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Cefuroxime

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Cefuroxime
Skeletal formula of cefuroxime
Ball-and-stick model of the cefuroxime molecule
Clinical data
Trade namesZinacef, Ceftin, Furacia, others
AHFS/Drugs.comMonograph
MedlinePlusa601206
License data
Pregnancy
category
  • B
Routes of
administration		Intramuscular, intravenous, by mouth
Drug classSecond-generation cephalosporin
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: WARNING[1]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability37% on an empty stomach, up to 52% if taken after food
Elimination half-life80 minutes
ExcretionUrine 66–100% unchanged
Identifiers
  • (6R,7R)-3-{[(Aminocarbonyl)oxy]methyl}-7-{[(2Z)-2-(2-furyl)-2-(methoxyimino)acetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.054.127 Edit this at Wikidata
Chemical and physical data
FormulaC16H16N4O8S
Molar mass424.38 g·mol−1
3D model (JSmol)
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)C(=N\OC)\c3occc3)COC(=O)N)C(=O)O
  • InChI=1S/C16H16N4O8S/c1-26-19-9(8-3-2-4-27-8)12(21)18-10-13(22)20-11(15(23)24)7(5-28-16(17)25)6-29-14(10)20/h2-4,10,14H,5-6H2,1H3,(H2,17,25)(H,18,21)(H,23,24)/b19-9+/t10-,14-/m1/s1 checkY
  • Key:JFPVXVDWJQMJEE-SWWZKJRFSA-N checkY
  (verify)

Cefuroxime, sold under the brand name Zinacef among others, is a second-generation cephalosporin[2] antibiotic used to treat and prevent a number of bacterial infections.[3] These include pneumonia, meningitis, otitis media, sepsis, urinary tract infections, and Lyme disease.[4] It is used by mouth or by injection into a vein or muscle.[4]

Common side effects include nausea, diarrhea, allergic reactions, and pain at the site of injection.[4] Serious side effects may include Clostridium difficile infection, anaphylaxis, and Stevens–Johnson syndrome.[4] Use in pregnancy and breastfeeding is believed to be safe.[5] It is a second-generation cephalosporin and works by interfering with a bacteria's ability to make a cell wall resulting in its death.[4]

Cefuroxime was patented in 1971, and approved for medical use in 1977.[6] It is on the World Health Organization's List of Essential Medicines.[7] In 2020, it was the 325th most commonly prescribed medication in the United States, with more than 800 thousand prescriptions.[8]

Medical uses

Cefuroxime is active against many bacteria including susceptible strains of Staphylococci and Streptococci, as well as a range of gram negative organisms.[9] As with the other cephalosporins, it is susceptible to beta-lactamase, although as a second-generation variety, it is less so. Hence, it may have greater activity against Haemophilus influenzae, Neisseria gonorrhoeae, and Lyme disease. Unlike other second-generation cephalosporins, cefuroxime can cross the blood-brain barrier.[10]

A systematic review found high quality evidence that injecting the eye with cefuroxime after cataract surgery will lower the chance of developing endophthalmitis after surgery.[11]

Side effects

Cefuroxime is generally well tolerated, and its side effects are usually transient. If ingested after food, this antibiotic is both better absorbed and less likely to cause its most common side effects of diarrhea, nausea, vomiting, headaches/migraines, dizziness, and abdominal pain compared to most antibiotics in its class.[medical citation needed]

Although a widely stated cross-allergic risk of about 10% exists between cephalosporins and penicillin, recent[when?] assessments have shown no increased risk for a cross-allergic reaction for cefuroxime and several other second-generation or later cephalosporins.[12]

Chemistry

Cefuroxime axetil is an acetoxyethyl ester prodrug of cefuroxime which is effective when taken by mouth.[13] It is a second-generation cephalosporin.

Trade names

In the U.S. it is marketed as Zinacef by Covis Pharmaceuticals since the company acquired the U.S. rights to the product from GSK.[14] GSK had continued marketing a pediatric oral suspension as Ceftin; however, this presentation was discontinued as of 24 June 2017.[15]

In Bangladesh, it is available as Kilbac by Incepta, Axim by Aristopharma, Rofurox by Radiant and Xorimax by Sandoz. In India, it is available as Ceftum and "Cefuall" by Allencia Biosciences in tablet form and Supacef in injection form by GSK.[16] In Poland, it is available as Zamur by Mepha, subsidiary of Teva Pharmaceutical Industries.[17] In Australia, the "first generic" form of Cefuroxime axetil, Pharmacor Cefuroxime (tablets) from Pharmacor Pty Ltd, was registered on 27 March 2017, by the Therapeutic Goods Administration.[18] Cefuroxime axetil is also available (in two strengths) as granules for oral suspension from Aspen Pharmacare Australia Pty Ltd under the brand name Zinnat cefuroxime.[19]

References

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 October 2023.
  2. ^ Katzung, Bertram (2018). Basic & Clinical Pharmacology. McGraw Hill. p. 803.
  3. ^ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 518. ISBN 9780857113382.
  4. ^ a b c d e "Cefuroxime Sodium Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 22 March 2019.
  5. ^ "Cefuroxime Use During Pregnancy". Drugs.com. Retrieved 3 March 2019.
  6. ^ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 493. ISBN 9783527607495.
  7. ^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  8. ^ "Cefuroxime – Drug Usage Statistics". ClinCalc. Retrieved 7 October 2022.
  9. ^ "Appendix 5 – Antibiotic overview". Wellington ICU Drug Manual. Retrieved 10 December 2020.
  10. ^ Root, Richard K.; Waldvogel, Francis; Corey, Lawrence; Stamm, Walter E. (1999). Clinical Infectious Diseases: A Practical Approach. Oxford University Press. p. 259. ISBN 9780195081039.
  11. ^ Gower EW, Lindsley K, Tulenko SE, Nanji AA, Leyngold I, McDonnell PJ (2017). "Perioperative antibiotics for prevention of acute endophthalmitis after cataract surgery". Cochrane Database Syst Rev. 2017 (2): CD006364. doi:10.1002/14651858.CD006364.pub3. PMC 5375161. PMID 28192644.
  12. ^ Pichichero ME (2006). "Cephalosporins can be prescribed safely for penicillin-allergic patients" (PDF). The Journal of Family Practice. 55 (2): 106–12. PMID 16451776. Archived from the original (PDF) on 24 February 2012.
  13. ^ Walter Sneader (23 June 2005). Drug Discovery: History. ISBN 9780471899792.
  14. ^ "Covis-pharma-sarl" (PDF). Archived from the original (PDF) on 8 August 2014. Retrieved 6 August 2012.
  15. ^ "FDA Drug Shortages". Food and Drug Administration (FDA). 20 March 2018.
  16. ^ "GlaxoSmithKline Pharmaceuticals Limited – Prescription Medicines – Anti-Infective". Gsk-india.com. 26 March 2013.
  17. ^ "Charakterystyka produktu lecznicznego" (PDF). Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych. 12 November 2015.
  18. ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". TGA. Therapeutic Goods Administration. 26 March 2018. Retrieved 30 July 2018.
  19. ^ "ARTG ID 81301". TGA. Therapeutic Goods Administration. Retrieved 30 July 2018.
  • "Cefuroxime". Drug Information Portal. U.S. National Library of Medicine.
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