Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Reteplase
Drug ID BADD_D01929
Description Human tissue plasminogen activator, purified, glycosylated, 355 residues purified from CHO cells. Retavase is considered a "third-generation" thrombolytic agent, genetically engineered to retain and delete certain portions of human tPA. Retavase is a deletion mutein of human tPA formed by deleting various amino acids present in endogenous human tPA. Retavase contains 355 of the 527 amino acids of native human tPA (amino acids 1-3 and 176-527), and retains the activity-related kringle-2 and serine protease domains of human tPA. Three domains are deleted from retavase - kringle-1, finger, and epidermal growth factor (EGF).
Indications and Usage For lysis of acute pulmonary emboli, intracoronary emboli, and management of myocardial infarction.
Marketing Status approved; investigational
ATC Code B01AD07
DrugBank ID DB00015
KEGG ID D05721
MeSH ID C087896
PubChem ID Not Available
TTD Drug ID D0T1UJ
NDC Product Code 72820-100; 68225-124; 10122-143; 10122-141
UNII DQA630RIE9
Synonyms reteplase | 173-527-plasminogen activator (human tissue-type), 173-L-serine-174-L-tyrosine-175-L-glutamine- | BM 06.022 | BM 06022 | BM-06.022 | Rapilysin | Retavase
Chemical Information
Molecular Formula Not Available
CAS Registry Number 133652-38-7
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)
Anaemia01.03.02.001--
Anaphylactoid reaction10.01.07.003; 24.06.03.007---
Arrhythmia02.03.02.001---
Atrioventricular block02.03.01.002---
Cardiac arrest02.03.04.001--
Cardiac failure02.05.01.001--
Cardiac tamponade02.06.01.001--
Cardiogenic shock02.05.01.003; 24.06.02.006---
Embolism venous24.01.01.003---
Gastrointestinal haemorrhage07.12.02.001; 24.07.02.009---
Haemorrhage intracranial17.08.01.008; 24.07.04.003--
Hypotension24.06.03.002--
Injection site haemorrhage08.02.03.005; 12.07.03.005; 24.07.01.010---
Mitral valve incompetence02.07.01.002---
Myocardial infarction02.02.02.007; 24.04.04.009--
Myocardial rupture02.04.02.002; 12.01.11.002---
Nausea07.01.07.001--
Pericardial effusion02.06.01.002--
Pericarditis02.06.02.001--
Pulmonary oedema02.05.02.003; 22.01.03.003--
Pyrexia08.05.02.003--
Venous thrombosis24.01.01.008---
Vomiting07.01.07.003--
Haemorrhage24.07.01.002---
Pulseless electrical activity02.03.04.020---
Genital haemorrhage21.10.05.002; 24.07.03.007---
Ischaemia24.04.02.004---
The 1th Page    1    Total 1 Pages
ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene