Product image of Optiray (Ioversol) supplied by GNH India

Optiray

Active Ingredient:
Ioversol
Origin:
EU

Optiray (Ioversol)

Ioversol, the active ingredient in Optiray, is a non‑ionic iodinated contrast media presented as a sterile solution for intraarterial and intravenous use. It enhances radiographic imaging by increasing X‑ray attenuation of tissues and is employed in diagnostic procedures such as angiography and computed tomography.

GNH India supplies Optiray as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, imaging centres and clinics worldwide, ensuring quality and regulatory compliance across markets. The company provides reliable logistics, temperature‑controlled shipping where required, and comprehensive documentation to meet import and local health authority requirements.

Manufacturer / TM Owner

Guerbet

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Indications & Clinical Uses

Optiray (ioversol) is used as a radiographic contrast agent to improve visualization of vascular and organ structures during imaging procedures.

  • Angiography: enhances visualization of blood vessels to aid diagnosis and interventional procedures.
  • Computed tomography (CT) imaging: provides contrast enhancement for better delineation of anatomical structures.
  • Urography: improves detection of urinary tract abnormalities by highlighting kidneys, ureters, and bladder.
  • Venography: facilitates clear imaging of the venous system for assessment of thrombosis or obstruction.

How It Works

  • Ioversol contains a high density of iodine atoms that absorb X‑ray photons. When administered intravenously or intra‑arterially, the iodine atoms increase the attenuation of X‑rays passing through blood, tissues and organs, creating a temporary difference in radiodensity between vascular structures and surrounding tissues. This contrast enhancement allows radiologists to distinguish anatomical details and pathological changes on fluoroscopic, CT or digital subtraction imaging studies.

Side Effects

Adverse reactions to Optiray are generally related to its iodine content and the physiological response to the injected solution.

Common Side Effects

  • Warmth or flushing sensation at the injection site.
  • Metallic taste in the mouth.
  • Nausea or mild vomiting.
  • Headache or dizziness.

Serious or Rare Side Effects

  • Severe allergic reactions, including anaphylaxis.
  • Acute kidney injury in susceptible patients.
  • Persistent hypotension or cardiovascular collapse.
  • Seizures or neurological disturbances.

Precautions & Warnings

Before administering Optiray, clinicians should evaluate patient-specific factors and follow handling guidelines to minimize risk.

  • Assess renal function: check serum creatinine and eGFR to determine suitability.
  • Review allergy history: identify prior reactions to iodinated contrast agents.
  • Use the lowest effective volume: limit iodine load especially in at‑risk patients.
  • Monitor vital signs: observe blood pressure and heart rate during and after injection.
  • Avoid in patients with known iodine hypersensitivity unless benefits outweigh risks.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Optiray may interact with certain medications, altering safety or efficacy.

Major Interactions (Avoid)

  • Metformin: concurrent use can increase risk of lactic acidosis in renal impairment; discontinue metformin before and after contrast administration.
  • Thyroid hormone preparations: excess iodine may exacerbate hyperthyroidism; monitor thyroid function.
  • Nephrotoxic drugs (e.g., aminoglycosides, amphotericin B): combined use raises risk of renal injury.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask tachycardia associated with contrast reactions.
  • ACE inhibitors or ARBs: can potentiate contrast‑induced nephropathy; consider temporary suspension.
  • Diuretics: may affect fluid balance and renal clearance of iodine.
  • NSAIDs: increase risk of renal dysfunction when combined with contrast.

Frequently Asked Questions

Optiray is a radiographic contrast agent containing ioversol that is used to improve the visibility of blood vessels, organs and urinary structures during imaging studies such as angiography, computed tomography (CT), urography and venography. The enhanced contrast helps radiologists detect abnormalities and guide interventional procedures.

Ioversol works by providing a high concentration of iodine atoms, which strongly absorb X‑ray photons. When injected into the bloodstream, the iodine increases the attenuation of X‑rays in the vessels and tissues it perfuses, creating a temporary difference in radiodensity that makes anatomical structures appear clearer on X‑ray‑based imaging modalities.

The dose of Optiray is individualized by the prescribing physician based on the specific imaging procedure, the patient’s body weight, renal function and the required level of contrast enhancement. No fixed dosing regimen is provided publicly; the healthcare professional calculates the appropriate volume for each case.

The safety of Optiray in pregnancy or while breastfeeding has not been definitively established. Because it contains iodine, which can cross the placenta and be secreted in breast milk, it should only be used when clearly needed and after careful risk‑benefit assessment by the treating physician.

To order Optiray, 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 the necessary import documentation.

Optiray (ioversol) is a low‑osmolality, non‑ionic iodinated contrast medium, which generally offers a lower incidence of discomfort and adverse reactions compared with older high‑osmolality agents. Compared with other low‑osmolality agents, its safety profile and image quality are comparable, while formulation differences may affect viscosity and injection rates.

Optiray should be stored at ambient temperature, preferably below 25 °C, in its original sealed container. It must be protected from direct light, moisture and extreme temperature fluctuations. No refrigeration is required for this injectable solution.

Optiray is administered by a trained healthcare professional either intravenously or intra‑arterially, depending on the imaging study. The solution is injected through a peripheral or central venous line, or directly into an arterial catheter, using a power injector or manual bolus as dictated by the imaging protocol.

The most serious risks include severe allergic reactions such as anaphylaxis, acute kidney injury especially in patients with pre‑existing renal impairment, persistent hypotension or cardiovascular collapse, and rare neurological events like seizures. Prompt recognition and management of these reactions are essential.

Optiray should be avoided in patients with a known hypersensitivity to ioversol or any other iodinated contrast media, in those with uncontrolled hyperthyroidism, and in individuals with severe renal impairment where the risk of contrast‑induced nephropathy outweighs the diagnostic benefit. The prescribing clinician must evaluate each case individually.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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