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Sulfoxone
Diasone (sulfoxone) is a small molecule pharmaceutical. Sulfoxone was first approved as Diasone sodium on 1982-01-01.
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Commercial
Therapeutic Areas
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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)
Sulfoxone sodium
Tradename
Company
Number
Date
Products
DIASONE SODIUMAbbVieN-006044 DISCN1982-01-01
1 products
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
J: Antiinfectives for systemic use
— J04: Antimycobacterials
— J04B: Drugs for treatment of lepra
— J04BA: Drugs for treatment of lepra
— J04BA03: Aldesulfone sodium
HCPCS
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Clinical
Clinical Trials
1 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Pneumocystis pneumoniaD011020EFO_0007448B59———1—1
Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameSULFOXONE
INNaldesulfone sodium
Description
Aldesulfone is a sulfonamide.
Classification
Small molecule
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
O=S(O)CNc1ccc(S(=O)(=O)c2ccc(NCS(=O)O)cc2)cc1
Identifiers
PDB—
CAS-ID144-75-2
RxCUI—
ChEMBL IDCHEMBL1570
ChEBI ID—
PubChem CID5351
DrugBankDB01145
UNII ID57OWB0Q221 (ChemIDplus, GSRS)
Target
Agency Approved
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Alternate
No data
Variants
Clinical Variant
No data
Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 136 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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10 adverse events reported
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