GNH USA

Europe — EMA

Metalyse

GNH USA supplies Metalyse (Tenecteplase), a thrombolytic agent for acute ST‑segment elevation myocardial infarction. Request a quote for global supply.

Tenecteplase

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What is Tenecteplase?

Tenecteplase, the active ingredient in Metalyse, is a thrombolytic agent presented as a powder for solution for injection for intravenous use. It facilitates rapid clot dissolution in the coronary arteries of adults experiencing an acute ST‑segment elevation myocardial infarction (STEMI), helping to restore blood flow and limit heart muscle damage. The drug is supplied in a sterile lyophilized form that is reconstituted immediately before administration under aseptic conditions.

GNH USA supplies Metalyse as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Tenecteplase used for?

Metalyse (tenecteplase) is a thrombolytic agent used in the management of acute coronary artery occlusion.

Acute myocardial infarction (STEMI): rapid reperfusion to restore coronary blood flow and limit myocardial injury.

What are the side effects of Tenecteplase?

Common Side Effects: - Bleeding at the injection site: mild to moderate bruising or hematoma. - Nausea: transient gastrointestinal discomfort. - Headache: mild to moderate intensity. - Hypotension: temporary drop in blood pressure. - Fever: low‑grade temperature elevation. - Dizziness: transient light‑headedness.

Serious or Rare Side Effects: - Intracranial hemorrhage: potentially life‑threatening bleeding in the brain. - Severe allergic reaction: anaphylaxis or angioedema. - Myocardial rupture: rare tearing of heart muscle. - Disseminated intravascular coagulation: abnormal clotting throughout the body. - Severe hypotension: profound drop in blood pressure requiring intervention. - Pulmonary hemorrhage: bleeding within the lungs.

What precautions apply to Tenecteplase?

Metalyse should be used only after careful assessment of bleeding risk and contraindications.

Assess bleeding risk: evaluate recent surgery, trauma, or active hemorrhage. Avoid in active internal bleeding: contraindicated when uncontrolled bleeding is present. Use with caution in uncontrolled hypertension: high blood pressure increases hemorrhagic risk. Monitor coagulation parameters during therapy: track PT/INR and aPTT as needed. Contraindicated in known hypersensitivity to tenecteplase or its excipients. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Tenecteplase interact with?

Tenalyse may interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Other thrombolytic agents: additive risk of severe bleeding. - Therapeutic anticoagulants (heparin, low‑molecular‑weight heparin, warfarin): increased anticoagulant effect. - Full‑dose antiplatelet drugs (e.g., clopidogrel, aspirin): heightened bleeding tendency.

Moderate Interactions (Monitor Closely): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): may amplify bleeding risk. - Selective serotonin reuptake inhibitors (SSRIs): potential platelet dysfunction. - Glycoprotein IIb/IIIa inhibitors: monitor for excessive bleeding.

Frequently asked questions

What is Metalyse used for?+
Metalyse is indicated for the rapid treatment of acute ST‑segment elevation myocardial infarction (STEMI) in adult patients. By dissolving the occluding coronary clot, it helps restore blood flow to the heart muscle and limits the extent of myocardial damage.
How does tenecteplase work?+
Tenecteplase is a recombinant tissue‑type plasminogen activator that binds to fibrin within a clot and converts plasminogen to plasmin. The resulting plasmin breaks down fibrin strands, leading to clot dissolution and reperfusion of the blocked coronary artery.
What is the usual dose of Metalyse?+
The dose of Metalyse is determined by the prescribing clinician based on the patient’s weight, clinical condition, and local guidelines. It is administered as a single intravenous bolus after reconstitution.
Is Metalyse safe in pregnancy or breastfeeding?+
Safety of tenecteplase in pregnancy and lactation has not been established. It should be used only if the potential maternal benefit justifies the potential risk to the fetus or infant, and only under specialist supervision.
How do I order Metalyse from GNH USA?+
To order Metalyse, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA 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 import documentation.
How does Metalyse compare with alteplase?+
Both tenecteplase (Metalyse) and alteplase are recombinant tissue‑type plasminogen activators, but tenecteplase has higher fibrin specificity, a longer half‑life, and can be given as a single bolus, whereas alteplase requires an initial bolus followed by an infusion. These differences can simplify administration and may reduce infusion‑related complications.
How should Metalyse be stored and handled?+
Metalyse is supplied as a lyophilized powder for reconstitution. Store it at 2‑8 °C, protected from light, and do not freeze or shake the vial. Keep the product in its original packaging until ready for use to maintain stability.
How is Metalyse administered?+
After reconstituting the powder with the appropriate diluent, Metalyse is given as a single intravenous bolus injection over a few seconds. Administration should be performed by qualified healthcare personnel under aseptic conditions.
What are the most serious risks associated with Metalyse?+
The most serious risks include intracranial hemorrhage, severe systemic bleeding, allergic reactions such as anaphylaxis, myocardial rupture, and disseminated intravascular coagulation. Prompt recognition and management of these events are essential.
Who should not use Metalyse?+
Metalyse is contraindicated in patients with active internal bleeding, recent intracranial or in‑trunk surgery, known hypersensitivity to tenecteplase or its excipients, uncontrolled hypertension, and in those who have received another thrombolytic agent within the previous 24 hours.
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
Tenecteplase
Route
Intravenous Use
Manufacturer
Boehringer Ingelheim International Gmbh
Origin
EU

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