Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H7N3O |
Molecular Weight | 137.1395 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
c1cnccc1C(=O)NN
InChI
InChIKey=QRXWMOHMRWLFEY-UHFFFAOYSA-N
InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)
DescriptionCurator's Comment:: Description was created based on several sources, including:
http://www.drugbank.ca/drugs/DB00951
http://www.rxlist.com/isoniazid-drug.htm
Curator's Comment:: Description was created based on several sources, including:
http://www.drugbank.ca/drugs/DB00951
http://www.rxlist.com/isoniazid-drug.htm
Isoniazid is a bactericidal agent active against organisms of the genus Mycobacterium, specifically M. tuberculosis, M. bovis and M. kansasii. Isoniazid is recommended for all forms of tuberculosis in which organisms are susceptible. Isoniazid is a prodrug and must be activated by bacterial catalase. Isoniazid inhibits InhA, the enoyl reductase from Mycobacterium tuberculosis, by forming a covalent adduct with the NAD cofactor. The most frequent adverse reactions to isoniazid are those affecting the nervous system and the liver.
CNS Activity
Sources: http://www.bmj.com/content/341/bmj.c4451
Curator's Comment:: Isoniazid easily crosses the blood-brain barrier.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1849 Sources: http://www.drugbank.ca/drugs/DB00951 |
0.75 nM [Ki] | ||
Target ID: P9WIE4|||Q50553 Gene ID: NA Gene Symbol: katG Target Organism: Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) Sources: http://www.drugbank.ca/drugs/DB00951 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | Isoniazid Approved Useall forms of tuberculos in which organisms are susceptible. However, active tuberculosis must be treated with multiple concomitant antituberculosis medications to prevent the emergence of drug resistance. Also is recommended as preventive therapy Launch Date2.73024E10 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
8.7 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg bw 2 times / week multiple, oral dose: 15 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
7.7 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg 2 times / week multiple, oral dose: 15 mg/kg route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
|
2.1 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 mg/kg bw 1 times / day multiple, oral dose: 5 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
|
2.8 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 μg/kg bw 1 times / day multiple, oral dose: 5 μg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16.6 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg bw 2 times / week multiple, oral dose: 15 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
3.1 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 mg/kg bw 1 times / day multiple, oral dose: 5 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
37.81 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg bw 2 times / week multiple, oral dose: 15 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
53.17 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg 2 times / week multiple, oral dose: 15 mg/kg route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
|
6.96 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 mg/kg bw 1 times / day multiple, oral dose: 5 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
|
9.71 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 μg/kg bw 1 times / day multiple, oral dose: 5 μg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
71.52 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
15 mg/kg bw 2 times / week multiple, oral dose: 15 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
11.06 ng × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25224007/ |
5 mg/kg bw 1 times / day multiple, oral dose: 5 mg/kg bw route of administration: Oral experiment type: MULTIPLE co-administered: |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
86% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/29735566/ |
unknown, unknown |
ISONIAZID plasma | Homo sapiens population: UNHEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Disc. AE: Nausea, Vomiting... AEs leading to discontinuation/dose reduction: Nausea Sources: Page: p.294Vomiting Grand mal seizure Lethargy Coma |
20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.295 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.295 |
Disc. AE: Nystagmus, Hyperreflexia... AEs leading to discontinuation/dose reduction: Nystagmus Sources: Page: p.295Hyperreflexia |
112 mg/kg single, oral (max) Overdose Dose: 112 mg/kg Route: oral Route: single Dose: 112 mg/kg Sources: |
unhealthy, 17 n = 1 Health Status: unhealthy Condition: Tuberculosis Age Group: 17 Sex: M Population Size: 1 Sources: |
Disc. AE: Lethargy, Seizures... AEs leading to discontinuation/dose reduction: Lethargy Sources: Seizures Coma Tachycardia |
25 g single, oral Overdose Dose: 25 g Route: oral Route: single Dose: 25 g Co-administed with:: pyridoxine, p.o(2.5 mg, single) Sources: Page: p.2 |
healthy, 20 n = 1 Health Status: healthy Age Group: 20 Sex: F Population Size: 1 Sources: Page: p.2 |
Disc. AE: Generalized tonic-clonic seizure... AEs leading to discontinuation/dose reduction: Generalized tonic-clonic seizure Sources: Page: p.2 |
900 mg 1 times / week multiple, oral Recommended Dose: 900 mg, 1 times / week Route: oral Route: multiple Dose: 900 mg, 1 times / week Co-administed with:: rifapentine, p.o(900 mg; 1/week) Sources: Page: p.2160 |
unhealthy, 25–47 n = 3986 Health Status: unhealthy Condition: Tuberculosis Age Group: 25–47 Sex: M+F Population Size: 3986 Sources: Page: p.2160 |
Disc. AE: Hepatotoxicity, Hypersensitivity... AEs leading to discontinuation/dose reduction: Hepatotoxicity (0.3%) Sources: Page: p.2160Hypersensitivity (2.9%) |
3000 mg single, oral Overdose Dose: 3000 mg Route: oral Route: single Dose: 3000 mg Sources: Page: 73/127 |
healthy, 7 n = 1 Health Status: healthy Age Group: 7 Sex: M Population Size: 1 Sources: Page: 73/127 |
Disc. AE: Seizures, Metabolic acidosis... AEs leading to discontinuation/dose reduction: Seizures (severe) Sources: Page: 73/127Metabolic acidosis Coma Oliguria |
900 mg 3 times / week multiple, oral Recommended Dose: 900 mg, 3 times / week Route: oral Route: multiple Dose: 900 mg, 3 times / week Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Tuberculosis Sources: Page: p.1 |
Disc. AE: Hepatitis... AEs leading to discontinuation/dose reduction: Hepatitis (grade 5) Sources: Page: p.1 |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Coma | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Grand mal seizure | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Lethargy | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Nausea | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Vomiting | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.294 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.294 |
Hyperreflexia | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.295 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.295 |
Nystagmus | Disc. AE | 20 g single, oral Overdose Dose: 20 g Route: oral Route: single Dose: 20 g Sources: Page: p.295 |
healthy, 16 n = 1 Health Status: healthy Age Group: 16 Sex: F Population Size: 1 Sources: Page: p.295 |
Coma | Disc. AE | 112 mg/kg single, oral (max) Overdose Dose: 112 mg/kg Route: oral Route: single Dose: 112 mg/kg Sources: |
unhealthy, 17 n = 1 Health Status: unhealthy Condition: Tuberculosis Age Group: 17 Sex: M Population Size: 1 Sources: |
Lethargy | Disc. AE | 112 mg/kg single, oral (max) Overdose Dose: 112 mg/kg Route: oral Route: single Dose: 112 mg/kg Sources: |
unhealthy, 17 n = 1 Health Status: unhealthy Condition: Tuberculosis Age Group: 17 Sex: M Population Size: 1 Sources: |
Seizures | Disc. AE | 112 mg/kg single, oral (max) Overdose Dose: 112 mg/kg Route: oral Route: single Dose: 112 mg/kg Sources: |
unhealthy, 17 n = 1 Health Status: unhealthy Condition: Tuberculosis Age Group: 17 Sex: M Population Size: 1 Sources: |
Tachycardia | Disc. AE | 112 mg/kg single, oral (max) Overdose Dose: 112 mg/kg Route: oral Route: single Dose: 112 mg/kg Sources: |
unhealthy, 17 n = 1 Health Status: unhealthy Condition: Tuberculosis Age Group: 17 Sex: M Population Size: 1 Sources: |
Generalized tonic-clonic seizure | Disc. AE | 25 g single, oral Overdose Dose: 25 g Route: oral Route: single Dose: 25 g Co-administed with:: pyridoxine, p.o(2.5 mg, single) Sources: Page: p.2 |
healthy, 20 n = 1 Health Status: healthy Age Group: 20 Sex: F Population Size: 1 Sources: Page: p.2 |
Hepatotoxicity | 0.3% Disc. AE |
900 mg 1 times / week multiple, oral Recommended Dose: 900 mg, 1 times / week Route: oral Route: multiple Dose: 900 mg, 1 times / week Co-administed with:: rifapentine, p.o(900 mg; 1/week) Sources: Page: p.2160 |
unhealthy, 25–47 n = 3986 Health Status: unhealthy Condition: Tuberculosis Age Group: 25–47 Sex: M+F Population Size: 3986 Sources: Page: p.2160 |
Hypersensitivity | 2.9% Disc. AE |
900 mg 1 times / week multiple, oral Recommended Dose: 900 mg, 1 times / week Route: oral Route: multiple Dose: 900 mg, 1 times / week Co-administed with:: rifapentine, p.o(900 mg; 1/week) Sources: Page: p.2160 |
unhealthy, 25–47 n = 3986 Health Status: unhealthy Condition: Tuberculosis Age Group: 25–47 Sex: M+F Population Size: 3986 Sources: Page: p.2160 |
Coma | Disc. AE | 3000 mg single, oral Overdose Dose: 3000 mg Route: oral Route: single Dose: 3000 mg Sources: Page: 73/127 |
healthy, 7 n = 1 Health Status: healthy Age Group: 7 Sex: M Population Size: 1 Sources: Page: 73/127 |
Metabolic acidosis | Disc. AE | 3000 mg single, oral Overdose Dose: 3000 mg Route: oral Route: single Dose: 3000 mg Sources: Page: 73/127 |
healthy, 7 n = 1 Health Status: healthy Age Group: 7 Sex: M Population Size: 1 Sources: Page: 73/127 |
Oliguria | Disc. AE | 3000 mg single, oral Overdose Dose: 3000 mg Route: oral Route: single Dose: 3000 mg Sources: Page: 73/127 |
healthy, 7 n = 1 Health Status: healthy Age Group: 7 Sex: M Population Size: 1 Sources: Page: 73/127 |
Seizures | severe Disc. AE |
3000 mg single, oral Overdose Dose: 3000 mg Route: oral Route: single Dose: 3000 mg Sources: Page: 73/127 |
healthy, 7 n = 1 Health Status: healthy Age Group: 7 Sex: M Population Size: 1 Sources: Page: 73/127 |
Hepatitis | grade 5 Disc. AE |
900 mg 3 times / week multiple, oral Recommended Dose: 900 mg, 3 times / week Route: oral Route: multiple Dose: 900 mg, 3 times / week Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Tuberculosis Sources: Page: p.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
yes [Ki 102 uM] | ||||
yes [Ki 110 uM] | ||||
yes [Ki 126 uM] | ||||
yes [Ki 13 uM] | ||||
yes [Ki 51.8 uM] | ||||
yes [Ki 60 uM] | ||||
yes [Ki >1000 uM] | ||||
Sources: https://pubmed.ncbi.nlm.nih.gov/8354023/ |
yes |
PubMed
Title | Date | PubMed |
---|---|---|
Hepatotoxicity of rifampicin and isoniazid in children. | 1975 May |
|
Antituberculosis activity of certain antifungal and antihelmintic drugs. | 1999 |
|
Comparative in vitro antimicrobial activities of the newly synthesized quinolone HSR-903, sitafloxacin (DU-6859a), gatifloxacin (AM-1155), and levofloxacin against Mycobacterium tuberculosis and Mycobacterium avium complex. | 1999 Dec |
|
High-dose isoniazid therapy for isoniazid-resistant murine Mycobacterium tuberculosis infection. | 1999 Dec |
|
Lymphocyte transformation test for the evaluation of adverse effects of antituberculous drugs. | 1999 Feb 25 |
|
[A case of pulmonary tuberculosis with acute renal failure caused by readministration of rifampicin]. | 1999 Nov |
|
Antimycobacterial activity of new ortho-, meta- and para-toluidine derivatives. | 1999 Nov-Dec |
|
Drug-induced lupus nephritis in HIV infection. | 1999 Oct |
|
Outcome of multidrug-resistant tuberculosis in human immunodeficiency virus-infected patients. | 1999 Sep |
|
Activity of moxifloxacin against mycobacteria. | 1999 Sep |
|
Genomic mutations in the katG, inhA and aphC genes are useful for the prediction of isoniazid resistance in Mycobacterium tuberculosis isolates from Kwazulu Natal, South Africa. | 2000 |
|
Diagnostic Standards and Classification of Tuberculosis in Adults and Children. This official statement of the American Thoracic Society and the Centers for Disease Control and Prevention was adopted by the ATS Board of Directors, July 1999. This statement was endorsed by the Council of the Infectious Disease Society of America, September 1999. | 2000 Apr |
|
Antimycobacterial activities of novel levofloxacin analogues. | 2000 Aug |
|
Acute isoniazid neurotoxicity during preventive therapy. | 2000 Feb |
|
Use of genomics and combinatorial chemistry in the development of new antimycobacterial drugs. | 2000 Feb 1 |
|
[Isoniazid-induced hepatic failure. Report of a case]. | 2000 Jan-Mar |
|
Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl-acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis. | 2000 Jul |
|
Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid. | 2000 Jul 4 |
|
A multicentre study of the early bactericidal activity of anti-tuberculosis drugs. | 2000 Jun |
|
Increased incidence of peripheral neuropathy with co-administration of stavudine and isoniazid in HIV-infected individuals. | 2000 Mar 31 |
|
Isoniazid affects multiple components of the type II fatty acid synthase system of Mycobacterium tuberculosis. | 2000 Nov |
|
Antepartum or postpartum isoniazid treatment of latent tuberculosis infection. | 2000 Nov |
|
Mutant prevention concentration as a measure of antibiotic potency: studies with clinical isolates of Mycobacterium tuberculosis. | 2000 Sep |
|
On-column amperometric detection of ofloxacin and pasiniazid in urine by capillary electrophoresis with an improved fractured joint and small detection cell. | 2001 Apr |
|
Evaluation of tuberculosis control by periodic or routine susceptibility testing in previously treated cases. | 2001 Apr |
|
Fatal and severe hepatitis associated with rifampin and pyrazinamide for the treatment of latent tuberculosis infection--New York and Georgia, 2000. | 2001 Apr 20 |
|
Ion interaction reagent reversed-phase high-performance liquid chromatography determination of anti-tuberculosis drugs and metabolites in biological fluids. | 2001 Apr 25 |
|
[Disseminated disease by Mycobacterium kansasii resistant to isoniazid and rifampin in patients] with AIDS]. | 2001 Feb |
|
Connatal tuberculosis in an extremely low birth weight infant: case report and management of exposure to tuberculosis in a neonatal intensive care unit. | 2001 Feb |
|
TB prevention in HIV clinics in New York City. | 2001 Feb |
|
Drug-resistant tuberculosis in Taipei, 1996-1999. | 2001 Feb |
|
Incentives vs outreach workers for latent tuberculosis treatment in drug users. | 2001 Feb |
|
Outbreak of multidrug-resistant tuberculosis at a methadone treatment program. | 2001 Jan |
|
Low rate of emergence of drug resistance in sputum positive patients treated with short course chemotherapy. | 2001 Jan |
|
Prevalence of drug-resistant tuberculosis in an HIV endemic area in northern Thailand. | 2001 Jan |
|
Does tuberculosis after kidney transplantation follow the trend of tuberculosis in general population? | 2001 Jan |
|
Can a nine-month regimen be used to treat isoniazid resistant tuberculosis diagnosed after standard treatment is started? | 2001 Jan |
|
Survey for tuberculosis in a tribal population in North Arcot District. | 2001 Mar |
|
Enhancement of antibiotic activity against poly-drug resistant Mycobacterium tuberculosis by phenothiazines. | 2001 Mar |
|
Mycobacterial FurA is a negative regulator of catalase-peroxidase gene katG. | 2001 Mar |
|
First randomised trial of treatments for pulmonary disease caused by M avium intracellulare, M malmoense, and M xenopi in HIV negative patients: rifampicin, ethambutol and isoniazid versus rifampicin and ethambutol. | 2001 Mar |
|
Active site structure of the catalase-peroxidases from Mycobacterium tuberculosis and Escherichia coli by extended X-ray absorption fine structure analysis. | 2001 Mar 9 |
|
Experimental in vitro efficacy study on the interaction of epiroprim plus isoniazid against Mycobacterium tuberculosis. | 2001 Mar-Apr |
|
Efficacy of chemotherapy for prostatic tuberculosis-a clinical and histologic follow-up study. | 2001 May |
Patents
Sample Use Guides
Adults: 5 mg/kg up to 300 mg daily in a single dose; or 15 mg/kg up to 900 mg/day, two or three times/week
Children: 10 mg/kg to15 mg/kg up to 300 mg daily in a single dose; or 20 mg/kg to 40 mg/kg up to 900 mg/day, two or three times/week
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/10582897
Curator's Comment:: MIC90 (minimum inhibitory concentration at which 90% of the test strains were inhibited) of isoniazid for Mycobacterium tuberculosis is 1.56 μg/ml.
1.56 μg/ml
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Classification Tree | Code System | Code | ||
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NDF-RT |
N0000175483
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4 (ETH/ISO)
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ATC |
J04AM01
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ATC |
J04AC01
Created by
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WHO-VATC |
QJ04AC51
Created by
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WHO-ATC |
J04AM04
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WHO-ATC |
J04AM06
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WHO-VATC |
QJ04AM01
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WHO-ATC |
J04AM05
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NCI_THESAURUS |
C280
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WHO-ATC |
J04AM03
Created by
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4 (ETH/ISO/PYR/RIF)
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4 (ETH/ISO/RIF)
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-VATC |
QJ04AM02
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WHO-VATC |
QJ04AM04
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LIVERTOX |
521
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WHO-VATC |
QJ04AM03
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FDA ORPHAN DRUG |
6585
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WHO-ATC |
J04AM08
Created by
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WHO-VATC |
QJ04AC01
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-VATC |
QJ04AM05
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ATC |
J04AM02
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4 (ISO/RIF)
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-VATC |
QJ04AM06
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4 (ISO/PYR/RIF)
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ATC |
J04AC51
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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WHO-ATC |
J04AM07
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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Code System | Code | Type | Description | ||
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1647
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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V83O1VOZ8L
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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1497
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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6038
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | RxNorm | ||
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M6502
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | Merck Index | ||
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SUB08326MIG
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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Isoniazid
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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CHEMBL64
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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4188
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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54-85-3
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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200-214-6
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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1349706
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | USP-RS | ||
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D007538
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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3767
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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DB00951
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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54-85-3
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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ISONIAZID
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | Description: Colourless crystals or a white, crystalline powder; odourless. Solubility: Soluble in 8 parts of water and in 40 parts of ethanol (~750 g/l) TS; very slightly soluble in ether R. Category: Tuberculostatic. Storage: Isoniazid should be kept in a well-closed container, protected from light. Definition: Isoniazid contains not less than 98.0% and not more than 101.0% of C6H7N3O, calculated with reference to the dried substance. | ||
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C600
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY | |||
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ISONIAZID
Created by
admin on Fri Jun 25 20:57:22 UTC 2021 , Edited by admin on Fri Jun 25 20:57:22 UTC 2021
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PRIMARY |
ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE (PARENT)
METABOLITE ACTIVE (PARENT)
METABOLITE INACTIVE (PARENT)
SALT/SOLVATE (PARENT)