Acivir Tablet Uses
For the treatment of viral infections due to herpes simplex virus (type I & II) and varicella zoster virus (herpes zoster & chickenpox). For the treatment of herpes simplex virus infections of the skin and mucous membranes including initial and recurrent genital herpes. For the prophylaxis of herpes simplex infections in immunocompromised patients.
Acyclovir exerts its antiviral effect on herpes simplex viruses (HSV) and varicella-zoster virus by interfering with DNA synthesis and inhibiting viral replication. The exact mechanisms of action against other susceptible viruses have not fully elucidated. In vitro studies with herpes simplex viruses indicate that acyclovir triphosphate is the pharmacologically active form of the drug; the triphosphate functions as both a substrate for and preferential inhibitor of viral DNA polymerase.
Absorption of Acyclovir from the GI tract is variable and incomplete. It is estimated that 15-30% of an oral dose of the drug is absorbed . Acyclovir is widely distributed into body tissues and fluids including the brain, kidney, saliva, lung, liver, muscle, spleen, uterus, vaginal mucosa and secretions, CSF, and herpetic vesicular fluid. The drug is also distributed into semen, achieving concentrations about 1.4 and 4 times those in plasma during chronic oral therapy at dosages of 400 mg and 1 g daily, respectively.
Plasma concentrations of Acyclovir appear to decline in a biphasic manner. In adults with normal renal function, the half-life of acyclovir in the initial phase averages 0.34 hours and the half-life in the terminal phase averages 2.1-3.5 hours.
Acivir Therapeutic Class
Herpes simplex & Varicella-zoster virus infections
Acivir Tablet Doses
Tablet: For the treatment of initial and recurrent episodes of herpes simplex infections in adults, 200 mg Acyclovir tablet should be taken 5 times daily (at 4 hours intervals omitting the night-time dose). Treatment should continue for 5 days and may be extended for up to 10 days in severe initial infections. For suppression of herpes simplex infections in adults, treatment with Acyclovir tablet should be continued at a dose of 200 mg 4 times daily or 400 mg twice daily for up to 1 year. If the patient remains recurrence free for up to 2-3 months, this dose can be reduced to 200 mg 3 times daily. After 1 year, treatment should be stopped to reassess patient's clinical status. For prophylaxis of herpes simplex infections in immune-compromised patients, 200 mg Acyclovir tablet should be taken four times daily at 6 hourly intervals for 7 days. In severely immune-compromised patients (e.g. after bone marrow transplantation) or in patients with impaired absorption from the gut, the dose can be doubled. For treatment of herpes zoster infections in adults, 800 mg Acyclovir tablet should be taken 5 times daily (at 4 hourly intervals) for 7 days.
Oral suspension: Children: HSV infections in children over 2 years should be given adult doses and children below 2 years should be given half of the adult dose.
Acivir Tablet Side Effects
Acyclovir is well tolerated when given orally. Skin rashes which, resolve after withdrawal of the drug have been reported with acyclovir. GI effects including nausea, vomiting, diarrhea, headache and abdominal pain have been reported in patients receiving oral acyclovir. The most common adverse effect is mild pain including transient burning and stinging at the site of application following acyclovir cream.
Concomitant administration of probenecid and acyclovir has reportedly increased the mean plasma half-life and decreased urinary excretion and renal clearance of acyclovir. Amphotericin B has been shown to potentiate the antiviral effect of acyclovir against pseudorabies virus in vitro when both drugs are added to the culture medium. Ketoconazole and acyclovir have shown dose-dependent, synergistic, antiviral activity against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) in in-vitro replication studies.
Acivir Uses During Pregnancy
Acyclovir has not been shown to be teratogenic in standard tests following subcutaneous administration in rats and rabbits. The drug does cross the placenta in humans. There are no adequate and controlled studies to date using acyclovir in pregnant women, and the drug should be used during pregnancy only when the potential benefits justify the possible risks to the fetus; the drug's potential for causing chromosomal damage at high concentrations should be considered.
Limited data indicate that acyclovir is distributed into milk, generally in concentrations greater than concurrent maternal plasma concentrations, and can be absorbed by nursing infants. Because of the potential for serious adverse reactions to acyclovir in nursing infants, a decision should be made whether to discontinue nursing or the drug, taking into account the importance of the drug to the woman.
Acyclovir is contraindicated in patients known to be hypersensitive to acyclovir. For the patients with severe renal impairment, a reduction of the doses is recommended.
Acivir Storage Condition
Acyclovir tablet and cream should be stored below 25° C in a cool and dry place.
Acivir Special Warning
HSV infections in children over 2 years should be given adult doses and children below 2 years should be given half of the adult dose.