Product image of Myoview (Tetrofosmin) supplied by GNH India

Myoview

Active Ingredient:
Tetrofosmin
Origin:
EU

Myoview (Tetrofosmin)

Tetrofosmin, the active ingredient in Myoview, is a radiopharmaceutical presented as a 0.5 mg lyophilized kit for intravenous use. It forms a technetium‑99m complex that localises in myocardial cells in proportion to blood flow, allowing single‑photon emission computed tomography (SPECT) to evaluate coronary artery disease, myocardial viability, and stress‑induced perfusion changes in adult patients.

GNH India supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies, clinics and research institutions worldwide through robust quality systems.

Manufacturer / TM Owner

Ge Healthcare Handels Gmbh

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Indications & Clinical Uses

Myoview (technetium‑99m tetrofosmin) is used in cardiac imaging to assess myocardial perfusion.

  • Coronary artery disease detection: Provides SPECT images of myocardial perfusion to identify obstructive lesions.
  • Myocardial viability assessment: Differentiates viable from non‑viable myocardium after infarction.
  • Stress‑test perfusion evaluation: Visualises blood flow changes during pharmacologic or exercise stress testing.

How It Works

  • Tetrofosmin is combined with technetium‑99m to create a lipophilic cationic complex that readily crosses cell membranes and accumulates in myocardial cells in proportion to regional blood flow, enabling high‑resolution SPECT imaging of cardiac perfusion patterns.

Side Effects

Adverse reactions may occur following intravenous administration of Myoview.

Common Side Effects

  • Nausea: Mild to moderate feeling of stomach upset.
  • Headache: Transient discomfort often resolving without intervention.
  • Injection site pain: Local discomfort at the venipuncture site.
  • Flushing: Warm sensation and reddening of the skin.
  • Dizziness: Temporary light‑headedness.

Serious or Rare Side Effects

  • Anaphylactic reaction: Severe allergic response requiring immediate medical attention.
  • Hypotension: Marked drop in blood pressure that may cause fainting.
  • Cardiac arrhythmia: Abnormal heart rhythm potentially leading to hemodynamic compromise.
  • Myocardial infarction: Rare occurrence of heart attack following administration.
  • Radiation‑induced skin injury: Localized skin changes at the injection site.

Precautions & Warnings

Myoview should be used with consideration of patient‑specific factors and handling requirements.

  • Pregnancy: Use only if the potential diagnostic benefit outweighs unknown fetal risk.
  • Breastfeeding: Discontinue nursing or withhold the drug until sufficient time has passed for clearance.
  • Renal impairment: Monitor patients with reduced kidney function as clearance may be altered.
  • Thyroid disorders: Caution in patients with hyperthyroidism due to possible iodine uptake interference.
  • Concomitant radiopharmaceuticals: Avoid simultaneous use of other technetium‑99m agents to prevent labeling competition.
  • Store at ambient temperature: Keep in original packaging, protect from light and moisture.

Avoid Interactions

Myoview may interact with other agents that affect radiotracer distribution or cardiac physiology.

Major Interactions (Avoid)

  • Concurrent technetium‑99m labeled agents: Can compete for labeling and reduce image quality.
  • High‑dose iodine contrast within 24 h: May interfere with myocardial uptake of the tracer.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: May blunt heart rate response during stress testing.
  • Calcium channel blockers: Can alter myocardial blood flow and affect perfusion images.
  • Thyroid hormone therapy: May influence radiotracer distribution in thyroid tissue.

Frequently Asked Questions

Myoview is a radiopharmaceutical used in single‑photon emission computed tomography (SPECT) to image myocardial perfusion. It helps clinicians detect coronary artery disease, assess myocardial viability after infarction, and evaluate blood flow changes during pharmacologic or exercise stress testing.

Tetrofosmin forms a technetium‑99m complex that is lipophilic and positively charged. After intravenous injection, the complex diffuses across cell membranes and accumulates in heart muscle cells proportionally to regional blood flow, allowing high‑resolution SPECT images of perfusion patterns.

The prescribed dose of Myoview is determined by the ordering physician based on the specific imaging protocol. The product is supplied as a lyophilized kit containing 0.5 mg tetrofosmin, which is reconstituted with technetium‑99m immediately before intravenous administration.

Safety data for Myoview in pregnancy are limited, so it should only be used when the diagnostic benefit justifies potential fetal exposure. Breastfeeding mothers should discontinue nursing or stop the drug until an appropriate clearance period has elapsed, as advised by a healthcare professional.

To order Myoview, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.

Myoview (technetium‑99m tetrofosmin) offers rapid myocardial uptake and a favorable imaging window, similar to technetium‑99m sestamibi but with slightly higher liver clearance, which can improve early image quality. Compared with thallium‑201, tetrofosmin provides lower radiation dose and better image resolution.

Myoview should be stored at ambient temperature, protected from light and moisture, and kept in its original sealed packaging until reconstitution. The lyophilized kit remains stable until it is mixed with technetium‑99m, after which it must be used promptly according to the manufacturer’s instructions.

Myoview is administered intravenously after reconstitution with technetium‑99m. The prepared solution is injected as a single bolus, typically followed by a short waiting period to allow myocardial uptake before SPECT image acquisition.

Serious risks include anaphylactic reactions, severe hypotension, cardiac arrhythmias, and, rarely, myocardial infarction. Because the product contains a radioactive tracer, radiation exposure is also a consideration, though it is generally low and within diagnostic limits.

Myoview is contraindicated in patients with known severe allergic reactions to tetrofosmin or any component of the kit, and in those who have received other technetium‑99m labeled agents within a short interval that could compromise image quality. Caution is advised for patients with uncontrolled thyroid disease or severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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