Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Capecitabine
Drug ID BADD_D00349
Description Capecitabine is an orally-administered chemotherapeutic agent used in the treatment of metastatic breast and colorectal cancers. Capecitabine is a prodrug, that is enzymatically converted to fluorouracil (antimetabolite) in the tumor, where it inhibits DNA synthesis and slows growth of tumor tissue.
Indications and Usage For the treatment of patients with metastatic breast cancer resistant to both paclitaxel and an anthracycline-containing chemotherapy regimen. May also be used in combination with docetaxel for the treatment of metastatic breast cancer in patients who have failed to respond to, or recurred or relasped during or following anthracycline-containing chemotherapy. Capecitabine is used alone as an adjuvant therapy following the complete resection of primary tumor in patients with stage III colon cancer when monotherapy with fluroprymidine is preferred. The use or capecitabine in combination regimens for advanced gastric cancer is currently being investigated.
Marketing Status approved; investigational
ATC Code L01BC06
DrugBank ID DB01101
KEGG ID D01223
MeSH ID D000069287
PubChem ID 60953
TTD Drug ID D00HCQ
NDC Product Code 55111-893; 82920-001; 72205-007; 72485-205; 62331-043; 16714-467; 51407-640; 55111-496; 55111-497; 61269-475; 65162-844; 15308-0714; 54893-0002; 59651-205; 64980-277; 70756-815; 68001-487; 69097-949; 72205-006; 63482-099; 72969-094; 16729-072; 59923-721; 61269-470; 0054-0271; 69539-019; 0093-7473; 64980-276; 0054-0272; 69097-948; 72606-554; 53104-7618; 55512-0015; 0004-1100; 51407-639; 67877-459; 68001-488; 69539-020; 35369-0010; 16729-073; 51407-096; 62756-238; 62756-239; 65162-843; 67877-458; 59651-204; 72485-204; 72606-555; 49452-1713; 68554-0033; 0004-1101; 0093-7474; 51407-095; 60687-149; 0378-2511; 70756-816; 53183-4009; 54245-7014; 65129-1241; 81955-0001; 16714-468; 59923-722
UNII 6804DJ8Z9U
Synonyms Capecitabine | N(4)-pentyloxycarbonyl-5'-deoxy-5-fluorocytidine | Xeloda
Chemical Information
Molecular Formula C15H22FN3O6
CAS Registry Number 154361-50-9
SMILES CCCCCOC(=O)NC1=NC(=O)N(C=C1F)C2C(C(C(O2)C)O)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)
Thrombocytopenia01.08.01.0020.011752%-
Thrombophlebitis24.01.02.0010.000224%-
Thrombosis24.01.01.006---
Thrombotic thrombocytopenic purpura01.08.01.005; 23.06.01.011; 24.07.06.0140.000112%
Thyroiditis05.02.04.0010.000168%-
Tic17.02.05.024; 19.11.04.001---
Tinnitus04.04.01.002; 17.04.07.004--
Tongue discolouration07.14.02.0060.001287%-
Tongue disorder07.14.01.0020.000492%-
Tongue oedema07.14.02.007; 10.01.05.008; 23.04.01.0090.000470%-
Tonsillitis11.01.13.006; 22.07.03.008---
Tooth abscess07.09.01.003; 11.01.04.003---
Tooth loss07.09.09.001; 12.01.17.0260.000683%-
Torsade de pointes02.03.04.005---
Toxic dilatation of intestine07.08.03.009---
Toxic encephalopathy12.03.01.027; 17.13.01.0040.000560%-
Toxic epidermal necrolysis10.01.01.006; 11.07.01.006; 12.03.01.015; 23.03.01.008--
Transient ischaemic attack17.08.04.001; 24.04.06.005--
Tremor17.01.06.002--
Trigger finger15.07.01.0050.000168%-
Trismus15.05.04.004; 17.01.03.0040.000492%
Tumour pain16.32.03.0030.000112%
Ulcer08.03.06.0010.000470%-
Upper gastrointestinal haemorrhage07.12.02.006; 24.07.02.024--
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Urethral disorder20.07.01.002---
Urinary incontinence17.05.01.008; 20.02.02.010--
Urinary retention20.02.02.011--
Urinary tract disorder20.08.01.0010.000224%-
Urinary tract infection11.01.14.004; 20.08.02.001--
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ADReCS-Target
Drug Name ADR Term Target
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