Loracarbef
Lorabid (loracarbef) is a small molecule pharmaceutical. Loracarbef was first approved as Lorabid on 1991-12-31. It is used to treat bacterial infections, female genital diseases, infectious bone diseases, infectious skin diseases, and joint diseases amongst others in the USA.
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Trade Name
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EMA
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Drug Products
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Labels
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Indications
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Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
bacterial infections | — | D001424 | A49 |
female genital diseases | EFO_0009549 | D005831 | N85 |
infectious bone diseases | — | D001850 | — |
infectious skin diseases | — | D012874 | — |
joint diseases | HP_0003040 | D007592 | M12.9 |
otitis media | EFO_0004992 | D010033 | H66.9 |
sinusitis | EFO_0007486 | D012852 | J32 |
urinary retention | HP_0000016 | D016055 | R33 |
Agency Specific
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Clinical
Indications Phases 4
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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 name | LORACARBEF |
INN | loracarbef |
Description | Loracarbef is a synthetic "carba" analogue of cefaclor, with carbon replacing sulfur at position 1. Used to treat a wide range of infections caused by both gram-positive and gram-negative bacteria. It has a role as an antibacterial drug and an antimicrobial agent. It is a conjugate acid of a loracarbef anion. It is a tautomer of a loracarbef zwitterion. |
Classification | Small molecule |
Drug class | antibiotics (carbacephem derivatives) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | N[C@@H](C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(Cl)CC[C@H]12)c1ccccc1.O |
Identifiers
PDB | — |
CAS-ID | 76470-66-1 |
RxCUI | 28981 |
ChEMBL ID | CHEMBL1200610 |
ChEBI ID | — |
PubChem CID | 5284585 |
DrugBank | DB00447 |
UNII ID | W72I5ZT78Z (ChemIDplus, GSRS) |
Target
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Variants
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Trends
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Safety
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Adverse Events
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39 adverse events reported
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