Optiray 300

— THERAPEUTIC CATEGORIES —
  • Imaging agents

Optiray 300 Generic Name & Formulations

General Description

Ioversol 636mg/mL; soln for intra-arterial or intravenous inj; contains organically bound iodine 300mg per mL.

Pharmacological Class

Radiopaque contrast agent.

How Supplied

OPTIRAY 300: Bottles (50mL)—25, 100mL, 150mL, 200mL—12, Syringes (100mL)—20, RFID-Tagged syringes (100mL)—20; OPTIRAY 320: Vials (20mL)—25, Bottles (50mL)—25, 100mL, 150mL, 200mL—12, Syringes (50mL, 75mL, 100mL, 125mL)—20, RFID-Tagged syringes (75mL, 100mL, 125mL)—20; OPTIRAY 350: Bottles (50mL)—25, 100mL, 150mL, 200mL—12, Syringes (50mL, 75mL, 100mL, 125mL)—20, RFID-Tagged syringes (100mL, 125mL)—20

Generic Availability

NO

Mechanism of Action

Intravascular injection of ioversol opacifies vessels in the path of the flow of the contrast medium, permitting visualization of the internal structures until significant hemodilution occurs.

Optiray 300 Indications

Indications

Cerebral arteriography. Computed tomography (CT) imaging of the head and body, venography, and intravenous (IV) excretory urography.

Optiray 300 Dosage and Administration

Adult

Individualize. Cerebral arteriography (carotid or vertebral arteries): 2–12mL; (aortic arch inj [four vessel study]): 20–50mL; both: may repeat as necessary; max 200mL. Peripheral arteriography (aortic-iliac runoff): 60mL (range 20–90mL); (common iliac, femoral): 40mL (range 10–50mL); (subclavian, brachial): 20mL (range 15–30mL); all: max 250mL. Venography: 50–100mL per extremity; max 250mL. CT (head): 50–150mL by infusion; (body): may give as 25–75mL bolus inj or 50–150mL by infusion, or combination of both. IV urography (usual dose): 50–75mL; (high dose): 1.6mL/kg; max 150mL.

Children

Not established.

Optiray 300 Contraindications

Contraindications

Symptomatic hyperthyroidism.

Optiray 300 Boxed Warnings

Boxed Warning

Risks with inadvertent intrathecal administration. For intra-arterial and intravenous use only.

Optiray 300 Warnings/Precautions

Warnings/Precautions

Inadvertent intrathecal administration; may cause death, convulsions, cerebral hemorrhage, coma, paralysis, arachnoiditis, acute renal failure, cardiac arrest, seizures, rhabdomyolysis, hyperthermia, and brain edema. History of previous reactions to a contrast agent and known allergies (eg, bronchial asthma, drug, or food) and other hypersensitivities; monitor. Should be administered by professional trained in use of radiopaque agents in appropriate facilities with emergency treatment readily available. Monitor for severe cardiovascular reactions. Risk of serious thromboembolic events (eg, MI, stroke) during angiographic procedures. Avoid angiography with homocystinuria. CHF. Dehydration. Diabetes. Advanced vascular disease. Multiple myeloma or other paraproteinemia. Hyperthyroidism. Autonomous thyroid nodule. Thyroid dysfunction (esp. children 0–3yrs); monitor. Pheochromocytoma or catecholamine-secreting paraganglioma: monitor closely. Homozygous sickle cell disease. History of severe cutaneous adverse reactions (SCAR); avoid. Hepatic or renal impairment. Use lowest effective dose. Maintain adequate hydration. Avoid extravasation. Elderly. Pregnancy. Nursing mothers: consider interrupting, pumping, and discarding breast milk for 8hrs after Optiray.

Optiray 300 Pharmacokinetics

Distribution

  • Ioversol does not bind to protein.

  • Volume of distribution: 0.26 L/kg body weight, consistent with distribution to the extracellular space.

Elimination

  • Renal (>95%).

  • Half-life: 1.5 hours.

  • Peak urine concentration occurs in the first 2 hours after administration.

Optiray 300 Interactions

Interactions

Increased risk of metformin-induced lactic acidosis; discontinue metformin at the time of, or prior to, Optiray in high risk patients (see full labeling). May antagonize radioactive iodine for thyroid carcinoma for up to 6–8wks. Defer in patients with hepatic impairment who recently received oral cholecystographic contrast agents. Caution with concomitant diuretics, nephrotoxic agents. Avoid laxatives, diuretics prior to administration. Protein-bound iodine or radioactive iodine uptake study results may not accurately reflect thyroid function for up to 16 days.

Optiray 300 Adverse Reactions

Adverse Reactions

Nausea; hypersensitivity reactions, acute kidney injury, cardiovascular reactions, SCAR (eg, SJS/TEN, DRESS). Also in children: fever.

Optiray 300 Clinical Trials

See Literature

Optiray 300 Note

Not Applicable

Optiray 300 Patient Counseling

See Literature