Цикловир

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Цикловир

Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Цикловир

The Identity of Цикловир (Aciclovir)

This section provides a factual overview of the drug Цикловир, focusing on its composition, classification, and general function.

Property Description
Active ingredient Aciclovir (INN) / Acyclovir
Form Tablet, Oral Suspension, Cream, Injection
Pharmacological class Direct Acting Antiviral Agent (DAA)
Common use Limiting the spread of herpesvirus infections
Origin Synthetic purine nucleoside analogue

What is Цикловир? Defining its Pharmaceutical Identity

Цикловир is a pharmaceutical preparation containing the active substance Aciclovir, which is categorically classified as a specialized direct acting antiviral (DAA). This medicine is chemically identified as a synthetic purine nucleoside analogue, meaning it is a laboratory-manufactured agent designed specifically to interfere with certain viral processes. Its recognition as an anti-herpesvirus agent establishes its targeted purpose against infections caused by viruses like the Herpes Simplex Virus (HSV) and Varicella Zoster Virus (VZV). This class of medication is clinically recognized for its ability to slow the growth and spread of the herpes virus in the body.

Aciclovir: Structure, Origin, and Available Forms

The Aciclovir compound is a synthetic drug and is a single-ingredient product, focusing its entire effect on its unique chemical action. The core substance is made available in several dosage forms, allowing for versatile delivery. These include tablets and oral suspensions for systemic administration, as well as topical creams and ophthalmic ointments for localized application. This diversity ensures the active substance can be delivered through the most appropriate route of administration.

How the Selective Action of Цикловир Serves its General Purpose

The general therapeutic purpose of Цикловир is to control and limit the reproduction of the targeted herpesviruses. This effect stems from its function as a selective inhibitor that is activated primarily within the infected cells. By interfering with viral DNA synthesis, the drug stops the virus from replicating itself. While this medication does not cure the infections, it helps relieve the pain and discomfort associated with viral sores and supports faster healing.

Regulatory References

  1. Acyclovir: MedlinePlus Drug Information

What side effects are possible with Цикловир?

Possible Side Effects and Safety Information

The safety characteristics of Цикловир (Aciclovir) are defined by formal regulatory classifications based on clinical trial and post-marketing data. Adverse reactions are grouped by the body system affected and assigned a frequency category, ranging from very common to very rare, as documented in official government prescribing information.

Adverse Reaction Frequency Classification

Classification Examples of Documented Effects
Very Common Headache, dizziness
Common Nausea, vomiting, diarrhea, abdominal pain, fatigue, fever, pruritus, rashes
Uncommon Urticaria (hives), accelerated diffuse hair loss
Rare Anaphylaxis, angioedema, acute renal failure, reversible hyperbilirubinemia
Very Rare Anaemia, leukopenia, thrombocytopenia, hepatitis, jaundice, confusion, convulsions

Key Safety Considerations

The official safety profile notes that Цикловир can affect several system-organ classes, including the Gastrointestinal System, Nervous System Disorders, Skin and Subcutaneous Tissue, and Renal and Urinary Disorders. Serious adverse reactions, though classified as rare or very rare, include acute renal failure, severe immune responses such as anaphylaxis, and neurological disturbances like confusion and convulsions.

Regulatory documents emphasize that specific safety considerations apply to certain populations. Older adults and patients with renal impairment are documented as being at increased risk for neurological and renal adverse reactions. The label also notes that renal injury is associated with drug crystallization in the renal tubules, a risk heightened by dehydration. Furthermore, some serious effects, particularly neurological reactions, may be more likely observed at the start of treatment or during dose escalation.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory profile for Цикловир overdosage is defined by documented manifestations in the central nervous system (CNS) and the renal system. Overdose presentations commonly involve gastrointestinal effects, such as nausea and vomiting, and CNS effects including agitation, confusion, hallucinations, and lethargy. More severe outcomes, which indicate a serious health scenario, include seizures and coma. Acute renal failure is an officially documented severe complication, often linked to the precipitation of the active substance in the kidney's tubules.

Regulatory guidance mandates seeking immediate emergency medical attention for any suspected overdose. It is specified that emergency services must be contacted immediately if an individual exhibits severe, life-threatening symptoms, such as collapse, seizure activity, or difficulty breathing. There is no specific antidote listed in the official labeling; therefore, management focuses on symptomatic and supportive care. Haemodialysis is documented as a procedural intervention that significantly enhances the removal of the drug and may be considered for symptomatic overdosage. Elderly patients and those with pre-existing renal impairment are noted in official documents to be at an increased risk of developing neurological side effects.

Therapeutic Uses of Цикловир

What Цикловир treats: Main Uses and Benefits

Цикловир is commonly used across conditions presenting with acute or disruptive episodes caused by the Herpes Simplex Virus (HSV) and Varicella Zoster Virus (VZV). This medication is applied across domains where additional symptomatic support is needed. It is primarily relevant for easing the acute burden of Herpes Zoster (shingles), genital herpes, cold sores (herpes labialis), and chickenpox (varicella), and for providing long-term suppressive management.

Symptom Relief and Therapeutic Benefits

The main therapeutic benefit is that Цикловир supports the process of healing and resolution of visible lesions and is relevant for easing the associated acute pain, burning, and itching that interfere with daily functioning. In clinical settings that involve acute or unstable symptom patterns, such as severe widespread infections, it assists with maintaining functional stability. For patients experiencing frequent recurrences, the long-term use is commonly used to help with significantly reducing the frequency of symptomatic recurrences.

“Its role is to support the patient during difficult episodes by easing distress and contributing to improved comfort during periods of heightened symptoms.”

It is relevant in situations requiring temporary assistance in symptom stabilization, particularly for immunocompromised patients where it may be applied in addressing symptoms related to heightened physiological activity in these individuals.


Therapeutic Focus: Acute Symptomatic Relief
Цикловир plays a role in managing symptoms related to acute sensory discomfort, used for managing symptoms associated with episodes where pain, tingling, or burning sensations are more noticeable.

Regulatory References

  1. Acyclovir MedlinePlus Drug Information

Eligibility and Restrictions for Use

Official Eligibility and Restrictions for Цикловир (Acyclovir)

Population Eligibility Status Constraint or Condition
Absolutely Contraindicated Patients with known hypersensitivity to Acyclovir, Valacyclovir, or any formulation component.
Conditional/Restricted Use Patients with impaired renal function, including older adults. Dose adjustments are required by regulatory authorities.
Conditional Use Pregnant or breastfeeding women. Use is permitted only when the potential clinical benefit outweighs the possibility of risk to the fetus or infant.
Established Use Adults and Pediatric Patients (typically starting from 3 months of age for systemic forms) with established safety and efficacy data.

The official regulatory profile defines who may and may not use Цикловир. The primary exclusion is based on a history of allergy to the drug or its precursor, Valacyclovir. Eligibility for all other populations is conditional on health factors that affect the drug's elimination. Specifically, because Цикловир is cleared by the kidneys, patients with reduced renal function—a group that includes many older adults—must have use restricted and monitored. Use in pregnant and nursing individuals is formally restricted by a required justification of clinical benefit over risk.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The official interaction profile for Aciclovir is defined by its primary elimination pathway through active renal tubular secretion. This pharmacokinetic mechanism leads to clinically significant interactions with medicines that compete for the same renal transport system, resulting in increased systemic exposure (AUC) of Aciclovir.

Documented Pharmacokinetic Interactions

Interacting Substance Official Interaction Outcome
Probenecid Significantly reduces Aciclovir renal clearance, increasing its half-life and plasma exposure.
Cimetidine Reduces Aciclovir renal clearance, leading to increased plasma concentration.
Mycophenolate Mofetil (MMF) Increases plasma exposure of both Aciclovir and the MMF inactive metabolite due to competition for renal tubular clearance.

Pharmacodynamic and Risk Interactions

Co-administration with potentially nephrotoxic agents is documented to increase the risk of renal dysfunction and/or the risk of reversible central nervous system symptoms. This additive risk is a key pharmacodynamic consideration.

The regulatory label also states that Aciclovir co-administration may increase the AUC of Theophylline by approximately 50%. Separately, Zidovudine co-administration has been associated with reports of fatigue.

Population and Administration Context

Elderly patients and patients with renal impairment are noted to be at increased risk of neurological side effects when combined with potentially nephrotoxic agents. Oral forms of the medicine may be taken with or without food.

Mechanism of Action

Selective Viral-Enzyme Activation

Цикловир's mechanism is defined by its status as an inactive pro-drug that requires the action of the viral enzyme Thymidine Kinase (TK) for its initial, rate-limiting phosphorylation. This enzyme, produced by the herpesvirus, converts Цикловир into a monophosphate intermediate. Subsequent phosphorylation steps by host cell kinases further produce the active metabolite, Aciclovir Triphosphate (ACV-TP). The mechanism provides for the preferential activation of the drug within virus-infected cells, allowing the active metabolite to concentrate at the replication site. This process dictates the selectivity of the drug's mechanism of action.


Obligate DNA Chain Termination

The activated metabolite, ACV-TP, is a molecular mimic of deoxyguanosine triphosphate (dGTP). ACV-TP engages the Viral DNA Polymerase as both a competitive inhibitor and a substrate that is incorporated into the growing viral DNA strand. Because the molecule lacks a critical binding site, its insertion causes obligate chain termination of the nascent viral DNA. The mechanistic consequence of chain termination is the suppression of active viral proliferation, restricting the synthesis of new infectious particles.


Mechanism Constraints

The effectiveness of the mechanism is intrinsically linked to the continuous activity of Viral Thymidine Kinase. When the virus is in its dormant (latent) phase, the absence of the activating enzyme means the mechanism does not engage the virus. This functional dependency restricts the mechanism's scope to the active replication phase.

Dosage and Administration Information

How to Use Цикловир (Acyclovir)

Цикловир is administered through multiple routes, including oral ingestion (tablets, suspension), intravenous infusion, and topical application (cream or ointment). The selection of the route and form depends on whether systemic or localized delivery of the active substance is necessary.


Administration Regimens and Timing

Standard regimens for oral administration typically involve doses of 200 mg, 400 mg, or 800 mg, with frequencies ranging from twice daily (for chronic suppression) up to five times daily for acute treatment courses. Oral forms may be taken with or without food, but administration requires the patient to maintain adequate hydration by drinking plenty of water.


Contextual Usage Principles

The duration of use is defined by the clinical context, ranging from short-term courses of 5 to 10 days for acute episodes to long-term suppressive cycles that may last up to 12 months before re-evaluation. For optimal use, therapy must be initiated as early as possible following the onset of initial signs or symptoms (prodrome).


Special Administration Requirements

Intravenous Цикловир requires strict procedural conditions: the powder must be reconstituted and diluted to a concentration not exceeding 7 mg/mL and administered as a slow infusion over a period of at least one hour. It must not be given by rapid or bolus injection. Furthermore, a dose reduction or interval extension is utilized in patients with renal impairment, with adjustments calculated based on Creatinine Clearance values.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Цикловир

Evidence for Use in Acute Herpes Zoster (Shingles)

The research base for managing acute shingles (Herpes Zoster) primarily involves short-term Randomized Controlled Trials (RCTs) and systematic reviews, often in older immunocompetent adults. Research examined outcomes related to physical discomfort and rash progression, specifically monitoring the rate of rash healing and the time until acute, zoster-associated pain (ZAP) resolved. Studies reported mixed findings when assessing the long-term risk of Postherpetic Neuralgia (PHN)—a form of long-term nerve pain—meaning the evidence regarding this specific outcome is not fully established.


Evidence for Suppressive Management of Genital Herpes

Long-term research, including RCTs and observational data, explored the use of Цикловир for managing recurrent genital herpes in adults. Researchers monitored outcomes describing episodic changes, particularly examining the count of symptomatic recurrences over periods up to 12 months or longer, and the frequency of asymptomatic viral shedding. Studies reported measurements related to the count of symptomatic outbreaks during the period of continuous use. Evidence is limited regarding the durability of these patterns after administration is stopped.


Evidence for Use in Herpes Simplex Infections of the Skin and Mouth

Short-term RCTs have evaluated the medicine for conditions like recurrent cold sores (Herpes Labialis) and primary mouth sores (PHG) in children. For cold sores, findings varied across studies regarding time-to-healing measurements, with the consistency of measured outcomes varying. For PHG, research examined measurements related to the duration of fever and the time until normal feeding resumed. Data for PHG are drawn from modest sample sizes, and the results apply only to the populations studied.


What the Research Record Shows is Still Uncertain

A synthesis of the available evidence highlights areas of uncertainty. The evidence quality varies when assessing the ability of Цикловир to prevent PHN, and certainty remains low on this specific long-term outcome. Furthermore, the durability of observed patterns, particularly after suppressive treatment is stopped, is not fully established, and comparative evidence against alternative treatments is limited in some areas.

Key Studies & References

  1. Prevention of VZV infection in immunosuppressed patients using antiviral agents (Review of randomized trials)
  2. Acyclovir: MedlinePlus Drug Information (General regulatory/patient information)

Frequently Asked Questions (FAQ)

Common questions about Цикловир (FAQ)


Q: How long can I use Цикловир?

A: Studies and official information indicate that for suppressive regimens, which are intended to prevent recurrent outbreaks, the medicine has been used in cycles of 6 to 12 months before use is re-evaluated. Long-term use has been reported to be generally well-tolerated in clinical data, with safety information often extending for periods up to several years.


Q: Can Цикловир be taken for prophylaxis (prevention)?

A: The medicine is described in official documents for use in suppressive regimens, which are intended to prevent recurrent outbreaks of genital herpes infections and may be used for prophylaxis in certain specified clinical situations.


Q: Can Цикловир affect the liver?

A: The medicine is documented as being minimally metabolized by the liver. However, official post-marketing reports have documented rare cases of mild and temporary elevations in liver enzymes, as well as hepatitis and jaundice.


Q: Do I need a prescription to buy Цикловир?

A: In many jurisdictions, the systemic forms of the medicine (tablets, capsules, and injections) are classified as prescription-only medications. Topical creams and ointments, however, may be available for purchase over-the-counter in some countries.


Q: Does Цикловир affect the effectiveness of birth control pills?

A: Official clinical experience and drug interaction analyses report no known or documented interactions between acyclovir and combined oral contraceptives (such as those containing ethinyl estradiol and norethindrone).


Q: Is Цикловир approved for use in children?

A: Official regulatory documents confirm that the use of systemic acyclovir is established and approved for use in pediatric patients. Specific dosing regimens are defined for children starting from typically 3 months of age.


Q: Can I use Цикловир during pregnancy?

A: The medicine is classified by the U.S. FDA as Pregnancy Category B. Official guidance indicates that its use is restricted to situations where the potential clinical benefit to the patient is judged to outweigh the potential risk to the fetus.


Q: Why do some people believe that Цикловир does not help them?

A: The drug’s action is functionally linked to the virus being in an active replication phase (not latent). This means it does not act against the virus when it is dormant. If lesions persist, low-level viral drug resistance is a factor that may be considered during monitoring.


Q: What should I do if I miss a dose of Цикловир?

A: Regulatory patient information describes the general guidance for a missed dose: it may be taken as soon as it is remembered, or skipped if it is almost time for the next scheduled dose. This is done to avoid doubling the amount taken.


Q: Are there any age restrictions for taking Цикловир?

A: There is no upper age limit for use, and the drug is approved for use in adults and children from 3 months of age. Older adults are noted to be at increased risk for certain neurological and renal side effects due to the possibility of reduced kidney function, which requires careful monitoring.


Q: Can Цикловир cause addiction or dependence?

A: The medicine is generally considered to have no known potential for abuse, addiction, or dependence. This is because it is not associated with the central nervous system effects, such as euphoria, that are typically produced by controlled substances.


Q: What is the difference between Цикловир tablets and cream?

A: The key difference lies in the route of administration and purpose. The tablet form is intended for systemic (whole-body) treatment of the infection. The cream is designed for topical/local application on the skin to treat superficial lesions like cold sores.


Q: Why do doctors prescribe Цикловир for different types of infections?

A: The medicine is classified as a single anti-herpesvirus agent whose targeted purpose is to act against a range of viruses within that family. This range includes both Herpes Simplex Virus (HSV) and Varicella Zoster Virus (VZV).


Q: How quickly is Цикловир eliminated from the body?

A: Official data indicates that the drug is eliminated primarily through the kidneys. Following administration, the plasma elimination half-life is described as typically brief.


Q: Does Цикловир contain lactose or gluten?

A: Many specific formulations of acyclovir tablets and capsules are documented to contain lactose monohydrate as an inactive ingredient. The presence of other specific excipients or fillers, such as gluten, varies depending on the specific manufacturer and product form.


Q: Why does Цикловир have different dosages?

A: Official product information indicates that the medicine is available in various oral dosages because different viral infections and different treatment goals—such as treating an acute episode versus long-term suppression—require different concentrations of the drug.


Q: What does research say about the long-term safety of Цикловир?

A: Clinical data and research indicate that the drug is often well-tolerated during continuous suppressive use for periods extending up to 10 years. Official reports state that adverse events are rare, mild, and generally show no evidence of cumulative toxicity over time.


Q: Why is Цикловир on the list of essential medicines?

A: Aciclovir is included in the World Health Organization (WHO) Model List of Essential Medicines. It is recognized as a vital treatment for a range of herpesvirus-related conditions, including Herpes Simplex infections, Zoster (shingles), Varicella (chickenpox), and Herpes simplex keratitis.


Q: Does Цикловир change blood test results?

A: The medicine has been associated with changes in certain laboratory parameters. These reports include mildly elevated serum enzyme values, such as transaminases, and, rarely, decreased counts of white blood cells or platelets.


Q: What is the maximum number of days I can apply Цикловир cream?

A: Official patient information describes that the duration of use for the cream for the approved indication of recurrent herpes labialis (cold sores) is typically 4 days.


Q: Can long-term use of Цикловир lead to viral resistance?

A: Official monitoring and studies indicate that viral resistance has been observed. However, the incidence is reported as very low in patients with normal immune function. Resistance is a consideration that should be monitored if lesions persist or recur frequently during treatment.


Q: How might Цикловир affect the immune system?

A: Research indicates that, in addition to its antiviral action, long-term use of the medicine may have the potential to modulate certain components of the host T-cell response. This effect relates to the immune reaction to specific viral antigens, such as those from Cytomegalovirus (CMV).

How should Цикловир be stored and disposed of?

How to Store and Dispose of Acyclovir

Acyclovir products, including tablets and intravenous powder, must be stored at controlled room temperature (20° to 25°C or 68° to 77°F). The tablets should be kept in a tight, light-resistant container and protected from excessive moisture. All forms must be stored out of the reach and sight of children.

For the intravenous solution, the reconstituted liquid must be used within 12 hours, and the subsequent diluted infusion solution must be used within 24 hours.

Disposal should follow official guidelines. Unused or expired medication should be disposed of by mixing it with an undesirable substance (e.g., used coffee grounds) and placing it in a sealed bag for the household trash, or by utilizing a drug take-back program. Acyclovir waste is classified as a Hazardous Drug (HD) and must be managed and disposed of to prevent environmental release.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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