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 intraarterial and intravenous use. It enhances radiographic imaging in diagnostic procedures for patients undergoing angiography, CT scans, and urography.

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

Manufacturer / TM Owner

Bracco Imaging S.P.A.

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Indications & Clinical Uses

  • Iomeron (iomeprol) is employed in diagnostic radiographic procedures that require enhanced vascular and tissue contrast.
  • Angiography: provides clear visualization of blood vessels and improves detection of vascular lesions.
  • CT imaging: enhances delineation of anatomical structures and pathology during computed tomography scans.
  • Urography: improves contrast of the urinary tract, aiding in the identification of stones, tumors, and structural abnormalities.

How It Works

  • Iomeprol contains high‑density iodine atoms that absorb X‑ray photons, increasing attenuation of the X‑ray beam. After intravenous or intra‑arterial administration, the agent distributes rapidly within the extracellular fluid and remains largely within the vascular compartment during the imaging window. The heightened attenuation creates a marked difference between enhanced and non‑enhanced tissues, allowing radiologists to distinguish anatomical details and pathological changes with greater clarity.

Side Effects

Iomeron may be associated with a range of adverse reactions, ranging from mild and transient to severe.

Common Side Effects

  • Warmth or flushing sensation during injection.
  • Metallic taste in the mouth.
  • Mild nausea or vomiting.
  • Headache.
  • Transient itching or urticaria.
  • Mild hypotension.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction.
  • Acute kidney injury, especially in patients with pre‑existing renal impairment.
  • Severe hypotension or cardiovascular collapse.
  • Pulmonary edema.
  • Persistent severe skin reactions such as Stevens‑Johnson syndrome.
  • Thyroid dysfunction due to iodine load.

Precautions & Warnings

Prior to administering Iomeron, clinicians should observe several precautionary measures to minimize risk.

  • Assess renal function: evaluate serum creatinine and eGFR before use.
  • Review allergy history: identify prior reactions to iodinated contrast agents.
  • Ensure adequate hydration: encourage fluid intake or intravenous hydration when appropriate.
  • Discontinue metformin in at‑risk patients: hold metformin in those with impaired renal function.
  • Monitor thyroid status: consider thyroid function tests in patients with known thyroid disease.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Iomeron can interact with certain medications and substances, affecting safety or efficacy.

Major Interactions (Avoid)

  • Metformin: risk of lactic acidosis in patients with reduced renal clearance.
  • Thyroid hormone preparations (levothyroxine, liothyronine): excess iodine may alter thyroid hormone levels.
  • Radiopharmaceuticals: iodine load can interfere with uptake of certain nuclear imaging agents.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may increase risk of contrast‑induced nephropathy.
  • Diuretics: can exacerbate renal impairment when combined with contrast.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may heighten renal toxicity.
  • Calcium channel blockers: monitor blood pressure as contrast may cause hypotension.

Frequently Asked Questions

Iomeron is a diagnostic radiographic contrast agent containing iomeprol. It is used to enhance the visibility of vascular structures and organs during imaging procedures such as angiography, computed tomography (CT) scans, and urography, helping radiologists obtain clearer images for accurate diagnosis.

Iomeprol works by providing high‑density iodine atoms that absorb X‑ray photons. When injected intravenously or intra‑arterially, it distributes in the extracellular fluid and remains within the vascular space during the imaging window, increasing X‑ray attenuation and creating a contrast difference between enhanced and surrounding tissues.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging study, patient weight, renal function, and clinical protocol. The healthcare provider calculates the appropriate volume and concentration to achieve optimal image quality while minimizing risk.

The safety of Iomeron in pregnancy and lactation has not been definitively established. It should be used only if the potential diagnostic benefit outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician in consultation with the patient.

To order Iomeron, submit an enquiry on the product page at gnhindia.com, specifying 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 any cold‑chain requirements), and necessary import documentation.

Iomeron (iomeprol) is a low‑osmolality, non‑ionic iodinated contrast medium, offering a favorable safety profile compared with high‑osmolality agents. Compared with other low‑osmolality agents, it provides similar image enhancement while generally causing fewer discomfort reactions, though individual tolerance can vary.

Iomeron should be stored at ambient temperature, below 25 °C, in its original sealed container. Protect the solution from direct sunlight, moisture, and freezing. Inspect the vial for particulate matter or discoloration before use, and discard if any abnormalities are observed.

Iomeron is supplied as a sterile solution for injection and is administered intravenously or intra‑arterially by a qualified healthcare professional. The injection is typically performed using a power injector or manual bolus, following the imaging protocol and aseptic technique.

The most serious risks include severe allergic reactions such as anaphylaxis, contrast‑induced acute kidney injury, significant hypotension or cardiovascular collapse, pulmonary edema, and rare but severe skin reactions. Prompt recognition and appropriate emergency management are essential if these events occur.

Iomeron should be avoided in patients with a known hypersensitivity to iodinated contrast media, uncontrolled severe asthma, recent severe allergic reactions, or those with critically impaired renal function where alternative imaging methods are feasible. The prescribing clinician must evaluate each patient’s risk factors before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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