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 Prescription
ATC Code L01EX02
DrugBank ID DB00398
KEGG ID D08524
MeSH ID D000077157
PubChem ID 216239
TTD Drug ID D0W5HK
NDC Product Code 0378-1201; 68554-0073; 12527-8488; 63850-8051; 47049-848; 50419-488; 43744-545
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
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Azotaemia20.01.01.0010.000799%Not Available
Back pain15.03.04.0050.010124%
Bacteraemia11.01.11.0010.000139%
Basal cell carcinoma23.08.02.001; 16.03.02.001--Not Available
Benign prostatic hyperplasia21.04.02.0010.001066%Not Available
Bile duct stone09.02.02.0030.000533%Not Available
Bladder cancer16.08.01.001; 20.03.04.001--Not Available
Blindness17.17.01.003; 06.02.02.0010.002131%Not Available
Blindness transient17.17.01.004; 06.02.02.0020.000533%Not Available
Blindness unilateral17.17.01.016; 06.02.02.0090.000533%Not Available
Blister12.01.06.002; 23.03.01.0010.039695%Not Available
Blood albumin decreased13.09.01.0010.000625%Not Available
Blood albumin increased13.09.01.0020.000533%Not Available
Blood bilirubin increased13.03.01.0080.023711%
Blood bilirubin unconjugated increased13.03.01.0240.000533%Not Available
Blood calcium decreased13.11.01.0020.000799%Not Available
Blood chloride increased13.11.01.0050.000533%Not Available
Blood cholesterol increased13.12.01.002--
Blood creatine increased13.13.01.0010.000533%Not Available
Blood creatine phosphokinase increased13.04.01.0010.002398%
Blood creatinine increased13.13.01.0040.006660%
Blood glucose decreased13.02.02.0010.002931%Not Available
Blood glucose increased13.02.02.0020.005328%Not Available
Blood lactate dehydrogenase increased13.04.02.0020.002131%
Blood lactic acid increased13.02.01.0150.000533%Not Available
Blood magnesium decreased13.11.01.0080.001066%Not Available
Blood potassium abnormal13.11.01.0240.000799%Not Available
Blood potassium decreased13.11.01.0100.002398%Not Available
Blood potassium increased13.11.01.0110.002664%Not Available
Blood pressure decreased13.14.03.0020.003996%Not Available
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