GNH USA

Europe — EMA

Myoview (Tetrofosmin)

GNH USA supplies Myoview (Tetrofosmin), a radiopharmaceutical for myocardial perfusion imaging and coronary artery disease detection. Request a quote today.

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What is Tetrofosmin?

Tetrofosmin, the active ingredient in Myoview, is a radiopharmaceutical presented as an injectable solution for intravenous use. It enables myocardial perfusion imaging to assess coronary artery disease in patients undergoing cardiac stress testing.

GNH USA supplies Myoview as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

What is Tetrofosmin used for?

Myoview is a radiopharmaceutical used in cardiac imaging to evaluate myocardial blood flow and detect coronary artery disease.

- Myocardial perfusion imaging: provides quantitative assessment of regional blood flow to the heart muscle. - Detection of coronary artery disease: helps identify obstructive lesions by comparing stress and rest perfusion. - Stress and rest cardiac SPECT: enables visualization of perfusion differences under pharmacologic or exercise stress and at rest.

What are the side effects of Tetrofosmin?

Myoview may cause a range of adverse reactions following administration.

Common Side Effects: - Nausea: mild to moderate discomfort after injection. - Flushing: transient warmth or redness of the skin. - Headache: mild to moderate intensity. - Dizziness or light‑headedness. - Injection‑site pain or irritation. - Mild hypotension.

Serious or Rare Side Effects: - Severe allergic reaction (anaphylaxis): rapid onset of airway swelling, rash, or shock. - Life‑threatening arrhythmia: abnormal heart rhythm requiring immediate care. - Marked hypotension: sudden drop in blood pressure. - Myocardial infarction: rare occurrence of heart attack post‑administration. - Pulmonary edema: fluid accumulation in the lungs. - Death: extremely rare but reported in severe reactions.

What precautions apply to Tetrofosmin?

Prior to Myoview administration, clinicians should consider several safety measures.

- Patient assessment: evaluate renal function and overall cardiac status. - Contraindications: avoid in individuals with known hypersensitivity to tetrofosmin or its excipients. - Pregnancy: use only if essential, as safety data are limited. - Breastfeeding: discontinue nursing or discontinue the drug, based on clinical judgment. - Drug interactions: review concurrent medications that affect myocardial blood flow. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Tetrofosmin interact with?

Myoview may interact with other agents that influence myocardial perfusion or radiotracer distribution.

Major Interactions (Avoid): - Dipyridamole stress agents: concurrent use can alter tracer uptake. - Other nuclear imaging agents: administration within 24 hours may cause cross‑interference. - High‑dose caffeine: may blunt stress‑induced perfusion changes.

Moderate Interactions (Monitor Closely): - Beta‑blockers: may reduce stress‑induced heart rate response. - Calcium channel blockers: can modify coronary vasodilation. - Nitrates: may affect myocardial blood flow patterns. - Antihypertensives: monitor blood pressure during imaging. - ACE inhibitors or ARBs: observe for altered perfusion signals.

Frequently asked questions

What is Myoview used for?+
Myoview is used as a cardiac imaging agent for myocardial perfusion scintigraphy. It helps physicians evaluate blood flow to the heart muscle during stress and rest conditions, facilitating the detection of coronary artery disease and assessment of myocardial viability.
How does tetrofosmin work?+
Tetrofosmin is a lipophilic radiotracer that enters cardiac cells in proportion to blood flow. Once inside, it localizes in the mitochondria of viable myocytes. The emitted gamma radiation is captured by SPECT cameras, producing detailed images of regional perfusion.
What is the usual dose of Myoview?+
The administered activity of Myoview is determined by the prescribing physician based on the imaging protocol, patient weight, and equipment specifications. The dose is delivered as a single intravenous injection immediately before the stress or rest imaging phase.
Is Myoview safe during pregnancy or breastfeeding?+
Safety data for tetrofosmin in pregnancy and lactation are limited. It is generally avoided unless the diagnostic benefit outweighs potential risk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.
How do I order Myoview from GNH USA?+
To order Myoview, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.
How does Myoview compare with other cardiac perfusion agents?+
Myoview (tetrofosmin) and technetium‑99m sestamibi are both technetium‑based perfusion tracers with similar imaging quality. Compared with thallium‑201, tetrofosmin offers lower radiation dose, faster imaging protocols, and better image resolution, making it a preferred choice in many modern nuclear cardiology labs.
What are the storage and handling requirements for Myoview?+
Myoview must be stored refrigerated at 2–8 °C, protected from light, and kept in its original container. It should not be frozen or shaken. Before use, allow the vial to reach room temperature if required by the imaging protocol.
How is Myoview administered?+
Myoview is administered by a qualified healthcare professional as an intravenous bolus injection. The injection is typically performed immediately before the stress or rest phase of a SPECT study, and imaging begins shortly after the tracer distributes within the myocardium.
What are the most serious risks associated with Myoview?+
Serious risks, although rare, include severe allergic reactions (anaphylaxis), life‑threatening arrhythmias, marked hypotension, myocardial infarction, and pulmonary edema. Patients should be monitored closely during and after injection, and emergency measures must be readily available.
Who should not receive Myoview?+
Myoview should not be given to individuals with a known hypersensitivity to tetrofosmin or any of its excipients. It is also contraindicated in patients with severe renal impairment, uncontrolled heart failure, or when pregnancy is confirmed unless the diagnostic benefit justifies the risk.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Tetrofosmin
Route
Intravenous Use
Manufacturer
Ge Healthcare As
Origin
EU

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