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Vizinect®

Patient Details

Vizinect®

Generic Name: Iodixanol
Iodine Content: 320 mg/mL
Dosage Forms: 20 mL, 50 mL, and 100 mL vials


1. What is Vizinect® and its Uses?

Vizinect® is an isotonic aqueous solution containing iodixanol, a non-ionic, dimeric contrast agent.

Indications in Adults:

  • Cardiac angiography

  • Cerebral angiography

  • Peripheral arteriography

  • Abdominal angiography (e.g., DSA)

  • Urography and venography

  • CT enhancement

  • Upper gastrointestinal tract studies

  • Arthrography and hysterosalpingography (HSG)

  • Spinal, chest, and cervical imaging

Indications in Children:

  • Cardiac angiography

  • Urography

  • CT enhancement

  • Upper gastrointestinal tract studies


2. Before Using Vizinect®

Contraindications:

  • Hypersensitivity to iodixanol or any component of the formulation

  • Thyrotoxicosis

  • Intrathecal administration (not approved)

Warnings & Precautions:

  • Allergy or asthma history: Use caution; premedication with corticosteroids or H1/H2 antagonists may be considered.

  • Risk of severe hypersensitivity reactions, including anaphylaxis; emergency medications and equipment should be available. Monitor patients closely for at least 30 minutes post-injection.

  • Thromboembolic events: Rarely, serious events such as myocardial infarction or stroke may occur. Proper catheter technique and hydration are essential.

  • Dehydration: Can lead to kidney injury, particularly in elderly, diabetic, or patients with multiple myeloma or renal impairment. Ensure adequate hydration before and after injection.

  • Cardiovascular or cerebrovascular disease: Use caution in patients with acute stroke, intracranial bleeding, altered blood-brain barrier, cerebral edema, or demyelinating disease.

  • Renal or hepatic impairment: Clearance of iodixanol may be significantly reduced; close monitoring required.

  • Metformin use: Suspend metformin at the time of contrast administration and for 48 hours afterward. Restart only after renal function is re-evaluated.

  • Special populations: Patients with hyperthyroidism, sickle cell disease, severe heart disease, pulmonary hypertension, atherosclerosis, seizure disorders, myasthenia gravis, or pheochromocytoma require special precautions.

Drug Interactions:

  • Loop diuretics: May increase nephrotoxicity risk

  • Metformin: Risk of lactic acidosis due to contrast-induced renal impairment

  • Radioactive iodine (I-123, I-131): Contrast may interfere with thyroid uptake for 6–8 weeks

  • Beta-blockers: May increase risk of hypersensitivity reactions

Pregnancy & Breastfeeding:

  • Safety not established in pregnancy; use only if benefits outweigh risks

  • Iodixanol is minimally excreted in breast milk; breastfeeding can usually continue

  • Neonatal thyroid function should be monitored after maternal contrast exposure

Pediatrics:

  • Safe in children >1 year for arterial and IV studies

  • Safety data for <1 year limited; close monitoring required in high-risk infants

  • Increased risk in children with kidney impairment, dehydration, asthma, or cyanotic/non-cyanotic heart disease

Elderly:

  • No major differences in safety compared to younger adults, but use caution due to possible comorbidities and organ dysfunction

Driving & Operating Machinery:

  • Avoid for 1 hour post-injection


3. Administration & Dosage

General Instructions:

  • Hydrate well before and after the procedure to minimize kidney risk

  • Not for intrathecal use; IV only

  • Dose, concentration, and injection rate adjusted for patient age, weight, vessel size, flow rate, and imaging technique

  • Warm to room or body temperature before injection

  • Avoid extravasation, especially in severe vascular disease

  • Injection rate should approximate normal blood flow

  • Do not mix with other drugs or nutrition lines

  • Dose tailored for optimal imaging of target vessels

Dosage:

  • Adults and children: Depends on procedure, age, weight, cardiac output, patient condition, and imaging technique

Overdose:

  • Rare; treat symptomatically

  • Maintain hydration and electrolytes

  • Monitor renal function for at least 3 days

  • Hemodialysis may be required to remove iodixanol


4. Side Effects

Common:

  • Discomfort, warmth, or pain at injection site

Less common:

  • Angina, chest pain, headache, migraine, dizziness, altered smell, paresthesia, rash, itching, taste changes, nausea

Severe hypersensitivity (rare):

  • Respiratory or skin reactions, angioedema, hypotension, fever, laryngeal edema, bronchospasm, pulmonary edema

  • Autoimmune patients: rare vasculitis or Stevens–Johnson-like syndrome

Procedure-specific common reactions:

  • HSG: abdominal pain, vaginal bleeding, headache, nausea, fever

  • Arthrography: injection site pain

  • GI: diarrhea, abdominal pain, nausea


5. Storage

  • Store below 30°C, protected from light and moisture, in the original box

  • Single-use only; discard any remaining solution

  • Keep out of reach of children

  • Do not use expired product


References

  1. GE Healthcare Visipaque PDF

  2. FDA Label Visipaque

  3. UpToDate 2023