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Drug ReportsCefpodoxime
Cefpodoxime
Cefpodoxime Proxetil (cefpodoxime) is a small molecule pharmaceutical. Cefpodoxime was first approved as Vantin on 1992-08-07. It is used to treat community-acquired infections, cystitis, escherichia coli infections, gonorrhea, and haemophilus infections amongst others in the USA.
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Study first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
stomatognathic diseasesD009057
respiratory tract diseasesD012140
otorhinolaryngologic diseasesD010038
urogenital diseasesD000091642
skin and connective tissue diseasesD017437
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
Brand Name
Status
Last Update
cefpodoxime proxetilANDA2024-10-10
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
— J01: Antibacterials for systemic use
— J01D: Other beta-lactam antibacterials in atc
— J01DD: Third-generation cephalosporins
— J01DD13: Cefpodoxime
— J01DD64: Cefpodoxime and beta-lactamase inhibitor
HCPCS
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Clinical
Clinical Trials
17 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_0000544———1113
Communicable diseasesD003141————11—2
Otitis mediaD010033EFO_0004992H66.9———1—1
OtitisD010031—————1—1
Otitis media with effusionD010034EFO_0007415H65.3———1—1
Pulmonary infarctionD054060EFO_1001408————1—1
Soft tissue infectionsD018461—————1—1
GastroenteritisD005759EFO_1001463K52.9———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NephrolithiasisD053040—N20.0——1—12
Kidney calculiD007669EFO_0004253N20——1—12
SinusitisD012852EFO_0007486J32——1——1
RhinosinusitisD000096825————1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
HypersensitivityD006967HP_0012393T78.40—1——12
AnaphylaxisD000707—T88.6—1———1
Drug hypersensitivityD004342EFO_0009482T88.7—1———1
Cephalosporin resistanceD018550—Z16.19—1———1
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C803————3
OsteomyelitisD010019EFO_0003102M861————1
NeuroblastomaD009447EFO_0000621—1————1
DiarrheaD003967HP_0002014R19.71————1
Healthy volunteers/patients———1————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Urinary tract infectionsD014552EFO_0003103N39.0————22
MicrobiotaD064307——————11
SepsisD018805HP_0100806A41.9————11
BlisterD001768——————11
Nut hypersensitivityD021184EFO_1001066—————11
StrokeD020521EFO_0000712I63.9————11
Traumatic brain injuriesD000070642—S06————11
Brain injuriesD001930—S06.9————11
AphasiaD001037HP_0002381R47.01————11
AnomiaD000849——————11
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCefpodoxime
INNcefpodoxime
Description
Cefpodoxime is a third-generation cephalosporin antibiotic with methoxymethyl and (2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamino substituents at positions 3 and 7, respectively, of the cephem skeleton. Given by mouth as its proxetil ester prodrug, it is used to treat acute otitis media, pharyngitis, and sinusitis. It has a role as an antibacterial drug. It is a cephalosporin and a carboxylic acid.
Classification
Small molecule
Drug classcephalosporins
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
COCC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)/C(=N\OC)c3csc(N)n3)[C@H]2SC1
Identifiers
PDB—
CAS-ID80210-62-4
RxCUI—
ChEMBL IDCHEMBL1672
ChEBI ID3504
PubChem CID6335986
DrugBankDB01416
UNII ID7R4F94TVGY (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
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Estimated US medical usage
Cefpodoxime
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Number of purchases
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 3,505 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1,105 adverse events reported
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