Product image of Imeron (Iomeprol) supplied by GNH India

Imeron

Active Ingredient:
Iomeprol
Origin:
EU

Imeron (Iomeprol)

Iomeprol, the active ingredient in Imeron, is an iodinated contrast agent presented as a 350 mg I/mL injection solution for intravenous use. It enhances radiographic imaging in diagnostic procedures such as computed tomography, angiography, urography and venography. It is indicated for use in adult and pediatric patients undergoing contrast‑enhanced imaging, where improved delineation of vascular and organ structures is required.

GNH India supplies Imeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company ensures consistent quality, regulatory compliance and reliable logistics for global distribution.

Manufacturer / TM Owner

Eurocontrast Gmbh

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Indications & Clinical Uses

Imeron (iomeprol) is an iodinated contrast agent used to improve X‑ray based imaging across several diagnostic procedures, delivering superior contrast enhancement and facilitating accurate clinical interpretation.

  • Contrast‑enhanced computed tomography: provides high‑contrast images of vascular and organ structures, aiding diagnosis.
  • Angiography: delineates blood vessels with enhanced radiopacity for accurate assessment and interventional planning.
  • Urography: enhances visualization of the urinary tract, facilitating detection of obstructions or lesions.
  • Venography: improves detection of venous pathology by increasing contrast between veins and surrounding tissues.

How It Works

  • After intravenous injection, iomeprol distributes rapidly within the extracellular fluid and vascular compartments. The molecule contains a high density of iodine atoms, each of which strongly absorbs X‑ray photons. This increased attenuation creates a radiopaque effect, making blood‑filled structures appear brighter on X‑ray, CT or fluoroscopic images. As a non‑ionic, low‑osmolality agent, iomeprol minimizes protein binding and reduces the risk of osmotic‑related adverse reactions while providing consistent image contrast.

Side Effects

Imeron may be associated with a range of adverse reactions following intravenous administration.

Common Side Effects

  • Warm sensation or flushing: transient feeling of heat or skin reddening.
  • Nausea or vomiting: mild gastrointestinal upset occurring shortly after injection.
  • Headache: temporary discomfort that usually resolves without treatment.
  • Mild urticaria or itching: limited skin rash that subsides spontaneously.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response that can include airway obstruction and shock.
  • Acute renal impairment: sudden decrease in kidney function, particularly in at‑risk patients.
  • Cardiovascular collapse: profound hypotension or arrhythmia requiring immediate medical intervention.

Precautions & Warnings

Before using Imeron, clinicians should observe several precautionary measures to reduce the risk of adverse events.

  • Assess renal function: evaluate serum creatinine and eGFR to determine suitability.
  • Review iodine allergy history: identify prior reactions to iodinated contrast media.
  • Ensure adequate hydration: encourage fluid intake before and after the procedure.
  • 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.
  • Store at ambient temperature: keep vials in original packaging, protect from light and moisture, and do not freeze.

Avoid Interactions

Imeron can interact with certain medications, influencing safety or efficacy.

Major Interactions (Avoid)

  • Cumulative iodine load: avoid concurrent use of other iodinated contrast agents.
  • Metformin in renal impairment: risk of lactic acidosis; consider temporary discontinuation.
  • Nephrotoxic drugs: concurrent aminoglycosides, NSAIDs or radiopharmaceuticals may increase kidney injury risk.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask tachycardia signs of contrast reaction.
  • Diuretics: can affect fluid balance and enhance renal stress.
  • Thyroid hormone therapy: excess iodine may alter thyroid function tests.

Frequently Asked Questions

Imeron is an iodinated contrast agent employed in diagnostic imaging procedures such as contrast‑enhanced computed tomography, angiography, urography and venography. By increasing the radiopacity of blood and extracellular fluid, it helps clinicians obtain clearer images of vascular and organ structures, facilitating accurate diagnosis and treatment planning.

Iomeprol contains a high concentration of iodine atoms that strongly absorb X‑ray photons. After intravenous injection, the compound distributes throughout the vascular and extracellular spaces, creating a radiopaque effect that makes blood‑filled structures appear brighter on X‑ray, CT or fluoroscopic images, thereby enhancing contrast between tissues.

The dose of Imeron is determined by the prescribing physician based on the specific imaging study, patient weight, renal function and the required level of contrast. The healthcare professional selects the appropriate volume and concentration for each procedure, ensuring optimal image quality while minimizing risk.

The safety of Imeron during pregnancy and lactation has not been established. It should be used only when the potential diagnostic benefit outweighs any possible risk to the fetus or infant, and the decision must be made by the treating physician after careful consideration of available alternatives.

To place an order, 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 necessary import documentation.

Imeron (iomeprol) is a non‑ionic, low‑osmolality iodinated contrast medium, offering a favorable safety profile compared with high‑osmolality agents. Its iodine concentration of 350 mg I/mL provides image enhancement comparable to other low‑osmolality agents, while its lower viscosity and osmolality are designed to reduce discomfort and adverse reactions.

Store at ambient temperature: keep the vials in the original packaging, protect from direct sunlight, moisture and extreme temperatures. Do not freeze the solution. Inspect the container for particulate matter before use and discard if the solution is discolored or cloudy.

Imeron is supplied as an injectable solution for intravenous use. It is typically administered through a peripheral or central venous line using a power injector or manual bolus, according to the imaging protocol. The injection rate and volume are set by the radiology team to achieve optimal contrast enhancement.

The most serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, and significant hypotension or cardiovascular collapse. Prompt recognition and emergency treatment are essential if these events occur.

Imeron should be avoided in patients with a known hypersensitivity to iodinated contrast media, a history of severe allergic reactions to similar agents, uncontrolled thyroid disease, or severe renal insufficiency where alternative imaging methods are feasible. The prescribing clinician must evaluate each patient’s risk before administration.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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