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Urokinase: Brands, Price & Uses in Bangladesh

Urokinase is a thrombolytic (fibrinolytic) enzyme administered only in a hospital setting under close medical supervision.

Forms:Injection

About Urokinase

Indications of Urokinase

Urokinase is a thrombolytic (fibrinolytic) enzyme administered only in a hospital setting under close medical supervision. Its use is classified by strength of evidence as follows:

Established / FDA-approved use

  • Acute massive pulmonary embolism (PE): Urokinase is indicated for the lysis of acute massive pulmonary emboli and pulmonary emboli accompanied by unstable hemodynamics, in adult patients where the diagnosis has been confirmed by objective means such as pulmonary angiography or lung scanning.

Established adjunct use

  • Clearance of occluded central venous access devices (catheter clearance): Urokinase is used to restore patency to intravenous catheters and cannulae obstructed by clotted blood, allowing the device to be used again without removal.

Urokinase is not used for routine or minor venous thrombosis, and it is not an antibiotic or anti-infective agent. Its use always requires administration by, or under the direct supervision of, medical personnel experienced in thrombolytic therapy, in a facility equipped for continuous clinical and laboratory monitoring.

Dosage & Administration of Urokinase

Dosing of Urokinase is highly specific to the indication, must be individualized, and is administered only by trained medical personnel using a calibrated infusion device with continuous monitoring. The following is a general summary; actual dosing must follow the treating physician's protocol and the current product labeling.

IndicationTypical Adult Dosing Regimen
Acute massive pulmonary embolismA loading dose (e.g., approximately 4,400 International Units per kilogram of body weight) infused over about 10 minutes, followed by a continuous intravenous infusion of approximately 4,400 International Units per kilogram per hour for approximately 12 hours, via a constant-infusion pump through a 0.22-micron in-line filter.
Clearance of occluded IV catheterA small, concentrated dose (e.g., 5,000–10,000 International Units) is instilled directly into the blocked catheter lumen and allowed to dwell for a defined period (commonly 30–60 minutes, sometimes longer), then aspirated; may be repeated once if the catheter remains occluded, per institutional protocol.

Concurrent anticoagulant (e.g., heparin) therapy is typically avoided during the Urokinase infusion itself and resumed afterward per protocol, due to additive bleeding risk (see Interactions).

Side Effects of Urokinase

The most important and frequent adverse reaction associated with Urokinase is bleeding, which can range from minor (e.g., oozing at puncture sites, bruising) to severe or fatal (e.g., intracranial hemorrhage, gastrointestinal or retroperitoneal bleeding). Other reported adverse effects include:

  • Hypersensitivity/allergic reactions (rash, itching, flushing, bronchospasm; rarely anaphylaxis).
  • Infusion-related reactions such as fever, chills, or transient hypoxia.
  • Reperfusion arrhythmias as a blocked vessel reopens (see Precautions).
  • Hypotension during infusion.
  • Nausea.

Patients should seek immediate medical attention for unusual bruising, bleeding that does not stop, severe headache, sudden weakness, confusion, or difficulty breathing during or after treatment.

Contraindications of Urokinase

Urokinase is contraindicated in patients with any of the following true absolute contraindications:

  • Known hypersensitivity to Urokinase or any component of the formulation.
  • Active internal bleeding.
  • Recent (within approximately 2 months) intracranial or intraspinal surgery, or recent intracranial or intraspinal trauma.
  • Intracranial neoplasm, arteriovenous malformation, or aneurysm.
  • Known bleeding diathesis (a significant, uncorrected bleeding disorder).
  • Severe uncontrolled hypertension.
  • Recent stroke (cerebrovascular accident).

Other clinical situations that raise bleeding risk without being absolute contraindications (e.g., recent major surgery, recent GI bleeding, pregnancy) are addressed under Precautions and Warnings and Pregnancy and Lactation rather than listed here.

Frequently Asked Questions about Urokinase

What is Urokinase used for?

Urokinase is a clot-dissolving (thrombolytic) medicine used mainly in hospitals to treat acute massive pulmonary embolism (a large blood clot in the lungs) and to clear blood clots blocking intravenous catheters.

Can I take Urokinase at home or by mouth?

No. Urokinase is given only as an intravenous infusion (or instilled into a blocked catheter) by trained hospital staff, with continuous monitoring. It is never a home or self-administered medicine.

What is the biggest risk with Urokinase?

The most important risk is bleeding, which can range from minor bruising to severe or fatal internal or brain bleeding. This is why Urokinase is only given after careful patient screening and with close monitoring by medical staff.

Is Urokinase safe during pregnancy?

Urokinase, like other thrombolytics, carries a real risk of bleeding for both mother and baby in pregnancy. It is used in pregnancy only for life-threatening conditions, such as a massive pulmonary embolism, when the doctor judges that the benefit outweighs the risk, and always under specialist hospital supervision.

Who should not receive Urokinase?

Urokinase should not be given to anyone with known allergy to it, active internal bleeding, a bleeding disorder, a recent stroke, recent brain or spinal surgery or injury, a brain tumor or aneurysm, or severe uncontrolled high blood pressure, because of the high risk of dangerous bleeding in these situations.

What happens if too much Urokinase is given?

An overdose mainly causes excessive bleeding. If this is suspected, the infusion is stopped immediately and the patient receives emergency medical treatment, which may include blood products; anyone who suspects an overdose should seek immediate emergency care.

Disclaimer

The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.

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