Skip to content
ClinCalc Pro
Menu
Thrombolytic — Peripheral Arterial Occlusion / DVT (Historical)

Streptokinase

Brand names: Streptase

Streptokinase is a fibrinolytic (thrombolytic) agent derived from streptococci that has been used to dissolve thrombi in conditions such as acute myocardial infarction, pulmonary embolism and acute arterial thromboembolism.

Dosing — being independently re-sourced

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 forms a complex with plasminogen that activates conversion of plasminogen to plasmin, which degrades fibrin and breaks down thrombus.

Prescribing in practice

  • It carries a major risk of serious haemorrhage and is contraindicated in active bleeding, recent haemorrhagic stroke and other conditions predisposing to bleeding.
  • Because antibodies develop, repeat administration between several days and a long period after a previous dose, or after streptococcal infection, may be ineffective and increase the risk of allergic reactions.
  • Anaphylactoid reactions and hypotension can occur during infusion.

Monitoring

Monitor for bleeding, blood pressure and signs of allergic reaction during and after administration.

Counselling the patient

  • Report any bleeding, severe headache or signs of an allergic reaction promptly.
  • Tell future healthcare staff that you have received this medicine, as it may not be suitable again.
  • Bruising and minor bleeding at puncture sites can occur.

Evidence & guidelines

The GISSI and ISIS-2 trials established the mortality benefit of streptokinase thrombolysis in acute myocardial infarction, though primary PCI is now preferred where available.

Reference: GISSI-1 Trial 1986; MHRA SPC Streptase; ESC/ESVS Peripheral Vascular Guidelines; 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.