3)

How to take dopamine hydrochloride

  • Dopamine is given as a continuous intravenous infusion by a trained clinician in a hospital setting. It must be diluted before use and must never be added to alkaline solutions such as sodium bicarbonate, which inactivate it.
  • The infusion is typically started at 2-5 mcg/kg/min and adjusted based on the patient's haemodynamic response; in more seriously ill patients, a clinician may start at around 5 mcg/kg/min and increase in 5-10 mcg/kg/min increments up to 20-50 mcg/kg/min as needed.
  • Blood pressure, ECG, urine output, and peripheral perfusion are monitored continuously during the infusion.
  • The infusion is given into a large vein (the antecubital fossa is preferred) to reduce the risk of extravasation. The infusion site is checked frequently.
  • The infusion must be tapered gradually when discontinuing; sudden cessation can cause marked hypotension.
(1) (2) (3)

Procedures and treatment changes

Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3) (4) (5) (6)

Missed dose

Not applicable. Dopamine is a continuous intravenous infusion under continuous monitoring. Any interruption is managed by the clinical team immediately.

Overdose

Overdose may cause an excessive rise in blood pressure. The clinical team will reduce or temporarily stop the infusion; because dopamine's effect wears off quickly, no other treatment is usually needed. If effects persist, an alpha-adrenergic blocking agent such as phentolamine may be considered. (1) (2)

Side effects

Dopamine's side effects are related to its dose-dependent cardiovascular and vasoconstrictive actions. The most serious risk, as with other IV vasopressors, is tissue ischaemia and necrosis from extravasation.

Fast heartbeat, extra heartbeats (ectopic beats), chest pain (anginal pain)

What to notice: These cardiac effects are commonly reported and monitored continuously via ECG.

What to do: The clinical team will adjust the infusion rate and treat any arrhythmias. (1) (2)

Headache, anxiety

What to notice: Patients may feel anxious or develop a headache.

What to do: Report to the attending nurse or doctor; they will assess whether the infusion needs adjustment. (1)

Nausea and vomiting

What to notice: Gastrointestinal upset has been reported.

What to do: Tell the clinical team, who can treat symptoms as needed. (1) (3)

Extravasation (tissue damage at the infusion site)

What to notice: Pain, swelling, pallor, cooling, or discolouration near the intravenous line. This is a medical emergency.

What to do: Alert the clinical team immediately. If extravasation occurs, the area will be infiltrated with phentolamine as soon as possible. (1) (2) (3)

Signs of tissue ischaemia (limb, gut, kidney)

What to notice: Cold, pale, painful, or mottled skin on limbs, decreased urine output, severe abdominal pain.

What to do: Inform the treating team immediately; they may need to adjust the infusion or administer phentolamine. (1) (3)

Cardiac arrhythmias

What to notice: Palpitations, irregular heartbeat, chest pain.

What to do: The clinical team will monitor the ECG continuously and treat any arrhythmias, which are rarely fatal ventricular arrhythmias. (1) (2)

Serious warnings

Extravasation and tissue necrosis — emergency

Symptoms: Persistent pain, blanching, swelling, or skin changes at the infusion site.

Action: The clinical team must stop the infusion immediately and infiltrate the area with 5-10 mg of phentolamine mesylate in 10-15 mL of 0.9% sodium chloride as soon as possible, ideally within 12 hours, to reverse vasoconstriction. (1) (2) (3)

Tissue ischaemia from vasoconstriction — emergency

Symptoms: Cool, pale limbs, decreased urine output, worsening perfusion, especially in patients with peripheral vascular disease.

Action: The clinical team will weigh the benefits of the infusion against the ischaemia risk and may give IV phentolamine to reverse it. (3)

Severe arrhythmias — emergency

Symptoms: Ventricular tachycardia, fibrillation, or other serious rhythm disturbances.

Action: Immediate cardiac monitoring and treatment as per critical-care protocols. Review contributing factors (anaesthetic interactions, digitalis co-therapy, tricyclic antidepressants). (1) (2)

Sudden hypotension and bradycardia with IV phenytoin — emergency

Symptoms: Sudden drop in blood pressure and heart rate, possibly progressing to cardiac arrest.

Action: The clinical team should avoid concurrent IV phenytoin during a dopamine infusion where possible and consider an alternative anticonvulsant. (3)

Sudden discontinuation — high

Symptoms: Marked hypotension can occur if the infusion is stopped abruptly.

Action: The infusion must be tapered gradually while expanding blood volume with intravenous fluids or another pressor agent as needed. (3)

Sulfite hypersensitivity reaction — high

Symptoms: Allergic-type reactions, including anaphylactic symptoms and asthmatic episodes (wheezing, difficulty breathing), particularly in people with asthma.

Action: Dopamine products contain sodium metabisulfite, a sulfite that can cause these reactions in susceptible people. The clinical team will monitor for signs of hypersensitivity and treat any reaction immediately; tell the clinical team about any known sulfite or asthma history before treatment if possible. (1) (3)

Interactions

Medicine or testEffectAction
Monoamine oxidase inhibitors (MAOIs)MAOIs potentiate and prolong dopamine's effect, risking severe hypertension.Patients on or recently (within 2-3 weeks) treated with MAOIs require a substantially reduced starting dopamine dose, about 1/10th the usual dose. (1) (2) (3)
Cyclopropane and halogenated hydrocarbon anaestheticsSensitise the heart muscle to dopamine, risking ventricular arrhythmias or hypertension.Use with extreme caution; avoid concurrent use if possible. (2) (3)
IV phenytoin (and other hydantoins)Risk of dose-dependent sudden hypotension, bradycardia, and possibly cardiac arrest.An alternative anticonvulsant should be considered if therapy is needed during a dopamine infusion. (3)
Ergot alkaloids (ergotamine, methysergide) and oxytocinMay cause excessive vasoconstriction, severe hypertension, and rupture of cerebral blood vessels.Concurrent use is not recommended. (3)
Tricyclic antidepressantsMay potentiate dopamine's cardiovascular effects, possibly causing arrhythmias, tachycardia, severe hypertension, or hyperpyrexia.Use with caution and monitor closely. (3)
Digitalis glycosidesIncreased risk of cardiac arrhythmias with concurrent use.Close ECG monitoring is advised if co-administration is necessary. (3)
Other vasopressors and oxytocic drugs (labour/delivery)Risk of severe hypertension.Avoid concurrent use where possible; monitor blood pressure closely. (1)

Pregnancy, breastfeeding, kidney/liver function, age

Pregnancy

Dopamine is a life-sustaining therapy for shock and should not be withheld due to pregnancy. There are no human data on its use in pregnant women; animal studies showed adverse effects at doses one-third the human starting dose. The clinical team will weigh benefits against potential fetal risk. (1) (3)

Breastfeeding

It is not known whether dopamine passes into breast milk. It is not recommended during breastfeeding unless the expected benefits outweigh potential risks, as judged by the clinical team. (3)

Children

Country labels differ: the US label describes dopamine use from birth through adolescence at similar weight-based dosing to adults, while the UK and New Zealand labels state that safety and effectiveness in children have not been established and it is not recommended for this age group. Use in children follows specialist judgment and the applicable local label. (1) (2) (3)

Elderly patients

No dose variation is specifically suggested for older adults, but close monitoring of blood pressure, urine output, and peripheral tissue perfusion is required. (3)

Peripheral vascular disease

Patients with conditions such as atherosclerosis, Buerger's disease, Raynaud's disease, diabetic endarteritis, or cold injury (e.g. frostbite) are more susceptible to peripheral ischaemia and gangrene, and are watched closely for changes in limb colour or temperature. (3)

Monitoring

Before starting

  • Confirm the need for vasopressor/inotrope support and correct hypovolaemia with a plasma expander, whole blood, or plasma.
  • Ensure appropriate intravenous access (large vein, antecubital fossa preferred) and a properly diluted solution, never mixed with alkaline solutions.
  • Review concomitant medications, especially MAOIs, IV phenytoin, ergot alkaloids, and anaesthetic agents.
  • Establish baseline blood pressure, heart rate, ECG, urine output, and peripheral perfusion.

During treatment

  • Continuously monitor blood pressure, ECG, urine output, and peripheral tissue perfusion.
  • Inspect the infusion site regularly for signs of extravasation; if suspected, stop the infusion and give the phentolamine antidote.
  • Watch for a disproportionate rise in diastolic pressure (a marked fall in pulse pressure), which may indicate excessive dosage and should prompt a rate reduction.
  • Adjust the infusion rate according to haemodynamic response, aiming for the lowest dose that maintains adequate perfusion.
(1) (2) (3)

Storage

Storage conditions vary by manufacturer and product. Diluted infusion solutions have been shown to be stable for 24 hours under specific dilution conditions; refer to the specific product labelling for exact storage and stability information.

Professional information

This is clinician-facing context only. Always refer to the current local product information and institutional protocols for dosing, administration, and safety guidance.

All regions

Indication: Acute hypotension / shock

Dose summary: Start at 2-5 mcg/kg/min (or 5 mcg/kg/min in more seriously ill patients), titrating in 5-10 mcg/kg/min increments based on haemodynamic response, up to a labelled maximum of 50 mcg/kg/min (rates above this have been used safely in advanced circulatory decompensation in some settings). MAOI pretreatment requires starting at about 1/10th the usual dose. The dose must be individualised; no fixed dose applies.

Renal context: Dopamine and its metabolites are almost completely excreted in urine; the effect of renal impairment is not fully known, so close monitoring is advised. (1) (2) (3)

Mechanism of action

Hepatic guidance

The effect of impaired liver function on dopamine metabolism is not fully known; close monitoring is advisable.

Overdose note

Overdose results in excessive blood pressure elevation. Reduce or temporarily discontinue the infusion; because dopamine's duration of action is short, no additional remedial measures are usually necessary. An alpha-adrenergic blocker (e.g. phentolamine) may be considered if effects persist. (1) (2) (3)

Frequently asked questions

Can I be given dopamine at home?

No. Dopamine is a powerful intravenous medicine used only in hospital intensive care, emergency, or operating-theatre settings. It requires continuous monitoring and adjustment by trained clinicians.

What happens if the medicine leaks out of the vein?

Leakage (extravasation) can cause serious tissue damage. The infusion site is checked frequently. If leakage is suspected, the clinical team will stop the infusion and promptly inject a specific antidote (phentolamine) to protect the tissue. (1) (2) (3)

Is intravenous dopamine the same as the brain chemical dopamine or a dopamine supplement?

This page is about the prescription intravenous vasopressor/inotrope drug dopamine hydrochloride (historically Intropin), used only in hospital critical care. It is not about dopamine as a brain neurotransmitter or any dietary supplement marketed to affect mood or motivation.

Can children be given dopamine?

This differs by country. The US label describes use in pediatric patients from birth through adolescence at similar weight-based doses to adults. The UK and New Zealand labels state that safety and effectiveness in children have not been established and do not recommend it for this age group. Any pediatric use is a specialist decision based on the applicable local label. (1) (2) (3)

What is the mechanism of action of dopamine hydrochloride?

Dopamine is a direct-acting catecholamine and natural precursor of noradrenaline and adrenaline, with dose-dependent effects: at low doses (about 0.5-2 mcg/kg/min) it acts on dopaminergic receptors causing renal/mesenteric vasodilation; at moderate doses (about 2-10 mcg/kg/min) it activates beta-1 receptors, increasing cardiac output and heart rate; at higher doses it activates alpha-adrenergic receptors, causing vasoconstriction and raising blood pressure. It is metabolised in tissues and blood by MAO and COMT. (1) (2) (3)

What is the generic name of Dopamine (intravenous)?

The generic name is dopamine hydrochloride. It is sold under brand names including Intropin (historical US brand), Dopamine Juno, Dopamine Hydrochloride Sterile (DBL), Sterile Dopamine Concentrate BP (Max Health, New Zealand), Dopamine Hydrochloride and 5% Dextrose Injection (Hospira/Baxter, Canada). (1) (2) (3) (4) (6)

What class of drug is dopamine hydrochloride?

Dopamine (intravenous) is classed as: Catecholamine vasopressor/inotrope (natural precursor of noradrenaline and adrenaline); dose-dependent dopaminergic, beta-adrenergic, and alpha-adrenergic effects. (1) (2) (3) (4) (6)

References

  1. DOPAMINE HYDROCHLORIDE injection, for intravenous use (Initial U.S. Approval: 1974)U.S. Food and Drug Administration (via DailyMed) · United States · accessed 2026-07-31 · source 1
  2. Dopamine Hydrochloride 40mg/ml Concentrate for Solution for Infusion - Summary of Product Characteristicselectronic Medicines Compendium (UK) · United Kingdom · accessed 2026-07-31 · source 2
  3. New Zealand Data Sheet - Sterile Dopamine Concentrate BP (Max Health Ltd) 200mg/5mLMedsafe, New Zealand Medicines and Medical Devices Safety Authority · New Zealand · accessed 2026-07-31 · source 3
  4. Dopamine medicinal product entry (brands: Dopamine Hydrochloride Sterile (DBL), Dopamine (Juno))healthdirect Australia (Australian Government-funded consumer health information service) · Australia · accessed 2026-07-31 · source 4
  5. DOPAMINE JUNO dopamine hydrochloride 200 mg/5 mL concentrated injection ampoules - ARTG entry 332320Therapeutic Goods Administration · Australia · accessed 2026-07-31 · source 5
  6. Health Canada Drug Product Database API query results for brand name 'dopamine'Health Canada (Drug Product Database, official public API) · Canada · accessed 2026-07-31 · source 6
  7. Centralised authorisation search - no dopamine hydrochloride entryEuropean Medicines Agency · European Union · accessed 2026-07-31 · source 7

Brand names by country

Single-ingredient dopamine hydrochloride names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.

Priority countries

United States

  • dopamine hydrochloride in dextrose1.6 mg/mL, 3.2 mg/mL · hospira, inc.
  • Dopamine Hydrochloride and Dextrose160 mg00mL, 320 mg00mL, 80 mg00mL · baxter healthcare corporation
  • DOPAMINE HCI40 mg/mL · hf acquisition co. llc, dba health first
  • DOPAMINE PHENOLIC6 [hp_X]/mL · energique, inc.
  • DOPAMINE HCI IN 5% DEXTROSE1.6 mg/mL · hf acquisition co llc, dba healthfirst

United Kingdom

  • Dopamine Hydrochloride 40mg/ml Concentrate for Solution for Infusion (2)current licensed product · 40 mg/mL (200 mg/5 mL ampoule) · Bowmed Ibisqus Limited / ADVANZ Pharma / Martindale Pharma; see current EMC SmPCs

Canada

  • Dopamine HCl Inj 4% (6)current regulator registration · 40 mg/mL · International Medication Systems Ltd. (DIN 00423823)
  • Dopamine Hydrochloride and 5% Dextrose Injection USP (6)current regulator registration · multiple strengths (DIN 00619698, 00619701, 00782394) · Hospira Healthcare ULC
  • Dopamine HCl / Dextrose 5% Inj USP (6)current regulator registration · 0.8 mg/mL, 1.6 mg/mL, 3.2 mg/mL (DIN 00761850, 00761826, 00761834) · Baxter Corporation

Australia

  • Dopamine Hydrochloride Sterile (DBL) (4)current register product · 200 mg/5 mL concentrate · See current TGA ARTG / healthdirect.gov.au listing
  • Dopamine (Juno) (5) (4)current register product · 200 mg/5 mL concentrated injection ampoules · Juno Pharmaceuticals Pty Ltd -- ARTG 332320

New Zealand

  • Sterile Dopamine Concentrate BP (3)current regulator label · 200 mg/5 mL (40 mg/mL) · Max Health Ltd; see current Medsafe data sheet
View brands in additional countries.

This page provides general medicine information, not a diagnosis, prescription, injection plan, emergency plan, or substitute for the specialist and current local product information.

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