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Alteplase

Fibrinolytic (recombinant tissue plasminogen activator) · freely accessible

For healthcare professionals. This information does not replace clinical judgement in the individual case; the current summary of product characteristics and the guidelines cited are authoritative.

Medically reviewed: Dr. med. univ. Daniel Pehböck, DESA, 01.11.2026

rt-PA

Fibrinolytic (recombinant tissue plasminogen activator)

Preparation: 1 mg/ml after reconstitution (e.g. 50 mg in 50 ml)

Acute ischaemic stroke (≤ 4.5 h)

  • 0.9 mg/kg i.v. – 10 % of this as a bolus over 1 min, remainder over 60 min[239]
    max. 90 mg · 1 mg/ml after reconstitution (e.g. 50 mg in 50 ml)

After exclusion of haemorrhage (CT/MRI), within 4.5 h of symptom onset. Do not delay thrombectomy in large-vessel occlusion.

Alteplase – Acute ischaemic stroke (≤ 4.5 h)
BW0.9 mg/kg
i.v. – 10 % of this as a bolus over 1 min, remainder over 60 min · 1 mg/ml after reconstitution
50 kg45 mg
45 ml
60 kg54 mg
54 ml
70 kg63 mg
63 ml
80 kg72 mg
72 ml
90 kg81 mg
81 ml
100 kg90 mg
90 ml
120 kg90 mg
90 ml max

High-risk pulmonary embolism (shock)

  • 100 mg i.v. – 10 mg bolus over 1–2 min, then 90 mg over 2 h[239]
    1 mg/ml after reconstitution (e.g. 50 mg in 50 ml) · = 100 ml
  • 0.6 mg/kg i.v. – accelerated regimen over 15 min (off-label, not licensed)[222]
    max. 50 mg · 1 mg/ml after reconstitution (e.g. 50 mg in 50 ml)

Body weight < 65 kg – total dose max. 1.5 mg/kg (SmPC). The accelerated regimen is listed in the 2019 ESC guideline but is explicitly not licensed (off-label, e.g. in extreme instability). Concomitant heparin therapy according to SmPC/ESC.

Alteplase – High-risk pulmonary embolism (shock)
BW0.6 mg/kg
i.v. – accelerated regimen over 15 min (off-label, not licensed) · 1 mg/ml after reconstitution
50 kg30 mg
30 ml
60 kg36 mg
36 ml
70 kg42 mg
42 ml
80 kg48 mg
48 ml
90 kg50 mg
50 ml max
100 kg50 mg
50 ml max
120 kg50 mg
50 ml max

Cardiac arrest with (suspected) pulmonary embolism

  • Consider fibrinolysis; ERC does not specify a dosing regimen. Commonly used is the accelerated ESC regimen 0.6 mg/kg (max. 50 mg), which ESC describes for administration over 15 min – an immediate bolus is to be distinguished from this; follow local protocol i.v. – off-label[1]

After thrombolysis, continue CPR for 60–90 min.

Contraindications

  • Previous intracranial haemorrhage or stroke of unknown origin
  • CNS damage, CNS tumour or AV malformation
  • Recent major trauma, surgery or head injury
  • Active bleeding, known bleeding tendency
  • Aortic dissection
  • In stroke, additionally observe the indication-specific criteria of the SmPC

Notes

  • In high-risk PE and during resuscitation, contraindications are relative – weigh benefit/risk.
  • Angio-oedema possible (especially with ACE inhibitors) during thrombolysis for stroke.
[239] Summary of product characteristics of the active substance (product reference in the app).
[222] Konstantinides SV, Meyer G, Becattini C et al. 2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism developed in collaboration with the European Respiratory Society (ERS). Eur Heart J 2020;41:543–603.
[1] Soar J, Böttiger BW et al. European Resuscitation Council Guidelines 2025 Adult Advanced Life Support. Resuscitation 2025;215 Suppl 1:110769 (Korrigendum 2026).
Reviewed: Dr. med. univ. Daniel Pehböck, DESA, 2026-11-01 (German original)

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