Product image of Imeron (Iomeprol) supplied by GNH India

Imeron

Active Ingredient:
Iomeprol
Origin:
EU

Imeron (Iomeprol)

Iomeprol, the active ingredient in Imeron, is an iodinated contrast media presented as a sterile solution for intra‑arterial, intra‑articular and intravenous use. It provides radiodensity to enhance image quality during diagnostic radiology procedures such as angiography, arthrography and computed tomography.

GNH India supplies Imeron 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

Imeron is an iodinated contrast agent used in diagnostic imaging procedures that require enhanced radiographic detail.

  • Angiography: improves visualization of blood vessels for diagnostic and interventional purposes.
  • Arthrography: delineates joint structures to aid in the assessment of cartilage, ligaments and menisci.
  • Computed Tomography (CT) imaging: increases contrast between tissues, facilitating detection of lesions and anatomical abnormalities.

How It Works

  • Iomeprol is a non‑ionic, water‑soluble iodinated contrast medium. Its iodine atoms have a high atomic number, which absorbs X‑ray photons and increases radiodensity of the administered area. After injection, the agent distributes rapidly within the extracellular fluid, remains largely unbound to plasma proteins, and provides transient contrast enhancement that improves the differentiation of anatomical structures on imaging studies.

Side Effects

Imeron may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Warmth or flushing sensation during injection.
  • Metallic taste or mild nausea.
  • Mild headache or transient dizziness.

Serious or Rare Side Effects

  • Severe allergic reactions, including anaphylaxis.
  • Acute kidney injury, especially in patients with pre‑existing renal impairment.
  • Thyroid dysfunction due to iodine load.
  • Cardiopulmonary arrest or severe hypotension.

Precautions & Warnings

Prior to administration, clinicians should consider several safety measures.

  • Renal Function Assessment: evaluate serum creatinine and eGFR, especially in at‑risk patients.
  • Allergy History Review: confirm no prior severe reactions to iodinated contrast.
  • Hydration: ensure adequate fluid intake before and after the procedure.
  • Hyperthyroidism Caution: avoid or use minimal dose in patients with uncontrolled thyroid disease.
  • Dose Optimization: employ the lowest effective volume for the specific imaging study.
  • Monitoring: observe patients for immediate and delayed reactions during and after injection.
  • Store at ambient temperature: keep in original container, protect from moisture and direct light.

Avoid Interactions

Imeron can interact with other substances that affect renal function or iodine handling.

Major Interactions (Avoid)

  • Concurrent administration of other iodinated contrast agents, which may cause cumulative iodine toxicity.
  • Use with nephrotoxic drugs (e.g., aminoglycosides, high‑dose NSAIDs) in patients with compromised renal function.

Moderate Interactions (Monitor Closely)

  • Co‑administration with diuretics may increase the risk of volume depletion and renal injury.
  • Thyroid hormone therapy in hyperthyroid patients may exacerbate thyroid hormone excess.
  • Beta‑blockers can mask early signs of anaphylactoid reactions, requiring careful monitoring.

Frequently Asked Questions

Imeron is an iodinated contrast agent used to enhance the visibility of blood vessels, joints and internal organs during imaging procedures such as angiography, arthrography and computed tomography (CT). The contrast improves the differentiation of structures, aiding accurate diagnosis.

Iomeprol contains iodine atoms that absorb X‑ray photons, increasing the radiodensity of the area where it is administered. After injection, it distributes in the extracellular fluid, providing temporary contrast that highlights vascular and tissue details on radiographic images.

The dose of Imeron is determined by the prescribing physician based on the specific imaging study, patient weight, renal function and the required level of contrast. Healthcare professionals calculate the appropriate volume to achieve optimal image quality while minimizing risk.

The safety of Imeron in pregnancy and lactation has not been definitively established. It should only be used when clearly needed and after a risk‑benefit assessment by the treating physician. Breastfeeding mothers should discuss potential exposure with their healthcare provider.

To order Imeron, 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 any cold‑chain requirements) and necessary import documentation.

Imeron (iomeprol) is a non‑ionic, low‑osmolality iodinated contrast medium, which generally offers a lower incidence of adverse reactions compared with older high‑osmolality agents. Its pharmacokinetic profile provides rapid distribution and clearance, making it suitable for a wide range of diagnostic procedures.

Imeron should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the solution from direct sunlight, moisture and extreme temperature fluctuations. Do not freeze the product, and inspect the container for any signs of damage before use.

Imeron is administered by a qualified healthcare professional via intra‑arterial, intra‑articular or intravenous injection, depending on the imaging study. The injection is typically performed using a power injector or manual bolus, following aseptic technique and the prescribed volume.

Serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, and thyroid dysfunction due to iodine load. Immediate medical attention is required if any signs of these reactions occur.

Imeron should be avoided in patients with a known hypersensitivity to iodinated contrast media, uncontrolled hyperthyroidism, severe renal insufficiency (eGFR < 30 mL/min/1.73 m²) unless benefits outweigh risks, and in individuals for whom alternative imaging methods without contrast are feasible.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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