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 injectable solution for intravenous use. It localizes in viable myocardial cells in proportion to regional blood flow, allowing clinicians to assess coronary artery disease, myocardial viability, and ischemia in adult patients undergoing cardiac imaging.

GNH India supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company provides reliable sourcing, regulatory support, and logistics for clinical and research facilities across multiple regions, ensuring timely delivery and compliance with local import requirements.

Manufacturer / TM Owner

Ge Healthcare As

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Indications & Clinical Uses

  • Tetrofosmin is used in cardiac imaging to evaluate myocardial perfusion and viability.
  • Coronary artery disease detection: Enables SPECT myocardial perfusion imaging to identify perfusion defects and assess the extent of coronary artery disease.
  • Myocardial viability assessment: Highlights viable myocardial tissue after ischemic injury, supporting decisions regarding revascularization.
  • Ischemia evaluation: Detects regional perfusion abnormalities during stress testing to differentiate reversible ischemia from scar tissue.

How It Works

  • After intravenous injection, tetrofosmin rapidly distributes into the myocardium, where it crosses cell membranes and accumulates in mitochondria of viable cardiac myocytes. Its uptake is proportional to regional blood flow, providing a quantitative map of perfusion. The radiolabeled compound emits gamma photons detectable by single‑photon emission computed tomography (SPECT), allowing visualization of perfusion patterns across the left ventricle.

Side Effects

Adverse reactions to Myoview are generally infrequent but may occur following administration of the radiopharmaceutical.

Common Side Effects

  • Mild nausea: transient feeling of queasiness after injection.
  • Headache: brief, mild headache reported in some patients.
  • Flushing: temporary warmth or redness at the injection site.

Serious or Rare Side Effects

  • Allergic reaction: urticaria, bronchospasm, or anaphylaxis requiring immediate medical attention.
  • Radiation‑induced skin erythema: localized reddening at the injection site persisting for days.
  • Cardiac arrhythmia: rare occurrence of new or worsening rhythm disturbances during imaging.

Precautions & Warnings

  • When using Myoview, several precautions should be observed to ensure patient safety and optimal image quality.
  • Pregnancy: avoid use unless clearly needed, as fetal radiation exposure cannot be excluded.
  • Breastfeeding: discontinue nursing for an appropriate period after administration, based on local guidelines.
  • Renal impairment: consider reduced clearance; adjust imaging timing if necessary.
  • Concurrent cardiac stress agents: verify compatibility with pharmacologic stress protocols.
  • Allergy history: screen for prior reactions to radiopharmaceuticals or iodine‑containing compounds.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Myoview may interact with other agents that affect cardiac imaging or radiation exposure.

Major Interactions (Avoid)

  • Thyroid hormone therapy: can alter iodine metabolism, potentially affecting radiotracer distribution.
  • High‑dose iodinated contrast: may compete for uptake pathways and reduce image quality.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt heart rate response during pharmacologic stress, influencing perfusion results.
  • Calcium channel blockers: can modify coronary vasodilation, requiring protocol adjustments.
  • Other radiopharmaceuticals: schedule sufficient interval to prevent cumulative radiation dose.

Frequently Asked Questions

Myoview is a radiopharmaceutical used in single‑photon emission computed tomography (SPECT) to assess myocardial perfusion, detect coronary artery disease, evaluate myocardial viability after ischemic injury, and identify reversible ischemia during stress testing.

Tetrofosmin is a lipophilic cation that crosses cardiac cell membranes and accumulates in the mitochondria of viable myocytes. Its uptake mirrors regional blood flow, and the emitted gamma photons are captured by SPECT cameras to produce detailed perfusion images of the heart.

The dose of Myoview is determined by the prescribing physician based on the patient’s weight, the imaging protocol, and regulatory guidelines. The prescriber selects the appropriate activity level to achieve optimal image quality while minimizing radiation exposure.

Myoview should be avoided in pregnancy unless the diagnostic benefit clearly outweighs the potential fetal radiation risk. Breastfeeding mothers are advised to discontinue nursing for a period recommended by local health authorities, as the radiotracer can be excreted in breast milk.

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

The primary alternatives are Technetium‑99m sestamibi and Thallium‑201. Compared with Thallium‑201, tetrofosmin offers a lower radiation dose and better image quality. Compared with Technetium‑99m sestamibi, tetrofosmin has similar diagnostic performance but may provide slightly higher myocardial uptake in certain stress protocols.

Myoview must be stored at 2‑8 °C in a refrigerator, protected from light, and never frozen or shaken. The vial should remain in its original packaging until use, and any unused portion should be discarded according to local radiation safety regulations.

Myoview is administered as an intravenous injection by a qualified healthcare professional. The injection is typically performed shortly before the SPECT imaging session, and the patient is monitored for any immediate reactions during and after the administration.

The most serious risks include severe allergic reactions such as anaphylaxis, radiation‑induced skin erythema at the injection site, and rare cardiac arrhythmias that may arise during the imaging procedure. Prompt medical intervention is required if any of these events occur.

Myoview should not be used in patients with known hypersensitivity to tetrofosmin or any component of the formulation, in pregnant women unless absolutely necessary, and in breastfeeding mothers who cannot suspend nursing. Caution is also advised for patients with severe renal impairment or uncontrolled thyroid disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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