Αναζήτηση Δραστικών

CEFUROXIME

Εμπορικές Ονομασίες

  • NIPOGALIN
    Μορφές: DR.PD.INJ
    Μορφές: F.C.TAB
  • CEFUR
    Μορφές: PD.I.SO.SU
    Μορφές: PD.I.S.INF
  • NORMAFENAC
    Μορφές: PD.INJ.SOL
    Μορφές: PD.I.S.INF
  • VEKFAZOLIN
    Μορφές: F.C.TAB
    Μορφές: DR.PD.INJ
  • YOKEL
    Μορφές: DR.PD.INJ
  • FEACEF
    Μορφές: F.C.TAB
  • ZINACEF
    Μορφές: PD.I.SO.SU
    Μορφές: PD.I.S.INF
  • ZINADOL
    Μορφές: F.C.TAB
    Μορφές: GRA.OR.SUS
  • MEDOXEM
    Μορφές: PD.INJ.SOL
    Μορφές: F.C.TAB
  • FREDYR
    Μορφές: DR.PD.INJ
  • RECEANT
    Μορφές: PD.I.S.INF
    Μορφές: PD.INJ.SOL
  • DRUGBANK - Cefuroxime
  • indication:

    For the treatment of many different types of bacterial infections such as bronchitis, sinusitis, tonsillitis, ear infections, skin infections, gonorrhea, and urinary tract infections.

  • pharmacology:

  • mechanism:

    Cefuroxime, like the penicillins, is a beta-lactam antibiotic. By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, it inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that cefuroxime interferes with an autolysin inhibitor.

  • toxicity:

    Allergic reactions might be expected, including rash, nasal congestion, cough, dry throat, eye irritation, or anaphylactic shock. Overdosage of cephalosporins can cause cerebral irritation leading to convulsions.

  • absorprion:

    Absorbed from the gastrointestinal tract. Absorption is greater when taken after food (absolute bioavailability increases from 37% to 52%).

  • halflife:

    Approximately 80 minutes following intramuscular or intravenous injection.

  • roouteelimination:

  • volumedistribution:

  • clearance: