Voriconazole, a broad-spectrum, triazole antifungal agent, is available as film-coated tablets for oral administration, a powder for oral suspension and as a lyophilised powder for solution for intravenous infusion. The structural formula is:

CAS number 137234-62-9 Voriconazole is designated chemically as (2R, 3S)-2-(2,4-difluorophenyl)-3-(5-fluoro-4- pyrimidinyl)-1-(1H -1,2,4-triazol-1-yl)-2-butanol with an empirical formula of C16H14F3N5O and a molecular weight of 349.3. Voriconazole drug substance is a white to off white powder. Its aqueous solubility is very low at 0.7 mg/mL at 25oC.

VFEND Tablets contain 50 mg or 200 mg of voriconazole and the following inactive ingredients: lactose, pregelatinised starch maize, croscarmellose sodium, povidone, magnesium stearate and a coating containing hypromellose, titanium dioxide, lactose and glycerol triacetate.

VFEND IV is a white lyophilised powder containing nominally 200 mg voriconazole in a 30 mL Type I clear glass vial. VFEND IV is intended for administration by intravenous infusion. It is a single dose, unpreserved product. The lyophilised powder contents of the VFEND 200 mg vials are intended for reconstitution with 19 mL Water for Injections to produce a solution containing 10 mg/mL voriconazole and 160 mg/mL of sulfobutyl betadex sodium (SBECD). The resulting solution is further diluted prior to administration as an intravenous infusion (see Dosage and Administration).

VFEND Powder for Oral Suspension is a white to off-white powder for oral suspension providing a white to off-white, orange flavoured suspension when reconstituted. Each bottle contains 45 g of powder for oral suspension. Following reconstitution, the volume of suspension is 75 mL, providing a usable volume of 70 mL of suspension at a voriconazole concentration of 40 mg/mL. The suspension contains the following inactive ingredients: sucrose, silica colloidal anhydrous, titanium dioxide, xanthan gum, sodium citrate, sodium benzoate, citric acid anhydrous, natural orange flavour.

Pharmacology

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Voriconazole is a triazole antifungal agent. Voriconazole's primary mode of action is the inhibition of fungal cytochrome P-450-mediated 14a-lanosterol demethylation, an essential step in ergosterol biosynthesis. Voriconazole is more selective than some other azole drugs for fungal as opposed to various mammalian cytochrome P-450 enzyme systems. The subsequent loss of normal sterols correlates with the accumulation of 14a-methyl sterols in fungi and may be responsible for its fungistatic/fungicidal activity.

In vitro, voriconazole displays broad-spectrum antifungal activity with high antifungal potency against Candida species (including fluconazole resistant C. krusei and resistant strains of C. glabrata and C. albicans) and fungicidal activity against all Aspergillus species tested. In addition, voriconazole shows in vitro activity against emerging fungal pathogens, such as Scedosporium or Fusarium, some isolates of which have limited susceptibility to existing antifungal agents. In addition, voriconazole exhibits in vitro fungicidal activity against some strains within these species. In animal studies there is a correlation between minimum inhibitory concentration values and efficacy against experimental mycoses. Furthermore, there appears to be a correlation between minimum inhibitory concentration values and clinical outcome for Candida species.

Clinical efficacy (with partial or complete response, see Clinical Experience) has been demonstrated for Aspergillus spp. including A. flavus, A. fumigatus, A. terreus, A. niger, A.

nidulans, Candida spp., including C. albicans, C. dubliniensis, C. glabrata, C. inconspicua,

C. krusei, C. parapsilosis, C. tropicalis and C. guilliermondii, Scedosporium spp., including

S. apiospermum, S. prolificans and Fusarium spp. Other treated fungal infections (with often partial or complete response) included isolated cases of Alternaria spp., Blastomyces dermatitidis, Blastoschizomyces capitatus, Cladosporium spp., Coccidioides immitis, Conidiobolus coronatus, Cryptococcus neoformans, Exserohilum rostratum, Exophiala spinifera, Fonsecaea pedrosoi, Madurella mycetomatis, Paecilomyces lilacinus, Penicillium spp including P. marneffei, Phialophora richardsiae, Scopulariopsis brevicaulis and Trichosporon spp including T. beigelii infections.

In vitro activity against clinical isolates has been observed for Acremonium spp., Alternaria spp., Bipolaris spp., Cladophialophora spp, Histoplasma capsulatum, with most strains being inhibited by concentrations of voriconazole in the range 0.05 to 2 ug/mL.

In vitro activity against the following pathogens has been shown, but the clinical significance is unknown:Curvularia spp. and Sporothrix spp. Specimens for fungal culture and other relevant laboratory studies (serology, histopathology) should be obtained to isolate and identify causative organisms prior to therapy. Therapy may be instituted before the results of the cultures and other laboratory studies are known; however, once these results become available, anti-infective therapy should be adjusted accordingly. Clinical isolates with decreased susceptibility to voriconazole have been identified. However, elevated Minimum Inhibitory Concentrations (MIC) did not always correlate with clinical failure and clinical success has been observed in patients infected with organisms resistant to other azoles. Correlation of in vitro activity with clinical outcome is difficult owing to the complexity of the patients studied in clinical trials; breakpoints for voriconazole remain to be established.

Pharmacokinetics

The pharmacokinetics of voriconazole have been characterised in healthy subjects, special populations and patients. During oral administration of 200 mg or 300 mg twice daily for 14 days in patients at risk of aspergillosis (mainly patients with malignant neoplasms of lymphatic or haematopoietic tissue), the observed pharmacokinetic characteristics of rapid and consistent absorption, accumulation and non-linear pharmacokinetics were in agreement with those observed in healthy subjects. The pharmacokinetics of voriconazole are non-linear due to saturation of its metabolism. Greater than proportional increase in exposure is observed with increasing dose. It is estimated that, on average, increasing the oral dose from 200 mg twice daily to 300 mg twice daily leads to a 2.5-fold increase in exposure (AUC) (area under the plasma concentration time curve over the 12-hour dosing interval) while increasing the intravenous dose from 3 mg/kg bd to 4 mg/kg bd produces a 2.3-fold increase in exposure. When the recommended intravenous or oral loading dose regimens are administered, plasma concentrations close to steady state are achieved within the first 24 hours of dosing. Without the loading dose,

accumulation occurs during twice daily multiple dosing with steady-state plasma voriconazole concentrations being achieved by day 6 in the majority of subjects.

Voriconazole is rapidly and almost completely absorbed following oral administration, with maximum plasma concentrations (Cmax) achieved 1 to 2 hours after dosing. The oral bioavailability of voriconazole is estimated to be 96%. Bioequivalence has been established between the 200 mg tablet and the 40 mg/mL oral suspension when administered as a 200 mg dose. When multiple doses of voriconazole are administered with high fat meals, Cmax and AUC of the tablets are reduced by 34% and 24%, respectively, and Cmax and AUC of the suspension are reduced by 58 % and 37 %, respectively. The absorption of voriconazole is not affected by changes in gastric pH.

The volume of distribution at steady state for voriconazole is estimated to be 4.6 L/kg, suggesting extensive distribution into tissues. Plasma protein binding is estimated to be 58%. Cerebrospinal fluid samples from eight patients in a compassionate programme showed detectable voriconazole concentrations in all patients.

studies showed that voriconazole is metabolised by the hepatic cytochrome P450 isoenzymes, CYP2C19, CYP2C9 and CYP3A4.

The inter-individual variability of voriconazole pharmacokinetics is high. In vivo studies indicated that CYP2C19 is significantly involved in the metabolism of voriconazole. This enzyme exhibits genetic polymorphism. For example, 15-20% of Asian populations may be expected to be poor metabolisers. For Caucasians and Blacks the prevalence of poor metabolisers is 3-5%. Studies conducted in Caucasian and Japanese healthy subjects have shown that poor metabolisers have, on average, 4-fold higher voriconazole exposure (AUC) than their homozygous extensive metaboliser counterparts. Subjects who are heterozygous extensive metabolisers have on average 2-fold higher voriconazole exposure than their homozygous extensive metaboliser counterparts. The major metabolite of voriconazole is the N-oxide, which accounts for 72% of the circulating radiolabelled metabolites in plasma. This metabolite has minimal antifungal activity and does not contribute to the overall efficacy of voriconazole.

Voriconazole is eliminated via hepatic metabolism with less than 2% of the dose excreted unchanged in the urine.

After administration of a radiolabelled dose of voriconazole, approximately 80% of the radioactivity is recovered in the urine after multiple intravenous dosing and 83% in the urine after multiple oral dosing. The majority (>94%) of the total radioactivity is excreted in the first 96 hours after both oral and intravenous dosing. The terminal half-life of voriconazole depends on dose and is approximately 6 hours at 3 mg/kg (intravenously) or 200 mg (orally). Because of non-linear pharmacokinetics, the terminal half-life is not useful in the prediction of the accumulation or elimination of voriconazole.

In 10 therapeutic studies, the median for the average and maximum plasma concentrations in individual subjects across the studies was 2425 ng/mL (inter-quartile range 1193 to 4380 ng/mL) and 3742 ng/mL (inter-quartile range 2027 to 6302 ng/mL), respectively. A positive association between mean, maximum or minimum plasma voriconazole concentration and efficacy in therapeutic studies was not found. PK/PD analyses of clinical trial data identified positive associations between plasma voriconazole concentrations and both LFT abnormalities and visual disturbances.

In an oral multiple dose study, Cmax and AUC for healthy young females were 83% and 113% higher, respectively, than in healthy young males (18-45 years). In the same study, no significant differences in Cmax and AUC were observed between healthy elderly males and healthy elderly females ( 65 years). In the clinical program, no dosage adjustment was made on the basis of gender. The safety profile and plasma concentrations observed in male and female patients were similar. Therefore, no dosage adjustment based on gender is necessary.

In an oral multiple dose study Cmax and AUC in healthy elderly males ( 65 years) were 61% and 86% higher, respectively, than in healthy young males (18-45 years). No significant differences in Cmax and AUC were observed between healthy elderly females ( 65 years) and healthy young females (18-45 years). In the therapeutic studies no dosage adjustment was made on the basis of age. A relationship between plasma concentrations and age was observed. The safety profile of voriconazole in young and elderly patients was similar and, therefore, no dosage adjustment is necessary for the elderly.

The recommended intravenous dose in paediatric patients is based on a population pharmacokinetic analysis of data pooled from 82 immunocompromised paediatric patients aged 2 to <12 years old who were evaluated in three pharmacokinetic studies (examining

single intravenous doses of 3 and 4 mg/kg twice daily, multiple intravenous doses of 3, 4, 6 and 8 mg/kg twice daily and multiple oral suspension doses of 4 and 6 mg/kg twice daily). The majority of patients received more than one dose level with a maximum duration of dosing of 30 days. A comparison of the paediatric and adult population pharmacokinetic data indicated that in order to obtain comparable exposures to those obtained in adults following intravenous maintenance doses of 4 mg/kg twice daily, intravenous maintenance doses of 7 mg/kg twice daily are required in paediatric patients. The higher intravenous maintenance dose in paediatric patients relative to adults reflects the higher elimination capacity in paediatric patients due to a greater liver mass to body mass ratio. In order to obtain comparable exposures to those obtained in adults following intravenous maintenance doses of 3 mg/kg twice daily, intravenous maintenance doses of 4 mg/kg twice daily are required in paediatric patients. Based on the population pharmacokinetic analysis, no loading dose or dosage adjustment according to age is warranted in patients aged 2 to <12 years old. The recommended oral dose in paediatrics is based on a population pharmacokinetic analysis data obtained from 47 immunocompromised paediatric patients aged 2 to <12 years old who were evaluated in a pharmacokinetic study examining multiple oral suspension doses of 4 to 6 mg/kg twice daily. A comparison of the paediatric and adult population pharmacokinetic data indicated that in order to obtain comparable exposures to those obtained in adults following a maintenance dose of 200 mg twice daily, the same dose of 200 mg of oral solution twice daily is required in paediatric patients, independent of body weight. In paediatric patients there is a general trend towards low bioavailability at lower body weights and high bioavailability at higher body weights (towards the extent demonstrated in adults). Based on the population pharmacokinetic analysis, no dosage adjustment according to age or weight is warranted in patients aged 2 to <12 years old at the 200 mg twice daily oral solution dosing regimen. A loading dose is not indicated in paediatric patients. Oral bioavailability may however be limited in paediatric patients with malabsorption and very low body weight for their age. In that case, intravenous voriconazole administration is recommended.

In a single oral dose (200 mg) study in subjects with normal renal function and mild (creatinine clearance 41-60 mL/min) to severe (creatinine clearance <20 mL/min) renal impairment, the pharmacokinetics of voriconazole were not significantly affected by renal impairment. The plasma protein binding of voriconazole was similar in subjects with different degrees of renal impairment. In patients with moderate to severe renal dysfunction (creatinine clearance < 50 mL/min), accumulation of the intravenous vehicle, SBECD, occurs. Oral voriconazole should be administered to patients with moderate to severe renal dysfunction including dialysis patients, unless an assessment of the benefit risk to the patient justifies the use of intravenous voriconazole. Serum creatinine levels should be closely monitored in these patients, and if increases occur, consideration should be given to changing to oral voriconazole therapy (see Dosage and Administration). A pharmacokinetic study in subjects with renal failure undergoing haemodialysis showed that voriconazole is dialysed with clearance of 121 mL/min. The intravenous vehicle, SBECD, is haemodialysed with clearance of 55 mL/min. A 4-hour haemodialysis session does not remove a sufficient amount of voriconazole to warrant dose adjustment.

Mean SBECD and voriconazole plasma concentrations were measured at the end of infusion on study days 3, 4 and 5 for both dialysis and normal subjects. The pharmacokinetic data indicated that exposure to SBECD was higher in dialysis subjects. There was no evidence of SBECD accumulation in normal subjects. Exposure to voriconazole was lower in the dialysis subjects. Combining the day 3, 4 and 5 data, the ratio of the post-infusion means (dialysis/normal subjects) was 455% (95% CI: 340%, 609%) for SBECD and 50% (95% CI: 32%, 80%) for voriconazole.

After a single oral dose (200 mg), AUC was 233% higher in subjects with mild to moderate hepatic cirrhosis (Child-Pugh A and B) compared with subjects with normal hepatic function. Protein binding of voriconazole was not affected by impaired hepatic function. In a multiple oral dose study, AUC was similar in subjects with moderate hepatic cirrhosis (Child-Pugh B) given maintenance doses of 100 mg twice daily and subjects with normal hepatic function given 200 mg twice daily. No pharmacokinetic data are available for patients with severe hepatic cirrhosis (Child-Pugh C) (see Dosage and Administration).

Clinical Trials

In clinical trials, 561 patients received voriconazole therapy for greater than 12 weeks, with 136 subjects receiving voriconazole for over 6 months.

The efficacy and survival benefit of voriconazole compared to conventional amphotericin B in the primary treatment of acute invasive aspergillosis was demonstrated in an open, randomised, multicentre study. The total duration of treatment was 12 weeks. Patients could be switched to Other Licensed Antifungal Therapy (OLAT) during the 12 week study period, either due to lack of efficacy of the initial randomised treatment (IRT) or for safety/tolerability reasons. Efficacy was assessed at 12 weeks (primary endpoint) and at the end of initial randomised therapy (IRT) by a Data Review Committee. Voriconazole was administered intravenously with a loading dose of 6 mg/kg every 12 hours for the first 24 hours followed by a maintenance dose of 4 mg/kg every 12 hours for a minimum of seven days, after which the oral formulation at a dose of 200 mg bd could be used. Patients in the comparator group received conventional amphotericin B as a slow infusion at a daily dose of 1.0-1.5 mg/kg/day.

In this study, 277 immunocompromised patients with invasive aspergillosis (modified intent to treat population) were evaluated. At week 12, a satisfactory global response (complete or partial resolution of all attributable symptoms, signs, radiographic/bronchoscopic abnormalities present at baseline) was seen in 53% of patients in the voriconazole group compared to 31% of patients in the comparator group. At the end of IRT, a satisfactory global response was seen in 53.5% of voriconazole treated patients compared to 21.8% of conventional amphotericin B treated patients. Subjects in the voriconazole group were treated longer than subjects in the amphotericin B group before switching to OLAT (median duration of IRT was 73 vs 12 days respectively). OLAT included liposomal amphotericin B formulations, itraconazole and flucytosine. Survival in the voriconazole group (71%) was greater than in the comparator group (58%) at week 12.

a MITT (modified intent to treat) population assessed by independent Data Review Committee b MITT population proportion of subjects alive

c Safety population discontinuations from initial randomised treatment due to adverse events/laboratory abnormalities (all causality)

Efficacy of Voriconazole in the Primary Treatment of Acute Invasive Aspergillosis
	Satisfactory Global Response	Survival at Week 12 b	Discontinuations due to AEs c
	Study 307/602 a	Study 307/602	Study 307/602
Voriconazole	76/144 (53%) e	102/144 (71%)	40/196 (20%)
Comparator	42/133 (31%) d, e	77/133 (58%)	103/185 (56%)
	P <0.0001	P=0.02	--

The results of this comparative trial confirmed the results of an earlier trial in the primary treatment of patients with acute invasive aspergillosis (Study 304). In this study, an overall success rate of 54% was seen in patients treated with voriconazole. Voriconazole successfully treated cerebral, sinus, pulmonary and disseminated aspergillosis in patients with bone marrow and solid organ transplants, haematological malignancies, cancer and AIDS.

The efficacy of voriconazole compared to the regimen of (conventional) amphotericin B followed by fluconazole in the primary treatment of candidaemia was demonstrated in an open comparative study (number 150-608). Three hundred and seventy (370) non-neutropenic patients with documented candidaemia (positive blood culture and clinical signs of infection) were included in the study, of which 248 were treated with voriconazole. The patient population was seriously ill, with approximately 50% of subjects in the intensive care unit and 40% mechanically ventilated at baseline. The median treatment duration was 15 days in both treatment arms. A successful response (resolution/improvement in all clinical signs and symptoms of infection, blood cultures negative for Candida, infected deep tissue sites negative for Candida) was seen in 41% of patients in both treatment arms 12 weeks after the End of Therapy (EOT). In this analysis, patients who did not have an assessment 12 weeks after EOT were set to failure. According to a secondary analysis, which compared response

rates at the latest time point most relevant to the evaluation of the patient (EOT, or 2, 6, or 12 weeks after EOT, which is more appropriate for this type of study), voriconazole and the regimen of amphotericin B followed by fluconazole had response rates of 65% and 71%, respectively. Forty-seven percent of isolated pathogens in the voriconazole treatment group were from non-albicans species, including C.glabrata and C.krusei, although C.albicans was the most commonly isolated species in the small subgroup of patients (n = 14) with confirmed deep tissue infections. When considering response at 12 weeks after EOT by pathogen, the success rates were comparable between voriconazole (43%) and amphotericin B followed by fluconazole (46%) for baseline Candida albicans infections. Success rates were more favourable with voriconazole (38.6%) than with amphotericin followed by fluconazole (32.3%) for baseline non-albicans infections.

Study 309/604 (the combined results of 2 open-label, non-comparative trials) assessed voriconazole in the treatment of fungal infections in patients refractory to, or intolerant of, other antifungal medications. Of the 301 patients assessed for efficacy, 87 patients had serious candidiasis: 38 had oesophageal candidiasis and 47 had invasive candidiasis, of which 26 patients had deep tissue Candida infections. The median duration of IV therapy was 11 days (range 1-138 days) and of oral therapy was 81 days (range 1-326 days). Overall 25/47 (53.2%) invasive candidiasis subjects had a successful response, with 16/47 (34.0%) having a complete response and 9/47 (19.1%) having a partial response; 6/47 (12.8%) were assessed as stable. Of the subjects with deep tissue Candida infection, 14/26 (53.8%) had a successful response, with 8/26 (30.8%) having a complete response, 6/26 (23.1%) having a partial response and 5/26 (19.2%) assessed as stable.

Study 150-305 was a randomised, double-blind, comparative study versus oral fluconazole in immunocompromised patients with endoscopically-proven oesophageal candidiasis. 200 patients were randomised to receive voriconazole (200 mg twice daily) and 191 to receive fluconazole (400 mg once daily on day 1 followed by 200 mg once daily from day 2 onwards). Over half of the patients in each group had advanced AIDS with CD4 cell counts < 50 cells/L. Outcome was assessed by repeat endoscopy at day 43 or the end of therapy. Voriconazole and fluconazole showed equivalent efficacy against oesophageal candidiasis in the per protocol and intention to treat analysis.

The efficacy, safety and tolerability of voriconazole in the treatment of systemic and invasive fungal infections in patients failing, or intolerant to other therapy, or for invasive fungal infections due to pathogens for which there is no licensed therapy was assessed in two, open,

non-comparative studies (Studies 309/604). A total of 301 patients were evaluated for efficacy, of whom 72 cases had invasive infections due to fungal pathogens other than Aspergillus spp. or Candida spp. Patients received an initial intravenous loading dose of 6 mg/kg q12h or an oral loading dose of 400 mg for the first 24 hours, followed by maintenance dosing with 4 mg/kg q12h or 200 mg bd, respectively, for up to 12 weeks. The primary endpoint was satisfactory global response at End of Therapy, defined as 'complete' or 'partial' global response. Overall 39/72 (54.2%) subjects with other (non-Aspergillus, non-Candida) serious fungal infections had a satisfactory global outcome at end of voriconazole therapy. In pooled analyses of patients enrolled across the development program, including those from the combined 309/604 studies, voriconazole was shown to be effective against the following additional fungal pathogens:

Scedosporium spp.- Successful response to voriconazole therapy was seen in 16 of 28 patients with S. apiospermum and in 2 of 7 patients with S. prolificans infection. In addition, a successful response was seen in 1 of 3 patients with mixed organism infections.

spp.- Seven of 17 patients were successfully treated with voriconazole. Of these seven patients, 3 had eye, 1 had sinus, and 3 had disseminated infection. Four additional patients with fusariosis had an infection caused by several organisms; two of them had a successful outcome.

The majority of patients receiving voriconazole treatment for rare fungal infections were intolerant of, or refractory to, prior antifungal therapy. Other successfully treated fungal infections included isolated cases of: Alternaria spp., Blastomyces dermatitidis, Blastoschizomyces capitatus, Cladosporium spp., Coccidioides immitis, Conidiobolus coronatus, Cryptococcus neoformans, Exserohilum rostratum, Exophiala spinifera, Fonsecaea pedrosoi, Madurella mycetomatis, Paecilomyces lilacinus, Penicillium spp including P. marneffei, Phialophora richardsiae, Scopulariopsis brevicaulis, and Trichosporon spp. including T. beigelii infections.

Sixty four (64) paediatric patients aged 9 months up to 15 years who had definite or probable invasive fungal infections, were treated with voriconazole. This population included 34 patients 2 to < 12 years old and 23 patients 12 - 15 years of age. The majority (59/64) had failed previous antifungal therapies. Therapeutic trials included eight patients aged 12-15 years, the remaining patients received voriconazole in the compassionate use programs. Underlying diseases in these patients included haematologic malignancies and aplastic anaemia (27 patients) and chronic granulomatous disease (14 patients). The most commonly treated fungal infection was aspergillosis (46/64; 71%). In addition, a successful response was seen in one patient with infection caused by Aspergillus fumigatus and Phialophora richardsiae. Other fungal infections were caused by Scedosporium, Candida, Fusarium, Conidiobolus, Alternaria and Trichosporon spp.

Clinical Outcome in Paediatric Patients by Age and Fungal Infection
Age (years)	Infection	Success/Treated
2 - <12 years	Aspergillosis	11/23
	Other	4/11
	Total	15/34
12-15 years	Aspergillosis	5/17
	Other	4/6
	Total	9/23

A placebo-controlled, randomised, single-dose, crossover study to evaluate the effect on the QT interval of healthy volunteers was conducted with three oral doses of voriconazole and ketoconazole. The placebo-adjusted mean maximum increases in QTc from baseline after 800, 1200 and 1600 mg of voriconazole were 5.1, 4.8, and 8.2 msec respectively and msec for ketoconazole 800 mg. No subject in any group had an increase in QTc of >=60 msec from baseline. No subject experienced an interval exceeding the potentially clinically relevant threshold of 500 msec. Subjects who were CYP2C19 genotype poor metabolisers were excluded from this study however the dose of 1600 mg voriconazole achieved plasma concentrations of approximately 5,400 to 16,900 ng/mL which covered the exposure seen in 95% of patients in Phase 2/3 trials where poor metabolisers were not excluded.

Contraindications

VFEND is contraindicated in patients with known hypersensitivity to voriconazole or to any of the excipients. Co-administration of the CYP3A4 substrates, pimozide or quinidine with voriconazole is contraindicated since increased plasma concentrations of these medicinal products can lead to QTc prolongation and rare occurrences of torsade de pointes (see Interactions).

Co-administration of voriconazole with rifabutin, rifampicin, carbamazepine and long-acting barbiturates (e.g. phenobarbitone) is contraindicated since these medicinal products are likely to decrease plasma voriconazole concentrations significantly (see Interactions). Co-administration with efavirenz at a dose of 400 mg once daily or above is contraindicated because efavirenz significantly decreases plasma voriconazole concentrations in healthy subjects at this dose (see Precautions; for lower doses of efavirenz see Interactions and Dosage and Administration). Co-administration of ergot alkaloids (ergotamine, dihydroergotamine), which are CYP3A4 substrates, is contraindicated since increased plasma concentrations of these medicinal products can lead to ergotism (see Interactions). Co-administration of voriconazole and sirolimus is contraindicated, since voriconazole is likely to increase plasma concentrations of sirolimus significantly (see Interactions). Co-administration of voriconazole and high-dose ritonavir (400 mg and above twice daily) is contraindicated because ritonavir significantly decreases plasma voriconazole concentrations in healthy subjects at this dose (see Interactions and, for lower doses, also see Precautions). Co-administration of voriconazole with St John's Wort is contraindicated (see Interactions).

Precautions

Caution should be used in prescribing voriconazole to patients with hypersensitivity to other azoles.

Cardiovascular: Some azoles, including voriconazole have been associated with QT interval prolongation. There have been rare cases of torsade de pointes in patients taking voriconazole who had risk factors, such as history of cardiotoxic chemotherapy, cardiomyopathy, hypokalemia and concomitant medications that may have been contributory. Voriconazole should be administered with caution to patients with these potentially proarrhythmic conditions. Electrolyte disturbances such as hypokalaemia, hypomagnesaemia and hypocalcaemia should be corrected prior to initiation of voriconazole therapy (see Dosage and Administration).

Anaphylactoid-type reactions, including flushing, fever, sweating, tachycardia, chest tightness, dyspnoea, faintness, nausea, pruritis and rash have been observed during administration of the intravenous formulation of voriconazole. Depending on the severity of symptoms, consideration should be given to stopping treatment.

In clinical trials, there have been uncommon cases of serious hepatic reactions during treatment with voriconazole (including clinical hepatitis, cholestasis and fulminant hepatic failure including fatalities). Instances of hepatic reactions were noted to occur primarily in patients with serious underlying medical conditions (predominantly haematological malignancy). Transient hepatic reactions, including hepatitis and jaundice, have occurred among patients with no other identifiable risk factors. Liver dysfunction has usually been reversible on discontinuation of therapy.

It is recommended that patients on voriconazole therapy should have their hepatic function routinely monitored. Patient management should include laboratory evaluation of hepatic function (particularly liver function tests and bilirubin). Discontinuation of voriconazole should be considered if clinical signs and symptoms consistent with liver disease develop (see Dosage and Administration).

The pharmacokinetic parameters of orally administered voriconazole are not affected by renal impairment. However, acute renal failure has been observed in severely ill patients undergoing treatment with voriconazole. Patients being treated with voriconazole are likely to be treated concomitantly with nephrotoxic medications and have concurrent conditions that may result in decreased renal function.

In patients with moderate to severe renal dysfunction (creatinine clearance <50 mL/min), including dialysis patients, accumulation of the intravenous vehicle SBECD occurs. Oral voriconazole should be administered to these patients, unless an assessment of the risk to the patient justifies the use of intravenous voriconazole. Patients should be monitored for the development of abnormal renal function. This should include laboratory evaluation, particularly serum creatinine .

Adults and children with risk factors for acute pancreatitis (e.g. recent chemotherapy, haematopoietic stem cell transplantation (HSCT)) should be monitored closely during VFEND treatment. Monitoring of serum amylase or lipase may be considered in this clinical situation.

Patients have rarely developed exfoliative cutaneous reactions, such as Stevens-Johnson syndrome, during treatment with voriconazole. If a patient develops an exfoliative cutaneous reaction voriconazole should be discontinued.

In addition, voriconazole has been associated with photosensitivity skin reaction. It is recommended that patients avoid intense or prolonged exposure to direct sunlight during voriconazole treatment. In patients with photosensitivity skin reactions and additional risk factors, squamous cell carcinoma of the skin and melanoma have been reported during long- term therapy. If a patient develops a skin lesion consistent with squamous cell carcinoma or melanoma, voriconazole discontinuation should be considered.

Periostitis has been reported in transplant patients during long- term voriconazole therapy. If a patient develops skeletal pain and radiologic findings compatible with periostitis, voriconazole should be discontinued.

Visual Adverse Events: There have been post-marketing reports of prolonged visual adverse events, including optic neuritis and papilloedema. These events occurred primarily in severely ill patients who had underlying conditions and/or concomitant medications which may have caused or contributed to these events (see Adverse Effects, Visual Disturbances).

Voriconazole may cause changes to vision, including blurring, altered/enhanced visual perception and/or photophobia. Patients must avoid potentially hazardous tasks, such as driving or operating machinery whilst experiencing these symptoms. Patients should be advised not to drive at night while taking voriconazole.

Paediatric Use: Safety and efficacy in paediatric subjects below the age of two years has not been established (see Clinical Trials). Hepatic function and pancreatic function should be monitored. Oral bioavailability may be limited in paediatric patients 2 to 12 years with malabsorption and very low body weight for age. In that case, intravenous voriconazole administration is recommended.

Everolimus (CYP3A4 substrate, P-gp substrate): Co-administration of voriconazole with everolimus is not recommended because voriconazole is expected to significantly increase everolimus concentrations. Currently there are insufficient data to allow dosing recommendations in this situation (see Interactions). Fluconazole (CYP2C9, CYP2C19 and CYP3A4 inhibitor): Co-administration of oral voriconazole and oral fluconazole resulted in significant increase in Cmax and AUC of voriconazole in healthy subjects. The reduced dose and/or frequency of voriconazole and f; luconazole that would reduce this effect have not been established. Monitoring for voriconazole associated adverse events is recommended if voriconazole is used sequentially after fluconazole (see Interactions).

Phenytoin (CYP2C9 substrate and potent CYP450 inducer): Careful monitoring of phenytoin levels is recommended when phenytoin is co-administered with voriconazole. Concomitant use of voriconazole and phenytoin should be avoided unless the benefit outweighs the risk (see Interactions).

Ritonavir (potent CYP450 inducer; CYP3A4 inhibitor and substrate): Co-administration of voriconazole and low dose ritonavir (100 mg twice daily) should be avoided unless an assessment of the benefit/risk justifies the use of voriconazole (see Interactions; for higher doses see Contraindications).

Methadone (CYP3A4 substrate): Increased plasma concentrations of methadone have been associated with toxicity including QT prolongation. Frequent monitoring for adverse events and toxicity related to methadone is recommended during co-administration. Dose reduction of methadone may be needed (see Interactions).

Short Acting Opiates (CYP3A4 substrate): Reduction in the dose of alfentanil, fentanyl and other short acting opiates similar in structure to alfentanil and metabolised by CYP3A4 (e.g. sufentanil) should be considered when co-administered with voriconazole (see Interactions). As the half life of alfentanil is prolonged in a 4-fold manner when alfentanil is co- administered with voriconazole and in an independent published study, concomitant use of voriconazole with fentanyl resulted in an increase in the mean AUC 0-[?] of fentanyl by 1.4- fold, frequent monitoring for opiate-associated adverse events (including a longer respiratory monitoring period) may be necessary.

Long Acting Opiates (CYP3A4 substrate): Reduction in the dose of oxycodone and other long-acting opiates metabolised by CYP3A4 (e.g. hydrocodone) should be considered when coadministered with voriconazole. Frequent monitoring for opiate-associated adverse events may be necessary (see Interactions).

VFEND Tablets contain lactose and should not be given to patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.

VFEND Powder for Oral Suspension contains sucrose (0.54 g/mL) and should not be given to patients with rare hereditary problems of fructose intolerance, sucrase-isomaltase deficiency or glucose-galactose malabsorption.

: Each vial of VFEND Powder for Injection contains 217.6 mg of sodium. This should be taken into consideration for patients on a controlled sodium diet.

Carcinogenic potential was studied in mice and rats at oral doses of up to 100 mg/kg/day and 50 mg/kg/day for 24 months, respectively. Hepatocellular adenoma appeared in male and female mice at 100 mg/kg/day and in female rats at 50 mg/kg/day. There was also an increased incidence of hepatocellular carcinoma in mice at 100 mg/kg/day. Although mean plasma drug concentrations indicated there is no safety margin in humans in terms of exposure, adenoma and carcinoma (as well as non-neoplastic changes) are known to occur in rodents after chronic administration of compounds that are hepatic enzyme inducers. Voriconazole showed no mutagenic potential in gene-mutation assays in bacterial (Salmonella typhimurium) and mammalian (Chinese hamster ovary) cells. While in vitro exposure of human lymphocytes to voriconazole produced equivocal effects on chromosomes, in vivo treatment of male and female mice at doses up to, and including the maximum tolerated dose produced no evidence of chromosome damage as determined by the micronucleus assay.

Fertility of male and female rats was not affected at oral doses of up to 50 mg/kg/day, corresponding to exposures 4-6 times the expected human exposure (based on AUC) at the maintenance dose.

There are no adequate studies in pregnant women. Studies in rats have shown reproductive toxicity, including teratogenicity (cleft palates) at oral doses of 10 mg/kg/day and disturbance of parturition (dystocia) at oral doses of 3 mg/kg/day, with exposures similar to or below those expected in humans at maintenance dosing. Voriconazole was not teratogenic in rabbits at oral doses of up to 100 mg/kg/day, but produced an increase in post-implantation loss and a decrease in foetal body weight, with exposures approximately 4 times the expected human exposure. VFEND must not be used during pregnancy except in patients with severe or potentially life-threatening fungal infections in whom VFEND may be used if the benefit to the mother clearly outweighs the potential risk to the foetus.

Women of childbearing potential must always use effective contraception during treatment (see Use in Pregnancy).

It is not known whether voriconazole is excreted in the milk of laboratory animals or in human breast milk. Voriconazole must not be used in nursing mothers unless the benefit clearly outweighs the risk.

Interactions

Unless otherwise specified, drug interaction studies have been performed in healthy male subjects, using multiple dosing to steady state with oral voriconazole at 200 mg twice daily. These results are relevant to other populations and routes of administration. This section addresses the effects of other medicinal products on voriconazole, the effects of voriconazole on other medicinal products and two-way interactions. The interactions for the first two sections are presented in the following order: contraindications, those requiring dosage adjustment, those requiring careful clinical and/or biochemical monitoring and finally those that have no significant pharmacokinetic interaction but may be of clinical interest in this therapeutic field.

Voriconazole is metabolised by cytochrome P450 isoenzymes, CYP2C19, CYP2C9 and CYP3A4. Inhibitors or inducers of these isoenzymes may increase or decrease voriconazole plasma concentrations, respectively.

The exposure to voriconazole is significantly reduced by the concomitant administration of the following agents:

Rifampicin (CYP450 inducer): Rifampicin (600 mg once daily) decreased the Cmax (maximum plasma concentration) and AUC (area under the plasma concentration time curve within a dose interval) of voriconazole by 93% and 96%, respectively. Co-administration of voriconazole and rifampicin is contraindicated (see Contraindications). Rifabutin (potent CYP450 inducer): Rifabutin (300 mg once daily) decreased the Cmax and AUC of voriconazole at 200 mg twice daily by 69% and 78%, respectively. During co- administration with rifabutin, the Cmax and AUC of voriconazole at 350 mg twice daily were 96% and 68% of the levels when administered alone at 200 mg twice daily. At a voriconazole dose of 400 mg twice daily Cmax and AUC were 104% and 87% higher, respectively, compared with voriconazole alone at 200 mg twice daily. Voriconazole at 400 mg twice daily increased Cmax and AUC of rifabutin by 195% and 331%, respectively. Co-administration of voriconazole with rifabutin is contraindicated (see Contraindications). Ritonavir (potent CYP450 inducer; CYP3A4 inhibitor and substrate): The effect of the co- administration of oral voriconazole (200 mg twice daily) and high dose (400 mg) and low dose (100 mg) oral ritonavir was investigated in two separate studies in healthy volunteers. High doses of ritonavir (400 mg twice daily) decreased the steady state Cmax and AUC of oral voriconazole by an average of 66% and 82% respectively, whereas low doses of ritonavir (100 mg twice daily) decreased the Cmax and AUC of oral voriconazole by an average of 24% and 39% respectively. Administration of voriconazole did not have a significant effect

on mean Cmax and AUC of ritonavir in the high dose study, although a minor decrease in steady state Cmax and AUC of ritonavir with an average of 25% and 13% respectively was observed in the low dose ritonavir interaction study. One outlier subject with raised voriconazole levels was identified in each of the ritonavir interaction studies. Co- administration of voriconazole and ritonavir (400 mg and above twice daily) is contraindicated (see Contraindications). Co-administration of voriconazole and low dose ritonavir (100 mg twice daily) should be avoided unless an assessment of the benefit/risk to the patient justifies the use of voriconazole (see Contraindications and Precautions).

Carbamazepine and phenobarbitone (CYP450 inducers): Although not studied, carbamazepine or phenobarbitone are likely to significantly decrease plasma voriconazole levels. Co-administration of voriconazole with carbamazepine and long acting barbiturates are contraindicated (see Contraindications).

Significant drug interactions that may require voriconazole dosage adjustment, or frequent monitoring of voriconazole related adverse events/toxicity:

Fluconazole (CYP2C9, CYP2C19 and CYP3A4 inhibitor): Coadministration of oral voriconazole and oral fluconazole resulted in significant increase in Cmax and AUC of voriconazole in healthy subjects. The clinical significance of this drug interaction has not been established and the coadministration of voriconazole and oral fluconazole is not recommended. Monitoring for voriconazole associated adverse events is recommended if voriconazole is used sequentially after fluconazole.

Minor or no significant pharmacokinetic interactions that require no dosage adjustment:

Cimetidine (non-specific CYP450 inhibitor and increases gastric pH): Cimetidine (400 mg twice daily) increased voriconazole Cmax and AUC by 18% and 23%, respectively. No dosage adjustment of voriconazole is recommended. Ranitidine (increases gastric pH): Ranitidine (150 mg twice daily) had no significant effect on voriconazole Cmax and AUC. Macrolide antibiotics: Erythromycin (CYP3A4 inhibitor; 1g twice daily) and azithromycin (500 mg once daily) had no significant effect on voriconazole Cmax and AUC.

Voriconazole inhibits the activity of cytochrome P450 isoenzymes, CYP2C19, CYP2C9 and CYP3A4. Therefore, there is potential for voriconazole to increase the plasma levels of drugs metabolised by these CYP450 isoenzymes. Voriconazole should be administered with caution in patients receiving concomitant medication that is known to prolong QT interval. When there is also a potential for voriconazole to increase the plasma levels of substances metabolised by CYP3A4 isoenzymes (certain antihistamines, quinidine, pimozide) co-administration is contraindicated (see below and Contraindications).

Pimozide and quinidine (CYP3A4 substrates): Although not studied, co-administration of voriconazole with pimozide or quinidine is contraindicated, since increased plasma concentrations of these drugs can lead to QTc prolongation and rare occurrences of torsade de pointes (see Contraindications). Sirolimus (CYP3A4 substrate): Voriconazole increased sirolimus (2 mg single dose) Cmax and AUC by 556% and 1014%, respectively. Co-administration of voriconazole and sirolimus is contraindicated (see Contraindications).

Ergot alkaloids (CYP3A4 substrates): Although not studied, voriconazole may increase the plasma concentrations of ergot alkaloids (ergotamine and dihydroergotamine) and lead to ergotism. Co-administration of voriconazole with ergot alkaloids is contraindicated (see Contraindications).

St John's Wort (CYP450 inducer; P-gp inducer): In a clinical study in healthy volunteers, St John's Wort exhibited a short initial inhibitory effect followed by induction of voriconazole metabolism. After 15 days of treatment with St John's Wort (300 mg three times daily), plasma exposure following a single 400 mg dose of voriconazole decreased by 40-60%. Therefore, concomitant use of voriconazole with St John's Wort is contraindicated (see Contraindications).

Interaction of voriconazole with the following agents may result in increased exposure to these drugs. Careful monitoring and/or dosage adjustment should be considered:

Cyclosporin (CYP3A4 substrate): In stable, renal transplant recipients, voriconazole increased cyclosporin Cmax and AUC by at least 13% and 70% respectively. When initiating voriconazole in patients already receiving cyclosporin, it is recommended that the cyclosporin dose be halved and cyclosporin level carefully monitored. Increased cyclosporin levels have been associated with nephrotoxicity. When voriconazole is discontinued, cyclosporin levels must be carefully monitored and the dose increased as necessary. Tacrolimus (CYP3A4 substrate): Voriconazole increased tacrolimus (0.1 mg/kg single dose) Cmax and AUC by 117% and 221%, respectively. When initiating voriconazole in patients already receiving tacrolimus, it is recommended that the tacrolimus dose be reduced to a third of the original dose and tacrolimus levels carefully monitored. Increased tacrolimus levels have been associated with nephrotoxicity. When voriconazole is discontinued, tacrolimus levels must be carefully monitored and the dose increased as necessary. Methadone (CYP3A4 substrate): Repeat dose administration of oral voriconazole (400 mg every 12 hours for 1 day, then 200 mg every 12 hours for 4 days) increased the Cmax and AUCt of pharmacologically active R-methadone by 31% (90% CI: 22%, 40%) and 47% (90% CI: 38%, 57%) respectively in subjects receiving a methadone maintenance dose (30-100 mg daily) (see Precautions).

Short Acting Opiates (CYP3A4 substrate): In an independent publication, steady-state administration of oral voriconazole increased the AUC[?] of a single dose of alfentanil by 6- fold. Reduction in the dose of alfentanil and other short acting opiates similar in structure to alfentanil and metabolised by CYP3A4 (e.g. sufentanil) should be considered when co- administered with voriconazole (see Precautions).

Fentanyl (CYP3A4 substrate): In an independent published study, concomitant use of voriconazole (400 mg q12h on Day 1, then 200 mg q12h on Day 2) with a single intravenous dose of fentanyl (5 ug/kg) resulted in an increase in the mean AUC0-[?] of fentanyl by 1.4-fold (range 1.12-1.60-fold). When voriconazole is co-administered with fentanyl, extended and frequent monitoring of patients for respiratory depression and other fentanyl-associated adverse events is recommended, and the fentanyl dose should be reduced if warranted. Oxycodone (CYP3A4 substrate): In an independent publication, co-administration of multiple doses of oral voriconazole (400 mg q12h on Day 1 followed by five doses of 200 mg q12h on Days 2 to 4) with a single 10 mg oral dose of oxycodone on Day 3 resulted in an increase in the mean Cmax and AUC0-[?] of oxycodone by 1.7-fold (range 1.4- to 2.2-fold) and 3.6-fold (range 2.7- to 5.6-fold) respectively. The mean elimination half-life of oxycodone was also increased by 2.0-fold (range 1.4- to 2.5-fold). A reduction in oxycodone dosage may be needed during voriconazole treatment to avoid opioid related adverse effects. Extended and frequent monitoring for adverse affects associated with oxycodone and other long-acting opiates metabolised by CYP3A4 is recommended.

(CYP3A4 substrate, P-gP substrate): Although not studied, voriconazole is likely to significantly increase the plasma concentrations of everolimus. Coadministration of voriconazole and everolimus is not recommended because voriconazole is expected to significantly increase everolimus concentrations.

(CYP2C9 substrate): Co-administration of voriconazole (300 mg twice daily) with warfarin (30 mg single dose) increased maximum prothrombin time by 93%. Close monitoring of prothrombin time is recommended if warfarin and voriconazole are co- administered.

(CYP2C9, CYP3A4 substrates): Although not studied, voriconazole may increase the plasma concentrations of coumarins and therefore may cause an increase in prothrombin time. If patients receiving coumarin preparations are treated simultaneously with voriconazole, the prothrombin time should be monitored at close intervals and the dosage of anticoagulants adjusted accordingly.

(CYP2C9 substrates): Although not studied, voriconazole may increase the plasma levels of sulphonylureas, (e.g. tolbutamide, glipizide, and glyburide) and therefore cause hypoglycaemia. Careful monitoring of blood glucose is recommended during co- administration.

Statins (CYP3A4 substrates): Although not studied clinically, voriconazole has been shown to inhibit lovastatin metabolism in vitro (human liver microsomes). Therefore, voriconazole is likely to increase plasma levels of statins that are metabolised by CYP3A4. It is recommended that dose adjustment of the statin be considered during co-administration. Increased statin levels have been associated with rhabdomyolysis. Benzodiazepines (CYP3A4 substrates): Although not studied clinically, voriconazole has been shown to inhibit midazolam metabolism in vitro (human liver microsomes). Therefore, voriconazole is likely to increase the plasma levels of benzodiazepines that are metabolised by CYP3A4 (e.g. midazolam, triazolam and alprazolam) and lead to a prolonged sedative effect. It is recommended that dose adjustment of the benzodiazepine be considered during co-administration.

(CYP3A4 substrates): Although not studied, voriconazole may increase the plasma levels of the vinca alkaloids (e.g. vincristine and vinblastine) and lead to neurotoxicity. It is therefore recommended that dose adjustment of the vinca alkaloid be considered.

Non-Steroidal Anti-Inflammatory Drugs (NSAIDs): Voriconazole increased Cmax and AUC of ibuprofen (400mg single dose) by 20% and 100% respectively. Voriconazole increased Cmax and AUC of diclofenac (50mg single dose) by 114% and 78% respectively. Frequent monitoring for adverse events and toxicity relating to NSAIDs is recommended. Adjustment of dosage of NSAIDs may be needed.

No significant pharmacokinetic interactions were observed when voriconazole was co- administered with the following agents. No dosage adjustment for these agents is recommended:

Prednisolone (CYP3A4 substrate): Voriconazole increased Cmax and AUC of prednisolone (60 mg single dose) by 11% and 34%, respectively. No dosage adjustment is recommended.

(P-glycoprotein mediated transport): Voriconazole had no significant effect on C

and AUC of digoxin (0.25 mg once daily). Mycophenolic acid (UDP-glucuronyl transferase substrate): Voriconazole had no effect on the Cmax and AUC of mycophenolic acid (1 g single dose).

Phenytoin (CYP2C9 substrates and potent CYP450 inducer): Concomitant use of voriconazole and phenytoin should be avoided unless the benefit outweighs the risk. Phenytoin (300 mg once daily) decreased the Cmax and AUC of voriconazole by 49% and 69%, respectively. Voriconazole (400 mg twice daily) increased Cmax and AUC of phenytoin (300 mg once daily) by 67% and 81%, respectively. Phenytoin may be co-administered with voriconazole if the maintenance dose of voriconazole is increased to 5 mg/kg intravenously twice daily or from 200 mg to 400 mg orally, twice daily (100 mg to 200 mg orally, twice daily in patients less than 40 kg). Careful monitoring of phenytoin plasma levels is recommended when phenytoin is co-administered with voriconazole. Omeprazole (CYP2C19 inhibitor; CYP2C19 and CYP3A4 substrate): Omeprazole (40 mg once daily) increased voriconazole Cmax and AUC by 15% and 41%, respectively. No dosage adjustment of voriconazole is recommended. Voriconazole increased omeprazole Cmax and AUC by 116% and 280%, respectively. When initiating voriconazole in patients already receiving omeprazole, it is recommended that the omeprazole dose be halved. The metabolism of other proton pump inhibitors which are CYP2C19 substrates may also be inhibited by voriconazole.

Fluconazole (CYP2C9, CYP2C19 and CYP3A4 inhibitor): Fluconazole (200 mg once daily) increased the Cmax and AUC of voriconazole by 57% and 79%, respectively. The Cmax and AUC of fluconazole were not determined. The reduced dose and/or frequency of voriconazole and fluconazole that would eliminate this effect have not been established. Monitoring for voriconazole-associated adverse events is recommended if voriconazole is used sequentially after fluconazole. Oral Contraceptives (CYP3A4 substrate): Co-administration of voriconazole and an oral contraceptive (norethisterone 1 mg and ethinylestradiol 0.035 mg once daily) in healthy female subjects resulted in increases in the Cmax and AUC of ethinylestradiol (36% and 61% respectively) and norethisterone (15% and 53% respectively). Voriconazole Cmax and AUC increased by 14% and 46% respectively. Oral contraceptives containing doses other than norethisterone 1 mg and ethinylestradiol 0.035 mg have not been studied. As the ratio between norethisterone and ethinylestradiol remained similar during interaction with voriconazole, their contraceptive activity would probably not be affected. Monitoring for adverse events related to oral contraceptives is recommended during co-administration. Indinavir (CYP3A4 inhibitor and substrate): Indinavir (800 mg three times daily) had no significant effect on voriconazole Cmax and AUC. Voriconazole did not have a significant effect on Cmax, Cmin and AUC of indinavir. Other HIV protease inhibitors (CYP3A4 substrates and inhibitors): In vitro studies suggest that voriconazole may inhibit the metabolism of HIV protease inhibitors (e.g. saquinavir, amprenavir and nelfinavir). In vitro studies also show that the metabolism of voriconazole may be inhibited by HIV protease inhibitors. Patients should be carefully monitored for drug toxicity during the co-administration of voriconazole and HIV protease inhibitors. Efavirenz (a non-nucleoside reverse transcriptase inhibitor [CYP450 inducer; CYP3A4 inhibitor and substrate]): Standard doses of voriconazole and efavirenz at a dose of 400 mg once daily or above is contraindicated (see Contraindications). In healthy subjects, steady state efavirenz (400 mg oral once daily) decreased the steady state Cmax and AUC of voriconazole by an average of 61% and 77%, respectively. In the same study, voriconazole at steady state (400 mg orally every 12 hours for 1 day, then 200 mg orally every 12 hours for 8 days) increased the steady state Cmax and AUC of efavirenz by an average of 38% and 44% respectively, in the same subjects. In a separate study in healthy subjects, voriconazole dose of 300mg twice daily in combination with low dose efavirenz (300mg once daily) did not lead to sufficient voriconazole exposure. Following co-administration of voriconazole 400 mg twice daily with efavirenz 300 mg orally once daily in healthy subjects, the AUC of voriconazole was decreased by 7%, and Cmax was increased by 23% , compared to voriconazole 200 mg twice daily alone. The AUC of efavirenz was increased by 17% and Cmax was equivalent compared to efavirenz 600 mg once daily alone. These differences were not considered to be clinically significant. Voriconazole may be co-administered with efavirenz if the voriconazole maintenance dose is increased to 400 mg twice daily and the efavirenz dose is reduced by 50% i.e. to 300 mg once

daily (see Dosage and Administration). When treatment with voriconazole is stopped, the initial dose of efavirenz should be restored. The concomitant use of intravenous voriconazole and oral efavirenz has not been studied. Other non-nucleoside reverse transcriptase inhibitors (NNRTIs) (CYP3A4 substrates, inhibitors or CYP450 inducers): In vitro studies show that the metabolism of voriconazole may be inhibited by delavirdine. Although not studied, the metabolism of voriconazole may be induced by nevirapine. Voriconazole may also inhibit the metabolism of NNRTIs. Patients should be carefully monitored for drug toxicity during the co-administration of voriconazole and NNRTIs.

Guidance on the Clinical Management of Drug Interactions
Contraindications	Dose adjustment of voriconazole	Dose adjustment and/or monitoring of other drugs	No dose adjustment of voriconazole or other drugs
Rifampicin Sirolimus Barbiturates (long acting) Carbamazepine Cisapride Pimozide Quinidine Ergot alkaloids St John's Wort Rifabutin Ritonavir (400 mg q12h) Efavirenz (400 mg q24h)	Phenytoin (1,3) Ritonavir (100 mg q12h) Efavirenz (1)	Cyclosporin (2,3) Tacrolimus (2,3) Omeprazole (2) Warfarin (4) Phenytoin (3) Sulphonylureas (5) Statins (7) Benzodiazepines (7) Vinca Alkaloids (7) Nevirapine (7) Efavirenz (1) HIV protease inhibitors (7) (excluding indinavir & ritonavir) Methadone (7) Oral Contraceptive (7) Short Acting Opiates including fentanyl (7) NSAIDs (7) Oxycodone (7)	Indinavir Mycophenolate mofetil Cimetidine Ranitidine Macrolide antibiotics Prednisolone Digoxin No established dosing recommendation Everolimus (8) Fluconazole (9)

Reduce dose (halve dose of cyclosporin and omeprazole, reduce dose to one third for tacrolimus)

Monitor for voriconazole associated adverse events if voriconazole is used sequentially after fluconazole

Adverse Effects

Clinical Trial Data

The safety of voriconazole is based on an integrated safety database of more than 2000 subjects (1655 patients in therapeutic studies). This represents a heterogeneous population, containing patients with haematological malignancy, HIV infected patients with oesophageal candidiasis and refractory fungal infections, non-neutropenic patients with candidaemia or aspergillosis and healthy volunteers. Five hundred and sixty one patients had a duration of voriconazole therapy of greater than 12 weeks, with 136 patients receiving voriconazole for over 6 months.

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The table below includes adverse reactions from therapeutic and/or compassionate/ extension studies, if possibly causally related. The most commonly reported adverse events were visual disturbances, fever, rash, vomiting, nausea, diarrhoea, headache, peripheral oedema and abdominal pain. The severity of the adverse events was generally mild to moderate. No clinically significant differences were seen when the safety data were analysed by age, race, or gender.

MedDRA System Organ Class Frequency *	Adverse Drug Reactions
Infections and infestations
Common	Sinusitis
Blood and lymphatic system disorders
Common	Thrombocytopenia, anaemia (including macrocytic, microcytic, normocytic, megaloblastic, aplastic), leukopenia, pancytopenia
Uncommon	Lymphadenopathy, agranulocytosis, eosinophilia, disseminated intravascular coagulation, marrow depression
Immune system disorders
Uncommon	Allergic reaction, anaphylactoid reaction
Endocrine disorders
Uncommon	Adrenal cortex insufficiency
Rare	Hyperthyroidism, hypothyroidism
Metabolism and nutrition disorders
Common	Hypokalaemia, hypoglycaemia
Uncommon	Hypercholesterolaemia, hyponatraemia
Psychiatric disorders
Common	Hallucinations, confusion, depression, anxiety, agitation
Nervous system disorders
Very common	Headache
Common	Dizziness, tremor, paraesthesia
Uncommon	Ataxia, brain oedema, hypertonia, hypoaesthesia, nystagmus, syncope, altered taste perception
Rare	Guillain-Barre syndrome, oculogyric crisis, extrapyramidal syndrome, hepatic coma, insomnia, encephalopathy, somnolence during infusion, convulsion, peripheral neuropathy
Eye disorders
Very Common	Visual disturbances (including altered/enhanced visual perception, blurred vision, colour vision change, photophobia)
Uncommon	Blepharitis, optic neuritis, papilloedema, scleritis, diplopia
Rare	Retinal haemorrhage, corneal opacity, optic atrophy

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Ear and labyrinth disorders
Uncommon	Vertigo
Rare	Hypoacusis, tinnitus
Cardiac disorders
Common	Lung oedema
Uncommon	Atrial arrhythmia , bradycardia, tachycardia, ventricular arrhythmia , ventricular fibrillation, supraventricular tachycardia, QT prolongation
Rare	Atrioventricular (AV) complete block, bundle branch block, nodal arrhythmia, torsade de pointes , ventricular tachycardia
Vascular disorders
Common	Hypotension, thrombophlebitis, phlebitis
Rare	Lymphangitis
Respiratory, thoracic and mediastinal disorders
Common	Respiratory distress syndrome
Gastrointestinal disorders
Very common	Nausea, vomiting, diarrhoea, abdominal pain
Common	Cheilitis, gastroenteritis
Uncommon	Constipation , duodenitis, dyspepsia, gingivitis, glossitis, pancreatitis, tongue oedema, peritonitis
Rare	Pseudomembranous colitis
Hepatobiliary disorders
Common	Elevated liver function tests (including AST (SGOT), ALT (SGPT), alkaline phosphatase, GGT, LDH, bilirubin), jaundice, cholestatic jaundice
Uncommon	Cholecystitis, cholelithiasis, enlarged liver, hepatitis, hepatic failure
Skin and subcutaneous tissue disorders
Very common	Rash
Common	Face oedema, pruritus, maculopapular rash, photosensitivity skin reaction, alopecia, exfoliative dermatitis, purpura
Uncommon	Fixed drug eruption, eczema, psoriasis, Stevens- Johnson syndrome, urticaria
Rare	Angioedema, discoid lupus erythematosis, erythema multiforme, toxic epidermal necrolysis, pseudoporphyria
Musculoskeletal, connective tissue and bone disorders
Common	Back pain
Uncommon	Arthritis
Renal and urinary disorders
Common	Creatinine increased, acute kidney failure, haematuria

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Uncommon	BUN increased, albuminuria, nephritis
Rare	Kidney tubular necrosis
General disorders and administration site conditions
Very common	Fever, peripheral oedema
Common	Chills, asthenia, chest pain, injection site reaction/inflammation, flu syndrome

*Frequencies are categorised as follows: very common 10%; common from 1% to <10%; uncommon from

0.1% to <1%; rare from 0.01% to <0.1%)

Adverse Events Reported in Comparative Therapeutic Studies 305 and 307/602 at a rate of 1% Possibly Related to Therapy or Causality Unknown
	Protocol 305 Voriconazole vs Fluconazole (oral therapy)		Protocol 307/602 Voriconazole vs Conventional Amphotericin B (IV/oral therapy)
	Vori N = 200 N (%)	Fluc N =191 N (%)	Vori N =196 N (%)	Ampho B * N = 185 N (%)
Body as a whole	-	-	7 (3.6)	25 (13.5)
Fever	-	-	7 (3.6)	25 (13.5)
Chills	-	-	-	36 (19.5)
Headache	-	-	7 (3.6)	8 (4.3)
Abdominal pain	-	-	5 (2.6)	6 (3.2)
Chest pain	-	-	4 (2.0)	2 (1.1)
Cardiovascular system
Tachycardia	-	-	5 (2.6)	5 (2.7)
Hypertension	-	-	-	2 (1.1)
Hypotension	-	-	-	3 (1.6)
Vasodilatation	-	-	2 (1.0)	2 (1.1)
Digestive system	2 (1.0)	3 (1.6)	14 (7.1)	29 (15.7)
Nausea	2 (1.0)	3 (1.6)	14 (7.1)	29 (15.7)
Vomiting	2 (1.0)	-	11 (5.6)	18 (9.7)
Liver function tests abnormal	6 (3.0)	2 (1.0)	9 (4.6)	4 (2.2)
Diarrhoea	-	-	3 (1.5)	6 (3.2)
Cholestatic jaundice	3 (1.5)	-	4 (2.0)	-
Dry mouth	-	-	3 (1.5)	-
Haemic and lymphatic system
Thrombocytopenia	-	-	2 (1.0)	2 (1.1)
Anaemia	-	-	-	5 (2.7)
Metabolic and Nutritional	10 (5.0)	3 (1.6)	6 (3.1)	4 (2.2)
Systems
Alkaline phosphatase increased
Hepatic enzymes increased	3 (1.5)	-	7 (3.6)	5 (2.7)
AST (SGOT) increased	8 (4.0)	2 (1.0)	-	-

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	Protocol 305 Voriconazole vs Fluconazole (oral therapy)		Protocol 307/602 Voriconazole vs Conventional Amphotericin B (IV/oral therapy)
	Vori N = 200 N (%)	Fluc N =191 N (%)	Vori N =196 N (%)	Ampho B * N = 185 N (%)
ALT (SGPT) increased	6 (3.0)	2 (1.0)	3 (1.5)	-
Hypokalaemia	-	-	-	36 (19.5)
Peripheral oedema	-	-	7 (3.6)	9 (4.9)
Hypomagnesaemia	-	-	2 (1.0)	10 (5.4)
Bilirubinaemia	-	-	-	3 (1.6)
Creatinine increased	-	-	-	59 (31.9)
Nervous system
Hallucinations	-	-	10 (5.1)	-
Dizziness	-	2 (1.0)	5 (2.6)	-
Skin and Appendages
Rash	3 (1.5)	1 (0.5)	13 (6.6)	7 (3.8)
Pruritus	-	-	2 (1.0)	2 (1.1)
Maculopapular rash	3 (1.5)	-	-	-
Special senses
Abnormal vision	31 (15.5)	8 (4.2)	55 (28.1)	1 (0.5)
Photophobia	5 (2.5)	2 (1.0)	7 (3.6)	-
Chromatopsia	2 (1.0)	-	2 (1.0)	-
Urogenital
Kidney function abnormal	-	-	4 (2.0)	40 (21.6)
Acute kidney failure	-	-	-	11 (5.9)

*Amphotericin B followed by other licensed antifungal therapy

Visual Disturbances

In clinical trials, voriconazole treatment-related visual disturbances were very common. In these studies, approximately 21% of subjects experienced altered/enhanced visual perception, blurred vision, colour vision change or photophobia. These visual disturbances were transient and fully reversible, with the majority spontaneously resolving within 60 minutes. There was evidence of attenuation with repeated doses of voriconazole. The visual disturbances were generally mild, rarely resulted in discontinuation and were not associated with long-term sequelae. Visual disturbances may be associated with higher plasma concentrations and/or doses. There have been post-marketing reports of prolonged visual adverse events (see

Precautions).

The mechanism of action is unknown, although the site of action is most likely to be within the retina. In a study in healthy volunteers investigating the impact of voriconazole on retinal function, voriconazole caused a decrease in the electroretinogram (ERG) waveform amplitude. The

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ERG measures electrical currents in the retina. The ERG changes did not progress over 29 days of treatment and were fully reversible on withdrawal of voriconazole. The long-term effect of voriconazole (median 169 days; range 5-353 days) on visual function was evaluated in subjects with paracoccioidomycoses. Voriconazole had no clinically relevant effect on visual function as assessed by testing visual acuity, visual fields, colour vision and contrast sensitivity. There were no signs of retinal toxicity. 17/35 voriconazole subjects experienced visual adverse events. These events did not lead to discontinuation, were generally mild, occurred in the first week of therapy and resolved during continued voriconazole therapy.

Dermatological Reactions

Dermatological reactions were common in patients treated with voriconazole. In clinical trials, rashes were reported by 19% (278/1493) of voriconazole treated patients, but these patients had serious underlying diseases and were receiving multiple concomitant medications. The majority of rashes were of mild to moderate severity. Patients have developed serious cutaneous reactions, including Stevens-Johnson syndrome (uncommon), toxic epidermal necrolysis (rare) and erythema multiforme (rare) during treatment with voriconazole. If patients develop a rash they should be monitored closely and voriconazole discontinued if lesions progress. Photosensitivity reactions have been reported, especially during long-term therapy (see Precautions).

Liver Function Tests

The overall incidence of clinically significant transaminase abnormalities in the voriconazole clinical program was 13.4% (200/1493) of subjects treated with voriconazole. Liver function test abnormalities may be associated with higher plasma concentrations and/or doses. The majority of abnormal liver function tests either resolved during treatment without dose adjustment or following dose adjustment, including discontinuation of therapy. Voriconazole has been infrequently associated with cases of serious hepatic toxicity, in patients with other serious underlying conditions. This includes cases of jaundice, and cases of hepatitis and hepatic failure leading to death (see Precautions).

Paediatric Use

The safety of voriconazole was investigated in 245 paediatric patients aged 2 to <12 years who were treated with voriconazole in pharmacokinetic studies (87 paediatric patients) and in compassionate use programs (158 paediatric patients). The adverse event profile of these 245 paediatrics was similar to adults although post-marketing data suggest that there might be a higher occurrence of skin reactions in the paediatric population compared to adults. There have been post-marketing reports of pancreatitis in paediatric patients.

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Infusion-Related Reactions

During infusion of the intravenous formulation of voriconazole in healthy subjects, anaphylactoid-type reactions, including flushing, fever, sweating, tachycardia, chest tightness, dyspnoea, faintness, nausea, pruritus and rash have occurred. Symptoms appeared immediately upon initiating the infusion (see Precautions).

Dosage and Administration

VFEND Tablets and Powder for Oral Suspension are to be taken at least one hour before or one hour following a meal. VFEND Powder for Oral Suspension requires reconstitution before use (see Administration and Incompatibilities - Powder for Oral Suspension). VFEND IV requires reconstitution and dilution prior to administration as an intravenous infusion (see Intravenous Administration). VFEND IV is not recommended for bolus injection. It is recommended that VFEND IV is administered at a maximum rate of 3 mg/kg per hour over 1 to 2 hours. Electrolyte disturbances such as hypokalaemia, hypomagnesaemia and hypocalcaemia should be corrected prior to initiation of voriconazole therapy (see Precautions, Cardiovascular).

Therapy must be initiated with the specified loading dose regimen of either intravenous or oral VFEND to achieve plasma concentrations on Day 1 that are close to steady state. On the basis of the high oral bioavailability (96%; see Pharmacokinetics), switching between intravenous and oral administration is appropriate when clinically indicated. Intravenous administration is not recommended for the treatment of oesophageal candidiasis; dosage recommendations for oesophageal candidiasis are provided in the following table.

Detailed information on dosage recommendations is provided in the following table:

If patient response at 3 mg/kg every 12 hours is inadequate, the intravenous maintenance dose may be increased to 4mg/kg every 12 hours. If patients are unable to tolerate 4mg/kg every 12 hours, reduce the intravenous dose to 3 mg/kg every 12 hours. Phenytoin may be co-administered with voriconazole if the maintenance dose of voriconazole is increased to 5 mg/kg intravenously every 12 hours. The loading dose regimen remains unchanged (see Precautions and Interactions). The dose recommendation for concomitant use of intravenous voriconazole and oral efavirenz has not been determined (see Interactions).

If patient response is inadequate, the maintenance dose may be increased to 300 mg twice daily for oral administration. For patients less than 40 kg the oral dose may be increased to 150 mg twice daily. If patients are unable to tolerate treatment at these higher doses reduce the oral dose by 50 mg steps to a minimum 200 mg twice daily (or 100 mg twice daily for patients less than 40 kg) maintenance dose. Phenytoin may be co-administered with voriconazole if the maintenance dose of voriconazole is increased from 200 to 400 mg twice daily orally (100 mg to 200 mg twice daily orally in patients less than 40 kg). The loading dose regimen remains unchanged (see Precautions and Interactions). When voriconazole is co-administered with efavirenz, the voriconazole maintenance dose should be increased to 400 mg every 12 hours and the efavirenz dose should be decreased to 300 mg every 24 hours (see Precautions and Interactions). Treatment duration depends upon patients' clinical and mycological response.

The pharmacokinetics of orally administered voriconazole are not affected by renal impairment. Therefore, no adjustment is necessary for oral dosing for patients with mild to severe renal impairment. In patients with moderate to severe renal dysfunction (creatinine clearance < 50 mL/min), including dialysis patients, accumulation of the intravenous vehicle, SBECD, occurs. Oral voriconazole should be administered to these patients, unless an assessment of the risk- benefit to the patient justifies the use of intravenous voriconazole. Serum creatinine levels should be closely monitored in these patients and, if increases occur, consideration should be given to changing to oral voriconazole therapy (see Pharmacokinetics, Renal Impairment).

No dose adjustment is necessary in patients with acute hepatic injury, manifested by elevated liver function tests (ALT, AST) (but continued monitoring of liver function tests for further elevations is recommended). It is recommended that the standard loading dose regimens be used but that the maintenance dose be halved in patients with mild to moderate hepatic cirrhosis (Child-Pugh A and B) receiving voriconazole. Voriconazole has not been studied in patients with severe chronic hepatic cirrhosis (Child- Pugh C). Voriconazole has been associated with elevations in liver function tests and

clinical signs of liver damage such as jaundice, and must only be used in patients with severe hepatic impairment if the benefit outweighs the potential risk. Patients with severe hepatic impairment must be carefully monitored for drug toxicity (see Adverse Effects).

Safety and efficacy in paediatric subjects below the age of 2 years has not been established (see Pharmacokinetics). Therefore, voriconazole is not recommended for children less than 2 years of age. The recommended maintenance dosing regimen in paediatric patients 2 to < 12 years is as follows:

Based on a population pharmacokinetic analysis in 82 immunocompromised patients aged 2 to < 12 years

* * Based on a population pharmacokinetic analysis in 47 immunocompromised patients aged 2 to < 12 years

If paediatric patients are unable to tolerate an intravenous dose of 7mg/kg twice daily, a dose reduction from 7mg/kg to 4mg/kg twice daily may be considered based on the population pharmacokinetic analysis and previous clinical experience. This provides equivalent exposure to 3mg/kg twice daily in adults (see Dosage and Administration, Use in Adults). Use in paediatric patients aged 2 to < 12 years with hepatic or renal insufficiency has not been studied (see Adverse Effects and Pharmacokinetics). These paediatric dose recommendations are based on studies in which VFEND was administered as the powder for oral suspension formulation. Bioequivalence between the powder for oral suspension and tablets has not been investigated in a paediatric population. Considering the assumed limited gastro-enteric transit time in paediatrics, the absorption of tablets may be different in paediatric compared to adult patients. Adolescents (12 -16 years of age) should be dosed as adults.

Pharmaceutical Precautions

VFEND IV Powder for Injection is supplied in single use vials. The powder should be reconstituted with 19 mL of Water for Injections. Shake thoroughly to give a clear concentrate containing 10 mg/mL of voriconazole and an extractable volume of 20 mL. It is recommended that a standard 20 mL (non-automated) syringe be used to ensure that the exact

amount (19.0 mL) of Water for Injections is dispensed. Discard the vial if a vacuum does not pull the diluent into the vial. For administration, the required volume of the reconstituted concentrate is added to a recommended compatible infusion solution (detailed below) to obtain a final solution containing voriconazole at a concentration between 0.5 mg/mL and 5 mg/mL. VFEND IV should be administered at a maximum rate of 3 mg/kg per hour over 1 to 2 hours and not as a bolus injection. VFEND IV contains no antimicrobial agent. To reduce microbiological hazard, use as soon as practicable after reconstitution. If storage is necessary, hold at 2 to 8C for not more than 24 hours. Product is for single use in one patient only. Discard any residue. Only clear solutions without particles should be used. Chemical and physical in-use stability has been demonstrated for 24 hours at 2 to 8C. The reconstituted solution can be diluted with:

5% Glucose and Compound Sodium Lactate Intravenous Infusion 5% Glucose and 0.45% Sodium Chloride Intravenous Infusion 5% Glucose Intravenous Infusion 5% Glucose in 20 mEq Potassium Chloride Intravenous Infusion 0.45% Sodium Chloride Intravenous Infusion 5% Glucose and 0.9% Sodium Chloride Intravenous Infusion The compatibility of VFEND IV with diluents other than those described above is unknown (see Intravenous Incompatibilities).

Voriconazole must not be infused concomitantly with any blood product or any short-term infusion of concentrated solution of electrolytes, even if the two infusions are running in separate lines. Electrolyte disturbances such as hypokalaemia, hypomagnesaemia and hypocalcaemia should be corrected prior to initiation of voriconazole therapy (see Precautions, Cardiovascular).

Voriconazole can be infused at the same time as other intravenous solutions containing (non- concentrated) electrolytes, but must be infused through a separate line.

Voriconazole can be infused at the same time as total parenteral nutrition, but must be infused in a separate line. If infused through a multiple-lumen catheter, TPN needs to be administered using a different port from the one used for voriconazole. Voriconazole must not be diluted with 4.2% Sodium Bicarbonate Infusion. Compatibility with other concentrations is unknown. VFEND IV must not be mixed with other medicinal products except those mentioned under Intravenous Administration.

Administration & Incompatibilities - Powder for Oral Suspension Reconstitution Instructions:

Reconstituted VFEND Powder for Oral Suspension should be shaken well before use. VFEND Powder for Oral Suspension should be administered using the syringe provided in the pack. VFEND Powder for Oral Suspension should not be mixed with any other medication. It is not intended that the reconstituted suspension be further diluted with water or other vehicles.

VFEND IV is a single dose unpreserved sterile lyophilised powder that should be stored below 30C. Following reconstitution of the lyophile with Water for Injections to 10 mg/mL, VFEND reconstituted concentrate can be stored at 2 to 8C in a refrigerator for up to 24 hours prior to use (see Dosage and Administration: Intravenous Administration). VFEND Powder for Oral Suspension should be stored at 2C to 8C (in a refrigerator) before reconstitution. Store reconstituted suspension below 30C. Discard suspension 14 days after reconstitution.

Overdosage

In clinical trials there were three cases of accidental overdose. All occurred in paediatric patients, who received up to five times the recommended intravenous dose of voriconazole. A single adverse event of photophobia of 10 minutes duration was reported. There is no known antidote to voriconazole. It is recommended that treatment of overdose is symptomatic and supportive. Monitor potassium, full blood count and liver function following an overdose. Consider administration of activated charcoal in the event of a potentially toxic ingestion. Activated charcoal is most effective when administered within one hour of ingestion. In patients who are not fully conscious or have impaired gag reflex, consideration should be given to administering activated charcoal via nasogastric tube once the airway is protected. Voriconazole is haemodialysed with a clearance of 121 mL/min. The intravenous vehicle, SBECD, is haemodialysed with a clearance of 55 mL/min. In an overdose, haemodialysis may assist in the removal of voriconazole and SBECD from the body. Contact the Poisons Information Centre for advice on the management of an overdose.

Presentation

VFEND 50 mg film-coated tablets are white, round tablets, debossed "Pfizer" on one side and "VOR50" on the reverse. VFEND 200 mg film-coated tablets are white, capsule-shaped tablets, debossed "Pfizer" on one side and "VOR200" on the reverse. PVC/Aluminium blisters of 2, 10, 14, 20, 28, 30, 50, 56 and 100 tablets in cartons. Not all pack sizes may be marketed.

VFEND IV 200 mg/vial is supplied as a sterile lyophilised powder in single use 30 mL clear glass vials. Packs of 1.

VFEND Powder for Oral Suspension is supplied in a 100 mL HDPE bottle. Each bottle contains 45 g of powder for oral suspension, providing a usable volume of 70 mL of suspension at a voriconazole concentration of 40 mg/mL, following reconstitution. A 5 mL syringe dispenser and a press-in bottle adaptor are also provided.

Medicine Classification

Name and Address

Pfizer New Zealand Ltd PO Box 3998 Auckland NEW ZEALAND Toll Free Number: 0800 736 363

	Success/total (%)
Treatment	PP	ITT
Voriconazole	113/115 (98%)	175/200 (88%)
Fluconazole	134/141 (95%)	171/191 (90%)

	Intravenous	Oral
		Patients 40 kg or above	Patients less than 40 kg
Serious invasive Candida infections Loading Dose Regimen (first 24 hours) Maintenance Dose (after first 24 hours)	6 mg/kg every 12 hours (for the first 24 hours) 3 mg/kg every 12 hours	400 mg or 10 mL every 12 hours (for the first 24 hours) 200 mg or 5 mL twice daily	200 mg or 5 mL every 12 hours (for the first 24 hours) 100 mg or 2.5 mL twice daily
Oesophageal Candidiasis Loading Dose Regimen (first 24 hours) Maintenance Dose (after first 24 hours)	Not recommended Not recommended	400 mg or 10 mL every 12 hours (for the first 24 hours) 200 mg or 5 mL twice daily	200 mg or 5 mL every 12 hours (for the first 24 hours) 100 mg or 2.5 mL twice daily
Invasive aspergillosis/ Scedosporium and Fusarium infections/ other serious fungal infections Loading Dose Regimen (first 24 hours) Maintenance Dose (after first 24 hours)	6 mg/kg every 12 hours (for the first 24 hours) 4 mg/kg every 12 hours	400 mg or 10 mL every 12 hours (for the first 24 hours) 200 mg or 5 mL twice daily	200 mg or 5 mL every 12 hours (for the first 24 hours) 100 mg or 2.5 mL twice daily

Loading Dose Regimen	No oral or intravenous loading dose is recommended
Maintenance Dose	Intravenous Dose *	Oral Dose * *
Maintenance Dose	7 mg/kg twice daily	200 mg twice daily

Description

Pharmacology

Actions

Pharmacokinetics

Clinical Trials

Indications

Contraindications

Precautions

Interactions

Adverse Effects

Dosage and Administration

Pharmaceutical Precautions

Overdosage

Presentation

Medicine Classification

Name and Address

Date of Preparation