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 370 MBq per vial injectable solution for intravenous use. It is used to assess myocardial perfusion and detect coronary artery disease in patients undergoing cardiac stress testing. The agent enables single‑photon emission computed tomography (SPECT) imaging to visualize blood flow distribution across the myocardium.

GNH India supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and procurement teams worldwide, ensuring reliable cold‑chain logistics and regulatory compliance for radiopharmaceuticals.

Manufacturer / TM Owner

Ge Healthcare Limited

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Indications & Clinical Uses

Myoview (tetrofosmin) is employed in cardiac imaging to evaluate myocardial blood flow and identify coronary artery disease.

  • Myocardial perfusion imaging: provides detailed images of blood flow to the heart muscle at rest and during stress.
  • Detection of coronary artery disease: highlights regions with reduced perfusion indicating possible arterial blockages.
  • Stress cardiac imaging: assesses myocardial perfusion response to pharmacologic or exercise stress.
  • Evaluation of myocardial viability: helps determine viable versus scarred myocardial tissue for therapeutic planning.

How It Works

  • Technetium‑99m tetrofosmin is a lipophilic complex that rapidly crosses cell membranes and accumulates in viable myocardial cells in proportion to regional blood flow. After intravenous injection, its gamma emissions are captured by SPECT cameras, producing images that reflect myocardial perfusion and enable detection of perfusion defects.

Side Effects

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

Common Side Effects

  • Nausea: mild transient nausea reported in some patients.
  • Headache: occasional mild headache during or after the procedure.
  • Injection site pain: mild discomfort at the venipuncture site.

Serious or Rare Side Effects

  • Anaphylactic reaction: rare severe allergic response requiring immediate medical attention.
  • Severe hypotension: uncommon drop in blood pressure following injection.
  • Radiation‑induced skin injury: very rare localized skin reaction at the injection site.
  • Cardiac arrhythmia: rare occurrence of abnormal heart rhythms.
  • Pulmonary embolism: extremely rare thrombotic event.

Precautions & Warnings

When using Myoview, several precautions should be observed to ensure patient safety and optimal image quality.

  • Pregnancy: avoid use unless clearly necessary, as fetal effects are unknown.
  • Breastfeeding: discontinue breastfeeding or consider alternative imaging, because radiotracer may be excreted in milk.
  • Renal impairment: assess kidney function, as reduced clearance may affect tracer distribution.
  • Allergies: screen for known hypersensitivity to technetium‑99m compounds.
  • Concomitant medications: inform the physician of drugs that may alter myocardial blood flow (e.g., vasodilators, beta‑blockers).
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Myoview may interact with certain drugs or conditions that influence myocardial blood flow or radiotracer distribution.

Major Interactions (Avoid)

  • Vasodilators (e.g., nitroglycerin): may alter perfusion patterns and affect image interpretation.
  • Beta‑blockers: can blunt stress response, leading to false‑negative results.
  • Calcium channel blockers: may modify coronary flow and impact tracer uptake.

Moderate Interactions (Monitor Closely)

  • Caffeine‑containing products: can interfere with pharmacologic stress agents, reducing test accuracy.
  • Antidepressants (SSRIs): may affect heart rate response during stress testing.
  • Thyroid hormones: altered metabolism may influence radiotracer kinetics.

Frequently Asked Questions

Myoview is a radiopharmaceutical containing tetrofosmin used in nuclear medicine to assess myocardial perfusion during rest and stress SPECT imaging, helping detect coronary artery disease and evaluate cardiac function.

Tetrofosmin, labeled with technetium‑99m, is a lipophilic complex that rapidly crosses cell membranes and accumulates in viable myocardial cells in proportion to regional blood flow. The emitted gamma photons are captured by a SPECT camera, producing images that reflect perfusion distribution.

The administered activity of Myoview is determined by the prescribing physician based on the imaging protocol, patient weight, and equipment specifications. Typical clinical practice uses a vial containing 370 MBq, but the exact dose is individualized and recorded on the order.

The safety of tetrofosmin in pregnancy has not been established, and it is classified as unknown. Because the radiopharmaceutical emits ionizing radiation, it should be avoided in pregnant patients unless essential. Breastfeeding mothers should discontinue nursing or consider alternatives, as the tracer may be secreted in milk.

To request Myoview, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details—including cold‑chain handling if needed—and assists with import documentation.

The primary alternative to tetrofosmin is technetium‑99m sestamibi. Both agents provide myocardial perfusion imaging, but tetrofosmin has slightly higher liver clearance, potentially improving image quality in the inferior wall. Choice between them depends on institutional preference, availability, and specific protocol requirements.

Myoview must be stored refrigerated at 2–8 °C in its original protective container, protected from light. Do not freeze or shake the vial. Before use, allow the product to reach room temperature if required by the imaging protocol, and handle only by trained personnel using aseptic technique.

Myoview is administered as a single intravenous injection, typically through a peripheral vein. The dose is injected rapidly, followed by a saline flush to ensure complete delivery. Imaging is performed after a short uptake period, which varies according to the stress protocol used (pharmacologic or exercise).

Although rare, serious adverse events include anaphylactic reactions, severe hypotension, and radiation‑induced skin injury at the injection site. Patients should be monitored for signs of allergic response, blood pressure changes, and any unexpected discomfort during and after the procedure.

Myoview is contraindicated in patients with known hypersensitivity to tetrofosmin or any technetium‑99m compounds. It should also be avoided in pregnant women unless the diagnostic benefit outweighs the risk, and in individuals where accurate perfusion assessment is impossible due to severe arrhythmias or uncontrolled heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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