Stem definition | Drug id | CAS RN |
---|---|---|
4741 | 843663-66-1 |
Dose | Unit | Route |
---|---|---|
86 | mg | O |
None
Date | Agency | Company | Orphan |
---|---|---|---|
Dec. 28, 2012 | FDA | JANSSEN THERAP | |
Jan. 19, 2018 | PMDA | Janssen Pharmaceutical KK |
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 |
---|---|---|---|---|---|---|
Electrocardiogram QT prolonged | 458.24 | 31.38 | 156 | 3230 | 59374 | 63426262 |
Neuropathy peripheral | 128.10 | 31.38 | 78 | 3308 | 113589 | 63372047 |
Hepatotoxicity | 127.02 | 31.38 | 54 | 3332 | 36987 | 63448649 |
Anaemia | 115.60 | 31.38 | 107 | 3279 | 293323 | 63192313 |
Off label use | 90.65 | 31.38 | 142 | 3244 | 674320 | 62811316 |
Intentional product use issue | 86.60 | 31.38 | 64 | 3322 | 127828 | 63357808 |
Drug-induced liver injury | 59.49 | 31.38 | 33 | 3353 | 40189 | 63445447 |
Vomiting | 55.23 | 31.38 | 103 | 3283 | 559514 | 62926122 |
Immune reconstitution inflammatory syndrome associated tuberculosis | 52.32 | 31.38 | 10 | 3376 | 360 | 63485276 |
Polyneuropathy | 49.04 | 31.38 | 21 | 3365 | 14568 | 63471068 |
Butterfly rash | 46.24 | 31.38 | 12 | 3374 | 1761 | 63483875 |
Aspartate aminotransferase increased | 45.48 | 31.38 | 38 | 3348 | 90239 | 63395397 |
Respiratory failure | 43.48 | 31.38 | 39 | 3347 | 101819 | 63383817 |
Meningitis tuberculous | 41.90 | 31.38 | 9 | 3377 | 584 | 63485052 |
Pyelonephritis chronic | 36.98 | 31.38 | 7 | 3379 | 239 | 63485397 |
Disturbance in social behaviour | 36.61 | 31.38 | 12 | 3374 | 3981 | 63481655 |
Herbal toxicity | 34.33 | 31.38 | 5 | 3381 | 31 | 63485605 |
Cardiopulmonary failure | 33.70 | 31.38 | 11 | 3375 | 3601 | 63482035 |
Hypomagnesaemia | 32.96 | 31.38 | 20 | 3366 | 28717 | 63456919 |
Product use in unapproved indication | 32.94 | 31.38 | 44 | 3342 | 179036 | 63306600 |
Deafness | 32.90 | 31.38 | 17 | 3369 | 17940 | 63467696 |
Psychotic disorder | 32.36 | 31.38 | 19 | 3367 | 25693 | 63459943 |
Gastroenteritis | 31.77 | 31.38 | 19 | 3367 | 26571 | 63459065 |
Alanine aminotransferase increased | 31.57 | 31.38 | 33 | 3353 | 103737 | 63381899 |
Hypokalaemia | 31.56 | 31.38 | 33 | 3353 | 103771 | 63381865 |
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 |
---|---|---|---|---|---|---|
Electrocardiogram QT prolonged | 709.24 | 31.96 | 233 | 3431 | 40719 | 34912548 |
Hepatotoxicity | 451.41 | 31.96 | 142 | 3522 | 21343 | 34931924 |
Intentional product use issue | 190.04 | 31.96 | 102 | 3562 | 59714 | 34893553 |
Neuropathy peripheral | 178.89 | 31.96 | 110 | 3554 | 83153 | 34870114 |
Off label use | 172.67 | 31.96 | 214 | 3450 | 419310 | 34533957 |
Anaemia | 106.45 | 31.96 | 126 | 3538 | 233209 | 34720058 |
Optic neuritis | 68.04 | 31.96 | 22 | 3642 | 3552 | 34949715 |
Drug resistance | 62.49 | 31.96 | 37 | 3627 | 25890 | 34927377 |
Tuberculosis | 59.11 | 31.96 | 25 | 3639 | 8552 | 34944715 |
Aspartate aminotransferase increased | 49.13 | 31.96 | 47 | 3617 | 67736 | 34885531 |
Polyneuropathy | 45.97 | 31.96 | 25 | 3639 | 14871 | 34938396 |
Vomiting | 43.48 | 31.96 | 86 | 3578 | 247535 | 34705732 |
Incorrect product administration duration | 43.35 | 31.96 | 17 | 3647 | 4794 | 34948473 |
Drug-induced liver injury | 39.69 | 31.96 | 29 | 3635 | 28803 | 34924464 |
Myelosuppression | 35.03 | 31.96 | 23 | 3641 | 19242 | 34934025 |
Toxic optic neuropathy | 32.64 | 31.96 | 9 | 3655 | 841 | 34952426 |
Psychotic disorder | 32.31 | 31.96 | 24 | 3640 | 24428 | 34928839 |
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 |
---|---|---|---|---|---|---|
Electrocardiogram QT prolonged | 1102.71 | 31.42 | 377 | 6509 | 90009 | 79647493 |
Hepatotoxicity | 542.29 | 31.42 | 193 | 6693 | 51159 | 79686343 |
Neuropathy peripheral | 297.17 | 31.42 | 172 | 6714 | 141133 | 79596369 |
Intentional product use issue | 259.75 | 31.42 | 162 | 6724 | 151950 | 79585552 |
Off label use | 250.09 | 31.42 | 345 | 6541 | 906870 | 78830632 |
Anaemia | 211.85 | 31.42 | 224 | 6662 | 444791 | 79292711 |
Polyneuropathy | 95.45 | 31.42 | 45 | 6841 | 24106 | 79713396 |
Aspartate aminotransferase increased | 92.01 | 31.42 | 84 | 6802 | 138557 | 79598945 |
Vomiting | 87.53 | 31.42 | 183 | 6703 | 665645 | 79071857 |
Optic neuritis | 86.07 | 31.42 | 32 | 6854 | 9488 | 79728014 |
Drug-induced liver injury | 84.71 | 31.42 | 59 | 6827 | 66058 | 79671444 |
Drug resistance | 79.52 | 31.42 | 48 | 6838 | 42165 | 79695337 |
Incorrect product administration duration | 72.01 | 31.42 | 30 | 6856 | 11992 | 79725510 |
Psychotic disorder | 70.14 | 31.42 | 44 | 6842 | 41358 | 79696144 |
Tuberculosis | 65.25 | 31.42 | 30 | 6856 | 15168 | 79722334 |
Myelosuppression | 61.26 | 31.42 | 40 | 6846 | 40256 | 79697246 |
Meningitis tuberculous | 59.68 | 31.42 | 15 | 6871 | 1190 | 79736312 |
Product use in unapproved indication | 57.47 | 31.42 | 88 | 6798 | 250271 | 79487231 |
Alanine aminotransferase increased | 53.54 | 31.42 | 68 | 6818 | 162502 | 79575000 |
Deafness | 53.21 | 31.42 | 29 | 6857 | 21008 | 79716494 |
Respiratory failure | 50.83 | 31.42 | 70 | 6816 | 180841 | 79556661 |
Hypokalaemia | 50.21 | 31.42 | 62 | 6824 | 143978 | 79593524 |
Cardiopulmonary failure | 47.67 | 31.42 | 19 | 6867 | 6782 | 79730720 |
Hepatitis toxic | 41.80 | 31.42 | 16 | 6870 | 5131 | 79732371 |
Optic neuropathy | 40.08 | 31.42 | 14 | 6872 | 3470 | 79734032 |
Pulmonary tuberculosis | 38.44 | 31.42 | 17 | 6869 | 7848 | 79729654 |
Treatment noncompliance | 37.23 | 31.42 | 33 | 6853 | 52235 | 79685267 |
Pain | 36.76 | 31.42 | 8 | 6878 | 703794 | 79033708 |
Butterfly rash | 36.66 | 31.42 | 11 | 6875 | 1685 | 79735817 |
Hypomagnesaemia | 36.19 | 31.42 | 31 | 6855 | 46880 | 79690622 |
Pneumothorax | 35.60 | 31.42 | 25 | 6861 | 28298 | 79709204 |
Drug ineffective | 34.44 | 31.42 | 26 | 6860 | 1080887 | 78656615 |
Fatigue | 32.75 | 31.42 | 20 | 6866 | 929707 | 78807795 |
Pyelonephritis chronic | 32.44 | 31.42 | 7 | 6879 | 284 | 79737218 |
Blood sodium decreased | 32.01 | 31.42 | 25 | 6861 | 33230 | 79704272 |
Toxic optic neuropathy | 31.64 | 31.42 | 9 | 6877 | 1144 | 79736358 |
Electrolyte imbalance | 31.43 | 31.42 | 24 | 6862 | 30857 | 79706645 |
None
Source | Code | Description |
---|---|---|
ATC | J04AK05 | ANTIINFECTIVES FOR SYSTEMIC USE ANTIMYCOBACTERIALS DRUGS FOR TREATMENT OF TUBERCULOSIS Other drugs for treatment of tuberculosis |
FDA CS | M0582947 | Diarylquinolines |
MeSH PA | D000900 | Anti-Bacterial Agents |
MeSH PA | D000890 | Anti-Infective Agents |
MeSH PA | D000995 | Antitubercular Agents |
FDA EPC | N0000186775 | Diarylquinoline Antimycobacterial |
CHEBI has role | CHEBI:33231 | antitubercular agents |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Pulmonary tuberculosis | indication | 154283005 | DOID:2957 |
Drug resistant tuberculosis | indication | 423709000 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 11.93 | acidic |
pKa2 | 8.89 | Basic |
pKa3 | 2.19 | Basic |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
---|---|---|---|---|---|---|---|---|---|---|
EQ 100MG BASE | SIRTURO | JANSSEN THERAP | N204384 | Dec. 28, 2012 | RX | TABLET | ORAL | 7498343 | Dec. 1, 2026 | TREATMENT OF PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS |
EQ 20MG BASE | SIRTURO | JANSSEN THERAP | N204384 | May 27, 2020 | RX | TABLET | ORAL | 7498343 | Dec. 1, 2026 | TREATMENT OF PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS |
EQ 100MG BASE | SIRTURO | JANSSEN THERAP | N204384 | Dec. 28, 2012 | RX | TABLET | ORAL | 8546428 | March 19, 2029 | TREATMENT OF PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS |
EQ 20MG BASE | SIRTURO | JANSSEN THERAP | N204384 | May 27, 2020 | RX | TABLET | ORAL | 8546428 | March 19, 2029 | TREATMENT OF PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
EQ 100MG BASE | SIRTURO | JANSSEN THERAP | N204384 | Dec. 28, 2012 | RX | TABLET | ORAL | Aug. 9, 2026 | INDICATED AS PART OF COMBINATION THERAPY IN THE TREATMENT OF PEDIATRIC PATIENTS (12 TO LESS THAN 18 YEARS OF AGE AND WEIGHING AT LEAST 30 KG) WITH PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS |
EQ 100MG BASE | SIRTURO | JANSSEN THERAP | N204384 | Dec. 28, 2012 | RX | TABLET | ORAL | May 27, 2027 | INDICATED AS PART OF COMBINATION THERAPY IN THE TREATMENT OF PEDIATRIC PATIENTS 5 YEARS AND OLDER TO LESS THAN 12 YEARS OF AGE AND WEIGHING AT LEAST 15 KG WITH PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS (MDR-TB) |
EQ 20MG BASE | SIRTURO | JANSSEN THERAP | N204384 | May 27, 2020 | RX | TABLET | ORAL | May 27, 2027 | INDICATED AS PART OF COMBINATION THERAPY IN THE TREATMENT OF PEDIATRIC PATIENTS 5 YEARS AND OLDER TO LESS THAN 12 YEARS OF AGE AND WEIGHING AT LEAST 15 KG WITH PULMONARY MULTI-DRUG RESISTANT TUBERCULOSIS (MDR-TB) |
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Potassium voltage-gated channel subfamily H member 2 | Ion channel | IC50 | 6.43 | CHEMBL | |||||
ATP synthase | Enzyme | INHIBITOR | CHEMBL | CHEMBL | |||||
ATP synthase subunit c | Enzyme | IC50 | 8.60 | CHEMBL | |||||
ATP synthase subunit c | Enzyme | Kd | 6.30 | CHEMBL |
ID | Source |
---|---|
78846I289Y | UNII |
D09872 | KEGG_DRUG |
4032353 | VUID |
N0000187065 | NUI |
845533-86-0 | SECONDARY_CAS_RN |
4032353 | VANDF |
C1664205 | UMLSCUI |
CHEBI:72292 | CHEBI |
BQ1 | PDB_CHEM_ID |
CHEMBL376488 | ChEMBL_ID |
5388906 | PUBCHEM_CID |
DB08903 | DRUGBANK_ID |
CHEMBL2105700 | ChEMBL_ID |
9316 | INN_ID |
C493870 | MESH_SUPPLEMENTAL_RECORD_UI |
11171 | IUPHAR_LIGAND_ID |
1364503 | RXNORM |
196758 | MMSL |
29035 | MMSL |
30320 | MMSL |
d07941 | MMSL |
014821 | NDDF |
014822 | NDDF |
1010553003 | SNOMEDCT_US |
714086004 | SNOMEDCT_US |
714087008 | SNOMEDCT_US |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
SIRTURO | HUMAN PRESCRIPTION DRUG LABEL | 1 | 59676-701 | TABLET | 100 mg | ORAL | NDA | 35 sections |
SIRTURO | HUMAN PRESCRIPTION DRUG LABEL | 1 | 59676-702 | TABLET | 20 mg | ORAL | NDA | 35 sections |