Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Vincristine
Drug ID BADD_D02360
Description Vincristine is an antitumor vinca alkaloid isolated from Vinca Rosea. It is marketed under several brand names, many of which have different formulations such as Marqibo (liposomal injection) and Vincasar. Vincristine is indicated for the treatment of acute leukaemia, malignant lymphoma, Hodgkin's disease, acute erythraemia, and acute panmyelosis. vincristine sulfate is often chosen as part of polychemotherapy because of lack of significant bone–marrow suppression (at recommended doses) and of unique clinical toxicity (neuropathy).
Indications and Usage Treatment of acute lymphocytic leukemia (ALL), Hodgkin lymphoma, non-Hodgkin lymphomas, Wilms' tumor, neuroblastoma, rhabdomyosarcoma. Liposomal vincristine is indicated for the treatment of relapsed Philadelphia chromosome-negative (Ph-) acute lymphoblastic leukemia (ALL).
Marketing Status approved; investigational
ATC Code L01CA02
DrugBank ID DB00541
KEGG ID D08679
MeSH ID D014750
PubChem ID 5978
TTD Drug ID D09QVV
NDC Product Code Not Available
UNII 5J49Q6B70F
Synonyms Vincristine | Leurocristine | Vincristine Sulfate | Sulfate, Vincristine | cellcristin | Citomid | Vincristin medac | Oncovin | Oncovine | Onkocristin | Vincasar | Farmistin | Vincasar PFS | PFS, Vincasar | Vincristin Bristol | Vintec | Vincrisul
Chemical Information
Molecular Formula C46H56N4O10
CAS Registry Number 57-22-7
SMILES CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8 N6C=O)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)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)
Abdominal distension07.01.04.0010.000168%
Abdominal pain07.01.05.0020.000504%
Acute abdomen07.01.06.015---
Acute lymphocytic leukaemia01.10.01.001; 16.01.01.0010.000112%-
Acute myeloid leukaemia01.10.05.001; 16.01.05.0010.000168%-
Acute respiratory failure14.01.04.004; 22.02.06.0010.000168%-
Adrenal disorder05.01.03.001---
Agitation17.02.05.012; 19.06.02.001--
Alopecia23.02.02.001--
Altered state of consciousness17.02.04.001; 19.07.01.003---
Anaemia01.03.02.0010.000448%
Anaphylactic shock10.01.07.002; 24.06.02.004---
Aphthous ulcer07.05.06.0020.000112%-
Areflexia17.02.01.0010.000112%-
Ascites02.05.04.002; 07.07.01.001; 09.01.05.0030.000112%
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.001---
Ataxia08.01.02.004; 17.02.02.001--
Atonic urinary bladder17.05.01.010; 20.03.03.004---
Azotaemia20.01.01.001---
Back pain15.03.04.005--
Blindness06.02.10.003; 17.17.01.003---
Blindness cortical06.02.10.004; 17.17.01.017---
Blood uric acid increased13.02.04.001---
Body temperature increased13.15.01.001---
Bone pain15.02.01.001--
Cardiac arrest02.03.04.0010.000280%
Cerebral haemorrhage17.08.01.003; 24.07.04.001---
Cerebral infarction17.08.01.004; 24.04.06.002---
Cholestasis09.01.01.0010.000168%-
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ADReCS-Target
Drug Name ADR Term Target
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