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Antiviral — CMV Treatment (IV) / Retinitis / Transplant

Ganciclovir

Brand names: Cymevene

Ganciclovir is an intravenous antiviral used to treat and prevent cytomegalovirus (CMV) disease, particularly CMV retinitis and other end-organ disease in immunocompromised and transplant patients.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It is phosphorylated by viral protein kinase and cellular kinases to ganciclovir triphosphate, which inhibits viral DNA polymerase and terminates viral DNA chain elongation.

Prescribing in practice

  • Profound, dose-related myelosuppression (neutropenia, anaemia and thrombocytopenia) is the principal toxicity and mandates close haematological monitoring with dose interruption if counts fall.
  • It is potentially teratogenic and carcinogenic and impairs fertility, so cytotoxic-handling precautions apply and effective contraception is required.
  • Renally excreted, so the dose must be adjusted to renal function and adequate hydration maintained.

Monitoring

Monitor full blood count frequently throughout treatment together with renal function to guide dosing.

Counselling the patient

  • Regular blood tests are essential to check your blood counts during treatment.
  • Use reliable contraception during and for a period after treatment, as this drug can harm a developing baby.
  • Report fever, sore throat, bruising or unusual bleeding promptly.

Evidence & guidelines

Ganciclovir is the established standard of care for CMV end-organ disease in immunocompromised patients, supported by long-standing transplant and HIV management guidance.

Reference: BHIVA HIV Guidelines; NICE Transplant Immunosuppression Guidance; Kimberlin Congenital CMV Trial NEJM 2015; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.