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 Prescription
ATC Code L01BC06
DrugBank ID DB01101
KEGG ID D01223
MeSH ID D000069287
PubChem ID 60953
TTD Drug ID D00HCQ
NDC Product Code 72205-007; 69097-948; 59923-722; 59651-204; 0378-2511; 55111-893; 55111-496; 0054-0272; 72205-006; 70756-816; 50268-154; 51407-095; 15308-0714; 16714-467; 62756-239; 67877-458; 64980-277; 55512-0015; 16729-072; 68001-487; 67877-459; 55111-497; 51079-510; 35369-0010; 54893-0002; 70756-815; 63482-099; 60687-149; 0004-1101; 62331-043; 72485-205; 53183-4009; 69539-019; 0004-1100; 65162-843; 16729-073; 72969-094; 62756-238; 16714-468; 68554-0033; 69097-949; 54245-7014; 72485-204; 62756-088; 0054-0271; 59651-205; 0093-7473; 72606-555; 76302-001; 69539-020; 65162-844; 53104-7618; 0378-2512; 51407-096; 81955-0001; 63759-0001; 49452-1713; 68001-488; 65129-1241; 64980-276; 0093-7474; 72606-554; 59923-721
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
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Gastrointestinal infection11.01.07.012; 07.19.02.0050.000799%Not Available
Gastrointestinal necrosis07.15.01.003; 24.04.08.0060.000278%
Gastrointestinal pain07.01.05.005--
Gastrointestinal perforation07.04.04.0010.000417%Not Available
Generalised oedema14.05.06.007; 08.01.07.0040.001066%
Genital ulceration23.07.03.004; 21.10.05.0010.000533%Not Available
Giardiasis11.06.06.001; 07.19.01.0150.000533%Not Available
Gingival bleeding24.07.02.010; 07.09.07.0010.001598%Not Available
Gingival pain07.09.04.0010.001066%
Gingivitis11.01.04.013; 07.09.03.0030.000533%
Glossitis07.14.01.0010.000533%Not Available
Glossodynia07.14.02.0010.001598%Not Available
Gout15.01.06.001; 14.09.01.001--Not Available
Granulocyte count decreased13.01.06.0050.000799%Not Available
Granulocytes abnormal13.01.06.034--Not Available
Granulocytopenia01.02.03.0030.001598%Not Available
Granuloma23.03.15.001; 08.01.05.0010.000533%Not Available
Haemangioma of liver24.03.06.006; 16.06.01.003; 09.04.01.0030.000799%Not Available
Haematemesis24.07.02.011; 07.12.02.002--Not Available
Haematochezia24.07.02.012; 07.12.02.003--Not Available
Haematoma24.07.01.001--
Haematuria24.07.01.047; 20.02.01.006--
Blood urine present13.13.02.002--Not Available
Haemoglobin13.01.05.018--Not Available
Haemoglobin abnormal13.01.05.0110.000799%Not Available
Haemoglobin decreased13.01.05.003--Not Available
Haemolysis01.06.04.0020.001066%
Haemolytic anaemia01.06.03.0020.001865%Not Available
Haemoptysis22.02.03.004; 02.01.02.006; 24.07.01.006--Not Available
Haemorrhoids24.10.02.002; 07.15.03.001--
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