Recommended Loading Dose of Acyclovir for Oral Herpes Outbreak
For an oral herpes outbreak, the recommended loading dose of acyclovir is 400 mg orally 3 times daily for 5 days, or alternatively 200 mg orally 5 times daily for 5 days, or 800 mg orally twice daily for 5 days. 1
Treatment Regimens for Oral Herpes (Cold Sores)
- Oral antiviral medications are significantly more effective than topical formulations for treating cold sores 2
- Treatment should be initiated during the prodrome or within 2 days of onset of lesions for maximum benefit 1
- The recommended dosing options for recurrent episodes (including oral herpes outbreaks) are:
Pharmacokinetics and Timing Considerations
- Peak plasma concentrations of acyclovir occur 1.5 to 2.5 hours after administration 3
- The oral bioavailability of acyclovir is relatively low at 15-30% 3
- The average plasma half-life is approximately 3 hours 3
- Early initiation of therapy is crucial for optimal effectiveness - treatment should begin within the first 72 hours of symptoms 4
Alternative Approaches
- Some evidence suggests that a single "stat" 800 mg dose of acyclovir taken at the first sensory signs of oral herpes may prevent lesions from appearing in many patients 5
- However, this single-dose approach is not part of standard guidelines and should be considered experimental 1
Special Considerations
- For immunocompromised patients, higher doses may be required:
- For HIV-infected patients, more aggressive therapy may be necessary with higher dosages 4, 2
- Patients should be counseled that acyclovir neither eradicates latent virus nor affects subsequent risk, frequency, or severity of recurrences after discontinuation 1, 4
Important Caveats
- Most immunocompetent patients with recurrent disease experience limited benefit from therapy 1
- Patients should be advised to abstain from activities that might spread the virus while lesions are present 1
- Higher doses of acyclovir (beyond standard recommendations) do not appear to provide additional clinical benefit but may increase the risk of adverse effects, particularly gastrointestinal symptoms 6