Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ceritinib
Drug ID BADD_D00414
Description Ceritinib is used for the treatment of adults with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) following failure (secondary to resistance or intolerance) of prior crizotinib therapy. About 4% of patients with NSCLC have a chromosomal rearrangement that generates a fusion gene between EML4 (echinoderm microtubule-associated protein-like 4) and ALK (anaplastic lymphoma kinase), which results in constitutive kinase activity that contributes to carcinogenesis and seems to drive the malignant phenotype. Ceritinib exerts its therapeutic effect by inhibiting autophosphorylation of ALK, ALK-mediated phosphorylation of the downstream signaling protein STAT3, and proliferation of ALK-dependent cancer cells. Following treatment with crizotinib (a first-generation ALK inhibitor), most tumours develop drug resistance due to mutations in key "gatekeeper" residues of the enzyme. This occurrence led to development of novel second-generation ALK inhibitors such as ceritinib to overcome crizotinib resistance. The FDA approved ceritinib in April 2014 due to a surprisingly high response rate (56%) towards crizotinib-resistant tumours and has designated it with orphan drug status.
Indications and Usage Ceritinib is a kinase inhibitor indicated for the treatment of patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) who have progressed on or are intolerant to crizotinib. This indication is approved under accelerated approval based on tumor response rate and duration of response. An improvement in survival or disease-related symptoms has not been established. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.
Marketing Status Prescription
ATC Code L01ED02
DrugBank ID DB09063
KEGG ID D10551
MeSH ID C586847
PubChem ID 57379345
TTD Drug ID D04LVK
NDC Product Code 0078-0694; 54893-0072
Synonyms ceritinib | 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine | Zykadia | LDK378
Chemical Information
Molecular Formula C28H36ClN5O3S
CAS Registry Number 1032900-25-6
SMILES CC1=CC(=C(C=C1C2CCNCC2)OC(C)C)NC3=NC=C(C(=N3)NC4=CC=CC=C4S(=O)(=O)C(C)C)Cl
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)
Abdominal discomfort07.01.06.0010.001865%Not Available
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.0020.009058%
Abdominal pain upper07.01.05.0030.002131%
Accommodation disorder06.02.04.001--Not Available
Acute hepatic failure09.01.03.0010.000533%Not Available
Adenocarcinoma16.16.01.0040.000139%Not Available
Alanine aminotransferase increased13.03.01.0030.005595%
Alopecia23.02.02.001--
Altered state of consciousness19.07.01.003; 17.02.04.0010.000278%Not Available
Amylase increased13.05.01.0090.000533%
Anaemia01.03.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.0010.000139%
Anxiety19.06.02.002--
Appendicitis07.19.01.001; 11.01.07.0010.000799%
Arrhythmia02.03.02.0010.000799%Not Available
Arthralgia15.01.02.001--
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.000533%
Aspartate aminotransferase increased13.03.01.0060.004529%
Asthenia08.01.01.001--Not Available
Atrial fibrillation02.03.03.002--
Back pain15.03.04.005--
Blister23.03.01.001; 12.01.06.0020.000533%Not Available
Blood bilirubin increased13.03.01.0080.001865%
Blood creatinine increased13.13.01.0040.004529%
Blood glucose increased13.02.02.0020.001332%Not Available
Blood lactate dehydrogenase increased13.04.02.0020.000208%
Blood potassium decreased13.11.01.0100.001066%Not Available
Bradycardia02.03.02.0020.000799%Not Available
Bronchitis22.07.01.001; 11.01.09.0010.000533%
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