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 an injection solution for intraarterial and intravenous use. It is marketed in the EU as a diagnostic radiographic contrast medium that increases X‑ray attenuation of blood and tissues, thereby improving visualization of vascular structures and organs during imaging studies.

GNH India supplies Imeron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bracco Imaging Deutschland Gmbh

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Indications & Clinical Uses

Imeron (iomeprol) is used in diagnostic imaging procedures that require vascular or organ contrast enhancement.

  • Angiography: provides enhanced visualization of blood vessels for accurate assessment.
  • Computed tomography (CT) imaging: improves delineation of anatomical structures and lesions.
  • Urography: highlights urinary tract anatomy for better diagnostic interpretation.
  • Contrast‑enhanced magnetic resonance imaging (MRI) (off‑label): offers supplementary contrast when required.
  • Other diagnostic imaging procedures requiring vascular or organ contrast: facilitates clearer imaging across various modalities.

How It Works

  • Iomeprol contains a high concentration of iodine atoms that absorb X‑ray photons more effectively than surrounding tissues. After intraarterial or intravenous injection, the agent distributes within the vascular and extracellular compartments, increasing the attenuation of X‑rays and thereby creating a contrast between blood‑filled structures and adjacent tissues. This enhanced attenuation allows radiologists to differentiate anatomical details and pathological changes during imaging studies.

Side Effects

Imeron may cause a range of adverse reactions following administration.

Common Side Effects

  • Warmth or flushing sensation during injection.
  • Metallic taste or mild nausea.
  • Headache or mild dizziness.
  • Transient injection site discomfort.
  • Mild vomiting.

Serious or Rare Side Effects

  • Severe allergic reactions, including anaphylaxis.
  • Acute kidney injury, especially in patients with pre‑existing renal impairment.
  • Hypotension or cardiovascular collapse.
  • Seizures or neurologic disturbances.
  • Life‑threatening pulmonary edema.

Precautions & Warnings

Prior to using Imeron, clinicians should consider several safety measures.

  • Assess renal function: evaluate serum creatinine and eGFR before administration.
  • Review allergy history: identify prior reactions to iodinated contrast agents.
  • Use the lowest effective dose: tailor volume to the specific imaging protocol.
  • Monitor vital signs: observe patients during and after injection for adverse events.
  • Avoid in patients with known severe iodine allergy: consider alternative imaging methods.
  • Store at ambient temperature: keep in original container, protect from light, and do not freeze.

Avoid Interactions

Imeron may interact with other medications, requiring careful management.

Major Interactions (Avoid)

  • Concurrent use of multiple iodinated contrast agents: increases total iodine load and risk of toxicity.
  • Co‑administration with nephrotoxic drugs (e.g., aminoglycosides, NSAIDs): may exacerbate renal impairment.
  • Use with high‑dose beta‑blockers: can mask contrast‑induced hypertension.

Moderate Interactions (Monitor Closely)

  • Combination with diuretics: may affect fluid balance and renal clearance.
  • Metformin therapy in patients with reduced renal function: temporary discontinuation recommended.
  • Anticoagulants: monitor for bleeding if contrast‑induced renal dysfunction occurs.

Frequently Asked Questions

Imeron is an iodinated contrast agent used to enhance the visibility of blood vessels and internal organs during diagnostic imaging procedures such as angiography, computed tomography (CT) scans, urography, and certain off‑label MRI studies.

Iomeprol contains iodine atoms that strongly absorb X‑ray photons. When injected, it distributes in the vascular and extracellular spaces, increasing X‑ray attenuation of blood and tissues, which creates a clear contrast between structures on the resulting images.

The dose of Imeron is determined by the prescribing physician based on the specific imaging protocol, patient size, and the diagnostic requirement. It is administered as an injection solution under controlled clinical conditions.

Safety of Imeron in pregnancy and lactation has not been established. It should only be used when clearly needed and after a careful risk‑benefit assessment by the healthcare provider.

To order Imeron, submit an enquiry on the product page at gnhindia.com with 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 import documentation.

Imeron (iomeprol) is a non‑ionic, low‑osmolality iodinated contrast medium, offering a favorable safety profile compared with older high‑osmolality agents. It provides comparable image quality while reducing the incidence of discomfort and adverse reactions.

Imeron should be stored at ambient temperature, protected from light, and kept in its original packaging. It must not be frozen or shaken vigorously to maintain solution integrity.

Imeron is administered by a trained healthcare professional as an intra‑arterial or intravenous injection. The volume and rate are adjusted according to the imaging study protocol and patient characteristics.

Serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, and cardiovascular events like hypotension or pulmonary edema. Immediate medical attention is required if these occur.

Imeron should be avoided in patients with a known severe allergy to iodinated contrast media, those with uncontrolled hyperthyroidism, and individuals with significant renal dysfunction unless the diagnostic benefit outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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