Therapeutic indications

valaciclovir hydrochloride monohydrate is indicated for the treatment of herpes zoster (shingles) and ophthalmic zoster in immunocompetent adults (see sections 4.4).

valaciclovir hydrochloride monohydrate is indicated for the treatment of herpes zoster in adult patients with mild or moderate immunosuppression (see section 4.4). Herpes simplex virus (HSV) infections valaciclovir hydrochloride monohydrate is indicated

•     for the treatment and suppression of HSV infections of the skin and mucous membranes including:

-          treatment of first-episode of genital herpes in immunocompetent adults and adolescents and in immunocompromised adults.

-          treatment of recurrences of genital herpes in immunocompetent adults and adolescents, and in immunocompromised adults.

-          suppression of recurrent genital herpes in immunocompetent adults and adolescents and in immunocompromised adults.

•     Treatment and suppression of recurrent ocular HSV infections in immunocompetent adults and adolescents and in immunocompromised adults (see section 4.4).

•     Clinical studies have not been conducted in HSV-infected patients immunocompromised for other causes than HIV-infection (see section 5.1).

Cytomegalovirus (CMV) infections:

•     Valaciclovir hydrochloride monohydrate is indicated for the prophylaxis of CMV infection and disease following solid organ transplantation in adults and adolescents (see section 4.4)

Varicella zoster virus (VZV) infections – herpes zoster and ophthalmic zoster

Patients should be advised to start treatment as soon as possible after a diagnosis of herpes zoster. There are no data on treatment started more than 72 hours after onset of the zoster rash.

Immunocompetent Adults

The dose in immunocompetent patients is 1000 mg three times daily for seven days (3000 mg total daily dose). This dose should be reduced according to creatinine clearance (see Renal impairment below).

Immunocompromised Adults

The dose in immunocompromised patients is 1000 mg three times daily for at least seven days (3000 mg total daily dose) and for 2 days following crusting of lesions. This dose should be reduced according to creatinine clearance (see Renal impairment below).

In immunocompromised patients, antiviral treatment is suggested for patients presenting within one week of vesicle formation or at any time before full crusting of lesions.

The dose is 500 mg of Valaciclovir hydrochloride monohydrate to be taken twice daily (1000 mg total daily dose). This dose should be reduced according to creatinine clearance (see Renal impairment below).

For recurrent episodes, treatment should be for three to five days. For initial episodes, which can be more severe, treatment may have to be extended to ten days. Dosing should begin as early as possible. For recurrent episodes of herpes simplex, this should ideally be during the prodromal period or immediately upon appearance of the first signs or symptoms. Valaciclovir hydrochloride monohydrate can prevent lesion development when taken at the first signs and symptoms of an HSV recurrence.

Herpes labialis

For herpes labialis (cold sores), valaciclovir hydrochloride monohydrate 2000 mg twice daily for one day is effective treatment in adults and adolescents. The second dose should be taken about 12 h (no sooner than 6 h) after the first dose. This dose should be reduced according to creatinine clearance (see Renal impairment below). When using this dosing regimen, treatment should not exceed one day, since this has been shown not to provide additional clinical benefit. Therapy should be initiated at the earliest symptom of a cold sore (e.g. tingling, itching or burning).

Immunocompromised Adults

For the treatment of HSV in immunocompromised adults, the dosage is 1000 mg twice daily for at least 5 days, following assessment of the severity of the clinical condition and immunological status of the patient. For initial episodes, which can be more severe, treatment may have to be extended to ten days. Dosing should begin as early as possible. This dose should be reduced according to creatinine clearance (see Renal impairment below). For maximum clinical benefit, the treatment should be started within 48 hours. A strict monitoring of the evolution of lesions is advised. 

Suppression of recurrences of herpes simplex virus (HSV) infections in adults and

The dose is 500 mg of Valaciclovir hydrochloride monohydrate to be taken once daily. Some patients with very frequent recurrences (≥ 10/year in absence of therapy) may gain additional benefit from the daily dose of 500 mg being taken as a divided dose (250 mg twice daily). This dose should be reduced according to creatinine clearance (see Renal impairment below).Treatment should be re-evaluated after 6 to 12 months of therapy.

Immunocompromised Adults

The dose is 500 mg of Valaciclovir hydrochloride monohydrate twice daily. This dose should be reduced according to creatinine clearance (see Renal impairment below). Treatment should be re-evaluated after 6 to 12 months of therapy.

Prophylaxis of cytomegalovirus (CMV) infection and disease in adults and adolescents (≥12 years)

The dosage of Valaciclovir hydrochloride monohydrate is 2000 mg four times a day, to be initiated as early as possible post-transplant. This dose should be reduced according to creatinine clearance (see Renal impairment below).

The duration of treatment will usually be 90 days, but may need to be extended in high-risk patients.

Special populations

Children

The efficacy of Valaciclovir hydrochloride monohydrate in children below the age of 12 years has not been evaluated.

Elderly

The possibility of renal impairment in the elderly must be considered and the dose should be adjusted accordingly (see Renal impairment below). Adequate hydration should be maintained.

Renal impairment

Caution is advised when administering Valaciclovir hydrochloride monohydrate to patients with impaired renal function. Adequate hydration should be maintained. The dose of Valaciclovir hydrochloride monohydrate should be reduced in patients with impaired renal function as shown in Table 1 below.

In patients on intermittent haemodialysis, the Valaciclovir hydrochloride monohydrate dose should be administered after the haemodialysis has been performed. The creatinine clearance should be monitored frequently, especially during periods when renal function is changing rapidly e.g. immediately after renal transplantation or engraftment. The Valaciclovir hydrochloride monohydrate dosage should be adjusted accordingly.

Hepatic impairment

Studies with a 1000 mg dose of valaciclovir hydrochloride monohydrate in adult patients show that dose modification is not required in patients with mild or moderate cirrhosis (hepatic synthetic function maintained). Pharmacokinetic data in adult patients with advanced cirrhosis (impaired hepatic synthetic function and evidence of portal-systemic shunting) do not indicate the need for dose adjustment; however, clinical experience is limited. For higher doses (4000 mg or more per day), see section 4.4.

Table 1: DOSAGE ADJUSTMENT FOR RENAL IMPAIRMENT

^aFor patients on intermittent haemodialysis, the dose should be given after dialysis on dialysis days.

^bFor HSV suppression in immunocompetent subjects with a history of ≥10 recurrences/year, better results may be obtained with 250 mg twice daily.

Hydration status

Care should be taken to ensure adequate fluid intake in patients who are at risk of dehydration, particularly the elderly.

Use in patients with renal impairment and in elderly patients

Aciclovir is eliminated by renal clearance, therefore the dose of valaciclovir hydrochloride monohydrate must be reduced in patients with renal impairment (see section 4.2). Elderly patients are likely to have reduced renal function and therefore the need for dose reduction must be considered in this group of patients. Both elderly patients and patients with renal impairment are at increased risk of developing neurological side-effects and should be closely monitored for evidence of these effects. In the reported cases, these reactions were generally reversible on discontinuation of treatment (see section 4.8).

Use of higher doses of valaciclovir hydrochloride monohydrate in hepatic impairment and liver transplantation

There are no data available on the use of higher doses of valaciclovir hydrochloride monohydrate (4000 mg or more per day) in patients with liver disease. Specific studies of valaciclovir hydrochloride monohydrate have not been conducted in liver transplantation, and hence caution should be exercised when administering daily doses greater than 4000 mg to these patients.

Use for zoster treatment

Clinical response should be closely monitored, particularly in immunocompromised patients. Consideration should be given to intravenous antiviral therapy when response to oral therapy is considered insufficient.

Patients with complicated herpes zoster, i.e. those with visceral involvement, disseminated zoster, motor neuropathies, encephalitis and cerebrovascular complications should be treated with intravenous antiviral therapy.

Moreover, immunocompromised patients with ophthalmic zoster or those with a high risk for disease dissemination and visceral organ involvement should be treated with intravenous antiviral therapy.

Transmission of genital herpes

Patients should be advised to avoid intercourse when symptoms are present even if treatment with an antiviral has been initiated. During suppressive treatment with antiviral agents, the frequency of viral shedding is significantly reduced. However, the risk of transmission is still possible. Therefore, in addition to therapy with valaciclovir hydrochloride monohydrate, it is recommended that patients use safer sex practices.

Use in ocular HSV infections

Clinical response should be closely monitored in these patients. Consideration should be given to intravenous antiviral therapy when response to oral therapy is unlikely to be sufficient.

Use in CMV infections

Data on the efficacy of valaciclovir hydrochloride monohydrate from transplant patients (~200) at high risk of CMV disease (e.g. donor CMV-positive/recipient CMV negative or use of antithymocyte globulin induction therapy) indicate that valaciclovir hydrochloride monohydrate should only be used in these patients when safety concerns preclude the use of valganciclovir or ganciclovir.

High dose valaciclovir hydrochloride monohydrate as required for CMV prophylaxis may result in more frequent adverse events, including CNS abnormalities, than observed with lower doses administered for other indications (see section 4.8). Patients should be closely monitored for changes in renal function, and doses adjusted accordingly (see section 4.2).

The combination of valaciclovir hydrochloride monohydrate with nephrotoxic medicinal products should be made with caution, especially in subjects with impaired renal function, and warrants regular monitoring of renal function. This applies to concomitant administration with aminoglycosides, organoplatinum compounds, iodinated contrast media, methotrexate, pentamidine, foscarnet, ciclosporin, and tacrolimus.

Aciclovir is eliminated primarily unchanged in the urine via active renal tubular secretion. Following 1000 mg valaciclovir hydrochloride monohydrate, cimetidine and probenecid reduce aciclovir renal clearance and increase the AUC of aciclovir by about 25% and 45%, respectively, by inhibition of the active renal secretion of aciclovir. Cimetidine and probenecid taken together with valaciclovir hydrochloride monohydrate increased aciclovir AUC by about 65%. Other medicinal products (including e.g. tenofovir) administered concurrently that compete with or inhibit active tubular secretion may increase aciclovir concentrations by this mechanism. Similarly, valaciclovir hydrochloride monohydrate administration may increase plasma concentrations of the concurrently administered substance.

In patients receiving higher aciclovir exposures from valaciclovir hydrochloride monohydrate (e.g., at doses for zoster treatment or CMV prophylaxis), caution is required during concurrent administration with drugs which inhibit active renal tubular secretion.

Increases in plasma AUCs of aciclovir and of the inactive metabolite of mycophenolate motefil, an immunosuppressant agent used in transplant patients, have been shown when the drugs are co-administered. No changes in peak concentrations or AUCs are observed with coadministration of valaciclovir hydrochloride monohydrate and mycophenolate mofetil in healthy volunteers. There is limited clinical experience with the use of this combination. 

Pregnancy

A limited amount of data on the use of valaciclovir hydrochloride monohydrate and a moderate amount of data on the use of aciclovir in pregnancy is available from pregnancy registries (which have documented the pregnancy outcomes in women exposed to valaciclovir hydrochloride monohydrate or to oral or intravenous aciclovir (the active metabolite of valaciclovir hydrochloride monohydrate); 111 and 1246 outcomes (29 and 756 exposed during the first trimester of pregnancy, respectively) and postmarketing experience indicate no malformative or foeto/neonatal toxicity. Animal studies do not show reproductive toxicity for valaciclovir hydrochloride monohydrate (see section 5.3). Valaciclovir hydrochloride monohydrate should only be used in pregnancy if the potential benefits of treatment outweigh the potential risk.

Breastfeeding

Aciclovir, the principle metabolite of valaciclovir hydrochloride monohydrate, is excreted in breast milk. However, at therapeutic doses of valaciclovir hydrochloride monohydrate, no effects on the breastfed newborns/infants are anticipated since the dose ingested by the child is less than 2% of the therapeutic dose of intravenous aciclovir for treatment of neonatal herpes (see Section 5.2). Valaciclovir hydrochloride monohydrate should be used with caution during breast feeding and only when clinically indicated.

Fertility

Valaciclovir hydrochloride monohydrate did not affect fertility in rats dosed by the oral route. At high parenteral doses of aciclovir testicular atrophy and aspermatogenesis have been observed in rats and dogs. No human fertility studies were performed with valaciclovir hydrochloride monohydrate, but no changes in sperm count, motility or morphology were reported in 20 patients after 6 months of daily treatment with 400 to 1000 mg aciclovir.

No studies on the effects on the ability to drive and use machines have been performed. The clinical status of the patient and the adverse reaction profile of Valaciclovir hydrochloride monohydrate hydrochloride monohydrate should be borne in mind when considering the patient`s ability to drive or operate machinery. Further, a detrimental effect on such activities cannot be predicted from the pharmacology of the active substance.

The most common adverse reactions (ARs) reported in at least one indication by patients treated with Valaciclovir hydrochloride monohydrate hydrochloride monohydrate in clinical trials were headache       and             nausea.            More   serious             ARs     such     as         thrombotic       thrombocytopenic purpura/haemolytic uraemic syndrome, acute renal failure and neurological disorders are discussed in greater detail in other sections of the label.

Undesirable effects are listed below by body system organ class and by frequency.

The following frequency categories are used for classification of adverse effects:

Very common         ≥ 1/10,

Common                 ≥1/100 to < 1/10,

Uncommon             ≥ 1/1,000 to < 1/100,

Rare                        ≥ 1/10,000 to < 1/1000,

Very rare                < 1/10,000

Clinical trial data have been used to assign frequency categories to ARs if, in the trials, there was evidence of an association with valaciclovir hydrochloride monohydrate.

For ARs identified from postmarketing experience, but not observed in clinical trials, the most conservative value of point estimate (“rule of three”) has been used to assign the AR frequency category. For ARs identified as associated with valaciclovir hydrochloride monohydrate from post-marketing experience, and observed in clinical trials, study incidence has been used to assign the AR frequency category. The clinical trial safety database is based on 5855 subjects exposed to valaciclovir hydrochloride monohydrate in clinical trials covering multiple indications (treatment of herpes zoster, treatment/suppression of genital herpes & treatment of cold sores).

Clinical Trial Data Nervous system disorders

Very common:    Headache

Gastrointestinal disorders

Common:           Nausea

Post Marketing Data Blood and lymphatic system disorders

Uncommon:         Leucopenia, thrombocytopenia

Leucopenia is mainly reported in immunocompromised patients.

Immune system disorders

Rare:                    Anaphylaxis

Psychiatric and nervous system disorders 

Common:            Dizziness

Uncommon:        Confusion, hallucinations, decreased consciousness, tremor, agitation

Rare:                    Ataxia, dysarthria, convulsions, encephalopathy, coma, psychotic symptoms. Neurological disorders, sometimes severe, may be linked to encephalopathy and include confusion, agitation convulsions, hallucinations, coma. These events are generally reversible and usually seen in patients with re impairment or with other predisposing factors (see section 4.4). In organ transplant patients receiving high d mg daily) of Valaciclovir hydrochloride monohydrate hydrochloride monohydrate for CMV prophylaxis, neurological reactions occurred more frequently compared with low used for other indications.

Respiratory, thoracic and mediastinal disorders                                                                                                       

Uncommon:Dyspnoea                                                                                                                                         

Gastrointestinal disorders

Common:            Vomiting, diarrhoea.

Uncommon:        Abdominal discomfort

Hepato-biliary disorders

Uncommon:        Reversible increases in liver function tests (e.g. bilirubin, liver enzymes).

Skin and subcutaneous tissue disorders

Common:            Rashes including photosensitivity, pruritus.

Uncommon:        Urticaria

Rare:                   Angioedema

Renal and urinary disorders

Uncommon:        Renal pain

Rare:            Renal impairment, acute renal failure (especially in elderly patients or in patients with impairment receiving higher than the recommended doses).

Renal pain may be associated with renal failure.

Intratubular precipitation of aciclovir crystals in the kidney has also been reported. Adequate fluid intake sho ensured during treatment (see section 4.4).

Additional information on special populations

There have been reports of renal insufficiency, microangiopathic haemolytic anaemia and thrombocytopenia (sometimes in combination) in severely immunocompromised adult patients, particularly those with advance disease, receiving high doses (8000 mg daily) of valaciclovir hydrochloride monohydrate for prolonged periods in clinical trials. These fin also been observed in patients not treated with valaciclovir hydrochloride monohydrate who have the same underlying or concurrent cor

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows co monitoring of the benefit/risk balance of the medicinal product follow below mentioned address.
• Saudi Arabia:

Other GCC States:

Please contact the relevant competent authority. 

Symptoms and Signs

Acute renal failure and neurological symptoms, including confusion, hallucinations, agitation, decreased consciousness and coma, have been reported in patients receiving overdoses of valaciclovir hydrochloride monohydrate. Nausea and vomiting may also occur. Caution is required to prevent inadvertent overdosing. Many of the reported cases involved renally impaired and elderly patients receiving repeated overdoses, due to lack of appropriate dosage reduction.

Treatment

Patients should be observed closely for signs of toxicity. Haemodialysis significantly enhances the removal of aciclovir from the blood and may, therefore, be considered a management option in the event of symptomatic overdose.

Antivirals for systemic use

Pharmacotherapeutic group: Nucleosides and nucleotides excluding reverse transcriptase inhibitors, ATC code: J05AB11

Mechanism of action

Valaciclovir hydrochloride monohydrate, an antiviral, is the L-valine ester of aciclovir. Aciclovir is a purine (guanine) nucleoside analogue.

Valaciclovir hydrochloride monohydrate is rapidly and almost completely converted in man to aciclovir and valine, probably by the enzyme referred to as valaciclovir hydrochloride monohydrate hydrolase.

Aciclovir is a specific inhibitor of the herpes viruses with in vitro activity against herpes simplex viruses (HSV) type 1 and type 2, varicella zoster virus (VZV), cytomegalovirus (CMV), EpsteinBarr Virus (EBV), and human herpes virus 6 (HHV-6). Aciclovir inhibits herpes virus DNA synthesis once it has been phosphorylated to the active triphosphate form.

The first stage of phosphorylation requires the activity of a virus-specific enzyme. In the case of HSV, VZV and EBV this enzyme is the viral thymidine kinase (TK), which is only present in virus-infected cells. Selectivity is maintained in CMV with phosphorylation, at least in part, being mediated through the phosphotransferase gene product of UL97. This requirement for activation of aciclovir by a virus-specific enzyme largely explains its selectivity.

The phosphorylation process is completed (conversion from mono- to triphosphate) by cellular kinases. Aciclovir triphosphate competitively inhibits the virus DNA polymerase and incorporation of this nucleoside analogue results in obligate chain termination, halting virus DNA synthesis and thus blocking virus replication.

Pharmacodynamic effects

Resistance to aciclovir is normally due to a thymidine kinase deficient phenotype which results in a virus which is disadvantaged in the natural host. Reduced sensitivity to aciclovir has been described as a result of subtle alterations in either the virus thymidine kinase or DNA polymerase. The virulence of these variants resembles that of the wild-type virus.

Monitoring of clinical HSV and VZV isolates from patients receiving aciclovir therapy or prophylaxis has revealed that virus with reduced sensitivity to aciclovir is extremely rare in the immunocompetent host and is found infrequently in severely immunocompromised individuals e.g. organ or bone marrow transplant recipients, patients receiving chemotherapy for malignant disease and people infected with the human immunodeficiency virus (HIV).

Clinical studies

Varicella Zoster Virus Infection

Valaciclovir hydrochloride monohydrate hydrochloride monohydrate accelerates the resolution of pain: it reduces the duration of and the proportion of patients with zoster-associated pain, which includes acute and, in patients older than 50 years, also post-herpetic neuralgia. Valaciclovir hydrochloride monohydrate hydrochloride monohydrate reduces the risk of ocular complications of ophthalmic zoster.

Intravenous therapy generally is considered standard for zoster treatment in immunocompromised patients; however, limited data indicate a clinical benefit of valaciclovir hydrochloride monohydrate in the treatment of VZV infection (herpes zoster) in certain immunocompromised patients, including those with solid organ cancer, HIV, autoimmune diseases, lymphoma, leukaemia and stem cell transplants.

Herpes Simplex Virus Infection

Valaciclovir hydrochloride monohydrate for ocular HSV infections should be given according to applicable treatment guidelines.

Studies of valaciclovir hydrochloride monohydrate treatment and suppression for genital herpes were performed in HIV/HSV coinfected patients with a median CD4 count of > 100cells/mm3. Valaciclovir hydrochloride monohydrate 500 mg twice daily was superior to 1000 mg once daily for suppression of symptomatic recurrences Valaciclovir hydrochloride monohydrate 1000 mg twice daily for treatment of recurrences was comparable to oral aciclovir 200 mg five times daily on herpes episode duration. Valaciclovir hydrochloride monohydrate has not been studied in patients with severe immune deficiency.

The efficacy of valaciclovir hydrochloride monohydrate for the treatment of other HSV skin infections has been documented. Valaciclovir hydrochloride monohydrate has shown efficacy in the treatment of herpes labialis (cold sores), mucositis due to chemotherapy or radiotherapy, HSV reactivation from facial resurfacing, and herpes gladiatorum. Based on historical aciclovir experience, valaciclovir hydrochloride monohydrate appears to be as effective as aciclovir for the treatment of erythema multiforme, eczema herpeticum and herpetic whitlow.

Valaciclovir hydrochloride monohydrate has been proven to reduce the risk of transmission of genital herpes in immunocompetent adults when taken as suppressive therapy and combined with safer sex practices. A double blind, placebo controlled study was conducted in 1,484 heterosexual, immunocompetent adult couples discordant for HSV-2 infection. Results showed significant reductions in risk of transmission: 75 % (symptomatic HSV-2 acquisition), 50 % (HSV-2 seroconversion), and 48 % (overall HSV-2 acquisition) for valaciclovir hydrochloride monohydrate compared to placebo. Among subjects participating in a viral shedding sub-study, valaciclovir hydrochloride monohydrate significantly reduced shedding by 73 % compared to placebo (see section 4.4 for additional information on transmission reduction).

Cytomegalovirus Infection (see section 4.4)

CMV prophylaxis with valaciclovir hydrochloride monohydrate in subjects receiving solid organ transplantation (kidney, heart) reduces the occurrence of acute graft rejection, opportunistic infections and other herpes virus infections (HSV, VZV). There is no direct comparative study versus valganciclovir to define the optimal therapeutic management of solid organ transplant patients.

Absorption

Valaciclovir hydrochloride monohydrate is a prodrug of aciclovir. The bioavailability of aciclovir from valaciclovir hydrochloride monohydrate is about 3.3 to 5.5-fold greater than that historically observed for oral aciclovir. After oral administration valaciclovir hydrochloride monohydrate is well absorbed and rapidly and almost completely converted to aciclovir and valine. This conversion is probably mediated by an enzyme isolated from human liver referred to as valaciclovir hydrochloride monohydrate hydrolase. The bioavailability of aciclovir from 1000 mg valaciclovir hydrochloride monohydrate is 54%, and is not reduced by food. Valaciclovir hydrochloride monohydrate pharmacokinetics is not doseproportional. The rate and extent of absorption decreases with increasing dose, resulting in a less than proportional increase in C_max over the therapeutic dose range and a reduced bioavailability at doses above 500 mg. Aciclovir pharmacokinetic (PK) parameter estimates following single doses of 250 to 2000 mg valaciclovir hydrochloride monohydrate to healthy subjects with normal renal function are shown below.

AUC         h.micrograms/mL 5.50 ± 0.82        11.1 ± 1.75      18.9 ± 4.51               29.5 ± 6.

C_max = peak concentration; T = time to peak concentration; AUC = area under the concentrationtime curve. Values for C and AUC denote mean ± standard deviation. Values for T denote median and range.

Peak plasma concentrations of unchanged valaciclovir hydrochloride monohydrate are only about 4% of peak aciclovir levels, occur at a median time of 30 to 100 min post-dose, and are at or below the limit of quantification 3 h after dosing. The valaciclovir hydrochloride monohydrate and aciclovir pharmacokinetic profiles are similar after single and repeat dosing. Herpes zoster, herpes simplex and HIV infection do not significantly alter the pharmacokinetics of valaciclovir hydrochloride monohydrate and aciclovir after oral administration of valaciclovir hydrochloride monohydrate compared with healthy adults. In transplant recipients receiving valaciclovir hydrochloride monohydrate 2000 mg 4 times daily, aciclovir peak concentrations are similar to or greater than those in healthy volunteers receiving the same dose. The estimated daily AUCs are appreciably greater.

Distribution

Binding of valaciclovir hydrochloride monohydrate to plasma proteins is very low (15%). CSF penetration, determined by CSF/plasma AUC ratio, is independent of renal function and was about 25% for aciclovir and the metabolite 8-OH-ACV, and about 2.5% for the metabolite

CMMG.

Biotransformation

After oral administration, valaciclovir hydrochloride monohydrate is converted to aciclovir and L-valine by first-pass intestinal and/or hepatic metabolism. Aciclovir is converted to a small extent to the metabolites 9(carboxymethoxy) methylguanine (CMMG) by alcohol and aldehyde dehydrogenase and to 8-hydroxy-aciclovir (8-OH-ACV) by aldehyde oxidase. Approximately 88% of the total combined plasma exposure is attributable to aciclovir, 11% to CMMG and 1% to 8-OH-ACV. Neither valaciclovir hydrochloride monohydrate nor aciclovir is metabolized by cytochrome P450 enzymes.

Elimination

Valaciclovir hydrochloride monohydrate is eliminated in the urine principally as aciclovir (greater than 80% of the recovered dose) and the aciclovir metabolite CMMG (about 14% of the recovered dose). The metabolite 8-OH-ACV is detected only in small amounts in urine (< 2% of the recovered dose). Less than 1% of the administered dose of valaciclovir hydrochloride monohydrate is recovered in the urine as unchanged drug. In patients with normal renal function the plasma elimination half-life of aciclovir after both single and multiple dosing with valaciclovir hydrochloride monohydrate is approximately 3 h.

Special Populations

Renal impairment

The elimination of aciclovir is correlated to renal function, and exposure to aciclovir will increase with increased renal impairment. In patients with end-stage renal disease, the average elimination half-life of aciclovir after valaciclovir hydrochloride monohydrate administration is approximately 14 hours, compared with about 3 hours for normal renal function (see section 4.2).

Exposure to aciclovir and its metabolites CMMG and 8-OH-ACV in plasma and cerebrospinal fluid (CSF) was evaluated at steady-state after multiple-dose valaciclovir hydrochloride monohydrate administration in 6 subjects with normal renal function (mean creatinine clearance 111 mL/min, range 91-144 mL/min) receiving 2000 mg every 6 hours and 3 subjects with severe renal impairment (mean CLcr 26 mL/min, range 17-31 mL/min) receiving 1500 mg every 12 hours. In plasma as well as CSF, concentrations of aciclovir, CMMG and 8-OH-ACV were on average 2, 4 and 5-6 times higher, respectively, at severe renal impairment compared with normal renal function.

Hepatic impairment

Pharmacokinetic data indicate that hepatic impairment decreases the rate of conversion of valaciclovir hydrochloride monohydrate to aciclovir but not the extent of conversion. Aciclovir half-life is not affected.

Pregnant women

A study of the pharmacokinetics of valaciclovir hydrochloride monohydrate and aciclovir during late pregnancy indicates that pregnancy does not affect the pharmacokinetics of valaciclovir hydrochloride monohydrate.

Transfer into breast milk

Following oral administration of a 500 mg dose of valaciclovir hydrochloride monohydrate, peak aciclovir concentrations (Cmax) in breast milk ranged from 0.5 to 2.3 times the corresponding maternal aciclovir serum concentrations. The median aciclovir concentration in breast milk was 2.24 micrograms/ml (9.95 micromoles/L). With a maternal valaciclovir hydrochloride monohydrate dosage of 500 mg twice daily, this level would expose a nursing infant to a daily oral aciclovir dosage of about 0.61 mg/kg/day. The elimination half-life of aciclovir from breast milk was similar to that for serum. Unchanged valaciclovir hydrochloride monohydrate was not detected in maternal serum, breast milk, or infant urine.

Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, and carcinogenic potential.

Valaciclovir hydrochloride monohydrate did not affect fertility in male or female rats dosed by the oral route.

Valaciclovir hydrochloride monohydrate was not teratogenic in rats or rabbits. Valaciclovir hydrochloride monohydrate is almost completely metabolised to aciclovir. Subcutaneous administration of aciclovir in internationally accepted tests did not produce teratogenic effects in rats or rabbits. In additional studies in rats, foetal abnormalities and maternal toxicity were observed at subcutaneous doses that produced plasma aciclovir levels of 100 micrograms/mL (>10-fold higher than 2000 mg single dose valaciclovir hydrochloride monohydrate in humans with normal renal function).

Valaciclovir Tablets 500mg:

The other ingredients are: Cellulose Microcrystalline, Crospovidone, Povidone, Purified water,    Magnesium Sterate.

Coating composition: Hypromellose, Titanium dioxide, Polyethylene glycol/Macrogol, Polysorbate 80.

NA

Store below 30ºC.

  Valaciclovir Tablets are supplied in Blister pack.

  Valaciclovir Tablets 500 mg- 5 x 10’s Alu-PVC Blister Pack

NA