Informational only — Not medical advice. Always consult a licensed healthcare provider.

Community data Updated 2 months ago
250 mg/50 ml
50 ml vial
৳1,000.00 per pack

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From ৳1,000.00 50 ml vial
Available as: 250 mg/50 ml · 50 ml vial

Indications & Uses

DOBUTamine Hameln is indicated for:

Pharmacology

Dobutamine Hydrochloride is a direct-acting inotropic agent. Its main action comes from stimulating adrenergic receptors in the heart. The chronotropic, hypertensive, arrhythmogenic and vasodilatory effects it produces are comparatively mild.

Unlike dopamine, Dobutamine Hydrochloride does not release norepinephrine, so its actions don't depend on norepinephrine stores in the heart. In humans it increases stroke volume and cardiac output. It also decreases ventricular filling pressure and total systemic and pulmonary vascular resistances.

Dosage Reference

Reference Information Only

Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.

Adults:

Dobutamine Hydrochloride has a short half-life, so it must be given as a continuous intravenous infusion. Once a constant rate infusion is started, or the rate is changed, the plasma dobutamine concentration reaches a steady state within about 10 minutes. Because of this, loading doses and bolus injections aren't necessary and are not recommended.

Recommended Dosage

In most patients, the infusion rate needed to increase cardiac output has ranged from 2.5 to 10 mcg/kg/min. Doses up to 20 mcg/kg/min are often required for adequate haemodynamic improvement. On rare occasions, rates up to 40 mcg/kg/min have been reported. The rate and the duration of therapy should be adjusted according to the patient's response. The indicators are haemodynamic parameters such as heart rate and rhythm, arterial pressure, and, whenever possible, cardiac output, measurements of ventricular filling pressures and signs of pulmonary congestion.

Concentrations up to 5,000 mg/L have been given to humans. The final volume should be decided by the patient's fluid requirements. Rather than stopping Dobutamine Hydrochloride suddenly, it is often advisable to lower the dose gradually.

Rates of Infusion Based on Concentration of Dobutamine Hydrochloride

The fluid infusion rate needed to deliver a specific dose depends on the concentration of Dobutamine Hydrochloride in the infusate. The table below is a guideline for the infusion rates (mL/kg/min) needed with 3 frequently used concentrations, 250, 500 and 1000 mg/L.

Dobutamine Injection was diluted to 250 micrograms/mL and 500 micrograms/mL with 0.9% Sodium Chloride Injection and 5% Glucose Injection. At these dilutions it was found to be stable for 24 hours at room temperature and in the presence of fluorescent light.

Side Effects

Heart rate, blood pressure and ventricular ectopic activity, hypotension, reactions at sites of intravenous infusion, miscellaneous.

Cautions & Contraindications

Warnings & Precautions

While Dobutamine Hydrochloride is being given, the heart rate and rhythm, the arterial blood pressure and the infusion rate should all be watched closely, as with any parenteral catecholamine. At the start of treatment, it's advisable to keep the patient on electrocardiographic monitoring until a stable response is reached.

Contraindications

Dobutamine Hydrochloride must not be given to anyone who has shown a hypersensitivity reaction to Dobutamine Hydrochloride before.

Pregnancy & Breastfeeding

Dobutamine Hydrochloride hasn't been studied in adequate, well-controlled trials in pregnant women. So it should not be used during pregnancy unless the possible benefit outweighs the possible risk to the foetus.

It isn't known whether this medicine passes into human milk. Many medicines do, so caution is needed when Dobutamine Hydrochloride is given to a nursing woman. If a mother needs dobutamine treatment, she should stop breastfeeding for as long as the treatment lasts.

⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

Storage

Store Dobutamine Hydrochloride below 30°C and keep it away from light and moisture. Keep it out of the reach of children.

Drug Interactions

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Moderate Spironolactone
Moderate Paracetamol
Moderate Nitroglycerin
Moderate Furosemide
Moderate Lidocaine
Moderate Folic Acid
Moderate Heparin Sodium

Common questions about DOBUTamine Hameln 250 mg/50 ml

What is DOBUTamine Hameln 250 mg/50 ml IV Injection?

DOBUTamine Hameln 250 mg/50 ml IV Injection is a medicine that contains Dobutamine Hydrochloride. It is made by ZAS Corporation. It belongs to the Inotropic-sympathomimetics group of medicines.

What is DOBUTamine Hameln used for?

DOBUTamine Hameln is used for: Edema.

What are the side effects of DOBUTamine Hameln?

Heart rate, blood pressure and ventricular ectopic activity, hypotension, reactions at sites of intravenous infusion, miscellaneous.

Can I take DOBUTamine Hameln during pregnancy or while breastfeeding?

Dobutamine Hydrochloride hasn't been studied in adequate, well-controlled trials in pregnant women. So it should not be used during pregnancy unless the possible benefit outweighs the possible risk to the foetus. Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

How should I store DOBUTamine Hameln?

Store Dobutamine Hydrochloride below 30°C and keep it away from light and moisture. Keep it out of the reach of children.

Can I take other medicines with DOBUTamine Hameln?

Some medicines can interact with Dobutamine Hydrochloride, for example: Spironolactone, Paracetamol, Nitroglycerin, Furosemide, Lidocaine, Potassium Chloride. Tell your doctor or pharmacist about every medicine you take.

Do I need a prescription for DOBUTamine Hameln?

DOBUTamine Hameln is a prescription (Rx) medicine. Take it as your doctor advises.

Last updated: 18 Aug 2026