Urokinase 25,000unit powder for solution for injection vials
Requires a prescription from a doctor or prescriber
Mammalian protein found in Homo sapiens
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Suspected adverse reactions reported for Urokinase
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Suspected adverse reactions reported for Urokinase
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Syner-KINASE 25,000unit powder for solution for injection vials
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
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Supply & safety information
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Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 16 · Randomised trials: 9 · 1981–2026
Showing the 50 most relevant studies, sorted by most relevant.
M. Look, W. van Putten, M. Duffy, et al.
Journal of the National Cancer Institute, 2002
- Breast Neoplasms
- Prognosis
- Urokinase-Type Plasminogen Activator
Evdoxia Kyriazopoulou, Garyphallia Poulakou, Haralampos Milionis, et al.
Nature Medicine, 2021
- COVID-19 Drug Treatment
- COVID-19
- SARS-CoV-2
G. Zoppo, R. Higashida, A. Furlan, et al.
Stroke, 1998
- Acute Disease
- Anticoagulants
- Cerebral Angiography
Akira Ogawa, Etsuro Mori, Kazuo Minematsu, et al.
Stroke, 2007
- Thrombolytic Therapy
- Acute Disease
- Cerebral Hemorrhage
SamuelZ. Goldhaber, John A. Heit, G.V.R.K. Sharma, et al.
The Lancet, 1988
- Acute Disease
- Clinical Trials as Topic
- Tissue Plasminogen Activator
Anne Thomson
Thorax, 2002
- Empyema
- Length of Stay
- Plasminogen Activators
M. Macleod, Stephen M. Davis, P. Mitchell, et al.
Cerebrovascular Diseases, 2005
Jiang T, Chen W, Liang G, et al.
2026
BackgroundLoculated pleural effusion caused by fibrinous septation often leads to incomplete drainage and prolonged hospitalization. Urokinase facilitates fibrin degradation; however, its overall efficacy and safety across different etiologies remain uncertain. This meta-analysis evaluated the clinical effectiveness and safety of intrapleural urokinase for loculated pleural effusions of various causes.MethodsA comprehensive search of PubMed, Embase, Cochrane Library, Web of Science, China National Knowledge Infrastructure (CNKI), Wanfang, and Chinese Biomedical Literature Database (CBM) was performed up to December 2024. Randomized controlled trials (RCTs) comparing urokinase plus standard drainage with drainage alone or with saline were included. Eligible studies enrolled patients with radiologically confirmed loculated or multiloculated pleural effusions and reported at least one quantitative efficacy or safety outcome. Trials using other fibrinolytics or steroids were excluded. The primary outcome was treatment success rate. Secondary outcomes included total drainage volume (mL), hospital stay (days), and adverse events. Data were synthesized using RevMan 5.4. Subgroup analyses were performed based on etiology and control group intervention (thoracentesis vs. catheter drainage).ResultsTwenty-five RCTs involving 1,990 patients (1,018 urokinase; 972 controls) met the inclusion criteria. Urokinase significantly improved treatment success rate [odds ratio (OR) =5.28, 95% confidence interval (CI): 3.98-7.01; Pvs. catheter drainage) showed consistent efficacy. Adverse events did not differ significantly between groups (P>0.05).ConclusionsIntrapleural urokinase appears to be a safe and effective adjunctive therapy for loculated pleural effusions of diverse etiologies, consistently improving drainage and clinical outcomes. Nevertheless, the certainty of evidence is limited by moderate study quality, dosing heterogeneity, and potential publication bias. Further high-quality randomized trials are warranted. This review was registered in PROSPERO (CRD42024581473).
Abstract licence: CC BY-NC-ND
Gungor AB, Pennathur P, Guran HS, et al.
2025
- Postoperative Complications
- Receptors, Urokinase Plasminogen Activator
- Biomarkers
Chang Liu, Chang-Yu Guo, Fengli Li, et al.
JAMA, 2025
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
152 found
Half-life
6.2 minutes
Mechanism
Urokinase is a serine protease.
Food interactions
1 warning
Human targets
9 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
6.2 minutes
[L12138]
Protein binding
Volume of distribution
11.5L
[L12138]
Metabolism
Elimination
[L12138]
Clearance
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Urokinase was granted FDA approval on 16 January 1978.[L12138]
[L12141]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 704 interactions
[L12141]
Treat patients with symptomatic and supportive measures which may include application of local pressure, administration of whole blood or plasma, and administration of aminocaproic acid.
[L12141]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L12138]
[L12138]
[L12138]
Proteins and enzymes this drug interacts with in the body
PMID:6447255
Cleavage of fibronectin and laminin leads to cell detachment and apoptosis.
Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be modulated by CSPG4. Binds to cells
PMID:15677461
Plays a role in localizing and promoting plasmin formation. Mediates the proteolysis-independent signal transduction activation effects of U-PA. It is subject to negative-feedback regulation by U-PA which cleaves it into an inactive form
PMID:15853774
Is a primary inhibitor of tissue-type plasminogen activator (PLAT) and urokinase-type plasminogen activator (PLAU). As PLAT inhibitor, it is required for fibrinolysis down-regulation and is responsible for the controlled degradation of blood clots .
PMID:17912461 PMID:8481516 PMID:9207454 PMID:21925150
As PLAU inhibitor, it is involved in the regulation of cell adhesion and spreading .
PMID:9175705
Acts as a regulator of cell migration, independently of its role as protease inhibitor .
PMID:15001579 PMID:9168821
It is required for stimulation of keratinocyte migration during cutaneous injury repair .
PMID:18386027
It is involved in cellular and replicative senescence .
PMID:16862142
Plays a role in alveolar type 2 cells senescence in the lung (By similarity).
Is involved in the regulation of cementogenic differentiation of periodontal ligament stem cells, and regulates odontoblast differentiation and dentin formation during odontogenesis PMID:25808697 PMID:27046084
Enzymes involved in drug metabolism — important for understanding drug interactions
Involved compounds
ATC B01AD04
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Urokinase
Additional database identifiers
Drugs Product Database (DPD)
2012
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9071
GenAtlas
PLG
GeneCards
PLG
GenBank Gene Database
X05199
GenBank Protein Database
387026
Guide to Pharmacology
2394
UniProt Accession
PLMN_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9053
GenAtlas
PLAUR
GeneCards
PLAUR
GenBank Gene Database
X51675
GenBank Protein Database
37605
UniProt Accession
UPAR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:8583
GenAtlas
SERPINE1
GeneCards
SERPINE1
GenBank Gene Database
X04429
GenBank Protein Database
35272
UniProt Accession
PAI1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:8584
GenAtlas
SERPINB2
GeneCards
SERPINB2
GenBank Gene Database
J02685
GenBank Protein Database
189545
UniProt Accession
PAI2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9052
GenAtlas
PLAU
GeneCards
PLAU
GenBank Gene Database
X02419
GenBank Protein Database
1834524
Guide to Pharmacology
2393
UniProt Accession
UROK_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:8723
GenAtlas
SERPINA5
GeneCards
SERPINA5
GenBank Gene Database
J02639
GenBank Protein Database
180550
UniProt Accession
IPSP_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6694
GenAtlas
LRP2
GeneCards
LRP2
GenBank Gene Database
U33837
GenBank Protein Database
1809240
UniProt Accession
LRP2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:11344
GenAtlas
ST14
GeneCards
ST14
GenBank Gene Database
AF118224
GenBank Protein Database
6647302
Guide to Pharmacology
2418
UniProt Accession
ST14_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:7821
GenAtlas
NID1
GeneCards
NID1
GenBank Gene Database
M30269
GenBank Protein Database
189209
UniProt Accession
NID1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:7158
GenAtlas
MMP12
GeneCards
MMP12
GenBank Gene Database
L23808
GenBank Protein Database
435970
Guide to Pharmacology
1636
UniProt Accession
MMP12_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q7119591), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.