Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Hydroxyurea
Drug ID BADD_D01110
Description An antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.
Indications and Usage For management of melanoma, resistant chronic myelocytic leukemia, and recurrent, metastatic, or inoperable carcinoma of the ovary and Sickle-cell anemia.
Marketing Status approved
ATC Code L01XX05
DrugBank ID DB01005
KEGG ID D00341
MeSH ID D006918
PubChem ID 3657
TTD Drug ID D07CWD
NDC Product Code 0904-6939; 35369-0006; 49452-3650; 55154-7143; 61269-403; 68084-284; 70518-3615; 51927-0072; 0555-0882; 55154-3554; 69315-164; 38779-1354; 42291-321; 71770-105; 49884-724; 17337-0023; 0003-6335; 0003-6337; 60429-265; 61269-835; 70518-0916; 55512-0003; 61269-402; 71770-120; 0003-0830; 51552-0851; 62049-135; 0003-6336; 61269-404; 10135-702; 71052-323; 17337-0022
UNII X6Q56QN5QC
Synonyms Hydroxyurea | Hydroxycarbamid | Oncocarbide | Hydrea
Chemical Information
Molecular Formula CH4N2O2
CAS Registry Number 127-07-1
SMILES C(=O)(N)NO
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)
Febrile neutropenia01.02.03.002; 08.05.02.0040.000392%
Feeling abnormal08.01.09.014---
Fibrosis08.03.01.0010.000112%-
Fluid retention14.05.06.002; 20.01.02.0030.000168%-
Folate deficiency14.12.02.006---
Gangrene11.02.01.003; 23.06.06.001; 24.04.05.003---
Gastric cancer07.21.02.001; 16.13.03.0010.000728%-
Gastric haemorrhage07.12.01.001; 24.07.02.0070.000224%
Gastric ulcer07.04.03.0020.000336%
Gastrointestinal disorder07.11.01.001---
Gastrointestinal haemorrhage07.12.02.001; 24.07.02.0090.000504%-
Generalised tonic-clonic seizure17.12.01.0020.000112%-
Gout14.09.01.001; 15.01.06.0010.000112%-
Haematemesis07.12.02.002; 24.07.02.0110.000224%-
Haematochezia07.12.02.003; 24.07.02.0120.000168%-
Haematoma24.07.01.0010.000336%
Haematuria20.02.01.006; 21.10.01.018; 24.07.01.0470.000224%
Haemoglobin13.01.05.018---
Haemolysis01.06.04.0020.000112%
Haemolytic anaemia01.06.03.0020.000336%-
Hallucination19.10.04.003--
Headache17.14.01.001--
Hemiparesis17.01.04.0010.000168%
Hemiplegia17.01.04.0020.000224%-
Hepatic failure09.01.03.0020.000112%
Hepatic function abnormal09.01.02.0010.001030%-
Hepatitis09.01.07.0040.000168%-
Hepatocellular injury09.01.07.0080.000112%-
Hepatosplenomegaly01.09.03.001; 09.01.05.0020.000168%-
Hepatotoxicity09.01.07.009; 12.03.01.0080.000112%-
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ADReCS-Target
Drug Name ADR Term Target
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