Product image of Multihance (Gadobenate Dimeglumine) supplied by GNH India

Multihance

Active Ingredient:
Gadobenate Dimeglumine
Origin:
EU

Multihance (Gadobenate Dimeglumine)

Gadobenate dimeglumine, the active ingredient in Multihance, is a gadolinium-based contrast agent presented as an injection solution for intravenous use. It enhances magnetic resonance imaging and is used in diagnostic imaging of various organ systems.

GNH India supplies Multihance as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bracco Imaging Deutschland Gmbh

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Indications & Clinical Uses

Multihance is used as a gadolinium‑based contrast agent for magnetic resonance imaging of several organ systems.

  • Central nervous system: improves lesion detection and delineation on T1‑weighted MRI.
  • Liver: enhances visualization of focal hepatic lesions and vascular structures.
  • Cardiovascular system: provides high‑contrast images of cardiac chambers, vessels, and myocardial perfusion.
  • Musculoskeletal system: clarifies soft‑tissue and joint pathology on MRI.

How It Works

  • Gadobenate dimeglumine is a chelated gadolinium complex that shortens the T1 relaxation time of nearby water protons. By increasing the T1 signal intensity, it produces brighter images on T1‑weighted MRI sequences, allowing better visualization of vascular structures and tissue contrast in the scanned region.

Side Effects

Multihance may cause a range of adverse reactions following intravenous administration.

Common Side Effects

  • Nausea: mild to moderate feeling of queasiness.
  • Headache: transient headache during or after injection.
  • Injection site discomfort: warmth or pain at the site of administration.
  • Dizziness: brief episodes of light‑headedness.
  • Mild hypertension: temporary rise in blood pressure.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Nephrogenic systemic fibrosis (NSF): rare fibrotic disorder in patients with severe renal impairment.
  • Severe hypotension: marked drop in blood pressure.
  • Cardiac arrest: extremely rare but life‑threatening event.
  • Acute kidney injury: sudden deterioration of renal function.

Precautions & Warnings

Before using Multihance, clinicians should consider several safety measures.

  • Renal function assessment: evaluate glomerular filtration rate prior to administration.
  • History of allergic reactions: screen for prior hypersensitivity to contrast media.
  • Pregnancy: use only if clearly needed; safety data are limited.
  • Concurrent nephrotoxic drugs: avoid or closely monitor renal function when combined with agents such as aminoglycosides or NSAIDs.
  • Gadolinium retention: consider cumulative exposure in patients requiring multiple contrast studies.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Multihance may interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Renal‑impairment agents: avoid concurrent high‑dose iodinated contrast agents.
  • Nephrotoxic drugs: avoid simultaneous use of aminoglycosides, NSAIDs, or other renal‑toxic medications.
  • Chelating agents: avoid co‑administration of deferoxamine or similar agents.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: monitor hemodynamic response during and after injection.
  • Diuretics: observe fluid balance and renal function.
  • Other MRI contrast agents: stagger dosing to reduce cumulative gadolinium load.

Frequently Asked Questions

Multihance is a gadolinium‑based contrast agent used to enhance magnetic resonance imaging (MRI) of the central nervous system, liver, cardiovascular system, and musculoskeletal structures, helping clinicians obtain clearer diagnostic images.

Gadobenate dimeglumine is a chelated gadolinium complex that shortens the T1 relaxation time of nearby water protons, increasing signal intensity on T1‑weighted MRI sequences and providing improved contrast between tissues.

The dose of Multihance is determined by the prescribing physician based on the specific imaging protocol, patient weight, and clinical indication. The healthcare professional sets the appropriate amount for each individual case.

Safety data for Multihance in pregnancy and lactation are limited. It should only be used when clearly needed, and the potential benefits must outweigh any potential risks to the fetus or infant.

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

Multihance offers high relaxivity, providing strong T1 signal enhancement, especially in liver and cardiovascular imaging. Compared with lower‑relaxivity agents, it may allow lower doses or improved lesion detection, but selection depends on the specific clinical scenario and patient factors.

Multihance should be stored at 2‑8 °C, kept refrigerated, protected from light, and never frozen or shaken. Use aseptic technique when preparing the injection and discard any solution that appears discolored or particulate.

Multihance is administered intravenously as an injection solution, typically as a rapid bolus followed by a saline flush. The administration protocol, including injection rate and volume, is defined by the imaging procedure and the prescribing radiologist.

The most serious risks include severe allergic reactions such as anaphylaxis, nephrogenic systemic fibrosis (NSF) in patients with severe renal impairment, and rare events like acute kidney injury or cardiac arrest. Prompt recognition and management are essential.

Multihance should be avoided in patients with known hypersensitivity to gadolinium‑based agents, those with severe renal dysfunction (eGFR <30 mL/min/1.73 m²) due to the risk of NSF, and in individuals where the diagnostic benefit does not outweigh potential risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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