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 agent presented as a solution for injection for intravenous use. It enhances radiographic imaging in diagnostic procedures and is employed in patients undergoing CT, angiography, and urography.

GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, imaging centres and clinics worldwide.

Manufacturer / TM Owner

Bracco Imaging Deutschland Gmbh

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Indications & Clinical Uses

Iomeron is an iodinated contrast agent used to improve visualization of vascular and urinary structures during radiographic procedures.

  • CT imaging: provides enhanced contrast for detailed cross‑sectional images.
  • Angiography: delineates blood vessels for diagnostic and interventional procedures.
  • Urography: highlights urinary tract anatomy for assessment of kidneys, ureters and bladder.

How It Works

  • Iomeprol contains iodine atoms that increase X‑ray attenuation. After intravenous injection, the molecule distributes rapidly into the vascular and extracellular compartments, where the iodine absorbs X‑ray photons, producing higher radiodensity on imaging. The transient enhancement allows clinicians to differentiate structures based on contrast differences.

Side Effects

Iomeron may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Warm sensation or flushing at the injection site.
  • Nausea or vomiting.
  • Mild headache.
  • Metallic taste in the mouth.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction.
  • Acute kidney injury, especially in patients with pre‑existing renal dysfunction.
  • Severe hypotension or cardiovascular collapse.

Precautions & Warnings

Before administering Iomeron, several safety measures should be observed.

  • Assess renal function: evaluate serum creatinine and eGFR.
  • Screen for iodine or contrast allergy: obtain detailed allergy history.
  • Use the lowest effective dose: tailor volume to the specific imaging study.
  • Monitor vital signs: observe blood pressure and heart rate during and after injection.
  • Avoid in patients with severe thyroid disease: iodine load may exacerbate conditions.
  • Store at ambient temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Iomeron can interact with other medicines, requiring attention to dosage and monitoring.

Major Interactions (Avoid)

  • Concurrent iodinated contrast agents: cumulative iodine load increases toxicity risk.
  • High‑dose NSAIDs: may potentiate renal impairment.
  • Metformin in patients with reduced renal function: risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect renal clearance of iodine.
  • ACE inhibitors or ARBs: potential alteration of renal function.
  • Beta‑blockers: may mask hypotensive responses during injection.

Frequently Asked Questions

Iomeron is used as a diagnostic imaging agent to enhance X‑ray based studies such as computed tomography (CT), angiography and urography. By increasing the radiodensity of blood vessels and extracellular spaces, it helps radiologists obtain clearer images for accurate diagnosis.

Iomeprol works by delivering iodine atoms into the bloodstream. Iodine strongly absorbs X‑ray photons, so when the solution is injected intravenously it temporarily raises the attenuation of X‑rays in vascular and extracellular compartments, creating a contrast difference that highlights anatomical structures on the scan.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging protocol, patient weight, renal function and the area to be examined. No fixed regimen is provided here; the healthcare professional calculates the appropriate volume for each individual case.

The safety of Iomeron during pregnancy and lactation has not been definitively established. It should only be used when the potential diagnostic benefit outweighs any possible risk to the fetus or infant, and the decision must 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 (including any cold‑chain needs) and required import documentation.

Iomeron (Iomeprol) is a low‑osmolality, non‑ionic iodinated contrast medium, offering a favorable safety profile compared with older high‑osmolality agents. Its viscosity and iodine concentration provide strong image enhancement while reducing the incidence of discomfort and adverse reactions relative to some alternatives.

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

Iomeron is administered as an intravenous injection by a qualified healthcare professional. The solution is typically injected through a peripheral or central vein using a power injector or manual bolus, depending on the imaging protocol and equipment used for the procedure.

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 or cardiovascular collapse. Immediate medical intervention is required if any of these events occur.

Iomeron should be avoided in patients with a known hypersensitivity to iodinated contrast media, those with uncontrolled severe thyroid disease, and individuals with markedly reduced renal function where the risk of contrast‑induced nephropathy is high. Contraindications must be confirmed by the prescribing clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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