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 non‑ionic iodinated contrast media presented as a solution for injection for intra‑arterial, intra‑articular, and intrathecal use. It enhances radiographic visualization of vascular and tissue structures during angiography, arthrography, myelography, CT imaging and other contrast‑enhanced examinations.
GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bracco Imaging S.P.A.

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Indications & Clinical Uses

Iomeron (iomeprol) is a non‑ionic iodinated contrast agent used to improve imaging of vascular and tissue structures.

  • Angiography: enhances visualization of blood vessels for diagnostic and interventional procedures.
  • Arthrography: improves delineation of joint spaces to assess cartilage and ligament integrity.
  • Myelography: provides contrast for spinal canal imaging to detect nerve root compression.
  • Computed tomography (CT) imaging: increases X‑ray attenuation for clearer cross‑sectional images.
  • Contrast‑enhanced radiographic examinations: facilitates detection of lesions and vascular abnormalities.

How It Works

  • Iomeprol contains a high density of iodine atoms that absorb X‑rays more effectively than surrounding tissues. When administered intra‑arterially, intra‑articular, or intrathecally, it distributes within the vascular or targeted compartment, increasing radiographic attenuation and thereby creating a stark contrast between the enhanced area and adjacent structures on imaging studies.

Side Effects

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

Common Side Effects

  • Warm sensation: transient feeling of heat during injection.
  • Nausea: mild upset stomach occurring shortly after administration.
  • Metallic taste: brief metallic flavor in the mouth.
  • Headache: mild to moderate headache post‑procedure.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Acute kidney injury: sudden decline in renal function, especially in patients with pre‑existing kidney disease.
  • Severe hypotension: marked drop in blood pressure that may necessitate intervention.

Precautions & Warnings

Before using Iomeron, clinicians should consider several safety measures.

  • Renal function assessment: evaluate serum creatinine and eGFR to identify patients at risk of contrast‑induced nephropathy.
  • Allergy history: review any prior reactions to iodinated contrast agents.
  • Hydration status: ensure adequate patient hydration to reduce renal risk.
  • Dose minimisation: use the lowest effective volume for the intended imaging study.
  • Vital sign monitoring: observe blood pressure and heart rate during and after injection.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Iomeron can interact with other substances that affect renal function or allergic risk.

Major Interactions (Avoid)

  • Concurrent iodinated contrast agents: may increase cumulative iodine load.
  • Nephrotoxic drugs (e.g., aminoglycosides, high‑dose NSAIDs): heighten risk of kidney injury.
  • Beta‑blockers: can mask contrast‑induced tachycardia.

Moderate Interactions (Monitor Closely)

  • Diuretics: may alter fluid balance and affect renal clearance.
  • ACE inhibitors or ARBs: potential additive effect on renal function.
  • Thyroid medications: excess iodine may interfere with thyroid hormone synthesis.

Frequently Asked Questions

Iomeron is a diagnostic contrast agent containing iomeprol, used to improve the visibility of vascular and tissue structures during imaging procedures such as angiography, arthrography, myelography, and computed tomography scans.

Iomeprol provides radiographic contrast by delivering a high concentration of iodine atoms that absorb X‑rays more strongly than surrounding tissues, thereby increasing attenuation and creating a clear distinction between the enhanced area and adjacent structures on the image.

The dose of Iomeron is determined by the prescribing clinician based on the specific imaging study, patient size, renal function and the required level of contrast enhancement. No fixed regimen is provided in public documentation.

The safety of Iomeron during pregnancy or lactation has not been definitively established. Use is generally avoided unless the diagnostic benefit outweighs potential risks, and the decision should be made 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 and any necessary import documentation.

Iomeron is a non‑ionic, low‑osmolality iodinated contrast medium, offering a lower incidence of adverse reactions compared with older high‑osmolality agents. Its iodine concentration provides strong X‑ray attenuation while maintaining a favorable safety profile for most patients.

Iomeron should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the solution from moisture, direct sunlight and extreme temperature fluctuations to maintain its stability.

Iomeron is supplied as a sterile solution for injection and is administered by a qualified healthcare professional via intra‑arterial, intra‑articular or intrathecal routes, depending on the imaging procedure being performed.

The most serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, and profound hypotension that may require immediate medical intervention.

Iomeron should be avoided in patients with known hypersensitivity to iodinated contrast media, severe renal insufficiency, uncontrolled hyperthyroidism, or in those who have experienced a prior severe reaction to a similar contrast agent.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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