Pyrazinamide
Rifater (pyrazinamide) is a small molecule pharmaceutical. Pyrazinamide was first approved as Pyrazinamide on 1982-01-01. It is used to treat mycobacterium infections and tuberculosis in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
infections | D007239 |
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Isoniazid
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Pyrazinamide
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Rifampin
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
RIFATER | Sanofi | N-050705 DISCN | 1994-05-31 | 1 products, RLD |
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Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
pyrazinamide | ANDA | 2023-03-31 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
mycobacterium infections | — | D009164 | A31.9 |
tuberculosis | EFO_0000774 | D014376 | A15-A19 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
— J04: Antimycobacterials
— J04A: Drugs for treatment of tuberculosis
— J04AK: Other drugs for treatment of tuberculosis in atc
— J04AK01: Pyrazinamide
— J04AM: Combinations of drugs for treatment of tuberculosis
— J04AM05: Rifampicin, pyrazinamide and isoniazid
— J04AM06: Rifampicin, pyrazinamide, ethambutol and isoniazid
HCPCS
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Clinical
Clinical Trials
77 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Tuberculosis | D014376 | EFO_0000774 | A15-A19 | 5 | 13 | 11 | 3 | 6 | 35 |
Pulmonary tuberculosis | D014397 | EFO_1000049 | A15 | — | 15 | 8 | 2 | 4 | 27 |
Hiv infections | D015658 | EFO_0000764 | B20 | 1 | 3 | 4 | 4 | 5 | 16 |
Multidrug-resistant tuberculosis | D018088 | EFO_0007381 | — | 4 | 7 | 1 | 1 | 11 | |
Spinal tuberculosis | D014399 | A18.01 | — | — | — | 1 | — | 1 | |
Hepatitis | D006505 | HP_0012115 | K75.9 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Hiv | D006678 | O98.7 | — | 2 | 1 | — | — | 3 | |
Acquired immunodeficiency syndrome | D000163 | EFO_0000765 | B20 | — | 1 | 2 | — | — | 2 |
Extensively drug-resistant tuberculosis | D054908 | — | 1 | 2 | — | — | 2 | ||
Anterior uveitis | D014606 | EFO_1000811 | — | — | 1 | — | — | 1 | |
Bacterial infections | D001424 | A49 | — | — | 1 | — | — | 1 |
Indications Phases 1
No data
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Body weight changes | D001836 | — | — | — | — | 1 | 1 | ||
Motor activity | D009043 | EFO_0003940 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | PYRAZINAMIDE |
INN | pyrazinamide |
Description | Pyrazinecarboxamide is a monocarboxylic acid amide resulting from the formal condensation of the carboxy group of pyrazinoic acid (pyrazine-2-carboxylic acid) with ammonia. A prodrug for pyrazinoic acid, pyrazinecarboxamide is used as part of multidrug regimens for the treatment of tuberculosis. It has a role as an antitubercular agent and a prodrug. It is a member of pyrazines, a N-acylammonia and a monocarboxylic acid amide. |
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | NC(=O)c1cnccn1 |
Identifiers
PDB | — |
CAS-ID | 98-96-4 |
RxCUI | 8987 |
ChEMBL ID | CHEMBL614 |
ChEBI ID | 45285 |
PubChem CID | 1046 |
DrugBank | DB00339 |
UNII ID | 2KNI5N06TI (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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65 adverse events reported
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