Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Urokinase
Drug ID BADD_D02320
Description Urokinase is an endogenous peptide that is cleaved in the presence of plasmin between lysine 158 and isoleucine 159 to yield active urokinase.[A191943] Urokinase remains connected between these 2 chains by a sulfhydryl bond.[A191943] Urokinase was granted FDA approval on 16 January 1978.[L12138]
Indications and Usage In Canada, urokinase is indicated for lysis of acute massive pulmonary emboli, acute thrombi obstructing coronary arteries, occlusive thromboemboli in peripheral arteries and grafts, and restoration of patency to intravenous catheters.[L12141]
Marketing Status approved; investigational; withdrawn
ATC Code B01AD04
DrugBank ID DB00013
KEGG ID D03341
MeSH ID D014568
PubChem ID Not Available
TTD Drug ID Not Available
NDC Product Code Not Available
UNII 83G67E21XI
Synonyms Urokinase-Type Plasminogen Activator | Urokinase Type Plasminogen Activator | Plasminogen Activator, Urokinase-Type | U-Plasminogen Activator | U Plasminogen Activator | U-PA | Urinary Plasminogen Activator | Urokinase | Renokinase | Abbokinase | Kidney Plasminogen Activator | Single-Chain Urokinase-Type Plasminogen Activator | Single Chain Urokinase Type Plasminogen Activator
Chemical Information
Molecular Formula Not Available
CAS Registry Number 9039-53-6
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Acidosis14.01.03.002--
Back pain15.03.04.005--
Bronchospasm22.03.01.004; 10.01.03.012--
Cardiac arrest02.03.04.001--
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Cerebrovascular disorder24.03.05.002; 17.08.02.002--Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.011--Not Available
Chills15.05.03.016; 08.01.09.001--
Cyanosis23.06.04.005; 02.11.04.004; 24.03.01.007; 22.02.02.007--
Dyspnoea02.11.05.003; 22.02.01.004--
Haematocrit decreased13.01.05.001--Not Available
Hemiplegia17.01.04.002--Not Available
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hypertension24.08.02.001--
Hypotension24.06.03.002--
Hypoxia22.02.02.003--
Mouth ulceration07.05.06.004--Not Available
Myocardial infarction24.04.04.009; 02.02.02.007--
Nausea07.01.07.001--
Pruritus23.03.12.001--
Pulmonary embolism24.01.06.001; 22.06.02.001--Not Available
Pulmonary oedema22.01.03.003; 02.05.02.003--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Tachycardia02.03.02.007--Not Available
Thrombocytopenia01.08.01.002--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Ventricular arrhythmia02.03.04.006--
Vomiting07.01.07.003--
Haemorrhage24.07.01.002--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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