GNH USA

Europe — EMA

Makro-Albumon

GNH USA supplies Makro-Albumon (Human Albumin Macroaggregates), an albumin product for lung perfusion imaging and pulmonary embolism assessment.

Human Albumin As Macroaggregates

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What is Human Albumin As Macroaggregates?

Human Albumin Macroaggregates, the active ingredient in Makro-Albumon, is an albumin drug presented as an injectable formulation for intravenous use. It is employed primarily in diagnostic imaging to assess pulmonary perfusion and related conditions. GNH USA supplies Makro-Albumon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Human Albumin As Macroaggregates used for?

Makro-Albumon is used in nuclear medicine procedures that evaluate pulmonary blood flow and related disorders. - Lung perfusion imaging: enables visualization of regional pulmonary blood flow for diagnostic assessment. - Pulmonary embolism detection: assists in identifying embolic obstruction of pulmonary arteries. - Pre‑operative lung function evaluation: provides functional information to guide surgical planning.

What are the side effects of Human Albumin As Macroaggregates?

Makro-Albumon may be associated with a range of adverse reactions following intravenous administration.

Common Side Effects: - Transient fever: mild temperature rise shortly after injection. - Mild hypotension: temporary drop in blood pressure. - Headache: short‑lasting discomfort. - Nausea: occasional feeling of queasiness. - Injection site discomfort: mild pain or irritation. - Flushing: brief redness of skin.

Serious or Rare Side Effects: - Anaphylactic reaction: severe allergic response requiring immediate medical attention. - Severe hypotension: marked blood pressure decline with possible syncope. - Pulmonary hypertension: abrupt increase in pulmonary arterial pressure. - Embolic complications: rare lodging of particles causing vascular blockage. - Acute respiratory distress: sudden breathing difficulty. - Cardiovascular collapse: life‑threatening circulatory failure.

What precautions apply to Human Albumin As Macroaggregates?

Prior to using Makro-Albumon, clinicians should consider several safety measures. - Allergy assessment: verify no known hypersensitivity to human albumin or related proteins. - Cardiac evaluation: avoid in patients with severe heart failure or uncontrolled hypertension. - Pulmonary status: contraindicated in severe pulmonary hypertension or acute respiratory distress. - Volume monitoring: watch for signs of fluid overload, especially when combined with other albumin products. - Concurrent radiopharmaceuticals: ensure appropriate timing to prevent imaging interference. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the vial.

What does Human Albumin As Macroaggregates interact with?

Makro-Albumon may interact with other agents administered intravenously.

Major Interactions (Avoid): - Other intravenous albumin solutions: risk of volume overload and circulatory strain. - High‑dose diuretics: may exacerbate hypotension.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., heparin, warfarin): potential alteration of bleeding risk. - Beta‑blockers: additive effect on blood pressure reduction. - Vasodilators (e.g., nitroglycerin): increased likelihood of hypotensive episodes. - Radiopharmaceuticals with overlapping emission spectra: may affect imaging interpretation.

Frequently asked questions

What is Makro-Albumon used for?+
Makro-Albumon is a sterile injectable containing human albumin macroaggregates that is used in nuclear medicine to perform lung perfusion scans. The procedure helps visualize blood flow in the pulmonary circulation, aiding in the diagnosis of pulmonary embolism, assessment of lung function before surgery, and evaluation of other pulmonary vascular conditions.
How does Human Albumin Macroaggregates work?+
The macroaggregated albumin particles are calibrated to a specific size range that allows them to become temporarily trapped in the small vessels of the lungs after intravenous injection. When labeled with a radiotracer, these particles emit gamma radiation that can be detected by a gamma camera, producing a detailed map of pulmonary perfusion.
What is the usual dose of Makro-Albumon?+
The dose of Makro-Albumon is determined by the prescribing physician based on the specific imaging protocol, patient weight, and clinical indication. Healthcare professionals calculate the appropriate activity of the radiolabeled preparation and the volume of macroaggregated albumin to administer for each individual case.
Is Makro-Albumon safe during pregnancy or breastfeeding?+
Safety data for Makro-Albumon in pregnant or breastfeeding individuals are limited. Because the product involves a radiopharmaceutical component, it is generally avoided unless the diagnostic benefit outweighs potential risks. Clinicians should discuss any concerns with the patient and consider alternative imaging methods when appropriate.
How do I order Makro-Albumon from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies, and procurement teams worldwide. After receiving the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including cold‑chain logistics if needed), and any required import documentation.
How does Makro-Albumon compare with other lung perfusion agents?+
Makro-Albumon uses human albumin macroaggregates as the carrier for the radiotracer, offering a well‑characterized particle size distribution that provides reliable capillary lodging. Compared with alternative agents such as technetium‑99m labeled macroaggregated albumin from other manufacturers, Makro-Albumon meets EU quality standards and is supplied with consistent sterility and particle uniformity, which can improve imaging reproducibility.
What are the storage and handling requirements for Makro-Albumon?+
Makro-Albumon must be stored refrigerated at 2‑8 °C. The vials should be kept in their original packaging, protected from light, and must not be frozen or shaken. Prior to administration, allow the product to reach room temperature if required by the imaging protocol, and inspect for any particulate matter or discoloration.
How is Makro-Albumon administered?+
Makro-Albumon is administered intravenously by a qualified healthcare professional. The prepared radiolabeled suspension is injected slowly, typically through a peripheral vein, while the patient is monitored for vital signs. The injection is followed by imaging with a gamma camera to capture the distribution of the radiotracer within the lungs.
What are the most serious risks associated with Makro-Albumon?+
The most serious risks include severe allergic reactions such as anaphylaxis, marked hypotension, and rare embolic events that can compromise pulmonary circulation. Patients should be observed closely during and after injection, and emergency measures must be readily available to manage any acute adverse reactions.
Who should not receive Makro-Albumon?+
Makro-Albumon is contraindicated in individuals with known hypersensitivity to human albumin or any component of the formulation, patients with severe pulmonary hypertension, uncontrolled heart failure, or those who have experienced a severe reaction to a previous macroaggregated albumin scan. Clinicians should evaluate each patient’s medical history before administration.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Human Albumin As Macroaggregates
Route
Intravenous Use
Manufacturer
Medi-Radiopharma Kft.
Origin
EU

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