Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Axitinib
Drug ID BADD_D00193
Description Axitinib is a second generation tyrosine kinase inhibitor that works by selectively inhibiting vascular endothelial growth factor receptors (VEGFR-1, VEGFR-2, VEGFR-3).[L6676] Through this mechanism of action, axitinib blocks angiogenesis, tumour growth and metastases. It is reported to exhibit potency that is 50-450 times higher than that of the first generation VEGFR inhibitors.[L6676] Axitinib is an indazole derivative.[A179398] It is most commonly marketed under the name Inlyta® and is available in oral formulations.
Indications and Usage Used in kidney cell cancer and investigated for use/treatment in pancreatic and thyroid cancer.
Marketing Status approved; investigational
ATC Code L01EK01
DrugBank ID DB06626
KEGG ID D03218
MeSH ID D000077784
PubChem ID 6450551
TTD Drug ID D01ZRI
NDC Product Code 0069-0145; 54893-0032; 68554-0088; 63539-026; 82920-028; 0069-0151; 65344-0033; 63539-044; 54893-0043
UNII C9LVQ0YUXG
Synonyms Axitinib | AG 013736 | AG013736 | AG-013736 | Inlyta
Chemical Information
Molecular Formula C22H18N4OS
CAS Registry Number 319460-85-0
SMILES CNC(=O)C1=CC=CC=C1SC2=CC3=C(C=C2)C(=NN3)C=CC4=CC=CC=N4
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)
Lower gastrointestinal haemorrhage07.12.03.011; 24.07.02.030--
Deep vein thrombosis24.01.02.003--Not Available
Blood pressure inadequately controlled24.06.01.0070.000112%Not Available
Plantar erythema23.03.06.0120.000112%Not Available
B-lymphocyte count decreased13.01.06.041--Not Available
Malignant neoplasm progression16.16.01.005--Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.0150.000224%Not Available
Ear congestion04.03.01.0100.000571%Not Available
Ear discomfort04.03.01.0050.000627%Not Available
Upper respiratory tract congestion22.12.03.0330.000761%Not Available
Lymphatic disorder01.09.01.003--Not Available
Nasal discomfort22.12.03.0120.000683%Not Available
Protein urine present13.13.02.006--Not Available
Epigastric discomfort07.01.02.0040.000571%Not Available
Musculoskeletal discomfort15.03.04.0010.000571%Not Available
Haemorrhoidal haemorrhage24.10.02.001; 07.15.03.0020.000302%
Cerebral disorder17.02.10.0170.000112%Not Available
Brain cancer metastatic17.20.04.001; 16.30.04.001--Not Available
Haemorrhage24.07.01.002--Not Available
Haemorrhage urinary tract24.07.01.007; 20.02.03.0050.000168%Not Available
Pneumatosis intestinalis07.11.01.0430.000560%Not Available
Hypoaesthesia oral07.05.05.003; 17.02.06.0210.000437%Not Available
Paraesthesia oral07.05.05.035; 17.02.06.0080.000302%Not Available
Cognitive disorder19.21.02.001; 17.03.03.003--
Cancer pain16.32.03.0040.001186%Not Available
Dysgraphia17.02.03.006--Not Available
Gastrointestinal toxicity12.03.01.019; 07.08.03.0060.000492%Not Available
Angiopathy24.03.02.0070.000168%Not Available
Metastases to central nervous system17.02.10.013; 16.22.02.004--Not Available
Skin toxicity12.03.01.020; 23.03.03.0320.000437%Not Available
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