Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sorafenib
Drug ID BADD_D02058
Description Sorafenib (rINN), marketed as Nexavar by Bayer, is a drug approved for the treatment of advanced renal cell carcinoma (primary kidney cancer). It has also received "Fast Track" designation by the FDA for the treatment of advanced hepatocellular carcinoma (primary liver cancer), and has since performed well in Phase III trials. Sorafenib is a small molecular inhibitor of Raf kinase, PDGF (platelet-derived growth factor), VEGF receptor 2 & 3 kinases and c Kit the receptor for Stem cell factor. A growing number of drugs target most of these pathways. The originality of Sorafenib lays in its simultaneous targeting of the Raf/Mek/Erk pathway.
Indications and Usage Sorafenib is indicated for the treatment of unresectable hepatocellular carcinoma and advanced renal cell carcinoma.
Marketing Status approved; investigational
ATC Code L01EX02
DrugBank ID DB00398
KEGG ID D08524
MeSH ID D000077157
PubChem ID 216239
TTD Drug ID D0W5HK
NDC Product Code 24979-715; 51407-760; 13668-682; 12527-8488; 63850-8051; 68554-0073; 51990-201; 0378-1201; 0480-5425; 47049-848; 43598-458; 50419-488
UNII 9ZOQ3TZI87
Synonyms Sorafenib | Nexavar | BAY 43-9006 | BAY 43 9006 | BAY 439006 | Sorafenib N-Oxide | Sorafenib N Oxide | BAY-673472 | BAY 673472 | BAY 545-9085 | BAY 545 9085 | BAY 5459085 | BAY-545-9085 | BAY5459085 | Sorafenib Tosylate | 4-(4-(3-(4-Chloro-3-trifluoromethylphenyl)ureido)phenoxy)pyridine-2-carboxylic acid methyamide-4-methylbenzenesulfonate
Chemical Information
Molecular Formula C21H16ClF3N4O3
CAS Registry Number 284461-73-0
SMILES CNC(=O)C1=NC=CC(=C1)OC2=CC=C(C=C2)NC(=O)NC3=CC(=C(C=C3)Cl)C(F)(F)F
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)
Bronchial obstruction22.03.01.0130.000112%
Bruxism19.11.03.001; 07.01.06.0080.000112%Not Available
Burning sensation17.02.06.001; 08.01.09.0290.002160%Not Available
Cachexia16.32.03.011; 14.03.02.001; 08.01.01.0090.000336%Not Available
Capillary leak syndrome08.01.07.012; 24.06.03.0010.000112%
Cardiac failure02.05.01.0010.001287%
Cardiac failure acute02.05.01.0050.000168%Not Available
Cardiac failure congestive02.05.01.002--Not Available
Cerebellar infarction24.04.06.007; 17.08.01.0130.000112%Not Available
Cerebral artery embolism24.01.04.001; 17.08.01.0010.000112%Not Available
Cerebral haemorrhage24.07.04.001; 17.08.01.003--Not Available
Cerebral infarction24.04.06.002; 17.08.01.0040.002406%Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Change of bowel habit07.02.03.0020.000112%Not Available
Cheilitis23.03.03.025; 07.05.01.0010.000246%
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.0110.003917%Not Available
Chills15.05.03.016; 08.01.09.0010.001679%
Cholangitis09.02.01.0020.000728%Not Available
Cholecystitis09.03.01.0010.000168%
Cholecystitis acute09.03.01.0030.000112%Not Available
Cholelithiasis09.03.01.0020.000280%Not Available
Choluria20.02.01.0210.000112%Not Available
Chromaturia20.02.01.0020.000862%
Circulatory collapse24.06.02.0010.000280%Not Available
Coagulopathy01.01.02.0010.000280%Not Available
Cold sweat23.02.03.002; 08.01.03.0240.000358%Not Available
Colitis ischaemic24.04.08.012; 07.08.01.0040.000392%Not Available
Coma17.02.09.0010.000783%Not Available
Coma hepatic09.01.03.005; 17.02.09.0020.000336%Not Available
Completed suicide19.12.01.001; 08.04.01.010--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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