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Visipaque 270 (IODIXANOL)

GE HealthCare · FDA-approved approved

Visipaque 270 works by increasing the density of fluids in the body, making them visible on X-ray images.

Visipaque 270 (iodixanol) is a radiographic contrast agent developed by GE Healthcare, currently owned by the same company. It is a small molecule drug used to enhance the visibility of internal structures during medical imaging procedures. Visipaque 270 is off-patent and has a generic manufacturer. It has a half-life of 2.1 hours and was FDA-approved in 1996. The exact target of Visipaque 270 is unknown.

At a glance

Generic nameIODIXANOL
SponsorGE HealthCare
Drug classRadiographic Contrast Agent
Therapeutic areaHematology
PhaseFDA-approved
First approval1996

Mechanism of action

Intravascular injection of iodixanol opacifies vessels in the path of flow of the contrast agent, permitting visualization of internal structures.In imaging of the body, iodinated contrast agents diffuse from the vascular into the extravascular space. In normal brain with an intact blood-brain barrier, contrast does not diffuse into the extravascular space. In patients with disrupted blood-brain barrier, contrast agent accumulates in the interstitial space in the region of disruption.

Approved indications

No approved indications tracked.

Boxed warnings

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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