Product image of Makro-Albumon (Macrosalb (99mtc)) supplied by GNH India

Makro-Albumon

Active Ingredient:
Macrosalb (99mtc)
Origin:
EU

Makro-Albumon (Macrosalb (99mtc))

Macrosalb, the active ingredient in Makro-Albumon, is a pharmaceutical compound presented as an intravenous preparation for clinical use. It is employed in specialized medical settings where plasma protein supplementation may be required.

GNH India supplies Makro-Albumon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide.

Manufacturer / TM Owner

Medi-Radiopharma Kft.

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Indications & Clinical Uses

Makro-Albumon is an intravenous albumin solution used in conditions where plasma oncotic pressure support is needed.

  • Hypoalbuminemia: helps restore normal serum albumin levels and oncotic pressure.
  • Acute volume depletion: contributes to plasma volume expansion during shock or major surgery.
  • Liver disease with ascites: may be used to manage fluid balance in selected patients.

How It Works

  • Macrosalb acts as a plasma protein replacement, increasing oncotic pressure within the vascular compartment. By expanding intravascular volume, it improves tissue perfusion and facilitates transport of endogenous substances such as hormones, drugs, and fatty acids. The molecule binds calcium and other ions, contributing to hemostasis and acid‑base balance.

Side Effects

Makro-Albumon, like other albumin solutions, may be associated with adverse reactions.

Common Side Effects

  • Fever or chills during infusion.
  • Mild hypotension or transient blood pressure changes.
  • Headache or dizziness.
  • Nausea or mild gastrointestinal discomfort.
  • Local irritation at the infusion site.
  • Transient increase in serum calcium levels.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reactions.
  • Volume overload leading to pulmonary edema.
  • Cardiac arrhythmias in susceptible patients.
  • Hemolysis or red blood cell aggregation.
  • Severe electrolyte disturbances.
  • Coagulopathy or bleeding complications.

Precautions & Warnings

Before using Makro-Albumon, consider the following safety measures.

  • Assess fluid status: evaluate for signs of overload or dehydration.
  • Cardiac function: monitor patients with heart failure or coronary disease.
  • Renal impairment: adjust volume administration in patients with reduced kidney function.
  • Electrolyte balance: check serum calcium and potassium levels prior to infusion.
  • Allergic history: verify no prior severe reactions to albumin products.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Makro-Albumon may interact with other agents affecting fluid balance or coagulation.

Major Interactions (Avoid)

  • Diuretics: concurrent use can exacerbate hypovolemia.
  • ACE inhibitors or ARBs: may increase risk of hypotension.
  • Anticoagulants: albumin can alter plasma protein binding, affecting drug levels.

Moderate Interactions (Monitor Closely)

  • Calcium channel blockers: monitor for additive blood pressure effects.
  • Immunosuppressants: observe for changes in drug pharmacokinetics.
  • Other plasma expanders: avoid cumulative volume overload.

Frequently Asked Questions

Makro-Albumon is an intravenous albumin solution used to support plasma oncotic pressure in conditions such as hypoalbuminemia, acute volume depletion, and certain liver diseases where fluid balance requires careful management.

Macrosalb functions as a plasma protein replacement, raising intravascular oncotic pressure. This helps retain fluid within the blood vessels, improves tissue perfusion, and facilitates transport of hormones, drugs, and electrolytes throughout the body.

The dose of Makro-Albumon is determined by the prescribing clinician based on the patient’s clinical condition, body weight, and laboratory parameters. No fixed regimen is provided here; the prescriber sets the appropriate amount.

Safety data for Makro-Albumon in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order, 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 needed) and import documentation.

Makro-Albumon is comparable to other intravenous albumin solutions in terms of its protein content and intended clinical uses. Differences may exist in manufacturing processes, purity specifications, and regulatory approvals, but the therapeutic intent—plasma volume expansion and oncotic support—is similar across products.

Makro-Albumon must be stored at 2‑8 °C, protected from light, and kept in its original packaging. Do not freeze or shake the vial, and ensure the cold‑chain is maintained during transport to preserve product stability.

Makro-Albumon is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate and total volume are adjusted according to the patient’s clinical status and monitoring parameters.

Serious risks include anaphylactic reactions, volume overload leading to pulmonary edema, severe electrolyte disturbances, and coagulopathy. Prompt recognition and management of these events are essential, and patients should be closely monitored during and after infusion.

Makro-Albumon should be avoided in patients with known hypersensitivity to albumin products, uncontrolled heart failure, severe renal impairment with fluid restriction, or active pulmonary edema. Clinicians must evaluate each patient’s condition before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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