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 is employed in myocardial perfusion imaging to evaluate coronary artery disease and assess myocardial viability in adult patients. The agent is administered under controlled conditions and interpreted by nuclear medicine specialists.

GNH India supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, diagnostic centres and cardiac imaging units worldwide, ensuring quality, regulatory compliance and reliable logistics across all markets today.

Manufacturer / TM Owner

Ge Healthcare S.R.L.

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Indications & Clinical Uses

Myoview is used in myocardial perfusion imaging to evaluate coronary blood flow and detect cardiac pathology.

  • Myocardial perfusion imaging: provides high‑resolution SPECT images of myocardial blood flow, allowing identification of perfusion defects and quantification of ischemic burden.
  • Coronary artery disease detection: facilitates non‑invasive assessment of coronary artery stenosis severity, supporting clinical decision‑making for medical or interventional therapy.
  • Myocardial viability assessment: distinguishes viable from scarred myocardium, guiding revascularization strategies in patients with left ventricular dysfunction.
  • Risk stratification: contributes to prognostic evaluation by correlating perfusion abnormalities with future cardiac events.

How It Works

  • Technetium‑99m tetrofosmin is a lipophilic cation that readily crosses cell membranes and accumulates in myocardial cells in proportion to regional blood flow. After intravenous injection, the technetium‑99m label emits gamma photons detected by SPECT cameras. Within the myocardium, tetrofosmin localizes in mitochondria, providing a quantitative image of perfusion that reflects coronary artery circulation. The rapid uptake and stable retention allow imaging within minutes, while clearance from non‑cardiac tissues reduces background activity.

Side Effects

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

Common Side Effects

  • Nausea: mild transient feeling of queasiness.
  • Headache: mild to moderate headache shortly after injection.
  • Dizziness: temporary light‑headedness.
  • Injection site pain: brief discomfort at the venipuncture site.
  • Flushing: transient warmth or redness of the skin.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Hypotension: marked drop in blood pressure post‑injection.
  • Arrhythmia: new or worsening cardiac rhythm disturbances.
  • Myocardial infarction: rare occurrence of heart attack following the procedure.
  • Severe bronchospasm: acute airway constriction in susceptible individuals.

Precautions & Warnings

When using Myoview, clinicians should observe specific precautions to ensure patient safety and optimal image quality.

  • Assess renal function: evaluate kidney performance as impaired clearance may affect tracer distribution.
  • Review allergy history: confirm no prior hypersensitivity to technetium‑99m compounds or tetrofosmin.
  • Ensure adequate hydration: encourage fluid intake to promote rapid renal elimination of excess tracer.
  • Avoid use in unstable cardiac patients: defer in individuals with severe heart failure or acute ischemia.
  • Monitor vital signs: observe blood pressure and heart rate during and after injection.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Myoview may interact with other agents that influence cardiac imaging or tracer distribution.

Major Interactions (Avoid)

  • Concurrent radiopharmaceuticals: administration of other nuclear medicine agents within 24 h can interfere with image interpretation.
  • Iodinated contrast media: use within 24 h may alter myocardial uptake and affect SPECT results.
  • High‑dose caffeine: ingestion shortly before the test can reduce tracer uptake and compromise image quality.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may modify heart rate and affect perfusion patterns, requiring adjustment of the imaging protocol.
  • Calcium channel blockers: can influence coronary vasodilation and alter tracer distribution.
  • Antioxidant supplements: high doses of vitamin C or E may affect radiotracer kinetics and should be documented.

Frequently Asked Questions

Myoview is a radiopharmaceutical used primarily for myocardial perfusion imaging. It helps visualize blood flow to the heart muscle, allowing clinicians to detect coronary artery disease, assess the extent of ischemia, and evaluate myocardial viability before therapeutic decisions.

Tetrofosmin, labeled with technetium‑99m, is a lipophilic cation that rapidly enters myocardial cells in proportion to regional blood flow. Once inside, it localizes in mitochondria, and the emitted gamma photons are captured by SPECT cameras to produce detailed perfusion images of the heart.

The administered activity of Myoview is determined by the prescribing physician based on patient weight, imaging protocol, and regulatory guidelines. Dosage is individualized and should follow the recommendations of nuclear medicine societies and local regulatory authorities.

Safety data for Myoview in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used when the potential diagnostic benefit outweighs any possible risk to the fetus or infant, and after thorough risk assessment.

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 worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Myoview (technetium‑99m tetrofosmin) offers rapid myocardial uptake and stable retention, providing high‑quality SPECT images. Compared with thallium‑201, it delivers lower radiation dose and faster imaging protocols. Relative to technetium‑99m sestamibi, tetrofosmin has similar diagnostic performance but may differ slightly in biodistribution and image timing.

Myoview must be stored at 2‑8 °C in a refrigerator, protected from light. The vial should not be frozen or shaken. Before use, allow the product to reach room temperature if required by the imaging protocol, and handle it using standard radiopharmacy safety procedures.

Myoview is administered as an intravenous injection by a qualified nuclear medicine professional. The dose is injected into a peripheral vein, and imaging typically begins a few minutes after administration, following the specific timing guidelines of the SPECT protocol being used.

Serious risks, although rare, include severe allergic reactions such as anaphylaxis, marked hypotension, cardiac arrhythmias, myocardial infarction, and severe bronchospasm. Immediate medical intervention is required if any of these events occur during or after the injection.

Myoview should be avoided in patients with known hypersensitivity to technetium‑99m compounds or tetrofosmin, those with unstable cardiac conditions (e.g., acute myocardial infarction, severe heart failure), and in pregnant women unless the diagnostic benefit justifies the potential risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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