Pefloxacin
Also called 1589-RB, Pefocin, Pefbid
Part of the metabolic pathway of Pefloxacin. See the timeline on the metabolic highway.
Overview
Pefloxacin is a quinolone antibiotic used to treat bacterial infections. Pefloxacin has not been approved for use in the United States. WP
Risks and side effects
Adverse effects
Tendinitis and rupture, usually of the Achilles tendon, are class-effects of the fluoroquinolones, most frequently reported with pefloxacin. The estimated risk of tendon damage during pefloxacin therapy has been estimated by the French authorities in 2000 to be 1 case per 23,130 treatment days as compared to ciprofloxacin where it has been estimated to be 1 case per 779,600.[1]
History
History
Pefloxacin was developed in 1979 and approved in France for human use in 1985.[3] WP
Chemistry
- Formula
- C17H20FN3O3 PC
- CAS number
- 70458-92-3 PC
- Molar mass (g/mol)
- 333.36 PC
- IUPAC name (computed by PubChem)
- 1-
ethyl- PC6- fluoro- 7- (4- methylpiperazin- 1- yl) - 4- oxoquinoline- 3- carboxylic acid - SMILES
- CCN1C=C(C(=O)
C2=CC(=C(C=C21) PCN3CCN(CC3) C) F) C(=O) O - InChIKey
- FHFYDNQZQSQIAI-
UHFFFAOYSA- PCN - PubChem CID
- 51081
- IUPAC name
- 1-
ethyl- WP6- fluoro- 7- (4- methylpiperazin- 1- yl) - 4- oxo- quinoline- 3- carboxylic acid
Harm reduction information
No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.
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Sources
- Journal / agency Khaliq Y, Zhanel GG. Musculoskeletal injury associated with fluoroquinolone antibiotics. Clin Plast Surg. October 2005. doi:10.1016/j.cps.2005.05.004 · PMID 16139623
- Journal / agency Casparian JM, Luchi M, Moffat RE, Hinthorn D. Quinolones and tendon ruptures. South. Med. J. May 2000. doi:10.1097/00007611-200093050-00008 · PMID 10832946
- Other http://www.bailii.org/ew/cases/EWHC/Patents/2008/2413.html. 15 October 2008
Text and values on this page are quoted from Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.