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, intraarticular and intrathecal use. It increases X‑ray attenuation, allowing clearer visualization of vascular and tissue structures during radiographic procedures.\n\nGNH 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 S.P.A.

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Indications & Clinical Uses

  • Iomeron is used in diagnostic imaging procedures that require enhanced vascular and tissue contrast.\n\n- Angiography: improves delineation of arterial and venous anatomy.\n- CT angiography: provides high‑resolution images of blood vessels in the head, neck and body.\n- Arthrography: enhances joint space visualization for orthopedic assessment.\n- Myelography: clarifies spinal canal structures during contrast‑enhanced studies.\n- Contrast‑enhanced CT of abdomen, pelvis and thorax: highlights organs and lesions for accurate diagnosis.

How It Works

  • Iomeprol supplies a high iodine content that absorbs X‑ray photons, thereby increasing attenuation of the X‑ray beam in the vascular and tissue compartments where it is administered. This heightened attenuation creates a contrast difference between enhanced structures and surrounding tissues, allowing radiologists to distinguish anatomical details and pathological changes during imaging examinations.

Side Effects

  • Adverse reactions may occur after administration of Iomeron.\n\nCommon Side Effects:\n- Warmth or flushing sensation at the injection site.\n- Metallic taste in the mouth.\n- Nausea or mild vomiting.\n- Transient headache.\n\nSerious or Rare Side Effects:\n- Anaphylactic or severe allergic reaction.\n- Acute renal impairment, especially in patients with pre‑existing kidney disease.\n- Hypotension or cardiovascular collapse.\n- Seizures or neurologic disturbances.\n- Pulmonary edema or severe respiratory distress.

Precautions & Warnings

  • Prior to using Iomeron, clinicians should consider several safety measures.\n\n- Renal function assessment: evaluate serum creatinine and eGFR.\n- Iodine allergy review: screen for previous contrast reactions.\n- Hydration: ensure adequate patient hydration before and after injection.\n- Dose minimisation: use the lowest effective volume for the intended study.\n- Thyroid monitoring: be aware of potential iodine‑induced thyroid dysfunction.\n- Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

  • Iomeron may interact with other medicines that affect renal function or iodine handling.\n\nMajor Interactions (Avoid):\n- Metformin: risk of lactic acidosis in patients with impaired renal function after contrast exposure.\n- Thyroid hormone therapy: excess iodine can alter thyroid hormone levels.\n\nModerate Interactions (Monitor Closely):\n- NSAIDs and other nephrotoxic drugs: increase risk of contrast‑induced nephropathy.\n- Diuretics: may exacerbate volume depletion and renal impairment.\n- Aminoglycoside antibiotics: additive renal toxicity potential.\n- Radiopharmaceutical iodine: cumulative iodine load may affect thyroid function.

Frequently Asked Questions

Iomeron is an iodinated contrast agent used to improve the visibility of blood vessels, organs and tissues during imaging procedures such as angiography, CT angiography, arthrography, myelography and contrast‑enhanced CT scans of the abdomen, pelvis and thorax.

Iomeprol contains a high concentration of iodine atoms that absorb X‑ray photons. When injected, it increases the attenuation of the X‑ray beam in the area where it circulates, creating a clear contrast between enhanced structures and surrounding tissues for detailed radiographic imaging.

The dose of Iomeron is individualized by the prescribing radiologist or physician based on the specific imaging study, patient size, renal function and the required level of contrast enhancement. Exact dosing is determined at the point of care.

Iomeron is classified as Pregnancy Category B, indicating that animal studies have not shown risk to the fetus and there are no adequate human studies. It should only be used if clearly needed, and breastfeeding mothers should discuss potential risks with their healthcare provider.

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 cold‑chain if required) and necessary import documentation.

Iomeron (Iomeprol) offers a high iodine concentration with a low osmolality profile, which can reduce the incidence of discomfort and adverse reactions compared with older high‑osmolality agents. Its safety and imaging performance are comparable to other modern low‑osmolality iodinated contrast media.

Iomeron should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the solution from moisture, direct sunlight and extreme temperatures. Do not freeze or shake the vial before use.

Iomeron is supplied as a sterile solution for injection and is administered intravenously, intra‑arterially, intra‑articularly or intrathecally by a qualified healthcare professional, following the imaging protocol for the specific diagnostic procedure.

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

Iomeron should be avoided in patients with known hypersensitivity to iodinated contrast media, uncontrolled severe renal insufficiency, active thyroid disease requiring iodine restriction, or in those who have had a recent severe reaction to another contrast agent. Clinical judgment is essential.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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