Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Darolutamide
Drug ID BADD_D02548
Description Darolutamide is a nonsteroidal androgen receptor antagonist for the treatment of castrate-resistant, non-metastatic prostate cancer (nmCRPC). This condition occurs in the majority of patients with advanced prostate cancer who have been treated with androgen receptor antagonists.[A189063] Though prior treatment for prostate cancer has been successful for these patients, the cancer eventually progresses to become resistant to existing therapies. This warrants further treatment. The goal of treatment with darolutamide is to delay the progression of prostate cancer to metastatic disease, increasing quality of life and life expectancy for those with advanced prostate cancer.[A189054,A189063] Darolutamide was developed by Bayer HealthCare Pharmaceuticals Inc. and approved by the FDA on July 30th, 2019.[L10887]
Indications and Usage This drug is indicated for the treatment of patients diagnosed with non-metastatic and castrate-resistant prostate cancer.[L10872]
Marketing Status approved; investigational
ATC Code L02BB06
DrugBank ID DB12941
KEGG ID D11045
MeSH ID C000607739
PubChem ID 67171867
TTD Drug ID D0DV6D
NDC Product Code 54893-0107; 50419-395; 52483-6300
UNII X05U0N2RCO
Synonyms darolutamide | Nubeqa | ORM-16497 | ODM-201 | ORM-16555
Chemical Information
Molecular Formula C19H19ClN6O2
CAS Registry Number 1297538-32-9
SMILES CC(CN1C=CC(=N1)C2=CC(=C(C=C2)C#N)Cl)NC(=O)C3=NNC(=C3)C(C)O
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)
Abdominal pain upper07.01.05.0030.000901%
Anaemia01.03.02.0010.001068%
Arrhythmia02.03.02.0010.000334%-
Atrial fibrillation02.03.03.0020.000334%
Bladder cancer16.08.01.001; 20.03.04.0010.000734%-
Cardiac failure congestive02.05.01.0020.000501%-
Cerebral infarction17.08.01.004; 24.04.06.0020.000334%-
Cerebrovascular accident17.08.01.007; 24.03.05.0010.000667%
Constipation07.02.02.0010.000501%
Dehydration14.05.05.0010.000667%
Delirium19.13.02.0010.000334%
Dementia17.03.01.001; 19.20.02.0010.000334%-
Diplopia06.02.06.002; 17.17.01.0050.000334%-
Dizziness02.11.04.006; 17.02.05.003; 24.06.02.0070.003036%
Drug eruption08.01.06.015; 10.01.01.005; 23.03.05.0010.000734%-
Dysphagia07.01.06.0030.003337%
Fatigue08.01.01.0020.009643%
Feeling abnormal08.01.09.0140.000901%-
Haematuria20.02.01.006; 21.10.01.018; 24.07.01.0470.000501%
Head discomfort17.02.05.0270.000334%-
Hemiparesis17.01.04.0010.000334%
Hepatic function abnormal09.01.02.0010.001401%-
Hepatotoxicity09.01.07.009; 12.03.01.0080.000334%-
Hypoaesthesia17.02.06.023; 23.03.03.0810.001301%-
Liver disorder09.01.08.0010.000501%-
Loss of consciousness17.02.04.0040.000501%-
Malaise08.01.01.0030.000834%
Metastases to spine15.09.03.007; 16.22.02.0070.000501%-
Mood altered19.04.02.0070.000334%-
Muscle spasms15.05.03.0040.001468%
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