Product image of Miozac (Dobutamine Hydrochloride) supplied by GNH India

Miozac

Active Ingredient:
Dobutamine Hydrochloride
Origin:
EU

Miozac (Dobutamine Hydrochloride)

Dobutamine Hydrochloride, the active ingredient in Miozac, is a Beta-1 adrenergic agonist presented as an injectable solution for intravenous use. It increases myocardial contractility and cardiac output in patients experiencing acute heart failure or cardiogenic shock. It is indicated for rapid hemodynamic support when conventional therapies are insufficient.

GNH India supplies Miozac as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals and intensive care units worldwide. The company adheres to stringent quality standards and provides reliable logistics for critical care medicines across global markets.

Manufacturer / TM Owner

Fisiopharma Srl

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Indications & Clinical Uses

  • Dobutamine acts as a beta‑1 adrenergic inotrope to improve cardiac performance in acute circulatory disorders.
  • Acute heart failure: enhances cardiac output and reduces symptoms of low perfusion.
  • Cardiogenic shock: restores hemodynamic stability by increasing contractility and blood pressure.
  • Low cardiac output states: supports circulation when other inotropes are inadequate.

How It Works

  • Dobutamine binds selectively to β1‑adrenergic receptors on myocardial cells, activating adenylate cyclase via Gs proteins. The resulting rise in intracellular cyclic AMP enhances calcium influx during systole, which strengthens myocardial contraction (positive inotropy) and modestly increases heart rate. This pharmacologic action raises stroke volume and cardiac output without significant peripheral vasoconstriction. The effect is dose‑dependent and rapidly reversible upon discontinuation, allowing clinicians to titrate therapy to the desired hemodynamic response.

Side Effects

Dobutamine may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Tachycardia: rapid increase in heart rate that may be symptomatic.
  • Hypertension: elevated blood pressure, sometimes requiring monitoring.
  • Headache: mild to moderate head discomfort occurring during infusion.
  • Nausea: feeling of sickness or urge to vomit, often transient.

Serious or Rare Side Effects

  • Myocardial ischemia: reduced blood flow to heart muscle that can cause chest pain.
  • Severe arrhythmias: life‑threatening irregular heart rhythms such as ventricular tachycardia.
  • Pulmonary edema: fluid accumulation in the lungs leading to breathing difficulty.
  • Anaphylactic reaction: severe allergic response with rash, swelling, and possible airway compromise.

Precautions & Warnings

When using Dobutamine, careful clinical monitoring and specific precautions are essential to ensure patient safety.

  • Cardiac monitoring: continuous ECG and arterial pressure monitoring should be maintained during infusion.
  • Dose titration: adjust infusion rate based on hemodynamic response and target parameters.
  • Renal impairment: monitor fluid balance and electrolytes closely in patients with kidney dysfunction.
  • Concomitant vasopressors: use with caution as combined effects may alter blood pressure.
  • Pregnancy: consider only if potential benefits justify potential risks to the fetus.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Dobutamine can interact with several medications, affecting its efficacy or safety profile.

Major Interactions (Avoid)

  • Beta‑blockers: may blunt Dobutamine’s inotropic effect, reducing therapeutic benefit.
  • MAO inhibitors: increase risk of hypertensive crisis when combined.
  • Tricyclic antidepressants: elevate risk of arrhythmias during therapy.
  • Non‑dihydropyridine calcium channel blockers: may potentiate negative inotropic actions.

Moderate Interactions (Monitor Closely)

  • Diuretics: electrolyte shifts can modify cardiac response to Dobutamine.
  • ACE inhibitors: additive hypotensive effect may require blood pressure monitoring.

Frequently Asked Questions

Miozac contains Dobutamine Hydrochloride and is used in hospital settings to provide rapid inotropic support for patients with acute heart failure or cardiogenic shock. By increasing the strength of heart muscle contractions, it helps improve cardiac output and stabilise blood pressure during critical episodes.

Dobutamine selectively stimulates β1‑adrenergic receptors on cardiac myocytes, activating a cascade that raises cyclic AMP levels. This enhances calcium entry during each heartbeat, producing a stronger contraction (positive inotropy) and modestly increasing heart rate, which together raise stroke volume and overall cardiac output.

The dosage of Miozac is individualized by the prescribing clinician. The infusion rate is titrated according to the patient’s hemodynamic response, target blood pressure, and cardiac output, with adjustments made under continuous monitoring in an intensive‑care environment.

Safety data for Dobutamine in pregnancy and lactation are limited. It should only be used when the potential maternal benefit outweighs any possible risk to the fetus, and breastfeeding decisions should be made in consultation with a healthcare professional.

To order Miozac, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and any necessary import documentation.

Both Dobutamine (Miozac) and dopamine act as inotropes, but Dobutamine is more β1‑selective, providing stronger contractility with less peripheral vasoconstriction. Dopamine has dose‑dependent effects that include dopaminergic and α‑adrenergic activity, which can raise systemic vascular resistance, whereas Dobutamine primarily enhances cardiac output with a milder impact on blood pressure.

Miozac should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Before use, inspect the solution for particulate matter or discoloration and allow it to reach room temperature if required for infusion.

Miozac is supplied as an injectable solution for intravenous infusion. It is administered through a controlled infusion pump, with the rate adjusted by the clinical team based on continuous monitoring of heart rate, blood pressure, and cardiac output to achieve the desired hemodynamic effect.

Serious risks include myocardial ischemia, severe arrhythmias such as ventricular tachycardia, pulmonary edema, and anaphylactic reactions. These events require immediate medical intervention and close monitoring during the infusion.

Miozac is contraindicated in patients with known hypersensitivity to Dobutamine, uncontrolled ventricular arrhythmias, or severe aortic stenosis. Caution is also advised in individuals with recent myocardial infarction, severe hypertension, or significant electrolyte disturbances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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