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Acyclovir dose for cold sores – medhelp, Common questions and answers about acyclovir dose for cold sores.
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Acyclovir is a synthetic purine nucleoside analogue with in vitro and in vivo inhibitory activity against herpes simplex virus types 1 (HSV-1), 2 (HSV-2) and varicella-zoster virus (VZV). Concentrations achieved in the cerebrospinal fluid are approximately 50% of plasma values.A  Plasma protein binding is relatively low (9% to 33%) and drug interactions involving binding site displacement are not anticipated.
The half-life and total body clearance of acyclovir are dependent on renal function as shown in Table 2. Consult DOSAGE AND ADMINISTRATION section for recommended adjustments in dosing based upon creatinine clearance.
Coadministration of probenecid with acyclovir has been shown to increase the mean acyclovir half-life and the area under the concentration-time curve.A  Urinary excretion and renal clearance were correspondingly reduced.


Patients less than 30 years of age and those who had the least severe neurologic involvement at time of entry into study had the best outcome with treatment with acyclovir.A  An additional controlled study performed in Europe demonstrated similar findings.
Acyclovir Sodium Injection is indicated for the treatment of initial and recurrent mucosal and cutaneous herpes simplex (HSV-1 and HSV-2) in immunocompromised patients. Acyclovir Sodium Injection is indicated for the treatment of severe initial clinical episodes of herpes genitalis in immuno-competent patients. Acyclovir Sodium Injection is indicated for the treatment of varicella-zoster (shingles) infections in immunocompromised patients.
Acyclovir Sodium Injection is contraindicated for patients who develop hypersensitivity to acyclovir or valacyclovir.
Acyclovir Sodium Injection is intended for intravenous infusion only, and should not be administered topically, intramuscularly, orally, subcutaneously, or in the eye.A  Intravenous infusions must be given over a period of at least 1 hour to reduce the risk of renal tubular damage (see PRECAUTIONS and DOSAGE AND ADMINISTRATION). Abnormal renal function (decreased creatinine clearance) can occur as a result of acyclovir administration and depends on the state of the patienta€™s hydration, other treatments, and the rate of drug administration.A  Concomitant use of other nephrotoxic drugs, pre-existing renal disease, and dehydration make further renal impairment with acyclovir more likely. Administration of acyclovir by intravenous infusion must be accompanied by adequate hydration. When dosage adjustments are required, they should be based on estimated creatinine clearance (see DOSAGE AND ADMINISTRATION). Approximately 1% of patients receiving intravenous acyclovir have manifested encephalopathic changes characterized by either lethargy, obtundation, tremors, confusion, hallucinations, agitation, seizures, or coma.A  Acyclovir should be used with caution in those patients who have underlying neurologic abnormalities and those with serious renal, hepatic, or electrolyte abnormalities, or significant hypoxia.


Acyclovir was tested in 16 in vitro and in vivo genetic toxicity assays.A  Acyclovir was positive in 5 of the assays. Hematologic and Lymphatic:A  Disseminated intravascular coagulation, hemolysis,leukocytoclastic vasculitis, leukopenia, lymphadenopathy.
Hepatobiliary Tract and Pancreas:A  Elevated liver function tests, hepatitis, hyperbilirubinemia,jaundice.
Urogenital:A  Renal failure, elevated blood urea nitrogen, elevated creatinine (see WARNINGS). CAUTION - RAPID OR BOLUS INTRAVENOUS INJECTION MUST BE AVOIDED (see WARNINGS and PRECAUTIONS). PATIENTS WITH ACUTE OR CHRONIC RENAL IMPAIRMENT: Refer to DOSAGE AND ADMINISTRATION section for recommended doses, and adjust the dosing interval as indicated in Table 5. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.



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