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 iodinated contrast media presented as a solution for injection for intraarterial, intraarticular, and intravenous use. It enhances radiographic imaging of vascular and joint structures in patients undergoing angiography, arthrography, CT, or other diagnostic procedures. It is marketed in the European Union and conforms to EU pharmacopoeial standards.

GNH India supplies Iomeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, imaging centres, diagnostic laboratories, and clinics worldwide, with a focus on quality assurance and regulatory compliance.

Manufacturer / TM Owner

Bracco Imaging S.P.A.

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Indications & Clinical Uses

Iomeron (iomeprol) is an iodinated contrast agent used to improve radiographic visualization of vascular and joint structures.

  • Angiography: Provides high‑contrast images of blood vessels to support diagnosis and interventional procedures.
  • Arthrography: Enhances joint space visualization, facilitating assessment of cartilage, ligaments, and intra‑articular pathology.
  • CT imaging: Increases tissue attenuation differences, allowing detailed cross‑sectional images of organs and vessels.
  • Vascular imaging: Improves delineation of arterial and venous anatomy during fluoroscopic and CT angiographic studies.

How It Works

  • Iomeprol is a non‑ionic, low‑osmolality iodinated contrast medium. Each molecule contains multiple iodine atoms that strongly absorb X‑ray photons, raising the radiodensity of the extracellular fluid and tissues into which it distributes. After intra‑arterial, intra‑articular, or intravenous administration, the agent rapidly equilibrates in the vascular and interstitial compartments, creating a pronounced contrast between blood vessels, organs, and surrounding structures on CT or fluoroscopic imaging.

Side Effects

Iomeron may be associated with a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Warm sensation or flushing: transient feeling of heat during injection.
  • Nausea or vomiting: mild gastrointestinal upset that usually resolves quickly.
  • Urticaria or mild skin rash: temporary itching or hives.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response that can be life‑threatening.
  • Acute renal impairment: sudden decrease in kidney function, particularly in patients with pre‑existing renal disease.
  • Severe hypotension or shock: marked drop in blood pressure requiring medical intervention.

Precautions & Warnings

Prior to administering Iomeron, several precautionary measures should be observed to minimize risk.

  • Assess renal function: evaluate serum creatinine and eGFR before use.
  • Review allergy history: check for prior reactions to iodinated contrast or iodine‑containing substances.
  • Use lowest effective dose: tailor volume to the specific imaging study.
  • Monitor vital signs: observe blood pressure, heart rate, and oxygen saturation during and after injection.
  • Avoid in known iodine hypersensitivity: contraindicated in patients with documented severe allergy to iodinated agents.
  • Store at ambient temperature: keep in original container, protect from moisture and direct light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent use of other iodinated contrast agents: cumulative iodine load may increase risk of toxicity.
  • Co‑administration with nephrotoxic drugs (e.g., aminoglycosides, NSAIDs): may exacerbate renal impairment.

Moderate Interactions (Monitor Closely)

  • Diuretics: may alter renal clearance of the contrast medium, requiring hydration monitoring.
  • Metformin: in patients with reduced kidney function, temporary discontinuation is advised to prevent lactic acidosis.
  • Thyroid medications: excess iodine can affect thyroid hormone synthesis, necessitating thyroid function monitoring.

Frequently Asked Questions

Iomeron is an iodinated contrast medium containing iomeprol. It is administered during radiographic procedures such as angiography, arthrography, computed tomography (CT) scans, and other vascular imaging studies to improve the visibility of blood vessels, joints, and organ structures.

Iomeprol works by providing a high concentration of iodine atoms that absorb X‑ray photons. When injected, it distributes in the vascular and interstitial spaces, increasing the radiodensity of those tissues and creating a clear contrast between vessels, organs, and surrounding structures on imaging modalities.

The dose of Iomeron is individualized by the prescribing physician based on the specific imaging study, patient size, renal function, and the route of administration. Healthcare professionals calculate the appropriate volume and concentration to achieve optimal image quality while minimizing risk.

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 recommended before administration to pregnant or nursing patients.

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. After submission, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details (including any cold‑chain requirements), 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. Compared with other low‑osmolality agents such as iohexol or iopamidol, iomeprol provides similar image quality while generally causing fewer discomfort‑related reactions, though individual patient factors influence the choice of agent.

Iomeron should be stored at ambient temperature, preferably below 25 °C. Keep the vial in its original packaging, protect it from direct sunlight, moisture, and extreme temperature fluctuations. Do not freeze the solution, and inspect the container for any particulate matter before use.

Iomeron is supplied as a sterile solution for injection and may be administered intra‑arterially, intra‑articularly, or intravenously, depending on the imaging procedure. The injection is typically performed by a qualified radiology or interventional specialist using aseptic technique, with the volume and rate adjusted to the specific diagnostic requirement.

The most serious risks include severe allergic reactions such as anaphylaxis, acute renal impairment especially in patients with pre‑existing kidney disease, and profound hypotension or shock that may require emergency medical intervention. Prompt recognition and appropriate management are essential if any of these events occur.

Iomeron is contraindicated in patients with a known severe hypersensitivity to iodinated contrast media or iodine‑containing substances. Caution is also advised for individuals with compromised renal function, uncontrolled thyroid disease, or a history of severe adverse reactions to contrast agents. The prescribing clinician should evaluate each patient’s medical history before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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