Stem definition | Drug id | CAS RN |
---|---|---|
uridine derivatives used as antiviral agents and as antineoplastics | 5029 | 4105-38-8 |
None
None
Date | Agency | Company | Orphan |
---|---|---|---|
Sept. 4, 2015 | FDA | WELLSTAT THERAPEUTICS CORP |
None
None
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Complication associated with device | 72.06 | 57.08 | 13 | 79 | 17483 | 79726813 |
None
Source | Code | Description |
---|---|---|
ATC | A16AX13 | ALIMENTARY TRACT AND METABOLISM OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS Various alimentary tract and metabolism products |
FDA Chemical/Ingredient | N0000007587 | Pyrimidines |
FDA Chemical/Ingredient | N0000175452 | Analogs/Derivatives |
FDA EPC | N0000191809 | Pyrimidine Analog |
CHEBI has role | CHEBI:49103 | drug metabolites |
CHEBI has role | CHEBI:77746 | Homo sapiens metabolite |
CHEBI has role | CHEBI:78675 | fundamental metabolites |
CHEBI has role | CHEBI:50266 | Prodrugs |
CHEBI has role | CHEBI:63726 | neuroprotective agents |
CHEBI has role | CHEBI:71031 | orphan drugs |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Hereditary orotic aciduria | indication | 16242007 | |
Antimetabolite overdose | indication | 295696001 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 9.68 | acidic |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
---|---|---|---|---|---|---|---|---|---|---|
10GM/PACKET | VISTOGARD | BTG INTL | N208159 | Dec. 11, 2015 | RX | GRANULE | ORAL | 7776838 | Aug. 17, 2027 | EMERGENCY TREATMENT OF ADULT & PEDIATRIC PATIENTS FOLLOWING FLUOROURACIL OR CAPECITABINE OVERDOSE,OR WHO EXHIBIT EARLY-ONSET,SEVERE OR LIFE-THREATENING CARDIAC OR CNS TOXICITY OR UNUSUALLY SEVERE ADVERSE REACTIONS WITHIN 96 HOURS |
None
None
ID | Source |
---|---|
2WP61F175M | UNII |
4035398 | VANDF |
4035399 | VANDF |
C0281351 | UMLSCUI |
CHEBI:90914 | CHEBI |
CHEBI:16704 | CHEBI |
URI | PDB_CHEM_ID |
CHEMBL2107381 | ChEMBL_ID |
20058 | PUBCHEM_CID |
DB09144 | DRUGBANK_ID |
9204 | INN_ID |
C000609666 | MESH_SUPPLEMENTAL_RECORD_UI |
DB02745 | DRUGBANK_ID |
11017 | RXNORM |
237553 | MMSL |
238118 | MMSL |
31371 | MMSL |
d05935 | MMSL |
005776 | NDDF |
016442 | NDDF |
57763003 | SNOMEDCT_US |
715619008 | SNOMEDCT_US |
C0041984 | UMLSCUI |
CHEMBL100259 | ChEMBL_ID |
58-96-8 | SECONDARY_CAS_RN |
6029 | PUBCHEM_CID |
D014529 | MESH_DESCRIPTOR_UI |
4566 | IUPHAR_LIGAND_ID |
WHI7HQ7H85 | UNII |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
VISTOGARD | HUMAN PRESCRIPTION DRUG LABEL | 1 | 69468-151 | GRANULE | 951 mg | ORAL | NDA | 25 sections |
XURIDEN | HUMAN PRESCRIPTION DRUG LABEL | 1 | 69468-152 | GRANULE | 951 mg | ORAL | NDA | 26 sections |
XURIDEN | HUMAN PRESCRIPTION DRUG LABEL | 1 | 69468-152 | GRANULE | 951 mg | ORAL | NDA | 26 sections |