Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Idelalisib
Drug ID BADD_D01130
Description Idelalisib is a phosphoinositide 3-kinase inhibitor indicated in the treatment of chronic lymphocytic leukemia (CLL), relapsed follicular B-cell non-Hodgkin lymphoma (FL), and relapsed small lymphocytic lymphoma (SLL). For the treatment of relapsed CLL, it is currently indicated as a second-line agent in combination with rituximab in patients for whom rituximab alone would be considered appropriate therapy due to other co-morbidities, while in the treatment of FL and SLL it is intended to be used in patients who have received at least two prior systemic therapies. More specifically, idelalisib targets P110δ, the delta isoform of the enzyme phosphatidylinositol-4,5-bisphosphate 3-kinase, also known as PI-3K. The PI-3Ks are a family of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival and intracellular trafficking, which in turn are involved in cancer. In contrast to the other class IA PI3Ks p110α and p110β, p110δ is principally expressed in leukocytes (white blood cells) and is important for the function of T cells, B cell, mast cells and neutrophils. By inhibiting this enzyme, idelalisib induces apoptosis of malignant cells and inhibits several cell signaling pathways, including B-cell receptor (BCR) signaling and C-X-C chemokine receptors type 5 and type 4 signalling, which are involved in trafficking and homing of B-cells to the lymph nodes and bone marrow. Treatment of lymphoma cells with idelalisib has been shown to result in inhibition of chemotaxis and adhesion, and reduced cell viability.
Indications and Usage Idelalisib is indicated in the treatment of chronic lymphocytic leukemia (CLL), relapsed follicular B-cell non-Hodgkin lymphoma (FL), and relapsed small lymphocytic lymphoma (SLL). For the treatment of relapsed CLL, it is currently indicated as a second-line agent in combination with rituximab in patients for whom rituximab alone would be considered appropriate therapy due to other co-morbidities, while in the treatment of FL and SLL it is intended to be used in patients who have received at least two prior systemic therapies.
Marketing Status Prescription
ATC Code L01EM01
DrugBank ID DB09054
KEGG ID D10560
MeSH ID C552946
PubChem ID 11625818
TTD Drug ID D0J5VR
NDC Product Code 61958-1701; 68578-0013; 63285-753; 61958-1702; 63285-754; 12651-122
Synonyms idelalisib | GS-1101 | Zydelig | CAL 101 | CAL101 | CAL-101
Chemical Information
Molecular Formula C22H18FN7O
CAS Registry Number 870281-82-6
SMILES CCC(C1=NC2=C(C(=CC=C2)F)C(=O)N1C3=CC=CC=C3)NC4=NC=NC5=C4NC=N5
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)
Abasia17.02.05.035; 08.01.02.007--Not Available
Staphylococcal bacteraemia11.02.05.0010.000533%Not Available
Deep vein thrombosis24.01.02.003--Not Available
Bronchopneumopathy22.02.07.0100.000208%Not Available
Sepsis syndrome11.01.11.012; 10.02.01.049--Not Available
Transaminases increased13.03.01.0150.005062%Not Available
Pneumonia necrotising22.07.01.011; 11.01.09.013--Not Available
Haemorrhage24.07.01.002--Not Available
Lung infection pseudomonal22.07.06.003; 11.02.12.002--Not Available
Cognitive disorder19.21.02.001; 17.03.03.003--
Toxic skin eruption10.01.01.008; 23.03.05.0030.000139%Not Available
Lung neoplasm malignant22.08.01.001; 16.19.02.0010.000208%Not Available
Dermatitis psoriasiform23.03.14.0040.000533%Not Available
Pseudomonal sepsis11.02.12.0030.000799%Not Available
Gastrointestinal toxicity12.03.01.019; 07.08.03.0060.000533%Not Available
Skin toxicity23.03.03.032; 12.03.01.0200.000533%Not Available
Blood alkaline phosphatase increased13.04.02.004--
Intervertebral discitis15.02.05.002; 12.02.13.001; 11.01.01.0020.000799%Not Available
Hepatic enzyme increased13.03.01.0190.002931%Not Available
Neurological symptom17.02.05.0100.000533%Not Available
Prostate cancer21.04.02.002; 16.25.01.0010.000139%Not Available
Pneumonia bacterial22.07.06.004; 11.02.01.0090.000533%Not Available
Cardiac disorder02.01.01.003--Not Available
Haematotoxicity12.03.01.025; 01.05.01.0070.002131%Not Available
Lung infection22.07.01.008; 11.01.09.0080.000486%
Ischaemic stroke17.08.01.018; 24.04.06.010--Not Available
Mantle cell lymphoma16.28.05.001; 01.15.05.0010.000139%Not Available
Pneumonia fungal22.07.08.002; 11.03.05.008--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Ill-defined disorder08.01.03.0490.000533%Not Available
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