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 sterile solution for injection for intra‑arterial, intrathecal, and intravenous use. It enhances radiographic imaging by providing radiodense contrast that improves visualization of vascular and tissue structures during diagnostic procedures.

GNH India supplies Iomeron 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

Iomeron, an iodinated contrast agent, is used in imaging procedures that require enhanced visualization of vascular and tissue structures.

  • Angiography: provides high‑contrast images of blood vessels to aid diagnosis and interventional planning.
  • Computed Tomography (CT) imaging: improves delineation of organs and lesions for accurate assessment.
  • Myelography: enhances cerebrospinal fluid spaces to facilitate evaluation of spinal pathology.

How It Works

  • Iomeprol contains multiple iodine atoms that strongly attenuate X‑ray photons. After injection, the iodine increases the radiodensity of blood vessels and tissues, creating a clear contrast between structures on X‑ray‑based imaging modalities such as CT, angiography, and myelography, thereby improving diagnostic detail.

Side Effects

Adverse reactions to Iomeron may range from mild to severe and should be monitored during and after administration.

Common Side Effects

  • Warm sensation or flushing at the injection site.
  • Nausea or vomiting.
  • Transient headache.
  • Metallic taste in the mouth.

Serious or Rare Side Effects

  • Severe allergic reaction or anaphylaxis.
  • Contrast‑induced nephropathy leading to acute kidney injury.
  • Cardiovascular collapse or severe hypotension.
  • Seizures or neurological disturbances.
  • Pulmonary edema or respiratory distress.

Precautions & Warnings

Prior to using Iomeron, clinicians should consider several safety measures to minimize risk.

  • Assess renal function: evaluate serum creatinine and eGFR before administration.
  • Screen for iodine or contrast media allergy: obtain detailed allergy history.
  • Use the lowest effective dose: tailor volume to patient size and imaging requirement.
  • Monitor vital signs: observe for reactions during and after injection.
  • Avoid in uncontrolled hyperthyroidism: iodine load may exacerbate thyroid activity.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Iomeron may interact with certain medications, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Thyroid hormone therapy: may increase risk of hyperthyroid crisis.
  • Metformin: risk of lactic acidosis in patients with renal impairment.
  • Loop diuretics: can potentiate renal toxicity.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may affect renal hemodynamics.
  • NSAIDs: increase risk of contrast‑induced nephropathy.
  • Calcium channel blockers: monitor blood pressure changes during injection.

Frequently Asked Questions

Iomeron is a diagnostic radiographic contrast agent containing iomeprol, employed to enhance visualization during imaging procedures such as angiography, computed tomography (CT) scans, and myelography, allowing clinicians to better assess vascular anatomy and cerebrospinal fluid spaces.

Iomeprol consists of iodine atoms that strongly absorb X‑ray photons. When injected, it increases the radiodensity of blood vessels and tissues, creating a clear contrast between structures on X‑ray‑based imaging modalities, thereby improving diagnostic accuracy.

The specific dose of Iomeron is determined by the prescribing physician based on the imaging study, patient weight, renal function, and the route of administration. Dosage calculations are individualized and should follow the relevant clinical guidelines.

Safety data for Iomeron in pregnancy and lactation are limited. It should only be used when clearly needed and after careful risk‑benefit assessment by the healthcare provider. Breastfeeding mothers should discuss potential exposure with their clinician.

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.

Iomeron (iomeprol) is a non‑ionic, low‑osmolality contrast medium, offering a favorable safety profile compared with older high‑osmolality agents. Its viscosity and iodine concentration provide high image quality while reducing the incidence of discomfort and adverse reactions relative to some alternative agents.

Iomeron should be stored at controlled room temperature, preferably below 25 °C, in its original sealed container. Protect the solution from direct sunlight, moisture and extreme temperature fluctuations. Do not freeze or shake the vial before use.

Iomeron is supplied as a sterile solution for injection and is administered intravenously, intra‑arterially, or intrathecally by a qualified healthcare professional. The injection rate and volume are adjusted according to the specific imaging protocol and patient characteristics.

The most serious risks include severe allergic reactions such as anaphylaxis, contrast‑induced nephropathy leading to acute kidney injury, and rare events like seizures or cardiovascular collapse. Prompt recognition and emergency management are essential if these reactions occur.

Iomeron is contraindicated in patients with known hypersensitivity to iomeprol or other iodinated contrast agents, those with uncontrolled hyperthyroidism, and individuals with severe renal impairment where alternative imaging strategies are preferred. Clinical judgment should guide use in other high‑risk populations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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