DRUG INTERACTIONS SECTION.

7 DRUG INTERACTIONS. Posaconazole is primarily metabolized via UDP glucuronosyltransferase and is substrate of p- glycoprotein (P-gp) efflux. Therefore, inhibitors or inducers of these clearance pathways may affect posaconazole plasma concentrations. Coadministration of drugs that can decrease the plasma concentrations of posaconazole should generally be avoided unless the benefit outweighs the risk. If such drugs are necessary, patients should be monitored closely for breakthrough fungal infections.Posaconazole is also strong inhibitor of CYP3A4. Therefore, plasma concentrations of drugs predominantly metabolized by CYP3A4 may be increased by posaconazole [see Clinical Pharmacology (12.3)].The following information was derived from data with Noxafil(R) oral suspension or early tablet formulation unless otherwise noted. All drug interactions with Noxafil(R) oral suspension, except for those that affect the absorption of posaconazole (via gastric pH and motility), are considered relevant to Posaconazole injection, Noxafil(R) delayed-release tablet, and Noxafil(R) PowderMix for delayed-release oral suspension as well.. Interaction DrugInteractionRifabutin, phenytoin, efavirenzAvoid coadministration unless the benefit outweighs the risks (7.6, 7.7, 7.8)Other drugs metabolized by CYP3A4 Consider dosage adjustment and monitor for adverse effects and toxicity (7.1, 7.10, 7.11)DigoxinMonitor digoxin plasma concentrations (7.12)FosamprenavirMonitor for breakthrough fungal infections (7.6). 7.1 Immunosuppressants Metabolized by CYP3A4. Sirolimus: Concomitant administration of Posaconazole with sirolimus increases the sirolimus blood concentrations by approximately 9-fold and can result in sirolimus toxicity. Therefore, posaconazole is contraindicated with sirolimus [see Contraindications (4.2) and Clinical Pharmacology (12.3)].Tacrolimus: Posaconazole has been shown to significantly increase the Cmax and AUC of tacrolimus. At initiation of posaconazole treatment, reduce the tacrolimus dose to approximately one-third of the original dose. Frequent monitoring of tacrolimus whole blood trough concentrations should be performed during and at discontinuation of Posaconazole treatment and the tacrolimus dose adjusted accordingly [see Warnings and Precautions (5.1) and Clinical Pharmacology (12.3)].Cyclosporine: Posaconazole has been shown to increase cyclosporine whole blood concentrations in heart transplant patients upon initiation of Posaconazole treatment. It is recommended to reduce cyclosporine dose to approximately three-fourths of the original dose upon initiation of Posaconazole treatment. Frequent monitoring of cyclosporine whole blood trough concentrations should be performed during and at discontinuation of Posaconazole treatment and the cyclosporine dose adjusted accordingly [see Warnings and Precautions (5.1) and Clinical Pharmacology (12.3)].. 7.2 CYP3A4 Substrates. Concomitant administration of Posaconazole with CYP3A4 substrates such as pimozide and quinidine may result in increased plasma concentrations of these drugs, leading to QTc prolongation and cases of torsades de pointes. Therefore, Posaconazole is contraindicated with these drugs [see Contraindications (4.3) and Warnings and Precautions (5.2)].. 7.3 HMG-CoA Reductase Inhibitors (Statins) Primarily Metabolized Through CYP3A4. Concomitant administration of Posaconazole with simvastatin increases the simvastatin plasma concentrations by approximately 10-fold. Therefore, Posaconazole is contraindicated with HMG-CoA reductase inhibitors primarily metabolized through CYP3A4 [see Contraindications (4.4) and Clinical Pharmacology (12.3)].. 7.4 Ergot Alkaloids. Most of the ergot alkaloids are substrates of CYP3A4. Posaconazole may increase the plasma concentrations of ergot alkaloids (ergotamine and dihydroergotamine) which may lead to ergotism. Therefore, Posaconazole is contraindicated with ergot alkaloids [see Contraindications (4.5)].. 7.5 Benzodiazepines Metabolized by CYP3A4. Concomitant administration of Posaconazole with midazolam increases the midazolam plasma concentrations by approximately 5-fold. Increased plasma midazolam concentrations could potentiate and prolong hypnotic and sedative effects. Concomitant use of Posaconazole and other benzodiazepines metabolized by CYP3A4 (e.g., alprazolam, triazolam) could result in increased plasma concentrations of these benzodiazepines. Patients must be monitored closely for adverse effects associated with high plasma concentrations of benzodiazepines metabolized by CYP3A4 and benzodiazepine receptor antagonists must be available to reverse these effects [see Warnings and Precautions (5.6) and Clinical Pharmacology (12.3)]. 7.6 Anti-HIV Drugs. Efavirenz: Efavirenz induces UDP-glucuronidase and significantly decreases posaconazole plasma concentrations [see Clinical Pharmacology (12.3)]. It is recommended to avoid concomitant use of efavirenz with Posaconazole unless the benefit outweighs the risks.Ritonavir and Atazanavir: Ritonavir and atazanavir are metabolized by CYP3A4 and Posaconazole increases plasma concentrations of these drugs [see Clinical Pharmacology (12.3)]. Frequent monitoring of adverse effects and toxicity of ritonavir and atazanavir should be performed during coadministration with Posaconazole.Fosamprenavir: Combining fosamprenavir with Posaconazole may lead to decreased posaconazole plasma concentrations. If concomitant administration is required, close monitoring for breakthrough fungal infections is recommended [see Clinical Pharmacology (12.3)]. 7.7 Rifabutin. Rifabutin induces UDP-glucuronidase and decreases posaconazole plasma concentrations. Rifabutin is also metabolized by CYP3A4. Therefore, coadministration of rifabutin with Posaconazole increases rifabutin plasma concentrations [see Clinical Pharmacology (12.3)]. Concomitant use of Posaconazole and rifabutin should be avoided unless the benefit to the patient outweighs the risk. However, if concomitant administration is required, close monitoring for breakthrough fungal infections as well as frequent monitoring of full blood counts and adverse reactions due to increased rifabutin plasma concentrations (e.g., uveitis, leukopenia) are recommended.. 7.8 Phenytoin. Phenytoin induces UDP-glucuronidase and decreases posaconazole plasma concentrations. Phenytoin is also metabolized by CYP3A4. Therefore, coadministration of phenytoin with Posaconazole increases phenytoin plasma concentrations [see Clinical Pharmacology (12.3)]. Concomitant use of Posaconazole and phenytoin should be avoided unless the benefit to the patient outweighs the risk. However, if concomitant administration is required, close monitoring for breakthrough fungal infections is recommended and frequent monitoring of phenytoin concentrations should be performed while coadministered with Posaconazole and dose reduction of phenytoin should be considered.. 7.10 Vinca Alkaloids. Most of the vinca alkaloids (e.g., vincristine and vinblastine) are substrates of CYP3A4. Concomitant administration of azole antifungals, including Posaconazole, with vincristine has been associated with serious adverse reactions [see Warnings and Precautions (5.7)]. Posaconazole may increase the plasma concentrations of vinca alkaloids which may lead to neurotoxicity and other serious adverse reactions. Therefore, reserve azole antifungals, including Posaconazole, for patients receiving vinca alkaloid, including vincristine, who have no alternative antifungal treatment options.. 7.11 Calcium Channel Blockers Metabolized by CYP3A4. Posaconazole may increase the plasma concentrations of calcium channel blockers metabolized by CYP3A4 (e.g., verapamil, diltiazem, nifedipine, nicardipine, felodipine). Frequent monitoring for adverse reactions and toxicity related to calcium channel blockers is recommended during coadministration. Dose reduction of calcium channel blockers may be needed.. 7.12 Digoxin. Increased plasma concentrations of digoxin have been reported in patients receiving digoxin and Posaconazole. Therefore, monitoring of digoxin plasma concentrations is recommended during coadministration.. 7.14 Glipizide. Although no dosage adjustment of glipizide is required, it is recommended to monitor glucose concentrations when Posaconazole and glipizide are concomitantly used.. 7.16 Venetoclax. Concomitant use of venetoclax (a CYP3A4 substrate) with posaconazole increases venetoclax (cmax and AUC 0-INF, which may increase venetoclax toxicities [see Contraindications (4.6), Warnings and Precautions (5.10)]. Refer to the venetoclax prescribing information for more information on the dosing instructions and the extent of increase in venetoclax exposure.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Pregnancy: Based on animal data, may cause fetal harm. (8.1)Pediatrics: Safety and effectiveness in patients younger than years of age have not been established. (8.4)Severe Renal Impairment: Monitor closely for breakthrough fungal infections. (8.6). Pregnancy: Based on animal data, may cause fetal harm. (8.1). Pediatrics: Safety and effectiveness in patients younger than years of age have not been established. (8.4). Severe Renal Impairment: Monitor closely for breakthrough fungal infections. (8.6). 8.1 Pregnancy. Risk SummaryBased on findings from animal data, Posaconazole may cause fetal harm when administered to pregnant women. Available data for use of Posaconazole in pregnant women are insufficient to establish drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. In animal reproduction studies, skeletal malformations (cranial malformations and missing ribs) and maternal toxicity (reduced food consumption and reduced body weight gain) were observed when posaconazole was dosed orally to pregnant rats during organogenesis at doses >=1.4 times the 400 mg twice daily oral suspension regimen based on steady-state plasma concentrations of Posaconazole in healthy volunteers. In pregnant rabbits dosed orally during organogenesis, increased resorptions, reduced litter size, and reduced body weight gain of females were seen at doses times the exposure achieved with the 400 mg twice daily oral suspension regimen. Doses of >= times the clinical exposure caused an increase in resorptions in these rabbits (see Data). Based on animal data, advise pregnant women of the potential risk to fetus.The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is to 4% and 15 to 20%, respectively.. Data. Animal DataPosaconazole resulted in maternal toxicity (reduced food consumption and reduced body weight gain) and skeletal malformations (cranial malformations and missing ribs) when given orally to pregnant rats during organogenesis (Gestational Days through 15) at doses >=27 mg/kg (>=1.4 times the 400 mg twice daily oral suspension regimen based on steady-state plasma concentrations of drug in healthy volunteers). The no-effect dose for malformations and maternal toxicity in rats was mg/kg, which is 0.7 times the exposure achieved with the 400 mg twice daily oral suspension regimen. No malformations were seen in rabbits dosed during organogenesis (Gestational Days through 19) at doses up to 80 mg/kg (5 times the exposure achieved with the 400 mg twice daily oral suspension regimen). In the rabbit, the no-effect dose was 20 mg/kg, while high doses of 40 mg/kg and 80 mg/kg (3 or times the clinical exposure) caused an increase in resorptions. In rabbits dosed at 80 mg/kg, reduction in body weight gain of females and reduction in litter size were seen.. 8.2 Lactation. Risk SummaryThere are no data on the presence of posaconazole in human milk, the effects on the breastfed infant, or the effects on milk production. Posaconazole is excreted in the milk of lactating rats. When drug is present in animal milk, it is likely that the drug will be present in human milk. The developmental and health benefits of breastfeeding should be considered along with the mothers clinical need for Posaconazole and any potential adverse effects on the breastfed child from Posaconazole or from the underlying maternal condition.. 8.4 Pediatric Use. The safety and effectiveness of Posaconazole injection for the prophylaxis of invasive Aspergillus and Candida infections have been established in pediatric patients aged and older who are at high risk of developing these infections due to being severely immunocompromised, such as HSCT recipients with GVHD or those with hematologic malignancies with prolonged neutropenia from chemotherapy.The safety and effectiveness of Posaconazole injection for the treatment of invasive aspergillosis have been established in pediatric patients aged 13 years and older.Use of Posaconazole in these age groups is supported by evidence from adequate and well-controlled studies of Posaconazole in adult and pediatric patients and additional pharmacokinetic and safety data in pediatric patients years of age and older [see Adverse Reactions (6.1), Clinical Pharmacology (12.3) and Clinical Studies (14)].The safety and effectiveness of Posaconazole have not been established in pediatric patients younger than years of age.. 8.5 Geriatric Use. No overall differences in the safety of Posaconazole injection were observed between geriatric patients and younger adult patients in the clinical trials; therefore, no dosage adjustment is recommended for any formulation of Posaconazole in geriatric patients. No clinically meaningful differences in the pharmacokinetics of Posaconazole were observed in geriatric patients compared to younger adult patients during clinical trials [see Clinical Pharmacology (12.3)].Of the 279 patients treated with Posaconazole injection in the Posaconazole Injection Study, 52 (19%) were greater than 65 years of age. Of the 230 patients treated with Noxafil(R) delayed-release tablets, 38 (17%) were greater than 65 years of age. Of the 288 patients randomized to Posaconazole injection/ Noxafil(R) delayed-release tablets in the Aspergillosis Treatment Study, 85 (29%) were >=65 years of age.No overall differences in the pharmacokinetics and safety were observed between elderly and young subjects during clinical trials, but greater sensitivity of some older individuals cannot be ruled out.. 8.6 Renal Impairment. Posaconazole Injection should be avoided in patients with moderate or severe renal impairment (eGFR <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection. In patients with moderate or severe renal impairment (eGFR <50 mL/min), receiving the Posaconazole injection, accumulation of the intravenous vehicle, SBECD, is expected to occur. Serum creatinine levels should be closely monitored in these patients, and, if increases occur, consideration should be given to changing to oral Posaconazole therapy [see Dosage and Administration (2.9) and Warnings and Precautions (5.5)].. 8.7 Hepatic Impairment. It is recommended that no dose adjustment of Posaconazole injection is needed in patients with mild to severe hepatic impairment (Child-Pugh Class A, B, or C) [see Dosage and Administration (2) and Warnings and Precautions (5.4)]. However, specific study has not been conducted with Posaconazole injection.. 8.8 Gender. The pharmacokinetics of posaconazole are comparable in males and females. No adjustment in the dosage of Posaconazole is necessary based on gender.. 8.9 Race. The pharmacokinetic profile of posaconazole is not significantly affected by race. No adjustment in the dosage of Posaconazole is necessary based on race.. 8.10 Weight. Pharmacokinetic modeling suggests that patients weighing greater than 120 kg may have lower posaconazole plasma drug exposure. It is, therefore, suggested to closely monitor for breakthrough fungal infections.

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. Calcineurin-Inhibitor Toxicity: Posaconazole increases concentrations of cyclosporine or tacrolimus; reduce dose of cyclosporine and tacrolimus and monitor concentrations frequently. (5.1)Arrhythmias and QTc Prolongation: Posaconazole has been shown to prolong the QTc interval and cause cases of TdP. Administer with caution to patients with potentially proarrhythmic conditions. Do not administer with drugs known to prolong QTc interval and metabolized through CYP3A4. (5.2)Electrolyte Disturbances: Monitor and correct, especially those involving potassium (K+), magnesium (Mg++), and calcium (Ca++), before and during Posaconazole therapy. (5.3)Hepatic Toxicity: Elevations in liver tests may occur. Discontinuation should be considered in patients who develop abnormal liver tests or monitor liver tests during treatment. (5.4)Renal Impairment: Posaconazole injection should be avoided in patients with moderate or severe renal impairment (creatinine clearance <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection. (5.5, 8.6)Concomitant Use with Midazolam: Posaconazole can prolong hypnotic/sedative effects. Monitor patients and benzodiazepine receptor antagonists should be available. (5.6, 7.5)Vincristine Toxicity: Concomitant administration of azole antifungals, including Posaconazole with vincristine has been associated with neurotoxicity and other serious adverse reactions; reserve azole antifungals, including Posaconazole, for patients receiving vinca alkaloid, including vincristine, who have no alternative antifungal treatment options. (5.7, 7.10)Venetoclax Toxicity: Concomitant administration of Posaconazole with venetoclax may increase venetoclax toxicities, including the risk of tumor lysis syndrome, neutropenia, and serious infections; monitor for toxicity and reduce venetoclax dose. (4.6, 5.10, 7.16). Calcineurin-Inhibitor Toxicity: Posaconazole increases concentrations of cyclosporine or tacrolimus; reduce dose of cyclosporine and tacrolimus and monitor concentrations frequently. (5.1). Arrhythmias and QTc Prolongation: Posaconazole has been shown to prolong the QTc interval and cause cases of TdP. Administer with caution to patients with potentially proarrhythmic conditions. Do not administer with drugs known to prolong QTc interval and metabolized through CYP3A4. (5.2). Electrolyte Disturbances: Monitor and correct, especially those involving potassium (K+), magnesium (Mg++), and calcium (Ca++), before and during Posaconazole therapy. (5.3). Hepatic Toxicity: Elevations in liver tests may occur. Discontinuation should be considered in patients who develop abnormal liver tests or monitor liver tests during treatment. (5.4). Renal Impairment: Posaconazole injection should be avoided in patients with moderate or severe renal impairment (creatinine clearance <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection. (5.5, 8.6). Concomitant Use with Midazolam: Posaconazole can prolong hypnotic/sedative effects. Monitor patients and benzodiazepine receptor antagonists should be available. (5.6, 7.5). Vincristine Toxicity: Concomitant administration of azole antifungals, including Posaconazole with vincristine has been associated with neurotoxicity and other serious adverse reactions; reserve azole antifungals, including Posaconazole, for patients receiving vinca alkaloid, including vincristine, who have no alternative antifungal treatment options. (5.7, 7.10). Venetoclax Toxicity: Concomitant administration of Posaconazole with venetoclax may increase venetoclax toxicities, including the risk of tumor lysis syndrome, neutropenia, and serious infections; monitor for toxicity and reduce venetoclax dose. (4.6, 5.10, 7.16). 5.1 Calcineurin-Inhibitor Toxicity. Concomitant administration of Posaconazole with cyclosporine or tacrolimus increases the whole blood trough concentrations of these calcineurin-inhibitors [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)]. Nephrotoxicity and leukoencephalopathy (including deaths) have been reported in clinical efficacy studies in patients with elevated cyclosporine or tacrolimus concentrations. Frequent monitoring of tacrolimus or cyclosporine whole blood trough concentrations should be performed during and at discontinuation of Posaconazole treatment and the tacrolimus or cyclosporine dose adjusted accordingly.. 5.2 Arrhythmias and QT Prolongation. Some azoles, including Posaconazole, have been associated with prolongation of the QT interval on the electrocardiogram. In addition, cases of torsades de pointes have been reported in patients taking Posaconazole.Results from multiple time-matched ECG analysis in healthy volunteers did not show any increase in the mean of the QTc interval. Multiple, time-matched ECGs collected over 12-hour period were recorded at baseline and steady-state from 173 healthy male and female volunteers (18-85 years of age) administered Noxafil(R) oral suspension 400 mg twice daily with high-fat meal. In this pooled analysis, the mean QTc (Fridericia) interval change from baseline was -5 msec following administration of the recommended clinical dose. decrease in the QTc(F) interval (-3 msec) was also observed in small number of subjects (n=16) administered placebo. The placebo-adjusted mean maximum QTc(F) interval change from baseline was <0 msec (-8 msec). No healthy subject administered Posaconazole had QTc(F) interval >=500 msec or an increase >=60 msec in their QTc(F) interval from baseline.Posaconazole should be administered with caution to patients with potentially proarrhythmic conditions. Do not administer with drugs that are known to prolong the QTc interval and are metabolized through CYP3A4 [see Contraindications (4.3) and Drug Interactions (7.2)].. 5.3 Electrolyte Disturbances. Electrolyte disturbances, especially those involving potassium, magnesium or calcium levels, should be monitored and corrected as necessary before and during Posaconazole therapy.. 5.4 Hepatic Toxicity. Hepatic reactions (e.g., mild to moderate elevations in alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase, total bilirubin, and/or clinical hepatitis) have been reported in clinical trials. The elevations in liver tests were generally reversible on discontinuation of therapy, and in some instances these tests normalized without drug interruption. Cases of more severe hepatic reactions including cholestasis or hepatic failure including deaths have been reported in patients with serious underlying medical conditions (e.g., hematologic malignancy) during treatment with Posaconazole. These severe hepatic reactions were seen primarily in subjects receiving the Noxafil(R) oral suspension 800 mg daily (400 mg twice daily or 200 mg four times day) in clinical trials. Liver tests should be evaluated at the start of and during the course of Posaconazole therapy. Patients who develop abnormal liver tests during Posaconazole therapy should be monitored for the development of more severe hepatic injury. Patient management should include laboratory evaluation of hepatic function (particularly liver tests and bilirubin). Discontinuation of Posaconazole must be considered if clinical signs and symptoms consistent with liver disease develop that may be attributable to Posaconazole.. 5.5 Renal Impairment. Posaconazole injection should be avoided in patients with moderate or severe renal impairment (eGFR <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection. In patients with moderate or severe renal impairment (eGFR <50 mL/min), receiving the Posaconazole injection, accumulation of the intravenous vehicle, SBECD, is expected to occur. Serum creatinine levels should be closely monitored in these patients, and, if increases occur, consideration should be given to changing to oral Posaconazole therapy [see Dosage and Administration (2.9) and Use in Specific Populations (8.6)].. 5.6 Midazolam Toxicity. Concomitant administration of Posaconazole with midazolam increases the midazolam plasma concentrations by approximately 5-fold. Increased plasma midazolam concentrations could potentiate and prolong hypnotic and sedative effects. Patients must be monitored closely for adverse effects associated with high plasma concentrations of midazolam and benzodiazepine receptor antagonists must be available to reverse these effects [see Drug Interactions (7.5) and Clinical Pharmacology (12.3)].. 5.7 Vincristine Toxicity. Concomitant administration of azole antifungals, including Posaconazole, with vincristine has been associated with neurotoxicity and other serious adverse reactions, including seizures, peripheral neuropathy, syndrome of inappropriate antidiuretic hormone secretion, and paralytic ileus. Reserve azole antifungals, including Posaconazole, for patients receiving vinca alkaloid, including vincristine, who have no alternative antifungal treatment options [see Drug Interactions (7.10)].. 5.10 Venetoclax Toxicity. Concomitant administration of Posaconazole, strong CYP3A4 inhibitor, with venetoclax may increase venetoclax toxicities, including the risk of tumor lysis syndrome (TLS), neutropenia, and serious infections. In patients with CLL/SLL, administration of Posaconazole during initiation and the ramp-up phase of venetoclax is contraindicated [see Contraindications (4.6)]. Refer to the venetoclax labeling for safety monitoring and dose reduction in the steady daily dosing phase in CLL/SLL patients.For patients with acute myeloid leukemia (AML), dose reduction and safety monitoring are recommended across all dosing phases when coadministering Posaconazole with venetoclax [see Drug Interactions (7.16)]. Refer to the venetoclax prescribing information for dosing instructions.

ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The following serious and otherwise important adverse reactions are discussed in detail in another section of the labeling:Hypersensitivity [see Contraindications (4.1)] Arrhythmias and QT Prolongation [see Warnings and Precautions (5.2)] Hepatic Toxicity [see Warnings and Precautions (5.4)] Hypersensitivity [see Contraindications (4.1)] Arrhythmias and QT Prolongation [see Warnings and Precautions (5.2)] Hepatic Toxicity [see Warnings and Precautions (5.4)] Adult Patients: Common adverse reactions in studies with Posaconazole in adults are diarrhea, nausea, fever, vomiting, headache, coughing, and hypokalemia. (6.1)Pediatric Patients: Common adverse reactions (incidence >20% receiving mg/kg Posaconazole injection in study in pediatric patients are pyrexia, febrile neutropenia, vomiting, mucosal inflammation, pruritus, hypertension, hypokalemia, and stomatitis. (6.1)To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Adult Patients: Common adverse reactions in studies with Posaconazole in adults are diarrhea, nausea, fever, vomiting, headache, coughing, and hypokalemia. (6.1). Pediatric Patients: Common adverse reactions (incidence >20% receiving mg/kg Posaconazole injection in study in pediatric patients are pyrexia, febrile neutropenia, vomiting, mucosal inflammation, pruritus, hypertension, hypokalemia, and stomatitis. (6.1). 6.1 Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of Posaconazole cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.. Clinical Trial Experience in AdultsClinical Trial Experience with Posaconazole Injection and Noxafil(R) Delayed-Release Tablets for the Treatment of Invasive AspergillosisThe safety of Posaconazole injection and Noxafil(R) delayed-release tablet was assessed in randomized, double-blind, active-controlled clinical study of Posaconazole injection and Noxafil(R) delayed-release tablets versus voriconazole for treatment of invasive aspergillosis (Aspergillosis Treatment Study). total of 575 (288 in Posaconazole arm, 287 in voriconazole arm) adult and pediatric patients 13 years of age and older with proven, probable or possible invasive aspergillosis were included. The median duration of treatment was 67 days for Posaconazole injection or Noxafil(R) delayed-release tablet and 64 days for voriconazole, with 55% to 60% of subjects starting treatment with the IV formulation of either drug. The median duration of the first instance of IV treatment (before switching to oral treatment or discontinuing or completing study treatment) was days for both groups. Table presents adverse reactions reported at an incidence of >=10% in either one of the groups in Aspergillosis Treatment Study.Adverse reactions leading to treatment discontinuation were reported for 33.9% of subjects. The most commonly reported adverse reactions (>2% of subjects) leading to treatment discontinuation were septic shock, respiratory failure, and bronchopulmonary aspergillosis in the Posaconazole arm, and septic shock and acute myeloid leukemia in the voriconazole arm.Table 7: Posaconazole Invasive Aspergillosis Treatment Study: Adverse Reactions in at Least 10% of Subjects Treated with Posaconazole Injection or Noxafil(R) Delayed-Release TabletsSystem Organ ClassPosaconazole injection or tablet (N 288), (%)Voriconazole injection or oral (N 287), (%)Blood and lymphatic system disorders Anemia25 (8.7)29 (10.1) Febrile neutropenia42 (14.6)38 (13.2)Gastrointestinal disorders Abdominal pain29 (10.1)24 (8.4) Constipation32 (11.1)23 (8.0) Diarrhea52 (18.1)52 (18.1) Nausea65 (22.6)51 (17.8) Vomiting52 (18.1)39 (13.6)General disorders and administration site conditions Edema peripheral32 (11.1)24 (8.4) Pyrexia81 (28.1)72 (25.1)Infections and infestations Pneumonia36 (12.5)26 (9.1)Investigations Alanine aminotransferase increased42 (14.6)37 (12.9) Aspartate aminotransferase increased38 (13.2)36 (12.5) Blood alkaline phosphatase increased21 (7.3)29 (10.1)Metabolism and nutrition disorders Hypokalemia82 (28.5)49 (17.1) Hypomagnesemia29 (10.1)18 (6.3)Nervous system disorders Headache35 (12.2)25 (8.7)Respiratory, thoracic and mediastinal disorders Cough30 (10.4)24 (8.4) Epistaxis32 (11.1)17 (5.9)The most frequently reported adverse reactions in the Posaconazole-treated group were pyrexia (28%), hypokalemia (28%), and nausea (23%).. Clinical Trial Experience with Posaconazole Injection for ProphylaxisMultiple doses of Posaconazole injection administered via peripheral venous catheter were associated with thrombophlebitis (60% incidence). Therefore, in subsequent studies, Posaconazole injection was administered via central venous catheter.The safety of Posaconazole injection has been assessed in 268 patients in clinical trial. Patients were enrolled in non-comparative pharmacokinetic and safety trial of Posaconazole injection when given as antifungal prophylaxis (Posaconazole Injection Study). Patients were immunocompromised with underlying conditions including hematological malignancy, neutropenia post-chemotherapy, GVHD, and post HSCT. This patient population was 55% male, had mean age of 51 years (range 18-82 years, 19% of patients were >=65 years of age), and were 95% white and 8% Hispanic. Ten patients received single dose of 200 mg Posaconazole injection, 21 patients received 200 mg daily dose for median of 14 days, and 237 patients received 300 mg daily dose for median of days.Table presents adverse reactions observed in patients treated with Posaconazole injection 300 mg daily dose in the Posaconazole Injection Study. Each patient received loading dose, 300 mg twice on Day 1. Following Posaconazole intravenous therapy, patients received Noxafil(R) oral suspension to complete 28 days of total Posaconazole therapy.Table 8: Posaconazole Injection Study: Adverse Reactions in at Least 10% of Subjects Treated with Posaconazole Injection 300 mg Daily DoseAdverse reactions reported in patients with an onset during the Posaconazole intravenous dosing phase of the study.+Adverse reactions reported with an onset at any time during the study in patients who were treated for up to 28 days of Posaconazole therapy.Body SystemPosaconazole Injection Treatment Phase n=237 (%)Posaconazole Injection Treatment Phase or Subsequent Noxafil(R) Oral Suspension Treatment Phase n=237 (%)+Subjects Reporting any Adverse Reaction220(93)235(99)Blood and Lymphatic System DisorderAnemia16(7)23(10)Thrombocytopenia17(7)25(11)Gastrointestinal DisordersAbdominal Pain Upper15(6)25(11)Abdominal Pain30(13)41(17)Constipation18(8)31(13)Diarrhea75(32)93(39)Nausea46(19)70(30)Vomiting29(12)45(19)General Disorders and Administration Site ConditionsFatigue19(8)24(10)Chills28(12)38(16)Edema Peripheral28(12)35(15)Pyrexia49(21)73(31)Metabolism and Nutrition DisordersDecreased appetite23(10)29(12)Hypokalemia51(22)67(28)Hypomagnesemia25(11)30(13)Nervous System DisordersHeadache33(14)49(21)Respiratory, Thoracic and Mediastinal DisordersCough21(9)31(13)Dyspnea16(7)24(10)Epistaxis34(14)40(17)Skin and Subcutaneous Tissue DisordersPetechiae20(8)24(10)Rash35(15)56(24)Vascular DisordersHypertension20(8)26(11)The most frequently reported adverse reactions with an onset during the Posaconazole intravenous phase of dosing with 300 mg once daily were diarrhea (32%), hypokalemia (22%), pyrexia (21%), and nausea (19%). These adverse reactions were consistent with those seen in studies with Noxafil(R) oral suspension.. Clinical Trial Experience in Pediatrics. Clinical Trial Experience in Pediatric Patients (2 to less than 18 Years of Age)The safety of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension for prophylaxis of invasive fungal infections has been assessed in an open label uncontrolled dose-ranging PK and safety study (Posaconazole injection/ Noxafil(R) PowderMix for delayed-release oral suspension Pediatric Study 1, NCT02452034); hereinafter referred to as Posaconazole Pediatric Study) in 115 immunocompromised pediatric patients to less than 18 years of age with known or expected neutropenia. Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension was administered at daily doses of up to mg/kg (twice daily on day 1) in three dose cohorts. All 115 subjects initially received Posaconazole injection for at least days, and 63 subjects were transitioned to Noxafil(R) PowderMix for delayed-release oral suspension. The mean overall treatment duration for all treated subjects was 20.6 days with 14.3 days (range: to 28 days) on Posaconazole injection and 11.6 days (range: to 18 days) on Noxafil(R) PowderMix for delayed-release oral suspension [see Clinical Pharmacology (12.3)]. Table 15 presents adverse reactions observed in greater than or equal to 10% of pediatric patients treated with Posaconazole in the Posaconazole Pediatric Study.Reported adverse reaction profile of Posaconazole in pediatric patients was consistent with the safety profile of Posaconazole in adults. The most common adverse reactions (occurring in greater than 20% of pediatric patients receiving mg/kg Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension daily dose) were pyrexia, febrile neutropenia, vomiting, mucosal inflammation, pruritus, hypertension, hypokalemia, and stomatitis.Table 15: Adverse Reactions in at Least 10% of Pediatric Patients Treated with Posaconazole Injection and Noxafil(R) PowderMix for Delayed-Release Oral SuspensionAdverse ReactionPosaconazole Injection andNoxafil(R) PowderMix for Delayed-Release Oral Suspension6 mg/kg Dose Cohort n=49 (%)Posaconazole Injection andNoxafil(R) PowderMix for Delayed-Release Oral SuspensionAll Dose Cohorts n=115 (%)Pyrexia16 (33)50 (43)Febrile neutropenia15 (31)25 (22)Vomiting12 (24)30 (26)Mucosal inflammation11 (22)32 (28)Pruritus11 (22)18 (16)Hypertension10 (20)20 (17)Hypokalemia10 (20)16 (14)Stomatitis10 (20)13 (11)Diarrhea9 (18)25 (22)Nausea9 (18)18 (16)Abdominal pain8 (16)20 (17)Decreased appetite7 (14)17 (15)Rash7 (14)18 (16)Alanine aminotransferase increased6 (12)8 (7)Headache6 (12)16 (14)Aspartate aminotransferase increased5 (10)8 (7)The number of patients receiving Posaconazole in the Posaconazole Pediatric Study who had changes in liver tests from Grade 0, 1, or at baseline to Grade or is presented in Table 16.Table 16: Posaconazole Pediatric Study: Changes in Liver Tests from CTC Grade 0, 1, or at Baseline to Grade or 4Change from Grade to at baseline to Grade or during the study. These data are presented in the form X/Y, where represents the number of patients who met the criterion as indicated, and represents the number of patients who had baseline observation and at least one post-baseline observation.CTC Common Toxicity Criteria; AST= Aspartate Aminotransferase; ALT= Alanine AminotransferaseNumber (%) of Patients with ChangePediatric Study 1Laboratory ParameterPosaconazole Injection and Noxafil(R) PowderMix for Delayed- Release Oral Suspension (6 mg/kg daily)n=49 (%)AST2/49 (4)ALT3/49 (6)Bilirubin0/48 (0)Alkaline Phosphatase0/48 (0). 6.2 Postmarketing Experience. The following adverse reaction has been identified during the post-approval use of Posaconazole. Because these reactions are reported voluntarily from population of uncertain size, it is not always possible to reliably estimate their frequency.Endocrine Disorders: Pseudoaldosteronism.

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. Posaconazole is an azole antifungal agent [see Clinical Pharmacology (12.4)].. 12.2 Pharmacodynamics. Exposure Response Relationship Prophylaxis: In clinical studies of neutropenic patients who were receiving cytotoxic chemotherapy for acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS) or hematopoietic stem cell transplant (HSCT) recipients with Graft versus Host Disease (GVHD), wide range of plasma exposures to posaconazole was noted following administration of Noxafil(R) oral suspension. pharmacokinetic-pharmacodynamic analysis of patient data revealed an apparent association between average posaconazole concentrations (Cavg) and prophylactic efficacy (Table 17). lower Cavg may be associated with an increased risk of treatment failure, defined as treatment discontinuation, use of empiric systemic antifungal therapy (SAF), or occurrence of breakthrough invasive fungal infections.Table 17: Noxafil(R) Oral Suspension Exposure Analysis (Cavg) in Prophylaxis TrialsCavg the average posaconazole concentration when measured at steady state Neutropenic patients who were receiving cytotoxic chemotherapy for AML or MDS+ HSCT recipients with GVHD Defined as treatment discontinuation, use of empiric systemic antifungal therapy (SAF), or occurrence of breakthrough invasive fungal infectionsProphylaxis in AML/MDSProphylaxis in GVHD+Cavg Range (ng/mL)Treatment Failure (%)Cavg Range (ng/mL)Treatment Failure (%)Quartile 190-32254.722-55744.4Quartile 2322-49037.0557-91520.6Quartile 3490-73446.8915-156317.5Quartile 4734-220027.81563-365017.5. Exposure Response Relationship Treatment of Invasive Aspergillosis:Across range of posaconazole plasma minimum concentrations (Cmin, range: 244 to 5663 ng/mL) following administration of Posaconazole injection and Noxafil(R) delayed-release tablets in patients treated for invasive aspergillosis in Aspergillosis Treatment Study, there was no association between posaconazole Cmin and treatment efficacy [see Clinical Pharmacology (12.3) and Clinical Studies (14.1)]. Similarly, across range of population pharmacokinetic model-predicted steady-state plasma average concentrations (Cavg, range: 589 to 6315 ng/mL), there was no association between posaconazole Cavg and treatment efficacy.. 12.3 Pharmacokinetics. General Pharmacokinetic Characteristics. Posaconazole InjectionPosaconazole injection exhibits dose proportional pharmacokinetics after single doses between 200 and 300 mg in healthy volunteers and patients. The mean pharmacokinetic parameters after single doses with Posaconazole injection in healthy volunteers and patients are shown in Table 18.Table 18: Summary of Mean Pharmacokinetic Parameters (%CV) in Healthy Volunteers (30-minute infusion via peripheral venous line) and Patients (90 minute infusion via central venous line) after Dosing with Posaconazole Injection on Day 1AUC0- Area under the plasma concentration-time curve from time zero to infinity; AUC0-12 Area under the plasma concentration- time curve from time zero to 12 hr after the first dose on Day 1; Cmax maximum observed concentration; 1/2 terminal phase half- life; CL total body clearance; N/D Not DeterminedDose (mg)nAUC0-(ng.hr/mL)AUC0-12(ng.hr/mL)Cmax(ng/mL)t1/2(hr)CL(L/hr)Healthy Volunteers200935400 (50)8840 (20)2250 (29)23.6 (23)6.5 (32)300946400 (26)13000 (13)2840 (30)24.6 (20)6.9 (27)Patients20030N/D5570 (32)954 (44)N/DN/D30022N/D8240 (26)1590 (62)N/DN/DTable 19 displays the pharmacokinetic parameters of posaconazole in patients following administration of Posaconazole injection 300 mg taken once day for 10 or 14 days following twice daily dosing on Day 1.Table 19: Arithmetic Mean (%CV) of PK Parameters in Serial PK-Evaluable Patients Following Dosing of Posaconazole Injection (300 mg)AUC0-24 area under the concentration-time curve over the dosing interval (i.e. 24 hours); Cav= time-averaged concentrations (i.e., AUC0-24h/24hr);Cmin POS trough level immediately before subject received the dose of POS on the day specified in the protocol; Cmax observed maximum plasma concentration; CV coefficient of variation, expressed as percent (%); Day study day on treatment; Tmax time of observed maximum plasma concentration. 300 mg dose administered over 90 minutes once day following twice daily dosing on Day 1+ Median (minimum-maximum)DayNCmax(ng/mL)Tmax+(hr)AUC0-24(nghr/mL)Cav (ng/mL)Cmin(ng/mL)10/14493280 (74)1.5 (0.98-4.0)36100 (35)1500 (35)1090 (44). Distribution:The mean volume of distribution of posaconazole after intravenous solution administration was 261 and ranged from 226-295 between studies and dose levels.Posaconazole is highly bound to human plasma proteins (>98%), predominantly to albumin.. Metabolism:Posaconazole primarily circulates as the parent compound in plasma. Of the circulating metabolites, the majority are glucuronide conjugates formed via UDP glucuronidation (phase enzymes). Posaconazole does not have any major circulating oxidative (CYP450 mediated) metabolites. The excreted metabolites in urine and feces account for ~17% of the administered radiolabeled dose.Posaconazole is primarily metabolized via UDP glucuronidation (phase enzymes) and is substrate for p-glycoprotein (P-gp) efflux. Therefore, inhibitors or inducers of these clearance pathways may affect posaconazole plasma concentrations. summary of drugs studied clinically with the oral suspension or an early tablet formulation, which affect posaconazole concentrations, is provided in Table 27. Table 27: Summary of the Effect of Coadministered Drugs on Posaconazole in Healthy Volunteers Ratio Estimate is the ratio of coadministered drug plus Posaconazole to Posaconazole alone for Cmax or AUC.+ The tablet refers to non-commercial tablet formulation without polymer.Coadministered Drug (Postulated Mechanism of Interaction)Coadministered Drug Dose/SchedulePosaconazole Dose/ScheduleEffect on Bioavailability of PosaconazoleChange in MeanCmax(ratio estimate; 90% CI of the ratio estimate)Change in Mean AUC(ratio estimate; 90% CI of the ratio estimate)Efavirenz400 mg once daily 10 and400 mg (oral45% 50%(UDP-G Induction)20 dayssuspension) twice daily 10 and 20 days(0.55; 0.47-0.66)(0.50; 0.43-0.60)Fosamprenavir700 mg twice daily x10 days200 mg once daily on the 1st 21%23%(unknown mechanism)day, 200 mg twice daily onthe 2nd day, then 4000.79 (0.71-0.89)0.77 (0.68-0.87)mg twice daily 8 DaysRifabutin(UDP-G Induction)300 mg once daily x17 days200 mg (tablets) oncedaily 10 days+ 43%(0.57; 0.43-0.75) 49%(0.51; 0.37-0.71)Phenytoin(UDP-G Induction)200 mg once daily x10 days200 mg (tablets) oncedaily 10 days+ 41%(0.59; 0.44-0.79) 50%(0.50; 0.36-0.71)In vitro studies with human hepatic microsomes and clinical studies indicate that posaconazole is an inhibitor primarily of CYP3A4. clinical study in healthy volunteers also indicates that posaconazole is strong CYP3A4 inhibitor as evidenced by >5-fold increase in midazolam AUC. Therefore, plasma concentrations of drugs predominantly metabolized by CYP3A4 may be increased by posaconazole. summary of the drugs studied clinically, for which plasma concentrations were affected by posaconazole, is provided in Table 28 [see Contraindications (4) and Drug Interactions (7.1) including recommendations].Table 28: Summary of the Effect of Posaconazole on Coadministered Drugs in Healthy Adult Volunteers and Patients Ratio Estimate is the ratio of coadministered drug plus Posaconazole to coadministered drug alone for Cmax or AUC.+ The tablet refers to non-commercial tablet formulation without polymer. The mean terminal half-life of midazolam was increased from hours to to 11 hours during coadministration with Posaconazole.Coadministered Drug (Postulated Mechanism of Interaction is Inhibition of CYP3A4 byposaconazole)Coadministered Drug Dose/SchedulePosaconazole Dose/ ScheduleEffect on Bioavailability of CoadministeredDrugsChange in MeanCmax(ratio estimate; 90% CI of the ratio estimate)Change in Mean AUC (ratio estimate; 90% CI of the ratio estimate)Sirolimus2-mg single oral dose400 mg (oral suspension) twice daily 16 days 572%(6.72; 5.62-8.03) 788%(8.88; 7.26-10.9)CyclosporineStable maintenance dose in heart transplant recipients200 mg (tablets) once daily 10 days+ cyclosporine whole blood trough concentrationsCyclosporine dose reductions of up to 29% were requiredTacrolimus0.05-mg/kg single oral dose400 mg (oral suspension) twice daily 7 days 121%(2.21; 2.01-2.42) 358%(4.58; 4.03-5.19)Simvastatin40-mg single oral dose100 mg (oral suspension)SimvastatinSimvastatinonce daily 13 days 841% 931%(9.41, 7.13-12.44)(10.31, 8.40-12.67)Simvastatin AcidSimvastatin Acid 817%634%(9.17, 7.36-11.43)(7.34, 5.82-9.25)200 mg (oral suspension)SimvastatinSimvastatinonce daily 13 days 1041% 960%(11.41, 7.99-16.29)(10.60, 8.63-13.02)Simvastatin AcidSimvastatin Acid851%748%(9.51, 8.15-11.10)(8.48, 7.04-10.23)Midazolam0.4-mg single200 mg (oral suspension) 30% 362%intravenous dose twice daily 7 days(1.3; 1.13-1.48)(4.62; 4.02-5.3)0.4-mg single400 mg (oral suspension)62%524%intravenous dose twice daily 7 days(1.62; 1.41-1.86)(6.24; 5.43-7.16)2-mg single oral dose200 mg (oral suspension) once daily 7 days 169%(2.69; 2.46-2.93) 470%(5.70; 4.82-6.74)2-mg single oral dose400 mg (oral suspension) twice daily 7 days 138%(2.38; 2.13-2.66) 397%(4.97; 4.46-5.54)Rifabutin300 mg once daily 17 days200 mg (tablets) once dailyx 10 days+ 31%(1.31; 1.10-1.57) 72%(1.72;1.51-1.95)Phenytoin200 mg once daily PO 10days200 mg (tablets) once dailyx 10 days+ 16%(1.16; 0.85-1.57) 16%(1.16; 0.84-1.59)Ritonavir100 mg once daily 14 days400 mg (oral suspension) twice daily 7 days 49%(1.49; 1.04-2.15) 80%(1.8;1.39-2.31)Atazanavir300 mg once daily 14 days400 mg (oral suspension) 155% 268%twice daily 7 days(2.55; 1.89-3.45)(3.68; 2.89-4.70)Atazanavir/ritonavir boosted300 mg/100 mg once daily400 mg (oral suspension) 53% 146%regimenx 14 daystwice daily 7 days(1.53; 1.13-2.07)(2.46; 1.93-3.13)Additional clinical studies demonstrated that no clinically significant effects on zidovudine, lamivudine, indinavir, or caffeine were observed when administered with Posaconazole 200 mg once daily; therefore, no dose adjustments are required for these coadministered drugs when coadministered with Posaconazole 200 mg once daily.. Excretion:Following administration of Noxafil(R) oral suspension, posaconazole is predominantly eliminated in the feces (71% of the radiolabeled dose up to 120 hours) with the major component eliminated as parent drug (66% of the radiolabeled dose). Renal clearance is minor elimination pathway, with 13% of the radiolabeled dose excreted in urine up to 120 hours (<0.2% of the radiolabeled dose is parent drug).Posaconazole injection is eliminated with mean terminal half-life (t 1/2 of 27 hours and total body clearance (CL) of 7.3 L/h.. Specific PopulationsNo clinically significant differences in the pharmacokinetics of posaconazole were observed based on age, sex, renal impairment, and indication (prophylaxis or treatment).. Race/Ethnicity:In population pharmacokinetic analysis of posaconazole, AUC was found to be 25% higher in Chinese patients relative to patients from other races/ethnicities. This higher exposure is not expected to be clinically relevant given the expected variability in posaconazole exposure.. Patients Weighing More Than 120 kg:Weight has clinically significant effect on posaconazole clearance. Relative to 70 kg patients, the Cavg is decreased by 25% in patients greater than 120 kg. Patients administered Posaconazole weighing more than 120 kg may be at higher risk for lower posaconazole plasma concentrations compared to lower weight patients [see Use in Specific Populations (8.10)].. Pediatric PatientsThe mean pharmacokinetic parameters after multiple-dose administration of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension in neutropenic pediatric patients to less than 18 years of age are shown in Table 29. Patients were enrolled into age groups and received Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension doses at mg/kg (0.6 to times the recommended dose) with maximum 300 mg dose once daily (twice daily on Day 1) [see Adverse Reactions (6.1)].Table 29: Summary of Steady-State Geometric Mean Pharmacokinetic Parameters (% Geometric CV) After Multiple Dosing with Posaconazole Injection and Noxafil(R) PowderMix for Delayed-Release Oral Suspension mg/kg in Pediatric Patients with Neutropenia or Expected NeutropeniaIV= Posaconazole injection; PFS= Noxafil(R) PowderMix for delayed-release oral suspension; AUC0-24 Area under the plasma concentration-time curve from time zero to 24 hr; Cmax maximum observed concentration; Cmin minimum observed plasma concentration; Tmax time of maximum observed concentration; CL /F apparent total body clearance 0.6 to times the recommended dose+ Cav time-averaged concentrations (i.e., AUC0-24 hr/24hr) Median (minimum-maximum) Clearance (CL for IV and CL/F for PFS)Age GroupDose TypeNAUC0-24 hr(ng.hr/mL)Cav+(ng/mL)Cmax(ng/mL)Cmin(ng/mL)T max (hr) CL/F(L/hr)2 to <7IV1731100130030606261.753.27years(48.9)(48.9)(54.1)(104.8)(1.57-1.83)(49.3)PFS723000960 (47.3)15105424.004.60(47.3)(43.4)(68.8)(2.17-7.92)(35.2)7 to 17 yearsIV2444200(41.5)1840(41.5)3340(39.4)1160(60.4)1.77(1.33-6.00)4.76(55.7)PFS1225000(184.3)1040(184.3)1370(178.5)713(300.6)2.78(0.00-4.00)8.39(190.3)Based on population pharmacokinetic model evaluating posaconazole pharmacokinetics and predicting exposures in pediatric patients, the exposure of steady-state posaconazole average concentration greater than or equal to 700 ng/mL in approximately 90% of patients is attained with the recommended dose of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension.The population pharmacokinetic analysis of posaconazole in pediatric patients suggests that age, sex, renal impairment and ethnicity have no clinically meaningful effect on the pharmacokinetics of posaconazole.A total of 12 patients 13 to 17 years of age received 600 mg/day (200 mg three times day) of Noxafil(R) oral suspension for prophylaxis of invasive fungal infections. Based on pharmacokinetic data in 10 of these pediatric patients, the mean steady-state Cav was similar between these patients and adults (>=18 years of age). In study of 136 neutropenic pediatric patients 11 months to less than 18 years treated with Noxafil(R) oral suspension, the exposure target of steady-state posaconazole Cavg between 500 ng/mL and less than 2500 ng/mL was attained in approximately 50% of patients instead of the pre-specified 90% of patients.. 12.4 Microbiology. Mechanism of Action:Posaconazole blocks the synthesis of ergosterol, key component of the fungal cell membrane, through the inhibition of cytochrome P-450 dependent enzyme lanosterol 14-demethylase responsible for the conversion of lanosterol to ergosterol in the fungal cell membrane. This results in an accumulation of methylated sterol precursors and depletion of ergosterol within the cell membrane thus weakening the structure and function of the fungal cell membrane. This may be responsible for the antifungal activity of posaconazole.. Resistance:Clinical isolates of Candida albicans and Candida glabrata with decreased susceptibility to posaconazole were observed in oral swish samples taken during prophylaxis with posaconazole and fluconazole, suggesting potential for development of resistance. These isolates also showed reduced susceptibility to other azoles, suggesting cross-resistance between azoles. The clinical significance of this finding is not known.. Antimicrobial Activity:Posaconazole has been shown to be active against most isolates of the following microorganisms, both in vitro and in clinical infections [see Indications and Usage (1)].. Microorganisms:Aspergillus spp. and Candida spp. Susceptibility Testing:For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see:https://www.fda.gov/STIC.

CLINICAL STUDIES SECTION.

14 CLINICAL STUDIES. 14.1 Treatment of Invasive Aspergillosis with Posaconazole Injection and Noxafil(R) Delayed-Release Tablets. Aspergillosis Treatment Study (NCT01782131) was randomized, double-blind, controlled trial which evaluated the safety and efficacy of Posaconazole injection and Noxafil(R) delayed-release tablets versus voriconazole for primary treatment of invasive fungal disease caused by Aspergillus species. Eligible patients had proven, probable, or possible invasive fungal infections per the European Organization for Research and Treatment of Cancer/Mycoses Study Group, EORTC/MSG criteria. Patients were stratified by risk for mortality or poor outcome where high risk included history of allogeneic bone marrow transplant, liver transplant, or relapsed leukemia undergoing salvage chemotherapy. The median age of patients was 57 years (range 14-91 years), with 27.8% of patients aged >=65 years; patients were pediatric patients 14-16 years of age, of whom were treated with Posaconazole and with voriconazole. The majority of patients were male (59.8%) and white (67.1%). With regard to risk factors for invasive aspergillosis, approximately two- thirds of the patients in the study had recent history of neutropenia, while approximately 20% with history of an allogeneic stem cell transplant. Over 80% of subjects in each treatment group had infection limited to the lower respiratory tract (primarily lung), while approximately 11% to 13% also had infection in another organ. Invasive aspergillosis was proven or probable in 58.1% of patients as classified by independent adjudicators blinded to study treatment assignment. At least one Aspergillus species was identified in 21% of the patients; A. fumigatus and A. flavus were the most common pathogens identified.Patients randomized to receive Posaconazole were given dose of 300 mg once daily (twice daily on Day 1) IV or tablet. Patients randomized to receive voriconazole were given dose of mg/kg twice daily Day followed by mg/kg twice daily IV, or oral 300 mg twice daily Day followed by 200 mg twice daily. The recommended initial route of administration was IV; however, patients could begin oral therapy if clinically stable and able to tolerate oral dosing. The transition from IV to oral therapy occurred when the patient was clinically stable. The protocol recommended duration of therapy was 84 days with maximum allowed duration of 98 days. Median treatment duration was 67 days for Posaconazole patients and 64 days for voriconazole patients. Overall, 55% to 60% of patients began treatment with the IV formulation with median duration of days for the initial IV dosing.The Intent to Treat (ITT) population included all patients randomized and receiving at least one dose of study treatment. All-cause mortality through Day 42 in the overall population (ITT) was 15.3% for Posaconazole patients compared to 20.6% for voriconazole patients for an adjusted treatment difference of -5.3% with 95% confidence interval of -11.6 to 1.0%. Consistent results were seen in patients with proven or probable invasive aspergillosis per EORTC criteria (see Table 30).Table 30: Posaconazole Injection and Noxafil(R) Delayed-Release Tablets Invasive Aspergillosis Treatment Study: All-Cause Mortality Through Day 42 Adjusted treatment difference based on Miettinen and Nurminens method stratified by randomization factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme.Posaconazole Injection and Delayed- Release TabletsVoriconazolePopulationNn (%)Nn (%)Difference (95% CI)Intent to Treat28844 (15.3)28759 (20.6)-5.3 (-11.6, 1.0)Proven/Probable Invasive Aspergillosis16331 (19.0)17132 (18.7)0.3 (-8.2, 8.8)Global clinical response at Week was assessed by blinded, independent adjudication committee based upon prespecified clinical, radiologic, and mycologic criteria. In the subgroup of patients with proven or probable invasive aspergillosis per EORTC criteria, the global clinical response of success (complete or partial response) at Week was seen in 44.8% for Posaconazole-treated patients compared to 45.6% for voriconazole-treated patients (see Table 31).Table 31: Posaconazole Injection and Noxafil(R) Delayed-Release Tablets Invasive Aspergillosis Treatment Study: Successful Global Clinical Response at Week Successful Global Clinical Response was defined as survival with partial or complete response+ Adjusted treatment difference based on Miettinen and Nurminens method stratified by randomization factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme.PosaconazoleVoriconazolePopulationNSuccessNSuccessDifference+ (95% CI)Proven/Probable Invasive Aspergillosis16373 (44.8)17178 (45.6)-0.6 (-11.2, 10.1).

CLINICAL TRIALS EXPERIENCE SECTION.

6.1 Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of Posaconazole cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.. Clinical Trial Experience in AdultsClinical Trial Experience with Posaconazole Injection and Noxafil(R) Delayed-Release Tablets for the Treatment of Invasive AspergillosisThe safety of Posaconazole injection and Noxafil(R) delayed-release tablet was assessed in randomized, double-blind, active-controlled clinical study of Posaconazole injection and Noxafil(R) delayed-release tablets versus voriconazole for treatment of invasive aspergillosis (Aspergillosis Treatment Study). total of 575 (288 in Posaconazole arm, 287 in voriconazole arm) adult and pediatric patients 13 years of age and older with proven, probable or possible invasive aspergillosis were included. The median duration of treatment was 67 days for Posaconazole injection or Noxafil(R) delayed-release tablet and 64 days for voriconazole, with 55% to 60% of subjects starting treatment with the IV formulation of either drug. The median duration of the first instance of IV treatment (before switching to oral treatment or discontinuing or completing study treatment) was days for both groups. Table presents adverse reactions reported at an incidence of >=10% in either one of the groups in Aspergillosis Treatment Study.Adverse reactions leading to treatment discontinuation were reported for 33.9% of subjects. The most commonly reported adverse reactions (>2% of subjects) leading to treatment discontinuation were septic shock, respiratory failure, and bronchopulmonary aspergillosis in the Posaconazole arm, and septic shock and acute myeloid leukemia in the voriconazole arm.Table 7: Posaconazole Invasive Aspergillosis Treatment Study: Adverse Reactions in at Least 10% of Subjects Treated with Posaconazole Injection or Noxafil(R) Delayed-Release TabletsSystem Organ ClassPosaconazole injection or tablet (N 288), (%)Voriconazole injection or oral (N 287), (%)Blood and lymphatic system disorders Anemia25 (8.7)29 (10.1) Febrile neutropenia42 (14.6)38 (13.2)Gastrointestinal disorders Abdominal pain29 (10.1)24 (8.4) Constipation32 (11.1)23 (8.0) Diarrhea52 (18.1)52 (18.1) Nausea65 (22.6)51 (17.8) Vomiting52 (18.1)39 (13.6)General disorders and administration site conditions Edema peripheral32 (11.1)24 (8.4) Pyrexia81 (28.1)72 (25.1)Infections and infestations Pneumonia36 (12.5)26 (9.1)Investigations Alanine aminotransferase increased42 (14.6)37 (12.9) Aspartate aminotransferase increased38 (13.2)36 (12.5) Blood alkaline phosphatase increased21 (7.3)29 (10.1)Metabolism and nutrition disorders Hypokalemia82 (28.5)49 (17.1) Hypomagnesemia29 (10.1)18 (6.3)Nervous system disorders Headache35 (12.2)25 (8.7)Respiratory, thoracic and mediastinal disorders Cough30 (10.4)24 (8.4) Epistaxis32 (11.1)17 (5.9)The most frequently reported adverse reactions in the Posaconazole-treated group were pyrexia (28%), hypokalemia (28%), and nausea (23%).. Clinical Trial Experience with Posaconazole Injection for ProphylaxisMultiple doses of Posaconazole injection administered via peripheral venous catheter were associated with thrombophlebitis (60% incidence). Therefore, in subsequent studies, Posaconazole injection was administered via central venous catheter.The safety of Posaconazole injection has been assessed in 268 patients in clinical trial. Patients were enrolled in non-comparative pharmacokinetic and safety trial of Posaconazole injection when given as antifungal prophylaxis (Posaconazole Injection Study). Patients were immunocompromised with underlying conditions including hematological malignancy, neutropenia post-chemotherapy, GVHD, and post HSCT. This patient population was 55% male, had mean age of 51 years (range 18-82 years, 19% of patients were >=65 years of age), and were 95% white and 8% Hispanic. Ten patients received single dose of 200 mg Posaconazole injection, 21 patients received 200 mg daily dose for median of 14 days, and 237 patients received 300 mg daily dose for median of days.Table presents adverse reactions observed in patients treated with Posaconazole injection 300 mg daily dose in the Posaconazole Injection Study. Each patient received loading dose, 300 mg twice on Day 1. Following Posaconazole intravenous therapy, patients received Noxafil(R) oral suspension to complete 28 days of total Posaconazole therapy.Table 8: Posaconazole Injection Study: Adverse Reactions in at Least 10% of Subjects Treated with Posaconazole Injection 300 mg Daily DoseAdverse reactions reported in patients with an onset during the Posaconazole intravenous dosing phase of the study.+Adverse reactions reported with an onset at any time during the study in patients who were treated for up to 28 days of Posaconazole therapy.Body SystemPosaconazole Injection Treatment Phase n=237 (%)Posaconazole Injection Treatment Phase or Subsequent Noxafil(R) Oral Suspension Treatment Phase n=237 (%)+Subjects Reporting any Adverse Reaction220(93)235(99)Blood and Lymphatic System DisorderAnemia16(7)23(10)Thrombocytopenia17(7)25(11)Gastrointestinal DisordersAbdominal Pain Upper15(6)25(11)Abdominal Pain30(13)41(17)Constipation18(8)31(13)Diarrhea75(32)93(39)Nausea46(19)70(30)Vomiting29(12)45(19)General Disorders and Administration Site ConditionsFatigue19(8)24(10)Chills28(12)38(16)Edema Peripheral28(12)35(15)Pyrexia49(21)73(31)Metabolism and Nutrition DisordersDecreased appetite23(10)29(12)Hypokalemia51(22)67(28)Hypomagnesemia25(11)30(13)Nervous System DisordersHeadache33(14)49(21)Respiratory, Thoracic and Mediastinal DisordersCough21(9)31(13)Dyspnea16(7)24(10)Epistaxis34(14)40(17)Skin and Subcutaneous Tissue DisordersPetechiae20(8)24(10)Rash35(15)56(24)Vascular DisordersHypertension20(8)26(11)The most frequently reported adverse reactions with an onset during the Posaconazole intravenous phase of dosing with 300 mg once daily were diarrhea (32%), hypokalemia (22%), pyrexia (21%), and nausea (19%). These adverse reactions were consistent with those seen in studies with Noxafil(R) oral suspension.. Clinical Trial Experience in Pediatrics. Clinical Trial Experience in Pediatric Patients (2 to less than 18 Years of Age)The safety of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension for prophylaxis of invasive fungal infections has been assessed in an open label uncontrolled dose-ranging PK and safety study (Posaconazole injection/ Noxafil(R) PowderMix for delayed-release oral suspension Pediatric Study 1, NCT02452034); hereinafter referred to as Posaconazole Pediatric Study) in 115 immunocompromised pediatric patients to less than 18 years of age with known or expected neutropenia. Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension was administered at daily doses of up to mg/kg (twice daily on day 1) in three dose cohorts. All 115 subjects initially received Posaconazole injection for at least days, and 63 subjects were transitioned to Noxafil(R) PowderMix for delayed-release oral suspension. The mean overall treatment duration for all treated subjects was 20.6 days with 14.3 days (range: to 28 days) on Posaconazole injection and 11.6 days (range: to 18 days) on Noxafil(R) PowderMix for delayed-release oral suspension [see Clinical Pharmacology (12.3)]. Table 15 presents adverse reactions observed in greater than or equal to 10% of pediatric patients treated with Posaconazole in the Posaconazole Pediatric Study.Reported adverse reaction profile of Posaconazole in pediatric patients was consistent with the safety profile of Posaconazole in adults. The most common adverse reactions (occurring in greater than 20% of pediatric patients receiving mg/kg Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension daily dose) were pyrexia, febrile neutropenia, vomiting, mucosal inflammation, pruritus, hypertension, hypokalemia, and stomatitis.Table 15: Adverse Reactions in at Least 10% of Pediatric Patients Treated with Posaconazole Injection and Noxafil(R) PowderMix for Delayed-Release Oral SuspensionAdverse ReactionPosaconazole Injection andNoxafil(R) PowderMix for Delayed-Release Oral Suspension6 mg/kg Dose Cohort n=49 (%)Posaconazole Injection andNoxafil(R) PowderMix for Delayed-Release Oral SuspensionAll Dose Cohorts n=115 (%)Pyrexia16 (33)50 (43)Febrile neutropenia15 (31)25 (22)Vomiting12 (24)30 (26)Mucosal inflammation11 (22)32 (28)Pruritus11 (22)18 (16)Hypertension10 (20)20 (17)Hypokalemia10 (20)16 (14)Stomatitis10 (20)13 (11)Diarrhea9 (18)25 (22)Nausea9 (18)18 (16)Abdominal pain8 (16)20 (17)Decreased appetite7 (14)17 (15)Rash7 (14)18 (16)Alanine aminotransferase increased6 (12)8 (7)Headache6 (12)16 (14)Aspartate aminotransferase increased5 (10)8 (7)The number of patients receiving Posaconazole in the Posaconazole Pediatric Study who had changes in liver tests from Grade 0, 1, or at baseline to Grade or is presented in Table 16.Table 16: Posaconazole Pediatric Study: Changes in Liver Tests from CTC Grade 0, 1, or at Baseline to Grade or 4Change from Grade to at baseline to Grade or during the study. These data are presented in the form X/Y, where represents the number of patients who met the criterion as indicated, and represents the number of patients who had baseline observation and at least one post-baseline observation.CTC Common Toxicity Criteria; AST= Aspartate Aminotransferase; ALT= Alanine AminotransferaseNumber (%) of Patients with ChangePediatric Study 1Laboratory ParameterPosaconazole Injection and Noxafil(R) PowderMix for Delayed- Release Oral Suspension (6 mg/kg daily)n=49 (%)AST2/49 (4)ALT3/49 (6)Bilirubin0/48 (0)Alkaline Phosphatase0/48 (0).

CONTRAINDICATIONS SECTION.

4 CONTRAINDICATIONS. Known hypersensitivity to posaconazole or other azole antifungal agents. (4.1)Coadministration of Posaconazole with the following drugs is contraindicated; Posaconazole increases concentrations and toxicities of:Sirolimus: (4.2, 5.1, 7.1)CYP3A4 substrates (pimozide, quinidine): can result in QTc interval prolongation and cases of torsades de pointes (TdP) (4.3, 5.2, 7.2)HMG-CoA Reductase Inhibitors Primarily Metabolized through CYP3A4 (4.4, 7.3)Ergot alkaloids (4.5, 7.4)Venetoclax: in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) at initiation and during the ramp of phase (4.6, 5.10, 7.16) Known hypersensitivity to posaconazole or other azole antifungal agents. (4.1). Coadministration of Posaconazole with the following drugs is contraindicated; Posaconazole increases concentrations and toxicities of:Sirolimus: (4.2, 5.1, 7.1)CYP3A4 substrates (pimozide, quinidine): can result in QTc interval prolongation and cases of torsades de pointes (TdP) (4.3, 5.2, 7.2)HMG-CoA Reductase Inhibitors Primarily Metabolized through CYP3A4 (4.4, 7.3)Ergot alkaloids (4.5, 7.4)Venetoclax: in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) at initiation and during the ramp of phase (4.6, 5.10, 7.16) Sirolimus: (4.2, 5.1, 7.1). CYP3A4 substrates (pimozide, quinidine): can result in QTc interval prolongation and cases of torsades de pointes (TdP) (4.3, 5.2, 7.2). HMG-CoA Reductase Inhibitors Primarily Metabolized through CYP3A4 (4.4, 7.3). Ergot alkaloids (4.5, 7.4). Venetoclax: in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) at initiation and during the ramp of phase (4.6, 5.10, 7.16). 4.1 Hypersensitivity. Posaconazole is contraindicated in persons with known hypersensitivity to posaconazole or other azole antifungal agents.. 4.2 Use with Sirolimus. Posaconazole is contraindicated with sirolimus. Concomitant administration of Posaconazole with sirolimus increases the sirolimus blood concentrations by approximately 9-fold and can result in sirolimus toxicity [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)].. 4.3 QT Prolongation with Concomitant Use with CYP3A4 Substrates. Posaconazole is contraindicated with CYP3A4 substrates that prolong the QT interval. Concomitant administration of Posaconazole with the CYP3A4 substrates, pimozide and quinidine may result in increased plasma concentrations of these drugs, leading to QTc prolongation and cases of torsades de pointes [see Warnings and Precautions (5.2) and Drug Interactions (7.2)].. 4.4 HMG-CoA Reductase Inhibitors Primarily Metabolized Through CYP3A4. Coadministration with the HMG-CoA reductase inhibitors that are primarily metabolized through CYP3A4 (e.g., atorvastatin, lovastatin, and simvastatin) is contraindicated since increased plasma concentration of these drugs can lead to rhabdomyolysis [see Drug Interactions (7.3) and Clinical Pharmacology (12.3)].. 4.5 Use with Ergot Alkaloids. Posaconazole may increase the plasma concentrations of ergot alkaloids (ergotamine and dihydroergotamine) which may lead to ergotism [see Drug Interactions (7.4)].. 4.6 Use with Venetoclax. Coadministration of Posaconzole with venetoclax at initiation and during the ramp-up phase is contraindicated in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) due to the potential for increased risk of tumor lysis syndrome [see Warnings and Precautions (5.10) and Drug Interactions (7.16)].

DOSAGE & ADMINISTRATION SECTION.

2 DOSAGE AND ADMINISTRATION. Posaconazole injection must be administered through an in-line filter.Administer Posaconazole injection by intravenous infusion over approximately 90 minutes via central venous line. (2.1)Do NOT administer Posaconazole injection as intravenous bolus injection. (2.1)Table 1: Recommended Dosage in Adult PatientsIndicationDosage Form, Dose, and Duration of TherapyTreatment of invasive AspergillosisPosaconazole Injection:Loading dose:300 mg Posaconazole injection intravenously twice day on the first day.Maintenance dose:300 mg Posaconazole injection intravenously once day thereafter. Recommended total duration of therapy is to 12 weeks. (2.2)Prophylaxis ofPosaconazole Injection:invasiveLoading dose: 300 mg Posaconazole injectionAspergillus andintravenously twice day on the first day.CandidaMaintenance dose: 300 mg Posaconazole injection intravenously once day thereafterinfectionsDuration of therapy is based on recovery from neutropenia or immunosuppression. (2.2, 2.3)For pediatric patients, see the Full Prescribing Information for dosing recommendations for Posaconazole injection, based on the age and indication associated with the dosage form. (1.1, 1.2, 2.1, 2.3). Posaconazole injection must be administered through an in-line filter.. Administer Posaconazole injection by intravenous infusion over approximately 90 minutes via central venous line. (2.1). Do NOT administer Posaconazole injection as intravenous bolus injection. (2.1). For pediatric patients, see the Full Prescribing Information for dosing recommendations for Posaconazole injection, based on the age and indication associated with the dosage form. (1.1, 1.2, 2.1, 2.3). 2.1 Important Administration Instructions. Posaconazole InjectionAdminister via central venous line, including central venous catheter or peripherally inserted central catheter (PICC), by slow intravenous infusion over approximately 90 minutes [see Dosage and Administration (2.4)].If central venous catheter is not available, Posaconazole injection may be administered through peripheral venous catheter by slow intravenous infusion over 30 minutes only as single dose in advance of central venous line placement or to bridge the period during which central venous line is replaced or is in use for other intravenous treatment.When multiple dosing is required, the infusion should be done via central venous line.Do NOT administer Posaconazole injection as an intravenous bolus injection.. Administer via central venous line, including central venous catheter or peripherally inserted central catheter (PICC), by slow intravenous infusion over approximately 90 minutes [see Dosage and Administration (2.4)].. If central venous catheter is not available, Posaconazole injection may be administered through peripheral venous catheter by slow intravenous infusion over 30 minutes only as single dose in advance of central venous line placement or to bridge the period during which central venous line is replaced or is in use for other intravenous treatment.. When multiple dosing is required, the infusion should be done via central venous line.. Do NOT administer Posaconazole injection as an intravenous bolus injection.. 2.2 Dosing Regimen in Adult Patients. Table 1: Dosing Regimens in Adult PatientsIndicationDose and FrequencyDuration of TherapyTreatment of invasive AspergillosisPosaconazole Injection:Loading dose:300 mg Posaconazole injection intravenously twice day on the first day.Maintenance dose:300 mg Posaconazole injection intravenously once day, starting on the second day.Switching between the intravenous and delayed-release tablets is acceptable. loading dose is not required when switching between formulations.Loading dose:1 dayMaintenance dose:Recommended total duration of therapy is to 12 weeks.Prophylaxis of invasive Aspergillusand Candida infectionsPosaconazole Injection:Loading dose:300 mg Posaconazole injection intravenously twice day on the first day.Maintenance dose:300 mg Posaconazole injection intravenously once day thereafter.Loading dose:1 dayMaintenance dose:Duration of therapy is based on recovery from neutropenia or immunosuppression.. 2.3 Dosing Regimen in Pediatric Patients (ages to less than 18 years of age). The recommended dosing regimen of Posaconazole for pediatric patients to less than 18 years of age is shown in Table [see Clinical Pharmacology (12.3)]. Table 2: Posaconazole Injection Dosing Regimens for Pediatric Patients (ages to less than 18 years of age)Recommended Pediatric Dosage and FormulationIndicationAgeInjectionDuration of therapyProphylaxis of invasive Aspergillusand Candida infectionsLess than or equal to 40 kg (2 to less than 18 years of age) Greater than 40 kg (2 to less than 18 years of age)Loading dose:6 mg/kg up to maximum of 300 mg twice daily on the first dayMaintenance dose:6 mg/kg up to maximum of 300 mg once dailyDuration of therapy is based on recovery from neutropenia or immunosuppression.Treatment of invasive Aspergillosis13 to less than 18 years of age regardless of weight.Loading dose:300 mg Posaconazole injection intravenously twice day on the first day.Maintenance dose:300 mg Posaconazole injection intravenously once day, starting on the second day.Switching between the intravenous and delayed-release tablets is acceptable. loading dose is not required when switching between formulations.Loading dose:1 dayMaintenance dose:Recommended total duration of therapy is to 12 weeks.. 2.4 Preparation, Intravenous Line Compatibility, and Administration of Posaconazole Injection. Preparation:Equilibrate the refrigerated vial of Posaconazole injection to room temperature.To prepare the required dose, aseptically transfer one vial (16.7 mL) of Posaconazole injection (containing 300 mg of posaconazole in solution) to an intravenous bag (or bottle) of compatible admixture diluent (as described in Table 5), to achieve final concentration of posaconazole that is between mg/mL and mg/mL. Use of other diluents is not recommended because they may result in particulate formation.Posaconazole injection is single-dose sterile solution without preservatives. Discard any unused portion from the vial.Once admixed, the diluted solution of Posaconazole in the intravenous bag (or bottle) should be used immediately. If not used immediately, the solution can be stored up to 24 hours refrigerated to 8C (36 to 46F). Discard any unused portion.Parenteral drug products should be inspected visually for particulate matter prior to administration, whenever solution and container permit. Once admixed, the solution of Posaconazole ranges from colorless to yellow. Variations of color within this range do not affect the quality of the product.. Equilibrate the refrigerated vial of Posaconazole injection to room temperature.. To prepare the required dose, aseptically transfer one vial (16.7 mL) of Posaconazole injection (containing 300 mg of posaconazole in solution) to an intravenous bag (or bottle) of compatible admixture diluent (as described in Table 5), to achieve final concentration of posaconazole that is between mg/mL and mg/mL. Use of other diluents is not recommended because they may result in particulate formation.. Posaconazole injection is single-dose sterile solution without preservatives. Discard any unused portion from the vial.. Once admixed, the diluted solution of Posaconazole in the intravenous bag (or bottle) should be used immediately. If not used immediately, the solution can be stored up to 24 hours refrigerated to 8C (36 to 46F). Discard any unused portion.. Parenteral drug products should be inspected visually for particulate matter prior to administration, whenever solution and container permit. Once admixed, the solution of Posaconazole ranges from colorless to yellow. Variations of color within this range do not affect the quality of the product.. Intravenous Line Compatibility:A study was conducted to evaluate physical compatibility of Posaconazole injection with injectable drug products and commonly used intravenous diluents during simulated Y-site infusion. Compatibility was determined through visual observations, measurement of particulate matter and turbidity. Compatible diluents and drug products are listed in Tables and below. Any diluents or drug products not listed in the tables below should not be co-administered through the same intravenous line (or cannula).Posaconazole injection can be infused at the same time through the same intravenous line (or cannula) with the following compatible diluents:Table 5: Compatible Diluents0.45% sodium chloride0.9% sodium chloride5% dextrose in water5% dextrose and 0.45% sodium chloride5% dextrose and 0.9% sodium chloride5% dextrose and 20 mEq potassium chloridePosaconazole injection can be infused at the same time through the same intravenous line (or cannula) with the following drug products prepared in 5% dextrose in water or sodium chloride 0.9%. Co-administration of drug products prepared in other diluents may result in particulate formation.Table 6: Compatible DrugsAmikacin sulfateCaspofunginCiprofloxacinDaptomycinDobutamine hydrochlorideFamotidineFilgrastimGentamicin sulfateHydromorphone hydrochlorideLevofloxacinLorazepamMeropenemMicafunginMorphine sulfateNorepinephrine bitartratePotassium chlorideVancomycin hydrochlorideIncompatible Diluents:Posaconazole injection must not be diluted with the following diluents:Lactated Ringers solution5% dextrose with Lactated Ringers solution4.2% sodium bicarbonateAdministration:Posaconazole injection must be administered through 0.22-micron polyethersulfone (PES) or polyvinylidene difluoride (PVDF) filter.Administer via central venous line, including central venous catheter or PICC by slow infusion over approximately 90 minutes. Posaconazole injection is not for bolus administration.If central venous catheter is not available, Posaconazole injection may be administered through peripheral venous catheter only as single dose in advance of central venous line placement or to bridge the period during which central venous line is replaced or is in use for other treatment.When multiple dosing is required, the infusion should be done via central venous line. When administered through peripheral venous catheter, the infusion should be administered over approximately 30 minutes. Note: In clinical trials, multiple peripheral infusions given through the same vein resulted in infusion site reactions [see Adverse Reactions (6.1)].. Posaconazole injection can be infused at the same time through the same intravenous line (or cannula) with the following compatible diluents:. Posaconazole injection can be infused at the same time through the same intravenous line (or cannula) with the following drug products prepared in 5% dextrose in water or sodium chloride 0.9%. Co-administration of drug products prepared in other diluents may result in particulate formation.. Posaconazole injection must be administered through 0.22-micron polyethersulfone (PES) or polyvinylidene difluoride (PVDF) filter.. Administer via central venous line, including central venous catheter or PICC by slow infusion over approximately 90 minutes. Posaconazole injection is not for bolus administration.. If central venous catheter is not available, Posaconazole injection may be administered through peripheral venous catheter only as single dose in advance of central venous line placement or to bridge the period during which central venous line is replaced or is in use for other treatment.. When multiple dosing is required, the infusion should be done via central venous line. When administered through peripheral venous catheter, the infusion should be administered over approximately 30 minutes. Note: In clinical trials, multiple peripheral infusions given through the same vein resulted in infusion site reactions [see Adverse Reactions (6.1)].. 2.9 Dosage Adjustments in Patients with Renal Impairment. Posaconazole injection should be avoided in patients with moderate or severe renal impairment (eGFR <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection.In patients with moderate or severe renal impairment (estimated glomerular filtration rate (eGFR) <50 mL/min), receiving the Posaconazole injection, accumulation of the intravenous vehicle, Betadex Sulfobutyl Ether Sodium (SBECD), is expected to occur. Serum creatinine levels should be closely monitored in these patients, and, if increases occur, consideration should be given to changing to oral Posaconazole therapy.. Posaconazole injection should be avoided in patients with moderate or severe renal impairment (eGFR <50 mL/min), unless an assessment of the benefit/risk to the patient justifies the use of Posaconazole injection.. In patients with moderate or severe renal impairment (estimated glomerular filtration rate (eGFR) <50 mL/min), receiving the Posaconazole injection, accumulation of the intravenous vehicle, Betadex Sulfobutyl Ether Sodium (SBECD), is expected to occur. Serum creatinine levels should be closely monitored in these patients, and, if increases occur, consideration should be given to changing to oral Posaconazole therapy.

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics. General Pharmacokinetic Characteristics. Posaconazole InjectionPosaconazole injection exhibits dose proportional pharmacokinetics after single doses between 200 and 300 mg in healthy volunteers and patients. The mean pharmacokinetic parameters after single doses with Posaconazole injection in healthy volunteers and patients are shown in Table 18.Table 18: Summary of Mean Pharmacokinetic Parameters (%CV) in Healthy Volunteers (30-minute infusion via peripheral venous line) and Patients (90 minute infusion via central venous line) after Dosing with Posaconazole Injection on Day 1AUC0- Area under the plasma concentration-time curve from time zero to infinity; AUC0-12 Area under the plasma concentration- time curve from time zero to 12 hr after the first dose on Day 1; Cmax maximum observed concentration; 1/2 terminal phase half- life; CL total body clearance; N/D Not DeterminedDose (mg)nAUC0-(ng.hr/mL)AUC0-12(ng.hr/mL)Cmax(ng/mL)t1/2(hr)CL(L/hr)Healthy Volunteers200935400 (50)8840 (20)2250 (29)23.6 (23)6.5 (32)300946400 (26)13000 (13)2840 (30)24.6 (20)6.9 (27)Patients20030N/D5570 (32)954 (44)N/DN/D30022N/D8240 (26)1590 (62)N/DN/DTable 19 displays the pharmacokinetic parameters of posaconazole in patients following administration of Posaconazole injection 300 mg taken once day for 10 or 14 days following twice daily dosing on Day 1.Table 19: Arithmetic Mean (%CV) of PK Parameters in Serial PK-Evaluable Patients Following Dosing of Posaconazole Injection (300 mg)AUC0-24 area under the concentration-time curve over the dosing interval (i.e. 24 hours); Cav= time-averaged concentrations (i.e., AUC0-24h/24hr);Cmin POS trough level immediately before subject received the dose of POS on the day specified in the protocol; Cmax observed maximum plasma concentration; CV coefficient of variation, expressed as percent (%); Day study day on treatment; Tmax time of observed maximum plasma concentration. 300 mg dose administered over 90 minutes once day following twice daily dosing on Day 1+ Median (minimum-maximum)DayNCmax(ng/mL)Tmax+(hr)AUC0-24(nghr/mL)Cav (ng/mL)Cmin(ng/mL)10/14493280 (74)1.5 (0.98-4.0)36100 (35)1500 (35)1090 (44). Distribution:The mean volume of distribution of posaconazole after intravenous solution administration was 261 and ranged from 226-295 between studies and dose levels.Posaconazole is highly bound to human plasma proteins (>98%), predominantly to albumin.. Metabolism:Posaconazole primarily circulates as the parent compound in plasma. Of the circulating metabolites, the majority are glucuronide conjugates formed via UDP glucuronidation (phase enzymes). Posaconazole does not have any major circulating oxidative (CYP450 mediated) metabolites. The excreted metabolites in urine and feces account for ~17% of the administered radiolabeled dose.Posaconazole is primarily metabolized via UDP glucuronidation (phase enzymes) and is substrate for p-glycoprotein (P-gp) efflux. Therefore, inhibitors or inducers of these clearance pathways may affect posaconazole plasma concentrations. summary of drugs studied clinically with the oral suspension or an early tablet formulation, which affect posaconazole concentrations, is provided in Table 27. Table 27: Summary of the Effect of Coadministered Drugs on Posaconazole in Healthy Volunteers Ratio Estimate is the ratio of coadministered drug plus Posaconazole to Posaconazole alone for Cmax or AUC.+ The tablet refers to non-commercial tablet formulation without polymer.Coadministered Drug (Postulated Mechanism of Interaction)Coadministered Drug Dose/SchedulePosaconazole Dose/ScheduleEffect on Bioavailability of PosaconazoleChange in MeanCmax(ratio estimate; 90% CI of the ratio estimate)Change in Mean AUC(ratio estimate; 90% CI of the ratio estimate)Efavirenz400 mg once daily 10 and400 mg (oral45% 50%(UDP-G Induction)20 dayssuspension) twice daily 10 and 20 days(0.55; 0.47-0.66)(0.50; 0.43-0.60)Fosamprenavir700 mg twice daily x10 days200 mg once daily on the 1st 21%23%(unknown mechanism)day, 200 mg twice daily onthe 2nd day, then 4000.79 (0.71-0.89)0.77 (0.68-0.87)mg twice daily 8 DaysRifabutin(UDP-G Induction)300 mg once daily x17 days200 mg (tablets) oncedaily 10 days+ 43%(0.57; 0.43-0.75) 49%(0.51; 0.37-0.71)Phenytoin(UDP-G Induction)200 mg once daily x10 days200 mg (tablets) oncedaily 10 days+ 41%(0.59; 0.44-0.79) 50%(0.50; 0.36-0.71)In vitro studies with human hepatic microsomes and clinical studies indicate that posaconazole is an inhibitor primarily of CYP3A4. clinical study in healthy volunteers also indicates that posaconazole is strong CYP3A4 inhibitor as evidenced by >5-fold increase in midazolam AUC. Therefore, plasma concentrations of drugs predominantly metabolized by CYP3A4 may be increased by posaconazole. summary of the drugs studied clinically, for which plasma concentrations were affected by posaconazole, is provided in Table 28 [see Contraindications (4) and Drug Interactions (7.1) including recommendations].Table 28: Summary of the Effect of Posaconazole on Coadministered Drugs in Healthy Adult Volunteers and Patients Ratio Estimate is the ratio of coadministered drug plus Posaconazole to coadministered drug alone for Cmax or AUC.+ The tablet refers to non-commercial tablet formulation without polymer. The mean terminal half-life of midazolam was increased from hours to to 11 hours during coadministration with Posaconazole.Coadministered Drug (Postulated Mechanism of Interaction is Inhibition of CYP3A4 byposaconazole)Coadministered Drug Dose/SchedulePosaconazole Dose/ ScheduleEffect on Bioavailability of CoadministeredDrugsChange in MeanCmax(ratio estimate; 90% CI of the ratio estimate)Change in Mean AUC (ratio estimate; 90% CI of the ratio estimate)Sirolimus2-mg single oral dose400 mg (oral suspension) twice daily 16 days 572%(6.72; 5.62-8.03) 788%(8.88; 7.26-10.9)CyclosporineStable maintenance dose in heart transplant recipients200 mg (tablets) once daily 10 days+ cyclosporine whole blood trough concentrationsCyclosporine dose reductions of up to 29% were requiredTacrolimus0.05-mg/kg single oral dose400 mg (oral suspension) twice daily 7 days 121%(2.21; 2.01-2.42) 358%(4.58; 4.03-5.19)Simvastatin40-mg single oral dose100 mg (oral suspension)SimvastatinSimvastatinonce daily 13 days 841% 931%(9.41, 7.13-12.44)(10.31, 8.40-12.67)Simvastatin AcidSimvastatin Acid 817%634%(9.17, 7.36-11.43)(7.34, 5.82-9.25)200 mg (oral suspension)SimvastatinSimvastatinonce daily 13 days 1041% 960%(11.41, 7.99-16.29)(10.60, 8.63-13.02)Simvastatin AcidSimvastatin Acid851%748%(9.51, 8.15-11.10)(8.48, 7.04-10.23)Midazolam0.4-mg single200 mg (oral suspension) 30% 362%intravenous dose twice daily 7 days(1.3; 1.13-1.48)(4.62; 4.02-5.3)0.4-mg single400 mg (oral suspension)62%524%intravenous dose twice daily 7 days(1.62; 1.41-1.86)(6.24; 5.43-7.16)2-mg single oral dose200 mg (oral suspension) once daily 7 days 169%(2.69; 2.46-2.93) 470%(5.70; 4.82-6.74)2-mg single oral dose400 mg (oral suspension) twice daily 7 days 138%(2.38; 2.13-2.66) 397%(4.97; 4.46-5.54)Rifabutin300 mg once daily 17 days200 mg (tablets) once dailyx 10 days+ 31%(1.31; 1.10-1.57) 72%(1.72;1.51-1.95)Phenytoin200 mg once daily PO 10days200 mg (tablets) once dailyx 10 days+ 16%(1.16; 0.85-1.57) 16%(1.16; 0.84-1.59)Ritonavir100 mg once daily 14 days400 mg (oral suspension) twice daily 7 days 49%(1.49; 1.04-2.15) 80%(1.8;1.39-2.31)Atazanavir300 mg once daily 14 days400 mg (oral suspension) 155% 268%twice daily 7 days(2.55; 1.89-3.45)(3.68; 2.89-4.70)Atazanavir/ritonavir boosted300 mg/100 mg once daily400 mg (oral suspension) 53% 146%regimenx 14 daystwice daily 7 days(1.53; 1.13-2.07)(2.46; 1.93-3.13)Additional clinical studies demonstrated that no clinically significant effects on zidovudine, lamivudine, indinavir, or caffeine were observed when administered with Posaconazole 200 mg once daily; therefore, no dose adjustments are required for these coadministered drugs when coadministered with Posaconazole 200 mg once daily.. Excretion:Following administration of Noxafil(R) oral suspension, posaconazole is predominantly eliminated in the feces (71% of the radiolabeled dose up to 120 hours) with the major component eliminated as parent drug (66% of the radiolabeled dose). Renal clearance is minor elimination pathway, with 13% of the radiolabeled dose excreted in urine up to 120 hours (<0.2% of the radiolabeled dose is parent drug).Posaconazole injection is eliminated with mean terminal half-life (t 1/2 of 27 hours and total body clearance (CL) of 7.3 L/h.. Specific PopulationsNo clinically significant differences in the pharmacokinetics of posaconazole were observed based on age, sex, renal impairment, and indication (prophylaxis or treatment).. Race/Ethnicity:In population pharmacokinetic analysis of posaconazole, AUC was found to be 25% higher in Chinese patients relative to patients from other races/ethnicities. This higher exposure is not expected to be clinically relevant given the expected variability in posaconazole exposure.. Patients Weighing More Than 120 kg:Weight has clinically significant effect on posaconazole clearance. Relative to 70 kg patients, the Cavg is decreased by 25% in patients greater than 120 kg. Patients administered Posaconazole weighing more than 120 kg may be at higher risk for lower posaconazole plasma concentrations compared to lower weight patients [see Use in Specific Populations (8.10)].. Pediatric PatientsThe mean pharmacokinetic parameters after multiple-dose administration of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension in neutropenic pediatric patients to less than 18 years of age are shown in Table 29. Patients were enrolled into age groups and received Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension doses at mg/kg (0.6 to times the recommended dose) with maximum 300 mg dose once daily (twice daily on Day 1) [see Adverse Reactions (6.1)].Table 29: Summary of Steady-State Geometric Mean Pharmacokinetic Parameters (% Geometric CV) After Multiple Dosing with Posaconazole Injection and Noxafil(R) PowderMix for Delayed-Release Oral Suspension mg/kg in Pediatric Patients with Neutropenia or Expected NeutropeniaIV= Posaconazole injection; PFS= Noxafil(R) PowderMix for delayed-release oral suspension; AUC0-24 Area under the plasma concentration-time curve from time zero to 24 hr; Cmax maximum observed concentration; Cmin minimum observed plasma concentration; Tmax time of maximum observed concentration; CL /F apparent total body clearance 0.6 to times the recommended dose+ Cav time-averaged concentrations (i.e., AUC0-24 hr/24hr) Median (minimum-maximum) Clearance (CL for IV and CL/F for PFS)Age GroupDose TypeNAUC0-24 hr(ng.hr/mL)Cav+(ng/mL)Cmax(ng/mL)Cmin(ng/mL)T max (hr) CL/F(L/hr)2 to <7IV1731100130030606261.753.27years(48.9)(48.9)(54.1)(104.8)(1.57-1.83)(49.3)PFS723000960 (47.3)15105424.004.60(47.3)(43.4)(68.8)(2.17-7.92)(35.2)7 to 17 yearsIV2444200(41.5)1840(41.5)3340(39.4)1160(60.4)1.77(1.33-6.00)4.76(55.7)PFS1225000(184.3)1040(184.3)1370(178.5)713(300.6)2.78(0.00-4.00)8.39(190.3)Based on population pharmacokinetic model evaluating posaconazole pharmacokinetics and predicting exposures in pediatric patients, the exposure of steady-state posaconazole average concentration greater than or equal to 700 ng/mL in approximately 90% of patients is attained with the recommended dose of Posaconazole injection and Noxafil(R) PowderMix for delayed-release oral suspension.The population pharmacokinetic analysis of posaconazole in pediatric patients suggests that age, sex, renal impairment and ethnicity have no clinically meaningful effect on the pharmacokinetics of posaconazole.A total of 12 patients 13 to 17 years of age received 600 mg/day (200 mg three times day) of Noxafil(R) oral suspension for prophylaxis of invasive fungal infections. Based on pharmacokinetic data in 10 of these pediatric patients, the mean steady-state Cav was similar between these patients and adults (>=18 years of age). In study of 136 neutropenic pediatric patients 11 months to less than 18 years treated with Noxafil(R) oral suspension, the exposure target of steady-state posaconazole Cavg between 500 ng/mL and less than 2500 ng/mL was attained in approximately 50% of patients instead of the pre-specified 90% of patients.

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Patient Information Posaconazole (poe sa KON zole) injectionWhat is PosaconazolePosaconazole (which refers to injection) is prescription medicine used in adults and children to help prevent or treat fungal infections that can spread throughout your body (invasive fungal infections). These infections are caused by fungi called Aspergillus or Candida. Posaconazole is used in people who have an increased chance of getting these infections due to weak immune system. These include people who have had hematopoietic stem cell transplantation (bone marrow transplant) with graft versus host disease or those with low white blood cell count due to chemotherapy for blood cancers (hematologic malignancies). Posaconazole injection is used for: prevention of fungal infections in adults and children years of age and older.treatment of fungal infections in adults and children 13 years of age and older. It is not known if Posaconazole is safe and effective in children under years of age.Who should not take PosaconazoleDo not take Posaconazole if you:are allergic to posaconazole, any of the ingredients in Posaconazole, or other azole antifungal medicines. See the end of this leaflet for complete list of ingredients in Posaconazole.are taking any of the following medicines:sirolimuspimozidequinidinecertain statin medicines that lower cholesterol (atorvastatin, lovastatin, simvastatin)ergot alkaloids (ergotamine, dihydroergotamine) have chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) and you have just started taking venetoclax or your venetoclax dose is being slowly increased. Ask your healthcare provider or pharmacist if you are not sure if you are taking any of these medicines. Do not start taking new medicine without talking to your healthcare provider or pharmacist.What should tell my healthcare provider before taking PosaconazoleBefore you take Posaconazole, tell your healthcare provider if you:are taking certain medicines that lower your immune system like cyclosporine or tacrolimus.are taking certain drugs for HIV infection, such as ritonavir, atazanavir, efavirenz, or fosamprenavir. Efavirenz and fosamprenavir can cause decrease in the Posaconazole levels in your body. Efavirenz and fosamprenavir should not be taken with Posaconazole.are taking midazolam, hypnotic and sedative medicine.are taking vincristine, vinblastine and other vinca alkaloids (medicines used to treat cancer).are taking venetoclax, medicine used to treat cancer.have or had liver problems.have or had kidney problems.have or had an abnormal heart rate or rhythm, heart problems, or blood circulation problems.are pregnant or plan to become pregnant. It is not known if Posaconazole will harm your unborn baby.are breastfeeding or plan to breastfeed. It is not known if Posaconazole passes into your breast milk. You and your healthcare provider should decide if you will take Posaconazole or breastfeed. You should not do both. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Posaconazole can affect the way other medicines work, and other medicines can affect the way Posaconazole works, and can cause serious side effects. Ask your healthcare provider or pharmacist for list of these medicines if you are not sure.Know the medicines you take. Keep list of them with you to show your healthcare provider or pharmacist when you get new medicine.How will take PosaconazoleTake Posaconazole exactly as your healthcare provider tells you to take it.Your healthcare provider will tell you how much Posaconazole to take and when to take it.Take Posaconazole for as long as your healthcare provider tells you to take it.If you take too much Posaconazole, call your healthcare provider or go to the nearest hospital emergency room right away.Posaconazole Injection is usually given over 30 to 90 minutes through plastic tube placed in your vein. Follow the instruction from your healthcare provider on how much Posaconazole you should take and when to take it.What are the possible side effects of Posaconazole Posaconazole may cause serious side effects, including:drug interactions with cyclosporine or tacrolimus. If you take Posaconazole with cyclosporine or tacrolimus, your blood levels of cyclosporine or tacrolimus may increase. Serious side effects can happen in your kidney or brain if you have high levels of cyclosporine or tacrolimus in your blood. Your healthcare provider should do blood tests to check your levels of cyclosporine or tacrolimus if you are taking these medicines while taking Posaconazole. Tell your healthcare provider right away if you have swelling in your arm or leg or shortness of breath.problems with the electrical system of your heart (arrhythmias and QTc prolongation). Certain medicines used to treat fungus called azoles, including posaconazole, the active ingredient in Posaconazole, may cause heart rhythm problems. People who have certain heart problems or who take certain medicines have higher chance for this problem. Tell your healthcare provider right away if your heartbeat becomes fast or irregular.changes in body salt (electrolytes) levels in your blood. Your healthcare provider should check your electrolytes while you are taking Posaconazole.liver problems. Some people who also have other serious medical problems may have severe liver problems that may lead to death, especially if you take certain doses of Posaconazole. Your healthcare provider should do blood tests to check your liver while you are taking Posaconazole. Call your healthcare provider right away if you have any of the following symptoms of liver problems:itchy skinnausea or vomitingyellowing of your eyes or skinfeeling very tiredflu-like symptomsincreased amounts of midazolam in your blood. If you take Posaconazole with midazolam, Posaconazole increases the amount of midazolam in your blood. This can make your sleepiness last longer. Your healthcare provider should check you closely for side effects if you take midazolam with Posaconazole.The most common side effects of Posaconazole in adults include:diarrheanauseafevervomiting headachecoughinglow potassium levels in the bloodThe most common side effects of Posaconazole in children include:feverfever with low white blood cell count (febrile neutropenia)vomitingredness and sores of the lining of the mouth, lips, throat, stomach, and genitals (mucositis or stomatitis) itchinghigh blood pressurelow potassium levels in the bloodTell your healthcare provider if you have any side effect that bothers you or that does not go away.These are not all the possible side effects of Posaconazole. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088How should store PosaconazolePosaconazole injectionStore Posaconazole Injection refrigerated at 36F to 46F (2C to 8C).Safely throw away medicine that is out of date or no longer needed. Keep Posaconazole and all medicines out of the reach of children. General information about the safe and effective use of Posaconazole.Medicines are sometimes prescribed for purposes other than those listed in Patient Information leaflet. Do not use Posaconazole for condition for which it was not prescribed. Do not give Posaconazole to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about Posaconazole that is written for health professionals.What are the ingredients in Posaconazole InjectionActive ingredient: posaconazole Inactive ingredients: Posaconazole injection: Betadex Sulfobutyl Ether Sodium (SBECD), edetate disodium, hydrochloric acid, sodium hydroxide, and water for injection. Manufactured by: Lake Zurich, IL 60047 www.fresenius-kabi.com/us 451564A This Patient Information has been approved by the U.S. Food and Drug Administration. Revised: 12/2023. prevention of fungal infections in adults and children years of age and older.. treatment of fungal infections in adults and children 13 years of age and older.. are allergic to posaconazole, any of the ingredients in Posaconazole, or other azole antifungal medicines. See the end of this leaflet for complete list of ingredients in Posaconazole.. are taking any of the following medicines:sirolimuspimozidequinidinecertain statin medicines that lower cholesterol (atorvastatin, lovastatin, simvastatin)ergot alkaloids (ergotamine, dihydroergotamine) sirolimus. pimozide. quinidine. certain statin medicines that lower cholesterol (atorvastatin, lovastatin, simvastatin). ergot alkaloids (ergotamine, dihydroergotamine). have chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) and you have just started taking venetoclax or your venetoclax dose is being slowly increased. are taking certain medicines that lower your immune system like cyclosporine or tacrolimus.. are taking certain drugs for HIV infection, such as ritonavir, atazanavir, efavirenz, or fosamprenavir. Efavirenz and fosamprenavir can cause decrease in the Posaconazole levels in your body. Efavirenz and fosamprenavir should not be taken with Posaconazole.. are taking midazolam, hypnotic and sedative medicine.. are taking vincristine, vinblastine and other vinca alkaloids (medicines used to treat cancer).. are taking venetoclax, medicine used to treat cancer.. have or had liver problems.. have or had kidney problems.. have or had an abnormal heart rate or rhythm, heart problems, or blood circulation problems.. are pregnant or plan to become pregnant. It is not known if Posaconazole will harm your unborn baby.. are breastfeeding or plan to breastfeed. It is not known if Posaconazole passes into your breast milk. You and your healthcare provider should decide if you will take Posaconazole or breastfeed. You should not do both. Take Posaconazole exactly as your healthcare provider tells you to take it.. Your healthcare provider will tell you how much Posaconazole to take and when to take it.. Take Posaconazole for as long as your healthcare provider tells you to take it.. If you take too much Posaconazole, call your healthcare provider or go to the nearest hospital emergency room right away.. Posaconazole Injection is usually given over 30 to 90 minutes through plastic tube placed in your vein. drug interactions with cyclosporine or tacrolimus. If you take Posaconazole with cyclosporine or tacrolimus, your blood levels of cyclosporine or tacrolimus may increase. Serious side effects can happen in your kidney or brain if you have high levels of cyclosporine or tacrolimus in your blood. Your healthcare provider should do blood tests to check your levels of cyclosporine or tacrolimus if you are taking these medicines while taking Posaconazole. Tell your healthcare provider right away if you have swelling in your arm or leg or shortness of breath.. problems with the electrical system of your heart (arrhythmias and QTc prolongation). Certain medicines used to treat fungus called azoles, including posaconazole, the active ingredient in Posaconazole, may cause heart rhythm problems. People who have certain heart problems or who take certain medicines have higher chance for this problem. Tell your healthcare provider right away if your heartbeat becomes fast or irregular.. changes in body salt (electrolytes) levels in your blood. Your healthcare provider should check your electrolytes while you are taking Posaconazole.. liver problems. Some people who also have other serious medical problems may have severe liver problems that may lead to death, especially if you take certain doses of Posaconazole. Your healthcare provider should do blood tests to check your liver while you are taking Posaconazole. Call your healthcare provider right away if you have any of the following symptoms of liver problems:. itchy skin. nausea or vomiting. yellowing of your eyes or skin. feeling very tired. flu-like symptoms. increased amounts of midazolam in your blood. If you take Posaconazole with midazolam, Posaconazole increases the amount of midazolam in your blood. This can make your sleepiness last longer. Your healthcare provider should check you closely for side effects if you take midazolam with Posaconazole.. diarrhea. nausea. fever. vomiting headache. coughing. low potassium levels in the blood. fever. fever with low white blood cell count (febrile neutropenia). vomiting. redness and sores of the lining of the mouth, lips, throat, stomach, and genitals (mucositis or stomatitis) itching. high blood pressure. low potassium levels in the blood. Store Posaconazole Injection refrigerated at 36F to 46F (2C to 8C).. Fresenius Kabi Logo.