Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Etoposide
Drug ID BADD_D00854
Description A semisynthetic derivative of podophyllotoxin that exhibits antitumor activity. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle.
Indications and Usage For use in combination with other chemotherapeutic agents in the treatment of refractory testicular tumors and as first line treatment in patients with small cell lung cancer. Also used to treat other malignancies such as lymphoma, non-lymphocytic leukemia, and glioblastoma multiforme.
Marketing Status approved
ATC Code L01CB01
DrugBank ID DB00773
KEGG ID D00125
MeSH ID D005047
PubChem ID 36462
TTD Drug ID D0B7EB
NDC Product Code 0378-3266; 0143-9510; 63323-104; 55361-0006; 68001-265; 0703-5656; 0143-9512; 16729-114; 0143-9511; 53183-8538; 57884-0008; 53104-7514; 0143-9376
UNII 6PLQ3CP4P3
Synonyms Etoposide | Eposide | Demethyl Epipodophyllotoxin Ethylidine Glucoside | Eto-GRY | Eto GRY | Etoposide, (5a alpha,9 alpha)-Isomer | Etoposide, (5S)-Isomer | Etoposide, alpha-D-Glucopyranosyl Isomer | Etoposide, alpha D Glucopyranosyl Isomer | alpha-D-Glucopyranosyl Isomer Etoposide | Etoposido Ferrer Farma | Exitop | Lastet | NSC-141540 | NSC 141540 | NSC141540 | Onkoposid | Riboposid | Toposar | Etoposide Teva | Teva, Etoposide | Vepesid | VP 16-213 | VP 16 213 | VP 16213 | VP-16 | VP 16 | VP16 | Vépéside-Sandoz | Vépéside Sandoz | Celltop | Etopos | Etomedac | Eposin | Etoposide, (5a alpha)-Isomer | Etoposide Pierre Fabre
Chemical Information
Molecular Formula C29H32O13
CAS Registry Number 33419-42-0
SMILES CC1OCC2C(O1)C(C(C(O2)OC3C4COC(=O)C4C(C5=CC6=C(C=C35)OCO6)C7=CC(=C(C(=C7)OC)O)OC) O)O
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)
Ulcer08.03.06.001--Not Available
Unresponsive to stimuli17.02.05.0310.000392%Not Available
Urethral disorder20.07.01.002--Not Available
Urinary tract disorder20.08.01.001--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Vein disorder24.03.02.015--Not Available
Venoocclusive liver disease12.02.09.039; 24.04.07.002; 09.01.06.0020.000112%
Vertigo17.02.12.002; 04.04.01.003--
Vomiting07.01.07.0030.001925%
Wheezing22.03.01.0090.000336%
Cardiotoxicity02.11.01.009; 12.03.01.0070.000280%Not Available
Brain oedema17.07.02.003; 12.01.10.0100.000112%
Neutropenic sepsis11.01.11.006; 01.02.03.007--Not Available
Muscle tightness15.05.03.007--Not Available
Lung cancer metastatic16.19.02.003; 22.08.01.004--Not Available
Musculoskeletal chest pain22.09.01.001; 15.03.04.0120.000112%
Acute coronary syndrome02.02.02.015; 24.04.04.011--Not Available
Haemodynamic instability24.03.02.0060.000224%Not Available
Lymphatic disorder01.09.01.003--Not Available
Inappropriate antidiuretic hormone secretion14.05.07.001; 05.03.03.0010.000224%Not Available
Febrile bone marrow aplasia01.03.03.007; 08.05.02.0050.000112%Not Available
Skin swelling23.03.03.0390.000168%Not Available
Bronchopleural fistula22.05.03.0010.000112%
Infusion site swelling12.07.05.003; 08.02.05.0020.000112%Not Available
Hypoaesthesia oral17.02.06.021; 07.05.05.0030.000112%Not Available
Ocular icterus06.08.03.009; 01.06.04.007; 09.01.01.0070.000112%Not Available
Nail pigmentation23.02.05.007--Not Available
Bicytopenia01.03.03.0100.000392%Not Available
Gastrointestinal toxicity12.03.01.019; 07.08.03.0060.000112%Not Available
Angiopathy24.03.02.007--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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