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)
Penile pain21.12.01.0080.000437%
Peptic ulcer07.04.07.0010.000112%Not Available
Pericardial effusion02.06.01.002--
Pericarditis02.06.02.0010.000280%
Peripheral coldness23.06.04.008; 24.04.03.006; 08.01.09.010--Not Available
Peripheral motor neuropathy17.09.03.0040.000112%
Peripheral sensory neuropathy17.09.03.0050.000806%
Peripheral vascular disorder24.03.01.0030.000392%Not Available
Peroneal nerve palsy17.09.02.003--Not Available
Personality change17.02.05.019; 19.05.01.006--
Petechiae24.07.06.004; 23.06.01.003; 01.01.03.0020.000392%Not Available
Pharyngeal oedema22.04.05.003; 10.01.05.016; 23.04.01.0160.000851%Not Available
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Phlebitis24.12.03.004; 12.02.01.0020.000246%
Photophobia17.17.02.006; 06.01.01.0040.000526%
Photosensitivity reaction23.03.09.003--
Platelet count decreased13.01.04.001--
Platelet disorder01.08.03.0010.000280%Not Available
Pleural disorder22.05.03.002--Not Available
Pleural effusion22.05.02.002--
Pleural fibrosis22.05.03.0030.000168%Not Available
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Pneumonitis22.01.01.0060.001108%
Pneumothorax22.05.02.0030.000504%
Pollakiuria20.02.02.007--
Polyneuropathy17.09.03.0120.000448%Not Available
Polyuria20.02.03.002--Not Available
Portal hypertension24.08.06.001; 09.01.06.0060.000224%
Portal vein thrombosis24.01.03.003; 09.01.06.0070.000168%
Premenstrual syndrome19.04.02.009; 17.14.01.019; 21.01.01.007--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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