CautionCymevene · Valcyte
Ganciclovir / Valganciclovir
Nucleoside analogue (anti-CMV)
Treats severe maternal/neonatal CMV — teratogenic, use only for life-threatening disease.
IV (ganciclovir)Oral (valganciclovir prodrug)
First-line for
- Symptomatic congenital CMV (neonatal valganciclovir × 6 months)
- CMV retinitis / pneumonitis / encephalitis in immunocompromised
- CMV prophylaxis post solid-organ transplant
Mechanism
Phosphorylated by CMV UL97 kinase to triphosphate → inhibits CMV DNA polymerase → chain termination.
“Teratogen — life-threatening CMV only”
- Neonatal valganciclovir × 6 mo improves hearing + NDI
- Use valaciclovir (not valganciclovir) for maternal HSV
Dosing
- Neonatal congenital CMV
- Valganciclovir 16 mg/kg PO BD × 6 months
- CMV retinitis (adult)
- Valganciclovir 900 mg PO BD × 21 d, then 900 mg OD
Contraindications
- AbsoluteANC <500 / platelets <25,000
- CautionPregnancy — only if life-threatening
- AbsoluteHypersensitivity to (val)ganciclovir or aciclovir
Side effects
- Myelosuppression (neutropenia ≫ anaemia ≫ thrombocytopenia)
- Nephrotoxicity
- Teratogenicity / carcinogenicity (animal data)
- Seizures (rare)
Fetal & maternal notes
- • Teratogenic in animal models — reserve for life-threatening maternal CMV under specialist supervision
- • Avoid breastfeeding during therapy
Key interactions
Zidovudine
AvoidAdditive marrow toxicity
Mycophenolate
Avoid↑ neutropenia
Imipenem
Caution↑ seizure risk
Probenecid
Caution↑ levels
Clinical pearls
- 💡 Maternal antenatal valaciclovir (8 g/day) under trial for primary maternal CMV — NOT ganciclovir
- 💡 Hold dose if ANC <500; weekly CBC during induction
Content last reviewed: REPLACE_ME (e.g. 2026-07)
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