
Uronase500000 IU/
Beacon Pharmaceuticals PLC
Urokinase is a thrombolytic (fibrinolytic) enzyme administered only in a hospital setting under close medical supervision.
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:
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.
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.
| Indication | Typical Adult Dosing Regimen |
|---|---|
| Acute massive pulmonary embolism | A 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 catheter | A 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).
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:
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.
Urokinase is contraindicated in patients with any of the following true absolute contraindications:
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.
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.