Product image of Iomeron (Iomeprol) supplied by GNH India

Iomeron

Active Ingredient:
Iomeprol
Origin:
EU

Iomeron (Iomeprol)

Iomeprol, the active ingredient in Iomeron, is an iodinated contrast media presented as a sterile solution for injection for intra‑arterial, intra‑articular, and intravenous use. It enhances radiographic visualization of vascular and tissue structures during diagnostic imaging procedures, aiding clinicians in accurate assessment.

GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, imaging centres and clinics worldwide, ensuring quality‑controlled manufacturing and reliable global distribution.

Manufacturer / TM Owner

Bracco Österreich Gmbh

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Indications & Clinical Uses

Iomeron, an iodinated contrast media, is employed in diagnostic imaging procedures that require enhanced X‑ray attenuation.

  • Angiography: provides high‑contrast vascular images to support diagnosis and interventional procedures.
  • Arthrography: delineates joint spaces and structures for accurate orthopedic evaluation.
  • Computed tomography (CT) imaging: improves soft‑tissue and organ visualization for comprehensive radiologic assessment.

How It Works

  • Iomeprol contains a high density of iodine atoms that absorb X‑ray photons, increasing attenuation of the X‑ray beam in the tissues where it distributes. After intravenous, intra‑arterial, or intra‑articular administration, the agent remains largely within the extracellular fluid and vascular compartments, creating a radiopaque contrast that highlights vessels, organs, and joint spaces on radiographic and CT images.

Side Effects

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

Common Side Effects

  • Warmth or flushing sensation during injection.
  • Metallic taste in the mouth.
  • Nausea or mild vomiting.
  • Headache.
  • Transient urticaria or skin itching.
  • Mild hypotension.

Serious or Rare Side Effects

  • Anaphylactoid or severe allergic reaction, including bronchospasm.
  • Acute kidney injury, especially in patients with pre‑existing renal impairment.
  • Thyroid function disturbances due to iodine load.
  • Seizures or neurologic events.
  • Cardiac arrhythmias or myocardial ischemia.

Precautions & Warnings

Prior to administering Iomeron, clinicians should observe several precautionary measures to minimize risk.

  • Assess renal function: evaluate serum creatinine and eGFR before use.
  • Review iodine allergy history: avoid in patients with known hypersensitivity to iodinated contrast.
  • Ensure adequate hydration: encourage fluid intake before and after the procedure.
  • Use the lowest effective dose: tailor volume to the specific imaging study.
  • Monitor thyroid status: consider thyroid function tests in patients at risk.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Iomeron can interact with other substances, influencing safety or efficacy.

Major Interactions (Avoid)

  • Concurrent administration of other iodinated contrast agents: increases total iodine load.
  • High‑dose iodine supplements or thyroid medications: may exacerbate thyroid dysfunction.
  • Nephrotoxic drugs (e.g., aminoglycosides, NSAIDs) in patients with renal impairment: heightens risk of kidney injury.

Moderate Interactions (Monitor Closely)

  • Metformin: temporary discontinuation may be required to prevent lactic acidosis in renal‑compromised patients.
  • Diuretics: may affect fluid balance and renal clearance of the contrast.
  • Beta‑blockers: may mask signs of contrast‑induced hypertension.

Frequently Asked Questions

Iomeron is an iodinated contrast agent used to improve the visibility of blood vessels, joints, and internal organs during diagnostic imaging procedures such as angiography, arthrography, and computed tomography (CT) scans.

Iomeprol contains iodine atoms that strongly absorb X‑ray photons. When injected, it distributes in the vascular and extracellular spaces, increasing X‑ray attenuation and creating a radiopaque outline of anatomical structures, which enhances image contrast on radiographs and CT scans.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging study, patient size, and clinical indication. Dosage is calculated to achieve optimal image quality while minimizing exposure.

Safety data for Iomeron in pregnancy and lactation are limited. It should only be used when clearly needed and after a risk‑benefit assessment by the healthcare provider. Breastfeeding mothers should discuss potential risks with their physician.

To order Iomeron, 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 if required) and import documentation.

Iomeron offers iodine concentration and viscosity comparable to other non‑ionic, low‑osmolality contrast media. It provides high‑quality image enhancement with a safety profile similar to its class, while formulation differences may affect injection pressure and patient tolerance.

Iomeron should be stored at room temperature, protected from light and moisture, and kept in its original packaging until use. Do not freeze the product, and inspect the vial for particulate matter before administration.

Iomeron is administered by a qualified healthcare professional via intravenous, intra‑arterial, or intra‑articular injection, depending on the imaging procedure. The injection is typically performed using a power injector or manual bolus under aseptic conditions.

The most serious risks include severe allergic reactions (anaphylaxis), acute kidney injury, especially in patients with pre‑existing renal dysfunction, and thyroid disturbances due to iodine overload. Immediate medical attention is required if any of these occur.

Iomeron should be avoided in individuals with a known hypersensitivity to iodinated contrast agents, severe renal impairment, uncontrolled hyperthyroidism, or in patients for whom the risk of contrast‑induced nephropathy outweighs the diagnostic benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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