Cefalotin
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This article needs additional citations for verification. (December 2009) |
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Names | |
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Clinical data | |
Pregnancy category |
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Routes of use | Intravenous |
External links | |
AHFS/Drugs.com | International Drug Names |
MedlinePlus | a682860 |
Legal | |
Legal status | |
Pharmacokinetics | |
Bioavailability | n/a |
Protein binding | 65 to 80% |
Metabolism | Liver |
Elimination half-life | 30 minutes to 1 hour |
Excretion | Kidney |
Chemical and physical data | |
Formula | C16H16N2O6S2 |
Molar mass | 396.43 g·mol−1 |
3D model (JSmol) | |
Melting point | 160 to 160.5 °C (320.0 to 320.9 °F) |
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Cefalotin (INN) /ˌsɛfəˈloʊtɪn/ or cephalothin (USAN) /ˌsɛfəˈloʊθɪn/ is a first-generation cephalosporin antibiotic.[1] It was the first cephalosporin marketed (1964) and continues to be widely used.[2] It is an intravenously administered agent with a similar antimicrobial spectrum to cefazolin and the oral agent cefalexin. Cefalotin sodium is marketed as Keflin (Lilly) and under other trade names.[3]
It is in the first-generation cephalosporin family of medications.[4]
References
- ↑ Hameed TK, Robinson JL (July 2002). "Review of the use of cephalosporins in children with anaphylactic reactions from penicillins". The Canadian Journal of Infectious Diseases. 13 (4): 253–8. doi:10.1155/2002/712594. PMC 2094874. PMID 18159398.
- ↑ Greenwood D (21 February 2008). Antimicrobial Drugs: Chronicle of a Twentieth Century Medical Triumph. OUP Oxford. pp. 128–. ISBN 978-0-19-953484-5.
- ↑ International Drug Names: Cefalotin
- ↑ Beauduy, Camille E.; Winston, Lisa G. (2020). "43. Beta-lactam and other cell wall - & membrane - active antibiotics". In Katzung, Bertram G.; Trevor, Anthony J. (eds.). Basic and Clinical Pharmacology (15th ed.). New York: McGraw-Hill. p. 830. ISBN 978-1-260-45231-0. Archived from the original on 2021-10-10. Retrieved 2021-11-30.
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