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 during diagnostic imaging procedures such as angiography, arthrography and myelography.

GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, clinics and imaging centres worldwide, ensuring quality, regulatory compliance, reliable logistics and dedicated technical support.

Manufacturer / TM Owner

Bracco Imaging S.P.A.

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Indications & Clinical Uses

  • Iomeron (iomeprol) is used as a radiographic contrast agent to improve X‑ray based imaging.
  • Angiography: provides clear delineation of blood vessels for accurate diagnosis.
  • Arthrography: enhances joint space visualization to assess cartilage and ligaments.
  • Myelography: improves contrast of the spinal canal for detailed evaluation of neural structures.
  • Other diagnostic imaging procedures requiring intra‑arterial, intra‑articular or intrathecal contrast: facilitates detailed anatomical assessment in specialized studies.

How It Works

  • Iomeprol contains multiple iodine atoms that strongly absorb X‑ray photons. When injected into vascular, joint or cerebrospinal spaces, the iodine increases attenuation of the X‑ray beam, creating radiodense areas that appear bright on the resulting images. This enhanced radiodensity allows clinicians to differentiate structures and detect pathology with greater clarity.

Side Effects

Adverse reactions to Iomeron can range from mild and transient to severe, though serious events are uncommon.

Common Side Effects

  • Warmth or flushing sensation during injection
  • Metallic taste in the mouth
  • Nausea or mild vomiting

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis) with respiratory distress
  • Contrast‑induced nephropathy leading to acute kidney injury
  • Significant hypotension or cardiovascular collapse

Precautions & Warnings

  • Before using Iomeron, several safety considerations should be observed.
  • Renal function assessment: evaluate serum creatinine and eGFR to identify risk of nephrotoxicity.
  • Allergy screening: confirm no known iodine or contrast media hypersensitivity.
  • Use lowest effective volume: limit exposure to the minimum required for diagnostic quality.
  • Vital sign monitoring: observe blood pressure and heart rate during and after injection.
  • Contraindication in severe hyperthyroidism: avoid use in uncontrolled thyroid disease.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent nephrotoxic agents (e.g., aminoglycosides, high‑dose NSAIDs): increase risk of renal injury.
  • Metformin in patients with reduced renal function: risk of lactic acidosis.
  • Radioactive iodine therapy (I‑131): iodine load may interfere with treatment.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask contrast‑induced tachycardia.
  • Diuretics: affect fluid balance and renal clearance.
  • ACE inhibitors or ARBs: may potentiate renal effects, monitor kidney function.

Frequently Asked Questions

Iomeron is an iodinated contrast agent used during diagnostic imaging procedures such as angiography, arthrography and myelography. It is injected into blood vessels, joints or the cerebrospinal fluid to improve the visibility of anatomical structures on X‑ray based studies.

Iomeprol contains iodine atoms that strongly absorb X‑ray photons. After injection, the iodine increases attenuation of the X‑ray beam, creating radiodense areas that appear bright on images. This enhanced contrast helps clinicians differentiate tissues and detect abnormalities more clearly.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging study, patient size, and clinical requirements. Dosage is individualized and should follow the recommendations in the product labeling and the radiologist’s protocol.

Safety data for Iomeron in pregnancy and lactation are limited. It should only be used when clearly needed and when the potential diagnostic benefit outweighs any possible risk to the fetus or infant. Consultation with a specialist is advised.

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, which generally results in fewer injection‑related sensations and a lower incidence of allergic reactions compared with older, high‑osmolality ionic agents. Its radiodensity is comparable, providing high‑quality images across a range of studies.

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

Iomeron is administered by a healthcare professional as an injection. It can be given intra‑arterially for vascular imaging, intra‑articularly for joint studies, or intrathecally for spinal imaging, always under strict aseptic technique and imaging guidance.

The most serious risks include severe allergic reactions (anaphylaxis), contrast‑induced nephropathy leading to acute kidney injury, and significant hypotension or cardiovascular collapse. Prompt recognition and appropriate medical management are essential if these events occur.

Iomeron should be avoided in patients with a known allergy to iodine or iodinated contrast media, severe renal impairment, uncontrolled hyperthyroidism, or in those who have experienced a prior severe reaction to a similar contrast agent. Clinical judgment is required for each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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