Adult

Ganciclovir

Warning

General Information

Special restricted formulary antimicrobial: For details see OUH netFormulary

IV ganciclovir requires manufacture by a specialist aseptic service unit. Contact the ward pharmacist as soon as the decision to treat with ganciclovir is made.   

Renal and hepatic impairment

Renal impairment

In oncology/ haematology settings use the regimen in the table below:

eGFR (mL/min/1.73m2)

Induction dose    

(up to the first 14-21 days of treatment)

Maintenance dose

(after induction therapy)

over 70

5mg/kg every 12 hours

5mg/kg every 24 hours

50-69

2.5mg/kg every 12 hours

2.5mg/kg every 24 hours

25-49

2.5mg/kg every 24 hours

1.25mg/kg every 24 hours

10-24

1.25mg/kg every 24 hours

0.625mg/kg every 24 hours

less than 10 or HD/CAPD

1.25mg/kg every 24 hours three times a week after haemodialysis

0.625mg/kg three times a week

(For HD /CAPD- give after haemodialysis)

 

In renal/ transplant/ infectious diseases settings use the regimen in the table below:

eGFR (mL/min/1.73m2)

Treatment dose

over 50

5mg/kg every 12 hours

25-50

2.5mg/kg every 12 hours

10-24

2.5mg/kg every 24 hours

less than 10 or HD/CAPD

1.25mg/kg every 24 hours

It is removed by haemodialysis- so give after haemodialysis on haemodialysis days

When dose adjusting, round +/- to the nearest 10mg.

 

Hepatic impairment

No information available for use in hepatic impairment.

Pregnancy and breastfeeding

Discuss with pharmacy.

Additional information

  • Cytotoxic precautions required for administration.
  • Risk of myelosuppression – monitor FBC before and during treatment. See local protocols for further advice.

References

  1. Renal Drug Database. Ganciclovir. Accessed via renaldrugdatabse.com 17/12/18; last updated 21/12/17
  2. BNF online accessed via www.medicinescomplete.com 17/12/18; last updated 31/5/18

Editorial Information

Next review date: 02 Mar 2026