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 visualization of vascular and tissue structures during procedures such as angiography, computed tomography, urography, cardiac catheterisation and peripheral vascular imaging.

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, an iodinated contrast agent, is used to improve visualization of vascular and organ structures in radiographic procedures.

  • Angiography: provides enhanced vessel delineation for diagnostic and interventional procedures.
  • Computed tomography (CT) imaging: increases tissue contrast to aid detection of lesions and anatomical detail.
  • Urography: highlights urinary tract anatomy for accurate assessment.
  • Cardiac catheterisation: improves coronary and cardiac chamber imaging during invasive studies.
  • Peripheral vascular imaging: clarifies arterial and venous pathways in limb studies.

How It Works

  • Iomeprol contains radiodense iodine atoms that absorb X‑ray photons, thereby increasing attenuation of the X‑ray beam. When injected into the bloodstream, these iodine atoms distribute within vascular and extracellular spaces, creating a temporary contrast between blood‑filled structures and surrounding tissues, which enhances image definition in X‑ray‑based modalities.

Side Effects

Adverse reactions to Iomeron may vary in frequency and severity.

Common Side Effects

  • Warmth or flushing sensation during injection.
  • Metallic or salty taste in the mouth.
  • Nausea or mild vomiting.
  • Transient headache.
  • Mild urticaria or skin itching.
  • Mild hypotension.

Serious or Rare Side Effects

  • Anaphylactoid or severe allergic reaction, including bronchospasm and shock.
  • Contrast‑induced nephropathy leading to acute kidney injury.
  • Thyroid dysfunction from iodine overload, such as hyperthyroidism or hypothyroidism.
  • Seizures or neurological disturbances.
  • Severe hypotension or cardiovascular collapse.
  • Pulmonary edema or acute respiratory distress.

Precautions & Warnings

When using Iomeron, clinicians should observe several safety measures.

  • Renal function assessment: evaluate baseline kidney function before administration.
  • Hydration status: ensure adequate patient hydration to reduce nephrotoxic risk.
  • Allergy history: screen for prior reactions to iodinated contrast agents.
  • Thyroid disease: consider potential iodine load in patients with thyroid disorders.
  • Pregnancy and lactation: use only if clearly needed; benefits must outweigh potential risks.
  • Store at ambient temperature: keep below 25°C, protect from light and moisture, retain in original container.

Avoid Interactions

Iomeron may interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Metformin: may precipitate lactic acidosis; discontinue before contrast administration.
  • Iodine‑containing drugs (e.g., amiodarone, potassium iodide): increase total iodine load.
  • ACE inhibitors or ARBs: can exacerbate contrast‑induced renal impairment.
  • Nephrotoxic agents (e.g., aminoglycosides, NSAIDs): heighten risk of kidney injury.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor fluid balance and renal function.
  • Beta‑blockers: observe hemodynamic response during cardiac procedures.
  • Thyroid hormone therapy: assess thyroid function after contrast exposure.
  • Anticoagulants: watch for bleeding if invasive imaging is performed.
  • Radiopharmaceuticals: consider cumulative radiation exposure.

Frequently Asked Questions

Iomeron is an iodinated contrast medium used to enhance X‑ray‑based imaging. It improves the visibility of blood vessels, organs and tissues during angiography, computed tomography (CT), urography, cardiac catheterisation and peripheral vascular studies, helping clinicians obtain clearer diagnostic images.

Iomeprol contains iodine atoms that strongly absorb X‑ray photons. After intravenous or intra‑arterial injection, the iodine distributes in the vascular and extracellular spaces, increasing X‑ray attenuation and creating a temporary contrast between blood‑filled structures and surrounding tissues, which sharpens image detail.

The dose of Iomeron is determined by the prescribing physician based on the specific imaging procedure, patient weight, renal function and the required level of contrast. Dosing is individualized and should follow the protocol established by the radiology or interventional team.

Safety data for Iomeron during pregnancy and lactation are limited. It should be used only when clearly necessary, and the potential diagnostic benefit must outweigh any possible risk to the fetus or infant. Clinicians should discuss the decision with the patient and consider alternative imaging strategies when possible.

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 requirements) and the necessary import documentation.

Iomeron (iomeprol) is a non‑ionic, low‑osmolality iodinated contrast medium, offering a favorable safety profile compared with older high‑osmolality agents. Compared with other low‑osmolality agents such as iohexol, iomeprol provides similar image quality but may have slightly lower rates of warmth sensation and mild nausea, though individual responses vary.

Iomeron should be stored at ambient temperature, preferably below 25 °C, protected from direct light and moisture. Keep the solution in its original, sealed container until use. Do not freeze the product, and avoid shaking the vial vigorously to maintain solution integrity.

Iomeron is administered by a qualified healthcare professional as an intravenous or intra‑arterial injection. The injection is typically performed using a power injector or manual bolus, following the dosing protocol set by the radiologist or interventionalist for the specific imaging study.

The most serious risks include severe allergic or anaphylactoid reactions, contrast‑induced nephropathy leading to acute kidney injury, and thyroid dysfunction from the iodine load. Prompt recognition and management of these events are essential, and patients with known risk factors should be closely monitored.

Iomeron should be avoided in patients with a documented hypersensitivity to iomeprol or any iodinated contrast media, those with severe renal impairment (e.g., eGFR < 30 mL/min/1.73 m²) unless benefits outweigh risks, and individuals with uncontrolled hyperthyroidism. Caution is also advised for patients with a history of severe asthma or cardiac instability.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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