Antiviral agent :Treatment of life- or sight-threatening cytomegalovirus (CMV) in immunocompromised peopleCMV prophylaxis in immunosuppressed patients secondary to organ transplantation
DOSE IN NORMAL RENAL FUNCTION
Induction/treatment of active CMV disease: 5 mg/kg 12 hourly for 14–21 daysMaintenance for CMV retinitis: 6 mg/kg per day for 5 days per week or 5 mg/kg daily until recovery of adequate immunity
<10           : See ‘Other Information’
DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Dialysed. 1.25 mg/kg every day
HD                     :Dialysed. 1.25 mg/kg every day, given post dialysis on dialysis days
HDF/high flux   :Dialysed. 1.25 mg/kg every day, given post dialysis on dialysis days
CAV/VVHD      :Dialysed. 2.5 mg/kg per day
IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugs
Antibacterials: increased risk of convulsions with imipenem-cilastatin
Antivirals: possibly increased didanosine concentration; avoid with lamivudine; profound myelosuppression with zidovudine – avoid if possibleIncreased risk of myelosuppression with other myelosuppressive drugsMycophenolate: concomitant treatment with ganciclovir and mycophenolate increase plasma levels of both drugs
ADMINISTRATION
Reconstition
Reconstitute 1 vial (500 mg) with 10 mL water for injection (50 mg/mL), then transfer dose to 100 mL sodium chloride 0.9%
Route
IV peripherally in fast-flowing vein or centrally – see below
Rate of Administration
Over 1 hour
Comments
May give 50% dose over 15 minutes after
HD                     : in washback (unlicensed)
<10           : 1.25 mg/kg 24 hourlyMonitor patient for myelosuppression, particularly in patients receiving prophylactic co-trimoxazole therapyPre-dialysis therapeutic blood levels in range 5–12 mg/LNot to be infused in concentrations over 10 mg/mL peripherally