Tenecteplase (Stroke)
Brand names: Metalyse
Tenecteplase is an intravenous fibrinolytic (a modified tissue plasminogen activator) used here for thrombolysis in acute ischaemic stroke within the licensed time window. This page concerns its stroke use rather than myocardial infarction.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It is a fibrin-specific plasminogen activator that converts plasminogen to plasmin at the clot surface, dissolving the occluding thrombus and restoring cerebral perfusion.
Prescribing in practice
- Intracranial haemorrhage is the principal hazard, so it is contraindicated where there is active bleeding, recent intracranial haemorrhage, recent surgery or trauma, or uncontrolled hypertension, and eligibility must follow stroke pathway criteria after imaging excludes haemorrhage.
- It is given as a single intravenous bolus, simplifying administration compared with alteplase infusion, and blood pressure must be controlled before and after treatment.
- Concomitant anticoagulants and recent antiplatelet exposure increase bleeding risk and must be factored into eligibility.
Monitoring
Monitor neurological status, blood pressure and for signs of bleeding closely during and after administration, with urgent imaging if deterioration occurs.
Counselling the patient
- Explain to the patient or family that this is an emergency clot-busting treatment carrying a risk of bleeding into the brain.
- Report any sudden worsening of symptoms, severe headache or new weakness immediately to staff.
- The team will monitor blood pressure and neurology frequently after the dose.
Evidence & guidelines
Randomised trials and stroke guidelines support intravenous tenecteplase as an alternative thrombolytic to alteplase for eligible acute ischaemic stroke patients.
Reference: AcT trial NEJM 2022; 388(4):308-318; TASTE trial NEJM 2023; 388(6):493-503; ESC/AHA Stroke Guidelines 2019; NICE NG128; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- CHA₂DS₂-VASc Score · Atrial Fibrillation
- CHADS₂ Score for AF Stroke Risk · Stroke Risk
- ATRIA Stroke Risk Score for Atrial Fibrillation · Stroke Risk
- CHA₂DS₂-VA Score for AF (2023) · Atrial Fibrillation
- RoPE Score for Patent Foramen Ovale · Structural Heart Disease
- GARFIELD-AF Risk Score for Atrial Fibrillation · Atrial Fibrillation
- Acute Stroke / TIA Assessment · NICE NG128; RCP Stroke Guidelines 2023
- Status Epilepticus (Adults) · NICE CG137; ESEM guidelines; RCP Neurology Guidelines
- Suspected Subarachnoid Haemorrhage · NICE NG228; RCEM 2023; AHA/ASA 2023
- Adult Head Injury · NICE NG232 (2023)
- Bell's Palsy / Facial Nerve Palsy · ENT UK 2017; AAN
- Vertigo Workup · ENT UK; NICE CKS