Lefamulin
| Clinical data | |
|---|---|
| Trade names | Xenleta | 
| Other names | BC-3781 | 
| AHFS/Drugs.com | Monograph | 
| License data | |
| Routes of administration | Intravenous, by mouth | 
| ATC code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| 
 | |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C28H45NO5S | 
| Molar mass | 507.73 g·mol−1 | 
| 3D model (JSmol) | |
| 
 | |
| 
 | |
Lefamulin, sold under the brand name Xenleta, is an antibiotic medication used it to treat adults with community-acquired bacterial pneumonia. It is taken by mouth or by injection into a vein.
Relatively common side effects include diarrhea, nausea, pain at the site of injection, and liver inflammation. It is a pleuromutilin antibiotic that inhibits the large subunit of bacterial ribosomes.
Lefamulin was approved for medical use in the United States in August 2019, and in the European Union in July 2020.