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Tenecteplase

TNKASE

What it isBioengineered tPA variant with greater fibrin specificity and a longer half-life; STEMI and, increasingly, ischemic stroke.

Why this oneA single bolus replaces alteplase’s infusion, which matters when transferring a stroke patient.

What limits itSame hemorrhage risk and same time window. Dosing differs from alteplase — the two are not interchangeable by volume.

FDA label

FDA dosingPopulationStartTargetMax
Acute ischemic stroke (AIS)AdultsWeight-based single IV bolus over 5 sec (<60 kg 15 mg; 60–<70 17.5 mg; 70–<80 20 mg; 80–<90 22.5 mg; ≥90 25 mg), within 3 h of symptom onsetSingle bolus25 mg
Acute ST elevation myocardial infarction (STEMI)AdultsWeight-based single IV bolus over 5 sec (<60 kg 30 mg; 60–<70 35 mg; 70–<80 40 mg; 80–<90 45 mg; ≥90 50 mg)Single bolus50 mg

Renal Undefined

Hepatic Undefined

Single-dose only

Instructions

Contraindications

Cautions

Adverse reactions

Pregnancy No human data; related thrombolytics not shown to increase birth defects; STEMI/AIS are life-threatening emergencies — do not withhold life-sustaining therapy

Lactation No data on presence in milk; weigh benefits of breastfeeding against clinical need

NO BOXED WARNINGS

Principal riskIntracranial hemorrhage; dosing differs from alteplase

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Tenecteplase ballicule

Tenecteplase ballicule: receptor binding, kinetics and half-life diagram

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