Product image of Iomeron (Iomeprol) supplied by GNH India

Iomeron

Active Ingredient:
Iomeprol
Origin:
EU

Iomeron (Iomeprol)

Iomeprol, the active ingredient in Iomeron, is a iodinated contrast agent presented as an injection solution for intravenous use. It enhances radiodensity by absorbing X‑rays, thereby improving the visibility of anatomical structures during diagnostic imaging procedures such as computed tomography, angiography and urography.

GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, imaging centres and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to facilitate import and distribution across multiple regions.

Manufacturer / TM Owner

Bracco Uk Ltd

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Indications & Clinical Uses

Iomeron is employed in diagnostic imaging to increase contrast between vascular and tissue structures.

  • Contrast‑enhanced radiographic imaging: provides clearer delineation of bones and soft tissues for accurate diagnosis.
  • Computed tomography (CT) scans: heightens attenuation differences, facilitating detection of lesions and vascular abnormalities.
  • Angiography: outlines blood vessels and vascular lesions, improving visualization for interventional procedures.

How It Works

  • Iomeprol is a non‑ionic, low‑osmolality iodinated compound that absorbs X‑ray photons. After intravenous injection, it rapidly distributes within the vascular and extracellular spaces, increasing the radiodensity of blood and surrounding tissues. The high atomic number of iodine causes greater attenuation of X‑rays, producing enhanced contrast on radiographic, CT and angiographic images, which aids clinicians in distinguishing anatomical details. This effect persists for the duration of the imaging study before the agent is cleared renally.

Side Effects

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

Common Side Effects

  • Warm sensation at injection site
  • Metallic taste in mouth
  • Nausea
  • Vomiting
  • Headache
  • Mild itching or rash

Serious or Rare Side Effects

  • Anaphylactic reaction (severe allergy)
  • Contrast‑induced nephropathy
  • Thyroid dysfunction (hyper‑ or hypothyroidism)
  • Severe hypotension
  • Cardiac arrhythmias

Precautions & Warnings

When using Iomeron, several precautionary measures should be observed to minimize risk.

  • Renal impairment: assess kidney function (eGFR) before administration.
  • History of iodine allergy: consider alternative contrast agents or pre‑medication.
  • Thyroid disease: monitor thyroid function tests as iodine load may affect hormone levels.
  • Pregnancy: use only if essential, after evaluating benefit‑risk ratio.
  • Hydration: ensure adequate fluid intake before and after the procedure to support renal clearance.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Iomeron can interact with certain medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Iodine‑containing drugs (e.g., amiodarone, potassium iodide): may increase total iodine burden and risk of toxicity.
  • Nephrotoxic agents (e.g., aminoglycosides, NSAIDs, radiocontrast‑enhancing chemotherapy): heighten risk of renal injury.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect renal clearance of the contrast medium.
  • Metformin: consider temporary discontinuation in patients with impaired renal function to prevent lactic acidosis.
  • Beta‑blockers: no direct pharmacokinetic interaction but monitor hemodynamic status during imaging.

Frequently Asked Questions

Iomeron is an iodinated contrast medium used in diagnostic imaging procedures such as computed tomography (CT), angiography, urography and other contrast‑enhanced radiographic studies to improve the visibility of anatomical structures.

Iomeprol contains iodine atoms that strongly absorb X‑ray photons. After intravenous injection it distributes in the vascular and extracellular spaces, raising the radiodensity of blood and tissues, which creates a clearer distinction between structures on X‑ray‑based images.

The dose of Iomeron is individualized and determined by the prescribing physician based on the type of imaging study, patient weight, renal function and the required level of contrast enhancement.

The safety of Iomeron in pregnancy and lactation has not been definitively established. It should be used only when clearly needed, after a careful benefit‑risk assessment by the healthcare professional.

To order Iomeron, 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 if required) and import documentation.

Iomeron is a non‑ionic, low‑osmolality iodinated agent, which generally offers lower incidence of discomfort and adverse reactions compared with high‑osmolality ionic agents. Its radiodensity and safety profile are comparable to other modern low‑osmolality contrast media used for similar imaging indications.

Iomeron should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Before use, allow the solution to reach room temperature if required and inspect for particulate matter or discoloration.

Iomeron is administered as an intravenous injection by a qualified healthcare professional. The solution is typically injected as a bolus or through a power injector, depending on the imaging protocol, to achieve optimal vascular and tissue enhancement.

The most serious risks include severe allergic reactions such as anaphylaxis, contrast‑induced nephropathy leading to acute kidney injury, and thyroid dysfunction due to iodine overload. Prompt recognition and appropriate medical management are essential if these events occur.

Iomeron should be avoided in patients with known severe iodine allergy, uncontrolled hyperthyroidism, severe renal impairment (eGFR < 30 mL/min/1.73 m²) unless benefits outweigh risks, and in pregnant women unless the diagnostic benefit justifies potential fetal exposure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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