Cefuroxime
Cefuroxime oral
CLINICAL USE
Antibacterial agent
DOSE IN NORMAL RENAL FUNCTION
125–500 mg every 12 hoursGonorrhoea: single dose of 1 g
PHARMACOKINETICS
Molecular weight                           :510.5 (as axetil) %Protein binding                           :50 %Excreted unchanged in urine     : 85–90 Volume of distribution (L/kg)       :0.13–1.8half-life – normal/ESRD (hrs)      :1.2/17 DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
20 to 50     : Dose as in normal renal function 10 to 20     : Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Dialysed. Dose as in normal renal function HD                     :Dialysed. Dose as in normal renal function HDF/high flux   :Dialysed. Dose as in normal renal function CAV/VVHD      :Dialysed. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAnticoagulants: effects of coumarins may be enhanced ADMINISTRATION
Reconstition
Route
Oral Rate of Administration
–Comments
Take with or after food .134 CEFUroXiME (PArEnTErAL)
CLINICAL USE
Antibacterial agent DOSE IN NORMAL RENAL FUNCTION
750 mg – 1.5 g every 6–8 hoursMeningitis: 3 g every 8 hours PHARMACOKINETICS
Molecular weight                           :446.4 (as sodium salt) %Protein binding                           :50 %Excreted unchanged in urine     : 85–90 Volume of distribution (L/kg)       :0.13–1.8half-life – normal/ESRD (hrs)      :1.2/17 DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
20 to 50     : 750 mg – 1.5 g every 8 hours 10 to 20     : 750 mg – 1.5 g every 8–12 hours <10           : 750 mg – 1.5 g every 12–24 hours DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :dialysed. Dose as in GFR <10           : mL/min HD                     :Dialysed. Dose as in GFR <10           : mL/min HDF/high flux   :Dialysed. Dose as in GFR <10           : mL/min CAV/VVHD      :Dialysed. Dose as in GFR=10–20 mL/min IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAnticoagulants: effects of coumarins may be enhanced ADMINISTRATION
Reconstition
IM: 1 mL of water for injection to each 250 mgIV bolus: 2 mL of water for injection to each 250 mg, but 15 mL of water for injection to 1.5 g IV infusion
: 1.5 g in 50 mL of water for injection Route
IM, IV Rate of Administration
IV bolus: over 3–5 minutes IV infusion
: over 30 minutes Comments
Do not mix in syringe with aminoglycoside antibioticsInjection may also be reconstituted with: sodium chloride 0.9%, glucose 5%, glucose saline, Hartmann’s solutionCefuroxime and metronidazole can be mixed (see manufacturer’s guidelines) OTHER INFORMATION
At high doses, take care in patients receiving concurrent treatment with potent diuretics such as furosemide, or aminoglycosides, as combination can adversely affect renal functionEach 750 mg vial ≡ 1.8 mmol sodiumCefuroxime (parenteral).
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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