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)
Dizziness postural02.11.04.008; 17.02.05.004; 24.06.02.0080.000470%Not Available
Dry throat22.12.03.005; 07.06.01.0050.000246%Not Available
Dysaesthesia23.03.03.077; 17.02.06.003--
Dysgeusia17.02.07.003; 07.14.03.0010.009089%
Dyspepsia07.01.02.0010.005865%
Dysphagia07.01.06.0030.012413%
Dyspnoea02.11.05.003; 22.02.01.0040.010633%
Dyspnoea exertional02.11.05.005; 22.02.01.0050.000694%Not Available
Ear haemorrhage04.03.01.002; 12.01.14.004; 24.07.01.0040.000112%Not Available
Ecchymosis24.07.06.002; 23.06.01.001; 01.01.03.0010.000112%Not Available
Electrocardiogram QT prolonged13.14.05.004--
Electrolyte imbalance14.05.01.0020.000526%Not Available
Embolism venous24.01.01.0030.000112%Not Available
Empyema11.01.08.020--Not Available
Enterocolitis07.08.03.0030.000168%
Eructation07.01.02.0030.000761%
Erythema multiforme23.03.01.003; 10.01.03.0150.000280%
Eye disorder06.08.03.0010.001097%Not Available
Eyelid ptosis06.05.01.002; 17.17.02.0040.000246%Not Available
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.003--
Fatigue08.01.01.0020.022386%
Febrile neutropenia08.05.02.004; 01.02.03.002--
Fibrosis08.03.01.0010.000112%Not Available
Flank pain20.02.03.006; 15.03.04.003; 08.01.08.0070.000168%
Flatulence07.01.04.0020.002507%
Fluid retention20.01.02.003; 14.05.06.0020.002686%Not Available
Gait disturbance15.03.05.013; 17.02.05.016; 08.01.02.002--
Gamma-glutamyltransferase increased13.03.04.024--
Gastric perforation12.02.03.007; 07.04.03.0010.000168%
Gastritis07.08.02.0010.000604%
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ADReCS-Target
Drug Name ADR Term Target
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