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 an injection kit for intravenous use. It enables myocardial perfusion imaging to assess coronary artery disease in adult patients, providing clinicians with functional information on regional blood flow. The product is authorized in the European Union and is used under physician supervision for diagnostic cardiac procedures.

GNH India supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with strict quality assurance and regulatory support.

Manufacturer / TM Owner

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Indications & Clinical Uses

  • Myoview (tetrofosmin) is used in cardiac imaging to evaluate myocardial blood flow.
  • Myocardial perfusion imaging (SPECT): Provides visual assessment of regional myocardial blood flow to detect perfusion defects.
  • Coronary artery disease evaluation: Helps identify areas of reduced perfusion indicative of obstructive coronary lesions.
  • Myocardial viability assessment: Differentiates viable from scarred myocardium to guide revascularization decisions.

How It Works

  • Tetrofosmin is a lipophilic cation that readily crosses cell membranes and is taken up by viable myocardial cells in proportion to regional blood flow. After intravenous injection, it accumulates in the mitochondria of perfused myocardium, allowing single‑photon emission computed tomography (SPECT) to generate images that reflect relative perfusion across the heart. The tracer’s rapid clearance from non‑cardiac tissues enhances contrast, and its physical half‑life permits imaging within minutes of administration.

Side Effects

Adverse reactions to Myoview are generally infrequent but may occur following intravenous administration.

Common Side Effects

  • Injection site pain: mild discomfort at the site of administration.
  • Nausea: transient feeling of queasiness.
  • Headache: mild to moderate headache.

Serious or Rare Side Effects

  • Allergic reaction: urticaria, bronchospasm, or anaphylaxis requiring immediate medical attention.
  • Cardiac arrhythmia: rare occurrence of rhythm disturbances during imaging.
  • Radiation exposure: low‑level ionizing radiation with cumulative risk, monitored per regulatory limits.

Precautions & Warnings

When using Myoview, clinicians should observe specific precautions to ensure patient safety and product integrity.

  • Patient selection: verify indication and assess for known hypersensitivity to tetrofosmin or similar agents.
  • Renal function: consider reduced clearance in severe renal impairment.
  • Thyroid status: avoid use in patients with uncontrolled hyperthyroidism due to iodine content.
  • Concurrent imaging agents: schedule sufficient interval after other radiopharmaceuticals to prevent interference.
  • Pregnancy and lactation: weigh potential risks versus benefits; use only if clearly justified.
  • Store at ambient temperature: keep below 25°C, in original packaging, protected from moisture and light.

Avoid Interactions

Myoview may interact with certain drugs or substances that affect its distribution, clearance, or imaging interpretation.

Major Interactions (Avoid)

  • Beta‑blockers: may alter myocardial blood flow and affect image interpretation.
  • Calcium channel blockers: can modify coronary vasomotor tone, influencing tracer uptake.
  • Thyroid hormones: excess may compete with radiotracer uptake.

Moderate Interactions (Monitor Closely)

  • Other radiopharmaceuticals: overlapping radiation dose requires timing adjustments.
  • Contrast agents used in CT: may interfere with subsequent SPECT imaging if administered too soon.
  • Caffeine‑containing products: can affect myocardial perfusion and should be avoided before the test.

Frequently Asked Questions

Myoview is a radiopharmaceutical used for myocardial perfusion imaging with single‑photon emission computed tomography (SPECT). It helps clinicians assess regional blood flow in the heart, detect perfusion defects, evaluate coronary artery disease, and determine myocardial viability for treatment planning.

Tetrofosmin is a lipophilic cation that crosses cell membranes and is taken up by viable myocardial cells in proportion to blood flow. After intravenous injection it accumulates in the mitochondria of well‑perfused heart muscle, allowing SPECT cameras to generate images that reflect relative perfusion across the myocardium.

The dose of Myoview is determined by the prescribing physician based on the specific imaging protocol, patient characteristics, and regulatory guidelines. Healthcare providers calculate the appropriate activity and volume for each examination; exact dosing information is not disclosed here.

Safety data for Myoview in pregnancy and lactation are limited. It should be used only when the potential diagnostic benefit outweighs any possible risk to the fetus or infant. Clinicians must evaluate each case individually and follow local regulatory recommendations.

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 cold‑chain if required) and necessary import documentation.

The primary alternatives for myocardial perfusion imaging are technetium‑99m sestamibi and thallium‑201. Compared with thallium‑201, tetrofosmin offers a lower radiation dose and faster imaging protocols. Relative to technetium‑99m sestamibi, Myoview provides comparable image quality with a slightly different biodistribution, allowing flexibility in certain clinical scenarios.

Myoview should be stored at ambient temperature, preferably below 25 °C. Keep the kit in its original packaging, protect it from moisture and direct light, and avoid freezing. Follow the manufacturer’s instructions for reconstitution and handle the product using standard aseptic techniques.

Myoview is administered as an intravenous injection, typically as part of a cardiac stress‑test protocol. The prepared solution is injected by qualified healthcare personnel, and imaging is performed shortly after administration according to the prescribed SPECT acquisition schedule.

Serious risks include allergic reactions such as urticaria, bronchospasm, or anaphylaxis, as well as rare cardiac arrhythmias that may occur during the imaging procedure. Additionally, patients receive a low dose of ionizing radiation; cumulative exposure should be monitored in accordance with regulatory limits.

Myoview should be avoided in individuals with known hypersensitivity to tetrofosmin or any component of the formulation, in patients with severe renal impairment, and in those with uncontrolled hyperthyroidism. Use in pregnant or breastfeeding women is reserved for situations where the diagnostic benefit clearly outweighs potential risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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