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Antiviral — nucleoside analogue (herpes zoster treatment) Pregnancy: Use should be considered only when the potential benefits outweigh the possibility of unknown risks; the post-marketing pregnancy registry has not shown an increase in birth defects compared with the general population. Breastfeeding: after 200 mg five times a day, aciclovir has been detected in breast milk at 0.6 to 4.1 times the corresponding plasma levels, potentially exposing nursing infants to up to 0.3 mg/kg/day — caution is advised in nursing women (§4.6).

Aciclovir 800mg Tablets (Ramsay Hunt Syndrome / Herpes Zoster Oticus)

Brand names: Zovirax, Aciclovir generic

Used in: Meningitis & Encephalitis Acute Red Eye

Aciclovir is an antiviral used for herpes simplex and varicella-zoster (chickenpox and shingles) infections.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 800 mg (treatment of varicella and herpes zoster infections)
Route: Oral — tablets may be dispersed in a minimum of 50 ml of water or swallowed whole with a little water; ensure patients on high doses of aciclovir are adequately hydrated
Frequency: Five times daily at approximately four-hourly intervals, omitting the night time dose; treatment should continue for seven days
SOURCE: eMC UK SPC, productName 'Aciclovir 200 mg Tablets' (https://www.medicines.org.uk/emc/product/4334/smpc), §4.2. VERBATIM: 'Treatment of varicella and herpes zoster infections: 800 mg Aciclovir should be taken five times daily at approximately four-hourly intervals, omitting the night time dose. Treatment should continue for seven days.' STRENGTH CAVEAT: the fetched SPC is the 200 mg tablet product, although its §4.2 states the 800 mg zoster regimen literally — confirm against the 800 mg tablet SPC before publishing. INDICATION CAVEAT: the SPC does not name Ramsay Hunt syndrome or herpes zoster oticus anywhere; the regimen above is the generic herpes zoster regimen and the clinician must confirm it is the one intended for this page. TIMING: dosing should begin as early as possible after the start of an infection; treatment of herpes zoster yields better results if initiated as soon as possible after the onset of the rash; treatment of chickenpox in immunocompetent patients should begin within 24 hours after onset of the rash. IMMUNOCOMPROMISED / IMPAIRED ABSORPTION: in severely immunocompromised patients (e.g. after marrow transplant) or in patients with impaired absorption from the gut, consideration should be given to intravenous dosing. OTHER INDICATIONS IN THE SAME SPC (not this page's indication): treatment of herpes simplex — 200 mg five times daily at approximately four hourly intervals omitting the night time dose for 5 days, extended in severe initial infections, and the dose can be doubled to 400 mg in severe immunocompromise or impaired gut absorption; suppression of herpes simplex in immunocompetent patients — 200 mg four times daily at approximately six-hourly intervals, or 400 mg twice daily at approximately twelve-hourly intervals, with titration down to 200 mg three times daily or twice daily, some patients may experience break-through infection on total daily doses of 800 mg, and therapy should be interrupted periodically at intervals of six to twelve months in order to observe possible changes in the natural history of the disease; prophylaxis of herpes simplex in immunocompromised patients — 200 mg four times daily at approximately six-hourly intervals (doubled to 400 mg in severe immunocompromise or impaired gut absorption), duration determined by the period at risk. ELDERLY: the possibility of renal impairment must be considered and the dosage adjusted accordingly; maintain adequate hydration on high oral doses. PAEDIATRIC — NOT carried into paedDose: the SPC states 'No specific data are available on the suppression of herpes simplex infections or the treatment of herpes zoster infections in immunocompetent children.' The only per-kg figure in this SPC belongs to the treatment of VARICELLA, not zoster — 'Dosing may be more accurately calculated as 20 mg/kg bodyweight (not to exceed 800 mg) Aciclovir four times daily', with fixed bands for varicella of 800 mg four times daily at 6 years and over, 400 mg four times daily at 2 to 5 years and 200 mg four times daily under 2 years, for five days. It has deliberately NOT been structured into paedDose because it is a different indication from this page and would otherwise be read as a paediatric zoster regimen. For treatment and prophylaxis of herpes simplex, children aged two years and over should be given adult dosages and children below the age of two years half the adult dose; for neonatal herpes virus infections intravenous aciclovir is recommended. Oral aciclovir should be used in the paediatric population mainly for non-severe skin and mucosa HSV infections; IV aciclovir should be used for neonatal HSV and severe HSV infections in immunocompromised children (§4.4). Verify all under-18 dosing against a children's formulary. No maximum dose for herpes zoster is stated anywhere in §4.2, so no maxDose is asserted in this draft.

Dose adjustments

Renal

Caution is advised in impaired renal function and adequate hydration should be maintained. Herpes zoster: severe renal impairment (creatinine clearance less than 10 ml/minute) — 800 mg twice daily at approximately twelve-hourly intervals; moderate renal impairment (creatinine clearance 10 to 25 ml/minute) — 800 mg three times daily at intervals of approximately eight hours. Herpes simplex: for severe renal impairment (creatinine clearance less than 10 ml/minute) an adjustment to 200 mg twice daily at approximately twelve-hourly intervals is recommended; otherwise the recommended oral doses will not lead to accumulation above levels established as safe by intravenous infusion. Both elderly patients and patients with renal impairment are at increased risk of neurological side effects and should be closely monitored (§4.4).

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to aciclovir or valaciclovir, or to any of the excipients

Side effects

  • Headache and dizziness (common)
  • Nausea, vomiting, diarrhoea and abdominal pains (common)
  • Pruritus and rashes including photosensitivity (common); urticaria and accelerated diffuse hair loss (uncommon); angioedema (rare)
  • Fatigue and fever (common)
  • Neurological effects — agitation, confusion, tremor, ataxia, dysarthria, hallucinations, psychotic symptoms, convulsions, somnolence, encephalopathy and coma (very rare; generally reversible and usually reported in patients with renal impairment or other predisposing factors). Anaphylaxis (rare); increases in blood urea and creatinine (rare); acute renal failure and renal pain (very rare)

Interactions

  • Probenecid and cimetidine — compete with active renal tubular secretion, increasing aciclovir AUC and reducing aciclovir renal clearance (§4.5)
  • Mycophenolate mofetil — increases in the plasma AUCs of aciclovir and of the inactive mycophenolate metabolite when co-administered; no dosage adjustment is necessary because of the wide therapeutic index of aciclovir (§4.5)
  • Theophylline — concomitant aciclovir increased the AUC of administered theophylline by approximately 50% in an experimental study in five male subjects; measure plasma concentrations during concomitant therapy (§4.5)
  • Other nephrotoxic drugs — the risk of renal impairment is increased by concomitant use (§4.4)

Clinical monograph

How it works

It is activated by viral thymidine kinase and then inhibits viral DNA polymerase, selectively blocking viral DNA replication.

Prescribing in practice

  • Start it early (e.g. within 72 hours of a shingles rash) for benefit.
  • It is renally cleared — reduce the dose in renal impairment and ensure good hydration, especially with intravenous use (risk of crystal nephropathy and neurotoxicity).
  • It is generally well tolerated by mouth.

Monitoring

For intravenous or high-dose use monitor renal function and hydration.

Counselling the patient

  • Start it as early as possible.
  • Drink plenty of fluids.
  • Complete the course.

Evidence & guidelines

Standard treatment for significant herpes simplex and varicella-zoster infection, most effective when started early, with renal dose adjustment.

Reference: NICE CKS Shingles; ENT-UK Ramsay Hunt Guidelines; Cochrane Review Zoster; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.