Valvir pills 1000mg, 7pcs

Composition

1 film-coated tablet contains:

Active ingredient:

valacyclovir hydrochloride hydrate 611.70 mg corresponding to 500 mg of valacyclovir;

excipients;

film coating.

Pharmacological action

Valvir is an antiviral drug. In humans, valacyclovir is rapidly and completely converted to acyclovir and L-valine by valacyclovir hydrolase. Acyclovir in vitro has specific inhibitory activity against Herpes simplex viruses types 1 and 2, Varicella zoster and Epstein-Barr, cytomegalovirus (CMV) and human herpes virus type 6.

Acyclovir inhibits the synthesis of viral deoxyribonucleic acid (DNA) immediately after phosphorylation and conversion to the active form of acyclovir triphosphate. The first stage of phosphorylation occurs with the participation of virus-specific enzymes. For Herpes simplex, Varicella zoster, and Epstein-Barr viruses, such an enzyme is viral thymidine kinase, which is present in virus-affected cells. Partial phosphorylation selectivity is preserved in CMV and is mediated through the phosphotransferase gene product UL 97. Activation of acyclovir by a specific viral enzyme greatly explains its selectivity.

The process of phosphorylation of acyclovir (conversion from mono – to triphosphate) is completed by cellular kinases. Acyclovir triphosphate competitively inhibits viral DNA polymerase and, being a nucleoside analog, is incorporated into viral DNA, which leads to an obligate (complete) chain break, stopping DNA synthesis and, consequently, blocking viral replication.

In immunocompromised patients, Herpes simplex and Varicella zoster viruses with reduced sensitivity to valacyclovir are extremely rare (less than 0.1%), but can sometimes be detected in patients with severe immune disorders, such as those with a bone marrow transplant, those receiving chemotherapy for malignancies, and those infected with the human immunodeficiency virus (HIV).

Resistance is caused by a deficiency of thymidine kinase of the virus, which leads to excessive spread of the virus in the host. Sometimes a decrease in sensitivity to acyclovir is due to the appearance of virus strains with a violation of the structure of viral thymidine kinase or DNA polymerase. The virulence of these varieties of the virus is similar to that of its wild strain.

Indications

• Treatment and prevention of recurrent infections of the skin and mucous membranes caused by the herpes simplex virus (including newly detected and recurrent genital herpes);
• Treatment of herpes zoster;
• Treatment of labial herpes;
• Reduction of genital herpes infection in a healthy partner, if it is taken as a suppressive therapy in combination with safe sex;
• Prevention of cytomegalovirus infection that occurs during organ transplantation (reduces the severity of acute graft rejection in patients with kidney transplants, the development of opportunistic infections and other viral infections caused by H. simplex and V. zoster viruses) for adults and children over 12 years of age.

Contraindications

-hypersensitivity to valacyclovir, acyclovir and other components of the drug;

– clinically expressed forms of HIV infection with a CD4+-lymphocyte content of less than 100 / µl;

– bone marrow transplantation

— – kidney transplantation;

– children (up to 12 years with CMV, up to 18 years – for other indications).

With caution:  liver failure (high doses of the drug), renal failure, pregnancy, lactation.

Side effects

The most common adverse reactions that occur with valacyclovir are headache and nausea, more serious adverse reactions: thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome, acute renal failure and neurological disorders.

Adverse reactions are listed below according to the classification by major system and organ and frequency of occurrence: very common – ≥ 1/10; often – ≥1/100 or < 1/10; sometimes – ≥ 1/1000 or < 1/100; rarely-1/10000 or < 1/1000; very rare —

From the digestive tract:  often — nausea; rarely-abdominal discomfort, including abdominal pain; vomiting, diarrhea; very rarely-reversible violations of functional liver tests, which are sometimes regarded as manifestations of hepatitis.

Blood and lymphatic system disorders:  very rarely — leukopenia (mainly in patients with reduced immunity), thrombocytopenia.

From the immune system:  very rarely — anaphylaxis.

Mental disorders and disorders of the nervous system:  often-headache; sometimes-agitation, including aggressive behavior; rarely-dizziness, confusion, hallucinations, decreased mental abilities; very rarely — agitation, tremor, ataxia, dysarthria; psychotic symptoms, including mania; depression, convulsions, encephalopathy, coma. These symptoms are reversible and usually occur in patients with impaired renal function or other diseases. In organ transplant patients receiving high doses of valacyclovir (8 g/day) for the prevention of CMV infection, neurological reactions develop more often than with lower doses.

Respiratory and mediastinal disorders:  sometimes-dyspnoea.

Skin and subcutaneous tissue disorders:  sometimes— rashes, including photosensitivity; rarely-itching.

Allergic reactions:  very rarely — urticaria, angioedema.

From the urinary system:  rarely-impaired renal function; very rarely-acute renal failure, renal colic (may be associated with impaired renal function).

Other services:  Cases of renal failure, microangiopathic hemolytic anemia, and thrombocytopenia (sometimes in combination) have been reported in patients with severe immune disorders, especially in patients with advanced acquired immune deficiency syndrome who receive high doses of valacyclovir (8 g/day) for a long time. Similar complications were reported in patients with the same medical conditions, but not receiving valacyclovir.

According to the available data, it is not possible to determine the frequency of some adverse reactions.

From the side of the senses:  visual impairment.

From the side of hematopoietic organs:  neutropenia, aplastic anemia, leukoplastic vasculitis, thrombotic thrombocytopenic purpura.

From the side of the skin:  erythema multiforme.

Laboratory parameters:  decreased hemoglobin, hypercreatininemia.

Other services:  dysmenorrhea, arthralgia, nasopharyngitis, respiratory tract infections, facial edema, high blood pressure, tachycardia, fatigue; in addition, children have fever, dehydration, rhinorrhea.

Interaction

No clinically significant interactions have been established.

Cimetidine and probenecid after taking 1 g of valacyclovir increase the AUC of acyclovir, reducing its renal clearance (however, dose adjustment of valacyclovir is not required due to the wide therapeutic index of acyclovir).

Caution should be exercised in the case of concomitant use of valacyclovir in high doses (4 g/ day) and drugs that compete with acyclovir for the elimination pathway (the latter is eliminated unchanged in the urine as a result of active tubular secretion), since there is a potential threat of an increase in plasma levels of one or both drugs or their metabolites. When acyclovir was co-administered with mycophenolate mofetil, an increase in the AUC of the first and inactive metabolite of the second was noted.

Caution should also be exercised when combining valacyclovir in high doses (4 g/ or higher) with drugs that affect renal function (for example, cyclosporine, tacrolimus).

How to take, course of use and dosage

Inside. Adults.

Herpes zoster — 1000 mg 3 times a day for 7 days.

Herpes simplex — 500 mg 2 times a day. In case of relapses, the course should be 3 or 5 days. In the first episode with a severe course, the duration of treatment can be increased to 10 days (in case of relapses, it is ideal to prescribe Valvir in the prodromal period or when the first symptoms of the disease appear, i. e. tingling, itching, burning).

For the treatment of labial herpes, it is effective to prescribe the drug at a dose of 2 g 2 times for 1 day: the second dose should be taken approximately 12 hours (but not earlier than 6 hours) after the first dose (do not use this dosage regimen for more than 1 day, since, as shown, this does not provide additional clinical benefits). Prevention of relapses of infections caused by the herpes simplex virus: in patients with preserved immunity-500 mg 1 time a day; with very frequent relapses (10 or more per year) – 250 mg 2 times a day; for adult patients with immunodeficiency-500 mg 2 times a day. The course duration is 4-12 months.

Prevention of infection with genital herpes of a healthy partner: infected hete Rozexual adults with preserved immunity and with the number of exacerbations up to 9 per year-500 mg 1 time a day for 1 year or more, every day with regular sexual activity, with irregular sexual contacts. Valvira should be started 3 days before the intended sexual contact (there are no data on the prevention of infection in other patient populations). Prevention of cytomegalovirus infection: adults and adolescents over 12 years of age – 2 g 4 times a day (as early as possible, after transplantation). The duration of the course is 90 days, but in patients with high risk, treatment may be longer.

Overdose

Currently, there are insufficient data on valacyclovir overdose.

Symptoms: A single overdose of acyclovir up to 20 g, which was partially absorbed from the gastrointestinal tract, was not accompanied by a toxic effect of the drug. When taking ultrahigh doses of acyclovir orally for several days, nausea, vomiting, headache, confusion developed; when administered intravenously, an increase in serum creatinine concentration, the development of renal failure, confusion, hallucinations, agitation, convulsions, coma.

Treatment: patients should be under close medical supervision for signs of toxic effects. Hemodialysis significantly enhances the removal of acyclovir from the blood and can be considered the method of choice in the management of patients with valacyclovir overdose.

Special instructions

Taking the drug in high doses for a long time in conditions accompanied by severe immunodeficiency (bone marrow transplantation, clinically expressed forms of HIV infection, kidney transplantation), led to the development of thrombocytopenic purpura and hemolytic-uremic syndrome, up to a fatal outcome. If side effects from the central nervous system occur (including agitation, hallucinations, confusion, delirium, convulsions and encephalopathy), the drug is discontinued.

Patients at risk of dehydration, especially elderly patients, should be adequately hydrated during treatment with Valvir. Patients with renal insufficiency have an increased risk of developing neurological complications.

In patients with impaired liver function in patients with mild or moderate cirrhosis of the liver (synthetic liver function is preserved), no dose adjustment of Valvir is required. The pharmacokinetic study in patients with severe cirrhosis of the liver (with impaired synthetic liver function and the presence of shunts between the portal system and the general vascular bed) also did not receive data indicating the need to adjust the dosage regimen; however, the clinical experience of using Valvir in this category of patients is organic. There are no data on the use of Valvir in high doses (4 g/ or more) in patients with liver disease, so caution should be exercised when prescribing the drug in high doses to this category of patients.

Elderly patients do not need to adjust the dose, except in cases of significant renal impairment. It is necessary to maintain an adequate water-electrolyte balance.

No specific studies have been conducted to investigate the effects of Valvir in patients undergoing liver transplantation. However, high-dose prophylactic use of acyclovir has been shown to reduce cytomegalovirus infection. Suppressive therapy with Valvir reduces the risk of transmission of genital herpes, but does not completely eliminate it and does not lead to a complete cure. During therapy with Valvir, the patient should take measures to ensure the safety of the partner during sexual contact.

Form of production

Pills.

Storage conditions

At a temperature not exceeding 25 °C

Shelf life

2 years

Active ingredient

Valacyclovir

Conditions of release from pharmacies

By prescription

Dosage form

Tablets

Purpose

For adults

Indications

Cytomegalovirus infection, Herpes