Acyclovir (Acyclovir) is a potent synthetic purine nucleoside analogue with strong antiviral properties, specifically targeting the herpes simplex virus (HSV) and varicella-zoster virus (VZV). It is prescribed for the management of viral infections affecting the skin, mucous membranes, and nervous system. By selectively inhibiting viral DNA synthesis and replication, Acyclovir helps reduce the severity and duration of outbreaks, promotes healing of sores, and limits the spread of the virus within the body. It is available in multiple formulations (including oral tablets, capsules, oral suspensions, topical creams or ointments, and intravenous injections), allowing tailored delivery based on the severity and site of the infection.
Acyclovir is an antiviral medicine in the nucleoside analogue class. It is used to treat infections caused by certain viruses, mainly those belonging to the herpesvirus family, including herpes simplex virus (HSV-1 and HSV-2) and varicella-zoster virus (VZV), which causes chickenpox and shingles.
After administration, acyclovir is converted inside virus-infected cells into its active form, acyclovir triphosphate. This activation depends on a viral enzyme called thymidine kinase, which is more active in infected cells than in healthy human cells. Once activated, acyclovir triphosphate inhibits viral DNA polymerase and gets incorporated into the growing viral DNA chain, leading to premature termination of DNA synthesis. This process helps stop viral replication and limits the spread of infection.
In clinical use, Acyclovir is prescribed for conditions such as cold sores, genital herpes, shingles, and chickenpox. It may also be used as suppressive therapy in patients with frequent recurrent herpes infections or in individuals with weakened immune systems to reduce the risk of viral reactivation.
Acyclovir does not eliminate the herpes virus completely from the body, as the virus remains dormant in nerve cells and may reactivate later. However, treatment helps reduce the severity and duration of symptoms, speeds up healing, and may reduce viral shedding when started early during an outbreak.
The medicine is available in multiple formulations, including oral tablets, oral suspension, topical cream, and intravenous injection. The choice of formulation depends on the type, location, and severity of infection, as well as the patient’s overall clinical condition. Treatment should always be taken under medical supervision, and adequate hydration is recommended during therapy, particularly with higher doses or intravenous use, to reduce the risk of kidney-related side effects.
Acyclovir may be indicated by your doctor for:
Treatment of initial and recurrent episodes of genital herpes infections.
Management of recurrent cold sores around the lips and mouth.
Treatment of acute shingles outbreaks to reduce pain and duration.
Management of chickenpox in both children and adults, particularly those at risk for severe disease.
Long-term prevention of recurrent herpes simplex infections in immunocompetent or immunocompromised individuals.
Intravenous treatment of serious viral brain infections.
Treatment of herpes simplex infections in newborns.
Acyclovir may provide benefits such as:
Acyclovir may cause side effects in some people, although many tolerate it well when used as prescribed. The type and likelihood of side effects can vary depending on the formulation and duration of use.
You must use Acyclovir exactly as prescribed by your doctor. Do not change the dose or frequency without medical advice.
Acyclovir is an antiviral drug that specifically blocks the replication of viral DNA.
After entering a virus-infected cell, Acyclovir is converted by the viral enzyme thymidine kinase into acyclovir monophosphate. It is then further converted by cellular enzymes into its active form: acyclovir triphosphate.
This active form works in two ways:
Competitive Inhibition: It competes with the natural building blocks of DNA for a spot in the viral DNA chain.
Chain Termination: Once acyclovir triphosphate is incorporated into the viral DNA strand, it acts as a "stop" signal because it lacks the necessary chemical group to attach the next building block. This permanently stops the viral DNA chain from growing.
Because healthy cells do not contain the viral thymidine kinase enzyme in significant amounts, very little active drug is produced in non-infected cells, making the treatment highly selective for the virus.
Acyclovir has been used extensively and is generally considered safe if the benefits outweigh the risks, but medical supervision is required.
Acyclovir passes into breast milk. While it is often considered compatible with breastfeeding, inform your healthcare provider before use.
Some patients may experience dizziness or tiredness. Avoid driving or operating machinery until you know how the medicine affects you.
No significant dose adjustments are typically required for liver disease, though overall health should be monitored.
Acyclovir is cleared by the kidneys. Patients with renal impairment require significant dose adjustments to prevent toxicity.
Alcohol does not directly interact with acyclovir, but it can worsen dehydration or dizziness; limit consumption during treatment.
Store Acyclovir at room temperature in a dry place away from direct sunlight and heat.
If you suspect an overdose, stop using the medicine and contact your doctor immediately or go to the nearest emergency department. Signs of a significant oral overdose may include agitation, seizures, or kidney failure.
If you miss a dose, take or use it as soon as you remember, unless it is almost time for your next dose. In that case, skip the missed dose and continue with your regular schedule. Never double the dose to compensate.
Therapeutic Class
Antiviral
Action Class
Antiviral (Viral DNA polymerase inhibitor)
Chemical Class
Purine nucleoside analogue
Habit Forming
No
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₹197.6
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₹197.6
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₹199.9
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₹199.9
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