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 solution for injection for intra‑arterial, intra‑articular and intravenous use. It provides radiographic contrast enhancement for imaging procedures such as angiography, CT scans and arthrography in adult and pediatric patients.
GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies, clinics and imaging centres worldwide.

Manufacturer / TM Owner

Bracco Imaging S.P.A.

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Indications & Clinical Uses

Iomeron is an iodinated contrast agent used to improve visualization in vascular and tissue imaging procedures.

  • Angiography: Enhances vascular visualization for diagnostic and interventional procedures.
  • CT imaging: Improves tissue contrast to aid detection of lesions and anatomical detail.
  • Arthrography: Provides clear joint space delineation for musculoskeletal assessment.

How It Works

  • Iomeprol contains a high concentration of iodine atoms that strongly attenuate X‑ray photons. When administered, the iodine molecules remain in the vascular and extracellular compartments, increasing the radiodensity of blood vessels and tissues. This heightened attenuation creates a contrast between structures on radiographic, computed‑tomography or fluoroscopic images, allowing clinicians to differentiate anatomical details more clearly.

Side Effects

Adverse reactions to Iomeron can range from mild to severe and should be monitored during and after administration.

Common Side Effects

  • Warmth or flushing sensation at the injection site.
  • Metallic taste or transient taste alteration.
  • Nausea or mild vomiting.
  • Headache or mild dizziness.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction.
  • Acute renal impairment, especially in patients with pre‑existing kidney disease.
  • Hypotension or cardiovascular collapse.
  • Seizures or neurological disturbances.
  • Pulmonary edema or severe respiratory distress.

Precautions & Warnings

Prior to using Iomeron, clinicians should consider several safety measures to minimize risk.

  • Renal function assessment: Evaluate serum creatinine and eGFR before administration.
  • Allergy history: Screen for prior reactions to iodinated contrast or iodine‑containing products.
  • Dose optimization: Use the lowest effective volume for the specific imaging study.
  • Vital sign monitoring: Observe blood pressure and heart rate during and after injection.
  • Contraindications: Avoid in patients with known severe iodine hypersensitivity.
  • Store at ambient temperature: Keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Iomeron may interact with other medications, influencing safety or efficacy.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., aminoglycosides, high‑dose NSAIDs): Increased risk of renal injury.
  • Radioactive iodine therapy: Potential interference with thyroid uptake studies.
  • Concurrent iodinated contrast agents: Cumulative iodine load may exacerbate toxicity.

Moderate Interactions (Monitor Closely)

  • Metformin: Risk of lactic acidosis in patients with impaired renal function; consider temporary discontinuation.
  • ACE inhibitors or ARBs: May affect renal perfusion; monitor kidney function.
  • Diuretics: Can exacerbate volume shifts; observe fluid balance.

Frequently Asked Questions

Iomeron is an iodinated contrast medium used to enhance the visibility of blood vessels, organs and joints during radiographic procedures such as angiography, computed tomography (CT) scans and arthrography. By increasing X‑ray attenuation, it helps clinicians obtain clearer diagnostic images.

Iomeprol contains a high density of iodine atoms that absorb X‑ray photons. When injected, the iodine remains in the vascular and extracellular spaces, raising the radiodensity of those areas. This creates a contrast difference between structures on X‑ray‑based imaging, allowing better delineation of anatomy.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging study, patient weight, renal function and the required level of contrast. Dosage calculations are individualized and should follow the relevant clinical guidelines.

The safety of Iomeron in pregnancy and lactation has not been definitively established. It should be used only if the potential diagnostic benefit justifies any potential risk to the fetus or infant, and after careful consideration by the treating 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 any cold‑chain requirements) and necessary import documentation.

Iomeron (iomeprol) is a non‑ionic, low‑osmolality iodinated contrast medium, offering a favorable safety profile compared with older high‑osmolality agents. It provides comparable image quality while typically causing fewer discomfort reactions and a lower incidence of renal adverse effects.

Iomeron should be stored at ambient temperature, below 25 °C, in its original sealed container. Protect the solution from moisture, direct sunlight and extreme temperatures. Do not freeze or shake the vial before use.

Iomeron is supplied as a sterile solution for injection and is administered intravenously, intra‑arterially or intra‑articularly by a qualified healthcare professional. The injection rate and volume are tailored to the imaging protocol and patient characteristics.

Serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, and cardiovascular events like hypotension or shock. Immediate medical attention is required if any of these reactions occur.

Iomeron should be avoided in patients with a known severe hypersensitivity to iodinated contrast media, those with uncontrolled hyperthyroidism, and individuals with significant renal dysfunction where alternative imaging strategies are feasible.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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