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whereas Acicvir 50 mg was statistically superior to placebo onlyfor remecation time.

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Acicvir should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.


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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Acicvir is rapidly and almost completely absorbed after oral administration.
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1 Dosing may be increased to 100 mg every four to six hours, but the daily dosage should not exceed 400 mg 1 and should be limited to 250 to 300 mg .
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The product information for Acicvir states that convulsions have been reported in patients using Acicvir at the recommended dose levels and that the risk
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In vitro studies indicate that Acicvir is unlikely to inhibit,
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A single i.m. dose of Acicvir is useful pre-treatment to minimize the risk of acid aspiration during operation,
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Acicvir may not work as well and may require higher doses to obtain the same effect as when originally taken.
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adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
1 Dosing may be increased to 100 mg every four to six hours, but the daily dosage should not exceed 400 mg 1 and should be limited to 250 to 300 mg .

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The analgesic activity of Acicvir is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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The suitability of Acicvir suppositories for inclusion in our hospital formulary,
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clinical trial was performed to assess the analgesic efficacy and reported side effects of Acicvir 100 mg, Acicvir 50 mg,
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Acicvir is administered as a racemate and both [-] and [+] forms of both Acicvir and M1 are detected in the circulation.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions).
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Acicvir should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
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The binding of Acicvir to human plasma proteins is approximately 20%,
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