Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Crizotinib
Drug ID BADD_D00535
Description Crizotinib an inhibitor of receptor tyrosine kinase for the treatment of non-small cell lung cancer (NSCLC). Verification of the presence of ALK fusion gene is done by Abbott Molecular's Vysis ALK Break Apart FISH Probe Kit. This verification is used to select for patients suitable for treatment. FDA approved in August 26, 2011.
Indications and Usage Crizotinib is used for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) that is anaplastic-lymphoma kinase (ALK)-positive as detected by a FDA-approved test.
Marketing Status approved
ATC Code L01ED01
DrugBank ID DB08865
KEGG ID D09731
MeSH ID D000077547
PubChem ID 11626560
TTD Drug ID D03ZBT
NDC Product Code 68724-1020; 53869-2231; 53869-2230; 0069-8140; 0069-8141
UNII 53AH36668S
Synonyms Crizotinib | PF-02341066 | PF-2341066 | PF 2341066 | PF2341066 | PF 02341066 | PF02341066 | Xalkori
Chemical Information
Molecular Formula C21H22Cl2FN5O
CAS Registry Number 877399-52-5
SMILES CC(C1=C(C=CC(=C1Cl)F)Cl)OC2=C(N=CC(=C2)C3=CN(N=C3)C4CCNCC4)N
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)
Mediastinal disorder22.09.03.001--Not Available
Neoplasm progression16.16.02.0050.049808%Not Available
Oesophageal disorder07.11.02.0010.000929%Not Available
Optic neuropathy17.04.05.005; 06.02.08.0020.000112%Not Available
Partial seizures17.12.03.0100.000168%Not Available
Decreased appetite14.03.01.005; 08.01.09.0280.011629%
Renal injury20.01.03.015; 12.01.05.0010.000112%Not Available
Blood disorder01.05.01.004--Not Available
Cardiac fibrillation02.03.02.0210.000112%Not Available
Disease progression08.01.03.0380.070067%
Neoplasm recurrence16.16.02.0040.000246%Not Available
Non-small cell lung cancer22.08.01.002; 16.19.01.0010.010185%Not Available
Pulmonary toxicity22.01.02.007; 12.03.01.0130.000448%Not Available
Hepatic lesion09.01.08.0050.000246%Not Available
Hepatobiliary disease09.01.08.003--Not Available
Metastasis16.22.01.0010.000246%Not Available
Renal impairment20.01.03.0100.005831%Not Available
Sinus disorder22.04.06.0020.000437%
Non-cardiac chest pain22.12.02.009; 08.01.08.0060.000246%
Erosive oesophagitis07.04.05.0040.000168%Not Available
Hypophagia19.09.01.004; 14.03.01.006; 07.01.06.0100.000660%Not Available
Cardiovascular event prophylaxis25.08.01.002--Not Available
Bone marrow failure01.03.03.0050.000728%
Cytopenia01.03.03.0120.000224%Not Available
Liver injury12.01.17.012; 09.01.07.0220.000392%Not Available
Organising pneumonia22.01.02.0080.000168%Not Available
Hypertransaminasaemia09.01.02.0050.000224%Not Available
Oropharyngeal discomfort22.12.03.015; 07.05.05.0080.000381%Not Available
Skin sensitisation23.03.03.052; 10.02.01.0380.000246%Not Available
Drug-induced liver injury09.01.07.023; 12.03.01.044--Not Available
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ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene