Prodrug Antiviral — HSV / VZV / CMV Prevention (Oral)
Pregnancy: Use with caution — aciclovir registry data show no increased birth defects; valaciclovir considered safe for HSV suppression in pregnancy
Valaciclovir
Brand names: Valtrex
Adult dose
Dose: Herpes zoster (shingles): 1 g 3 times daily × 7 days; Genital herpes (first episode): 500 mg twice daily × 10 days; Recurrent genital herpes: 500 mg twice daily × 3–5 days; HSV suppression: 500 mg once daily; CMV prevention (transplant): 2 g 4 times daily × 90 days
Route: Oral
Frequency: 1–4 times daily (indication-dependent)
Max: 4 g/day (CMV prevention — high dose); 3 g/day (zoster)
Prodrug of aciclovir — L-valyl ester increases bioavailability from 15–20% (aciclovir oral) to 54–70%. Start within 72 hours of rash onset for herpes zoster — ideally within 48 hours. High-dose (2 g QDS) for CMV prevention is an unlicensed dose in most countries — used in transplant centres as alternative to valganciclovir.
Paediatric dose
Route:
Seek specialist opinion — not licensed in paediatrics; IV aciclovir preferred in children for severe HSV/VZV; some specialist centres use valaciclovir in adolescents for suppression therapy
Dose adjustments
Renal
CrCl 30–49: reduce zoster dose to 1 g BD; CrCl 10–29: 1 g OD (zoster), 500 mg OD (HSV); CrCl <10: 500 mg OD; haemodialysis: dose post-dialysis
Hepatic
No dose adjustment required
Clinical pearls
- Zoster timing critical: start within 72 hours of rash onset (ideally <48 hours) — reduces duration of acute neuritis and risk of post-herpetic neuralgia; no benefit if started after 72 hours in immunocompetent (unless new lesions still appearing)
- Immunocompromised patients (HIV, transplant): treat regardless of timing — disseminated zoster risk; use IV aciclovir if systemic involvement (visceral, ophthalmologic, neurological)
- High-dose CMV prophylaxis (2 g QDS): less expensive than valganciclovir — used in some transplant centres; evidence from VALGANCICLOVIR vs high-dose valaciclovir trials (non-inferior in some studies)
- Neurological toxicity at high doses or in renal failure: confusion, agitation, hallucinations — ensure dose reduction in renal impairment; TMA is a rare but serious complication in immunosuppressed at very high doses
Contraindications
- Hypersensitivity to valaciclovir or aciclovir
Side effects
- Headache
- Nausea
- Dizziness
- Neurological effects (confusion, hallucinations — especially in renal failure)
- Thrombotic microangiopathy (TMA — at high doses in immunocompromised; rare)
- Renal impairment (high doses — ensure adequate hydration)
Interactions
- Probenecid/cimetidine — increase aciclovir levels (reduce tubular secretion)
- Nephrotoxic drugs — additive renal toxicity
- Ciclosporin — additive nephrotoxicity
Monitoring
- Renal function (especially at high doses)
- Neurological status
- FBC (high-dose TMA risk)
- Clinical response (lesion healing, pain)
Reference: BNFc; BNF 90; BASHH Herpes Guidelines 2014; BHIVA HIV Guidelines; Cochrane Review: Antivirals for Herpes Zoster; PHE Shingles Treatment Guidance. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- Framingham Risk Score · Cardiovascular Risk
- SCORE2-Diabetes 10-Year CVD Risk in Type 2 Diabetes · Cardiovascular Risk
- DOAC Score for Selecting Direct Oral Anticoagulant in Non-Valvular AF · Anticoagulation
- PFO-Associated Stroke Causal Likelihood (PASCAL) Classification · Stroke Prevention
- PCP-HF Risk Score (Pooled Cohort Equations to Prevent Heart Failure) · Heart Failure Prevention
- CHADS-65 Score for Atrial Fibrillation · Atrial Fibrillation
Pathways