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Cefuroxime, sold under the brand name Zinacef among others, is an antibiotic used to treat and prevent a number of bacterial infections.[1] These include pneumonia, meningitis, otitis media, sepsis, urinary tract infections, and Lyme disease.[2] It is used by mouth or by injection into a vein or muscle.[2]

Cefuroxime
Skeletal formula of cefuroxime
Ball-and-stick model of the cefuroxime molecule
Clinical data
Trade namesZinacef, Ceftin, others
AHFS/Drugs.comMonograph
MedlinePlusa601206
Pregnancy
category
  • B
Routes of
administration
Intramuscular, intravenous, by mouth
Drug classSecond-generation cephalosporin
ATC code
Legal status
Legal status
  • 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
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
ECHA InfoCard100.054.127 Edit this at Wikidata
Chemical and physical data
FormulaC16H16N4O8S
Molar mass424.38 g·mol−1
3D model (JSmol)
  (verify)

Common side effects include nausea, diarrhea, allergic reactions, and pain at the site of injection.[2] Serious side effects may include Clostridium difficile infection, anaphylaxis, and Stevens-Johnson syndrome.[2] Use in pregnancy and breastfeeding is believed to be safe.[3] It is a second-generation cephalosporin and works by interfering with a bacteria's ability to make a cell wall resulting in its death.[2]

Cefuroxime was patented in 1971 and approved for medical use in 1977.[4] It is available as a generic medication.[1] A week of treatment when taken by mouth in the United Kingdom costs the NHS about £18 as of 2019.[1] In the United States, the wholesale cost of this amount is about US$8.50.[5] In 2016, it was the 291st most prescribed medication in the United States, with more than a million prescriptions.[6]

Contents

Medical usesEdit

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 most other second-generation cephalosporins, cefuroxime can cross the blood-brain barrier.

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.[7]

Side effectsEdit

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.[citation needed]

Although a widely stated cross-allergic risk of about 10% exists between cephalosporins and penicillin, recent assessments have shown no increased risk for a cross-allergic reaction for cefuroxime and several other second-generation or later cephalosporins.[8]

ChemistryEdit

Cefuroxime axetil is an acetoxyethyl ester prodrug of cefuroxime which is effective when taken by mouth.[9] It is a second-generation cephalosporin.

Trade namesEdit

In US it is available as Zinacef by Covis Pharmaceuticals as the company acquired the US rights of the product from GSK.[10] GSK had continued marketing a pediatric oral suspension as Ceftin; however, this presentation was discontinued as of June 24, 2017.[11]

In Bangladesh it is available as Kilbac by Incepta and Xorimax by Sandoz. In India it is available as Ceftum in tablet form and Supacef in injection form by GSK.[12] In Poland it is available as Zamur by Mepha, subsidiary of Teva Pharmaceutical Industries.[13] 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.[14] 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.[15]

ReferencesEdit

  1. ^ a b c British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 518. ISBN 9780857113382.
  2. ^ a b c d e "Cefuroxime Sodium Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 22 March 2019.
  3. ^ "Cefuroxime Use During Pregnancy". Drugs.com. Retrieved 3 March 2019.
  4. ^ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 493. ISBN 9783527607495.
  5. ^ "NADAC as of 2019-02-27". Centers for Medicare and Medicaid Services. Retrieved 3 March 2019.
  6. ^ "The Top 300 of 2019". clincalc.com. Retrieved 22 December 2018.
  7. ^ 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. 2: CD006364. doi:10.1002/14651858.CD006364.pub3. PMC 5375161. PMID 28192644.
  8. ^ 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.
  9. ^ Walter Sneader. "Drug Discovery: History".
  10. ^ http://www.covispharma.ch/assets/pdf/covis-pharma-acquires-portfolio-of-drugs-from-glaxosmithkline.pdf
  11. ^ "FDA Drug Shortages". www.accessdata.fda.gov.
  12. ^ "GlaxoSmithKline Pharmaceuticals Limited – Prescription Medicines – Anti-Infective". Gsk-india.com. 26 March 2013.
  13. ^ "Charakterystyka produktu lecznicznego" (PDF). Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych. 12 November 2015.
  14. ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". TGA. Therapeutic Goods Administration. Retrieved 30 July 2018.
  15. ^ "ARTG ID 81301". TGA. Therapeutic Goods Administration. Retrieved 30 July 2018.

External linksEdit