netilmicin
netilmicin.JPG

CLINICAL USE

Antibacterial agent

DOSE IN NORMAL RENAL FUNCTION

IM, IV: 4–7.5 mg/kg daily, as a single daily dose or in divided doses every 8 or 12 hoursUrinary tract infection: 150 mg daily for 5 days

PHARMACOKINETICS

  • Molecular weight                           :1441.6 (as sulphate)
  • %Protein binding                           :<5
  • %Excreted unchanged in urine     : 80
  • Volume of distribution (L/kg)       :0.16–0.3
  • half-life – normal/ESRD (hrs)      :2–2.5/35–72

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : 4–7.5 mg/kg once daily. Monitor levels
  • 10 to 20     : 3–4 mg/kg once daily. Monitor levels
  • <10           : 2 mg/kg once daily. Monitor levels

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Dialysed. IV: 2 mg/kg on alternate daysIP: 7.5–10 mg/L per exchange. Monitor levels
  • HD                     :Dialysed. Administer 2 mg/kg at the end of each dialysis session. Monitor levels
  • HDF/high flux   :Dialysed. Administer 2 mg/kg at the end of each dialysis session. Monitor levels
  • CAV/VVHD      :Dialysed. Dose as in GFR=10–20 mL/min. Monitor levels

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugsBotulinum toxin: neuromuscular block enhanced (risk of toxicity)
  • Ciclosporin: increased risk of nephrotoxicityCytotoxics: increased risk of nephrotoxicity and possibly of ototoxicity with platinum compounds
  • Diuretics: increased risk of ototoxicity with loop diureticsMuscle relaxants: effects of non- depolarising muscle relaxants and suxamethonium enhancedParasympathomimetics: antagonism of effect of neostigmine and pyridostigmine
  • Tacrolimus: increased risk of nephrotoxicity

    ADMINISTRATION

    Reconstition

    Route

    IM, IP, IV bolus or infusion

    Rate of Administration

    IV bolus: Administer over 3–5 minutes

    IV infusion

    : Administer over 0.5–2 hours

    Comments

    Add to 50–200 mL of sterile water for injection, sodium chloride 0.9%, glucose 5% or 10%IM and IV dose are identical. Calculate on mg/kg lean body weight, or actual weight, whichever is lower

    OTHER INFORMATION

    Netilmicin serum concentrations should be monitored and used for basis of dosage adjustment, otherwise follow guidelines in the SPC according to serum creatinine/creatinine clearanceOnce-daily administration of netilmicin may lead to transient peak concentrations of 20–30 micrograms/mL. Other dosage regimens will result in peak levels not exceeding 12 micrograms/mL. Prolonged levels above 16 micrograms/mL should be avoided. If trough levels are monitored they will usually be 3 micrograms/mL or less with the recommended dosage. Increasing trough concentrations above 4 micrograms/mL should be avoided.



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