HOW SUPPLIED SECTION.

16HOW SUPPLIED/STORAGE AND HANDLING. ZYVOX I.V. Injection is available in single-dose, ready-to-use flexible plastic infusion bags in foil laminate overwrap. The infusion bags and ports are not made with natural rubber latex. The infusion bags are available in the following package sizes:600 mg/300 mL (2 mg/mL) linezolid 10NDC 0009-7807-02. Store at 25oC (77oF). Protect from light. It is recommended that the infusion bags be kept in the overwrap until ready to use. Protect infusion bags from freezing.

LACTATION SECTION.

8.2Lactation. Risk SummaryLinezolid is present in breast milk. Based on data from available published case reports, the daily dose of linezolid that the infant would receive from breastmilk would be approximately 6% to 9% of the recommended therapeutic infant dose (10 mg/kg every hours). There is no information on the effects of linezolid on the breastfed infant; however, diarrhea and vomiting were the most common adverse reactions reported in clinical trials in infants receiving linezolid therapeutically [see Adverse Reactions (6.1) and (see Clinical Considerations). There is no information on the effects of linezolid on milk production. The developmental and health benefits of breastfeeding should be considered along with the mothers clinical need for linezolid and any potential adverse effects on the breastfed child from linezolid or from the underlying maternal condition.. Clinical ConsiderationsAdvise lactating women to monitor breastfed infant for diarrhea and vomiting.

MECHANISM OF ACTION SECTION.

12.1Mechanism of Action. ZYVOX is an antibacterial drug [see Microbiology (12.4) ].

ADVERSE REACTIONS SECTION.

6ADVERSE REACTIONS. Most common adverse reactions (>5% of adult and/or pediatric patients treated with ZYVOX) include: diarrhea, vomiting, headache, nausea, and anemia. (6)To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc. at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.. AdultsThe safety of ZYVOX formulations was evaluated in 2,046 adult patients enrolled in seven Phase comparator-controlled clinical trials, who were treated for up to 28 days.Of the patients treated for uncomplicated skin and skin structure infections (uSSSIs), 25.4% of ZYVOX-treated and 19.6% of comparator-treated patients experienced at least one drug-related adverse event. For all other indications, 20.4% of ZYVOX -treated and 14.3% of comparator-treated patients experienced at least one drug-related adverse event.Table shows the incidence of all-causality, treatment-emergent adverse reactions reported in at least 1% of adult patients in these trials by dose of ZYVOX.Table 2. Incidence (%) of Treatment-Emergent Adverse Reactions Occurring in >1% of Adult Patients Treated with ZYVOX in Comparator-Controlled Clinical TrialsADVERSE REACTIONSUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg by mouth every 12 hours (n=548)Clarithromycin 250 mg by mouth every 12 hours (n=537)ZYVOX 600 mg every 12 hours (n=1498)All Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. (n=1464)Headache8.88.45.74.4Diarrhea8.26.18.36.4Nausea5.14.56.64.6Vomiting2.01.54.32.3Dizziness2.63.01.81.5Rash1.11.12.32.6Anemia0.402.11.4Taste alteration1.82.01.00.3Vaginal moniliasis1.81.31.10.5Oral moniliasis0.501.71.0Abnormal liver function tests0.40.21.60.8Fungal infection1.50.20.30.2Tongue discoloration1.300.30Localized abdominal pain1.30.61.20.8Generalized abdominal pain0.90.41.21.0Of the patients treated for uSSSIs, 3.5% of ZYVOX-treated and 2.4% of comparator-treated patients discontinued treatment due to drug-related adverse events. For all other indications, discontinuations due to drug-related adverse events occurred in 2.1% of ZYVOX-treated and 1.7% of comparator-treated patients. The most common reported drug-related adverse events leading to discontinuation of treatment were nausea, headache, diarrhea, and vomiting.. Pediatric PatientsThe safety of ZYVOX formulations was evaluated in 215 pediatric patients ranging in age from birth through 11 years, and in 248 pediatric patients aged through 17 years (146 of these 248 were age through 11 and 102 were age 12 to 17). These patients were enrolled in two Phase comparator-controlled clinical trials and were treated for up to 28 days. In the study of hospitalized pediatric patients (birth through 11 years) with Gram-positive infections, who were randomized to (linezolid: vancomycin), mortality was 6.0% (13/215) in the linezolid arm and 3.0% (3/101) in the vancomycin arm. However, given the severe underlying illness in the patient population, no causality could be established.Of the pediatric patients treated for uSSSIs, 19.2% of ZYVOX-treated and 14.1% of comparator-treated patients experienced at least one drug-related adverse event. For all other indications, 18.8% of ZYVOX-treated and 34.3% of comparator-treated patients experienced at least one drug-related adverse event.Table shows the incidence of all-causality, treatment-emergent adverse reactions reported in more than 1% of pediatric patients (and more than patient) in either treatment group in the comparator-controlled Phase trials.Table 3. Incidence (%) of Treatment-Emergent Adverse Reactions Occurring in 1% of Pediatric Patients (and >1 Patient) in Either Treatment Group in Comparator-Controlled Clinical TrialsADVERSE REACTIONSUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg by mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOX(n=248)Cefadroxil(n=251)ZYVOX(n=215)Vancomycin(n=101)Diarrhea7.88.010.812.1Vomiting2.96.49.49.1Headache6.54.00.90Anemia005.67.1Thrombocytopenia004.72.0Nausea3.73.21.90Generalized abdominal pain2.42.80.92.0Localized abdominal pain2.42.80.51.0Loose stools1.60.82.33.0Eosinophilia0.40.81.91.0Pruritus at non-application site0.80.41.42.0Vertigo1.20.400Of the pediatric patients treated for uSSSIs, 1.6% of ZYVOX-treated and 2.4% of comparator-treated patients discontinued treatment due to drug-related adverse events. For all other indications, discontinuations due to drug-related adverse events occurred in 0.9% of ZYVOX-treated and 6.1% of comparator-treated patients.. Laboratory AbnormalitiesZYVOX has been associated with thrombocytopenia when used in doses up to and including 600 mg every 12 hours for up to 28 days. In Phase comparator-controlled trials, the percentage of adult patients who developed substantially low platelet count (defined as less than 75% of lower limit of normal and/or baseline) was 2.4% (range among studies: 0.3 to 10.0%) with ZYVOX and 1.5% (range among studies: 0.4 to 7.0%) with comparator. In study of hospitalized pediatric patients ranging in age from birth through 11 years, the percentage of patients who developed substantially low platelet count (defined as less than 75% of lower limit of normal and/or baseline) was 12.9% with ZYVOX and 13.4% with vancomycin. In an outpatient study of pediatric patients aged from through 17 years, the percentage of patients who developed substantially low platelet count was 0% with ZYVOX and 0.4% with cefadroxil. Thrombocytopenia associated with the use of ZYVOX appears to be dependent on duration of therapy (generally greater than weeks of treatment). The platelet counts for most patients returned to the normal range/baseline during the follow-up period. No related clinical adverse events were identified in Phase clinical trials in patients developing thrombocytopenia. Bleeding events were identified in thrombocytopenic patients in compassionate use program for ZYVOX; the role of linezolid in these events cannot be determined [see Warning and Precautions (5.1) ].Changes seen in other laboratory parameters, without regard to drug relationship, revealed no substantial differences between ZYVOX and the comparators. These changes were generally not clinically significant, did not lead to discontinuation of therapy, and were reversible. The incidence of adult and pediatric patients with at least one substantially abnormal hematologic or serum chemistry value is presented in Tables 4, 5, 6, and 7.Table 4. Percent of Adult Patients who Experienced at Least One Substantially Abnormal<75% (<50% for neutrophils) of Lower Limit of Normal (LLN) for values normal at baseline; <75% (<50% for neutrophils) of LLN and of baseline for values abnormal at baseline. Hematology Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg every 12 hoursClarithromycin 250 mg every 12 hoursZYVOX 600 mg every 12 hoursAll Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. Hemoglobin (g/dL)0.90.07.16.6Platelet count (x 103/mm3)0.70.83.01.8WBC (x 103/mm3)0.20.62.21.3Neutrophils (x 103/mm3)0.00.21.11.2Table 5. Percent of Adult Patients who Experienced at Least One Substantially Abnormal>2 Upper Limit of Normal (ULN) for values normal at baseline; >2 ULN and >2 baseline for values abnormal at baseline. Serum Chemistry Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg every 12 hoursClarithromycin 250 mg every 12 hoursZYVOX 600 mg every 12 hoursAll Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. AST (U/L)1.71.35.06.8ALT (U/L)1.71.79.69.3LDH (U/L)0.20.21.81.5Alkaline phosphatase (U/L)0.20.23.53.1Lipase (U/L)2.82.64.34.2Amylase (U/L)0.20.22.42.0Total bilirubin (mg/dL)0.20.00.91.1BUN (mg/dL)0.20.02.11.5Creatinine (mg/dL)0.20.00.20.6Table 6. Percent of Pediatric Patients who Experienced at Least One Substantially Abnormal<75% (<50% for neutrophils) of Lower Limit of Normal (LLN) for values normal at baseline;<75% (<50% for neutrophils) of LLN and <75% (<50% for neutrophils, <90% for hemoglobin if baseline <LLN) of baseline for values abnormal at baseline. Hematology Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg by mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOXCefadroxilZYVOXVancomycinHemoglobin (g/dL)0.00.015.712.4Platelet count (x 103/mm3)0.00.412.913.4WBC (x 103/mm3)0.80.812.410.3Neutrophils (x 103/mm3)1.20.85.94.3Table 7. Percent of Pediatric Patients who Experienced at Least One Substantially Abnormal>2 Upper Limit of Normal (ULN) for values normal at baseline; >2 ULN and >2 (>1.5 for total bilirubin) baseline for values abnormal at baseline. Serum Chemistry Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously/by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOX CefadroxilZYVOXVancomycinALT (U/L)0.00.010.112.5Lipase (U/L)0.41.2------Amylase (U/L)------0.61.3Total bilirubin (mg/dL)------6.35.2Creatinine (mg/dL)0.40.02.41.0. 6.2Postmarketing Experience. The following adverse reactions have been identified during postapproval use of ZYVOX. Because these reactions are reported voluntarily from population of uncertain size, it is not always possible to reliably estimate their frequency or establish causal relationship to drug exposure;Myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) [see Warnings and Precautions (5.1) ]; sideroblastic anemia.Peripheral neuropathy, and optic neuropathy sometimes progressing to loss of vision [see Warnings and Precautions (5.2) ].Lactic acidosis [see Warnings and Precautions (5.7) ]. Although these reports have primarily been in patients treated for longer than the maximum recommended duration of 28 days, these events have also been reported in patients receiving shorter courses of therapy.Serotonin syndrome has been reported in patients receiving concomitant serotonergic agents, including antidepressants such as selective serotonin reuptake inhibitors (SSRIs) and opioids, and ZYVOX [see Warnings and Precautions (5.3) ].Convulsions [see Warnings and Precautions (5.8) ].Anaphylaxis, angioedema, bullous skin disorders including severe cutaneous adverse reactions (SCAR) such as toxic epidermal necrolysis and Stevens-Johnson syndrome, and hypersensitivity vasculitis.Superficial tooth discoloration and tongue discoloration have been reported with the use of linezolid. The tooth discoloration was removable with professional dental cleaning (manual descaling) in cases with known outcome.Hypoglycemia, including symptomatic episodes [see Warnings and Precautions (5.9) ].Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) [see Warnings and Precautions (5.10) ].. Myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) [see Warnings and Precautions (5.1) ]; sideroblastic anemia.. Peripheral neuropathy, and optic neuropathy sometimes progressing to loss of vision [see Warnings and Precautions (5.2) ].. Lactic acidosis [see Warnings and Precautions (5.7) ]. Although these reports have primarily been in patients treated for longer than the maximum recommended duration of 28 days, these events have also been reported in patients receiving shorter courses of therapy.. Serotonin syndrome has been reported in patients receiving concomitant serotonergic agents, including antidepressants such as selective serotonin reuptake inhibitors (SSRIs) and opioids, and ZYVOX [see Warnings and Precautions (5.3) ].. Convulsions [see Warnings and Precautions (5.8) ].. Anaphylaxis, angioedema, bullous skin disorders including severe cutaneous adverse reactions (SCAR) such as toxic epidermal necrolysis and Stevens-Johnson syndrome, and hypersensitivity vasculitis.. Superficial tooth discoloration and tongue discoloration have been reported with the use of linezolid. The tooth discoloration was removable with professional dental cleaning (manual descaling) in cases with known outcome.. Hypoglycemia, including symptomatic episodes [see Warnings and Precautions (5.9) ].. Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) [see Warnings and Precautions (5.10) ].

INDICATIONS & USAGE SECTION.

1INDICATIONS AND USAGE. ZYVOX is an oxazolidinone-class antibacterial indicated in adults and children for the treatment of the following infections caused by susceptible Gram-positive bacteria: Nosocomial pneumonia (1.1); Community-acquired pneumonia (1.2); Complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis (1.3); Uncomplicated skin and skin structure infections (1.4); Vancomycin-resistant Enterococcus faecium infections. (1.5)Limitations of Use (1.6):ZYVOX is not indicated for the treatment of Gram-negative infections.The safety and efficacy of ZYVOX formulations given for longer than 28 days have not been evaluated in controlled clinical trials.To reduce the development of drug-resistant bacteria and maintain the effectiveness of ZYVOX formulations and other antibacterial drugs, ZYVOX should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. (1.7). ZYVOX is not indicated for the treatment of Gram-negative infections.. The safety and efficacy of ZYVOX formulations given for longer than 28 days have not been evaluated in controlled clinical trials.. 1.1Nosocomial Pneumonia. ZYVOX is indicated for the treatment of nosocomial pneumonia caused by Staphylococcus aureus (methicillin-susceptible and -resistant isolates) or Streptococcus pneumoniae [see Clinical Studies (14) ].. 1.2Community-acquired Pneumonia. ZYVOX is indicated for the treatment of community-acquired pneumonia caused by Streptococcus pneumoniae, including cases with concurrent bacteremia, or Staphylococcus aureus (methicillin-susceptible isolates only) [see Clinical Studies (14) ].. 1.3Complicated Skin and Skin Structure Infections. ZYVOX is indicated for the treatment of complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis, caused by Staphylococcus aureus (methicillin-susceptible and -resistant isolates), Streptococcus pyogenes, or Streptococcus agalactiae. ZYVOX has not been studied in the treatment of decubitus ulcers [see Clinical Studies (14) ].. 1.4Uncomplicated Skin and Skin Structure Infections. ZYVOX is indicated for the treatment of uncomplicated skin and skin structure infections caused by Staphylococcus aureus (methicillin-susceptible isolates only) or Streptococcus pyogenes [see Clinical Studies (14) ].. 1.5Vancomycin-resistant Enterococcus faecium Infections. ZYVOX is indicated for the treatment of vancomycin-resistant Enterococcus faecium infections, including cases with concurrent bacteremia [see Clinical Studies (14) ].. 1.6Limitations of Use. ZYVOX is not indicated for the treatment of Gram-negative infections. It is critical that specific Gram-negative therapy be initiated immediately if concomitant Gram-negative pathogen is documented or suspected [see Warnings and Precautions (5.4) ].The safety and efficacy of ZYVOX formulations given for longer than 28 days have not been evaluated in controlled clinical trials [see Clinical Studies (14) ]. ZYVOX is not indicated for the treatment of Gram-negative infections. It is critical that specific Gram-negative therapy be initiated immediately if concomitant Gram-negative pathogen is documented or suspected [see Warnings and Precautions (5.4) ].. The safety and efficacy of ZYVOX formulations given for longer than 28 days have not been evaluated in controlled clinical trials [see Clinical Studies (14) ]. 1.7Usage. To reduce the development of drug-resistant bacteria and maintain the effectiveness of ZYVOX and other antibacterial drugs, ZYVOX should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

ANIMAL PHARMACOLOGY & OR TOXICOLOGY SECTION.

13.2Animal Toxicology and/or Pharmacology. Target organs of linezolid toxicity were similar in juvenile and adult rats and dogs. Dose- and time-dependent myelosuppression, as evidenced by bone marrow hypocellularity/decreased hematopoiesis, decreased extramedullary hematopoiesis in spleen and liver, and decreased levels of circulating erythrocytes, leukocytes, and platelets have been seen in animal studies. Lymphoid depletion occurred in thymus, lymph nodes, and spleen. Generally, the lymphoid findings were associated with anorexia, weight loss, and suppression of body weight gain, which may have contributed to the observed effects.In rats administered linezolid orally for months, non-reversible, minimal to mild axonal degeneration of sciatic nerves was observed at 80 mg/kg/day; minimal degeneration of the sciatic nerve was also observed in male at this dose level at 3-month interim necropsy. Sensitive morphologic evaluation of perfusion-fixed tissues was conducted to investigate evidence of optic nerve degeneration. Minimal to moderate optic nerve degeneration was evident in male rats after months of dosing, but the direct relationship to drug was equivocal because of the acute nature of the finding and its asymmetrical distribution. The nerve degeneration observed was microscopically comparable to spontaneous unilateral optic nerve degeneration reported in aging rats and may be an exacerbation of common background change.These effects were observed at exposure levels that are comparable to those observed in some human subjects. The hematopoietic and lymphoid effects were reversible, although in some studies, reversal was incomplete within the duration of the recovery period.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.

13.1Carcinogenesis, Mutagenesis, Impairment of Fertility. Lifetime studies in animals have not been conducted to evaluate the carcinogenic potential of linezolid. Neither mutagenic nor clastogenic potential was found in battery of tests including: assays for mutagenicity (Ames bacterial reversion and CHO cell mutation), an in vitro unscheduled DNA synthesis (UDS) assay, an in vitro chromosome aberration assay in human lymphocytes, and an in vivo mouse micronucleus assay.Linezolid did not affect the fertility or reproductive performance of adult female rats given oral doses of up to 100 mg/kg/day for 14 days prior to mating through Gestation Day 7. It reversibly decreased fertility and reproductive performance in adult male rats when given at doses >= 50 mg/kg/day, with exposures approximately equal to or greater than the expected human exposure level (exposure comparisons are based on AUCs). The reversible fertility effects were mediated through altered spermatogenesis. Affected spermatids contained abnormally formed and oriented mitochondria and were non-viable. Epithelial cell hypertrophy and hyperplasia in the epididymis was observed in conjunction with decreased fertility. Similar epididymal changes were not seen in dogs.In sexually mature male rats exposed to drug as juveniles, mildly decreased fertility was observed following treatment with linezolid through most of their period of sexual development (50 mg/kg/day from days to 36 of age, and 100 mg/kg/day from days 37 to 55 of age), with exposures up to 1.7 times greater than mean AUCs observed in pediatric patients aged months to 11 years. Decreased fertility was not observed with shorter treatment periods, corresponding to exposure in utero through the early neonatal period (gestation day through postnatal day 5), neonatal exposure (postnatal days to 21), or to juvenile exposure (postnatal days 22 to 35). Reversible reductions in sperm motility and altered sperm morphology were observed in rats treated from postnatal day 22 to 35.

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1Mechanism of Action. ZYVOX is an antibacterial drug [see Microbiology (12.4) ].. 12.2Pharmacodynamics. In randomized, positive- and placebo-controlled crossover thorough QT study, 40 healthy subjects were administered single ZYVOX 600 mg dose via 1 hour IV infusion, single ZYVOX 1,200 mg dose via 1 hour IV infusion, placebo, and single oral dose of positive control. At both the 600 mg and 1,200 mg ZYVOX doses, no significant effect on QTc interval was detected at peak plasma concentration or at any other time.. 12.3Pharmacokinetics. The mean pharmacokinetic parameters of linezolid in adults after single and multiple oral and intravenous doses are summarized in Table 8. Plasma concentrations of linezolid at steady-state after oral doses of 600 mg given every 12 hours are shown in Figure 1.Table 8. Mean (Standard Deviation) Pharmacokinetic Parameters of Linezolid in AdultsDose of LinezolidCmax mcg/mLCmin mcg/mLTmax hrsAUC AUC for single dose AUC0-; for multiple dose AUC0- mcgh/mLt1/2 hrsCLmL/minCmax Maximum plasma concentration; Cmin Minimum plasma concentration; Tmax Time to Cmax; AUC Area under concentration-time curve; t1/2 Elimination half-life; CL Systemic clearance400 mg tablet single dose Data dose-normalized from 375 mg 8.10(1.83)---1.52(1.01)55.10(25.00)5.20(1.50)146(67) every 12 hours11.00(4.37)3.08(2.25)1.12(0.47)73.40(33.50)4.69(1.70)110(49)600 mg tablet single dose12.70(3.96)---1.28(0.66)91.40(39.30)4.26(1.65)127(48) every 12 hours21.20(5.78)6.15(2.94)1.03(0.62)138.00(42.10)5.40(2.06)80(29)600 mg IV injection Data dose-normalized from 625 mg, intravenous dose was given as 0.5-hour infusion. single dose12.90(1.60)---0.50(0.10)80.20(33.30)4.40(2.40)138(39) every 12 hours15.10(2.52)3.68(2.36)0.51(0.03)89.70(31.00)4.80(1.70)123(40)600 mg oral suspension single dose11.00(2.76)---0.97(0.88)80.80(35.10)4.60(1.71)141(45)Figure 1. Plasma Concentrations of Linezolid in Adults at Steady-State Following Oral Dosing Every 12 Hours (Mean +- Standard Deviation, n=16). Figure 1. AbsorptionLinezolid is extensively absorbed after oral dosing. Maximum plasma concentrations are reached approximately to hours after dosing, and the absolute bioavailability is approximately 100%. Therefore, linezolid may be given orally or intravenously without dose adjustment.Linezolid may be administered without regard to the timing of meals. The time to reach the maximum concentration is delayed from 1.5 hours to 2.2 hours and Cmax is decreased by about 17% when high fat food is given with linezolid. However, the total exposure measured as AUC0- is similar under both conditions.. DistributionAnimal and human pharmacokinetic studies have demonstrated that linezolid readily distributes to well-perfused tissues. The plasma protein binding of linezolid is approximately 31% and is concentration-independent. The volume of distribution of linezolid at steady-state averaged 40 to 50 liters in healthy adult volunteers.Linezolid concentrations have been determined in various fluids from limited number of subjects in Phase volunteer studies following multiple dosing of linezolid. The ratio of linezolid in saliva relative to plasma was 1.2 to and the ratio of linezolid in sweat relative to plasma was 0.55 to 1.. MetabolismLinezolid is primarily metabolized by oxidation of the morpholine ring, which results in two inactive ring-opened carboxylic acid metabolites: the aminoethoxyacetic acid metabolite (A), and the hydroxyethyl glycine metabolite (B). Formation of metabolite is presumed to be formed via an enzymatic pathway whereas metabolite is mediated by non-enzymatic chemical oxidation mechanism in vitro. In vitro studies have demonstrated that linezolid is minimally metabolized and may be mediated by human cytochrome P450. However, the metabolic pathway of linezolid is not fully understood.. ExcretionNonrenal clearance accounts for approximately 65% of the total clearance of linezolid. Under steady-state conditions, approximately 30% of the dose appears in the urine as linezolid, 40% as metabolite B, and 10% as metabolite A. The mean renal clearance of linezolid is 40 mL/min which suggests net tubular reabsorption. Virtually no linezolid appears in the feces, while approximately 6% of the dose appears in the feces as metabolite B, and 3% as metabolite A.A small degree of nonlinearity in clearance was observed with increasing doses of linezolid, which appears to be due to lower renal and nonrenal clearance of linezolid at higher concentrations. However, the difference in clearance was small and was not reflected in the apparent elimination half-life.. Specific Populations. Geriatric PatientsThe pharmacokinetics of linezolid are not significantly altered in elderly patients (65 years or older). Therefore, dose adjustment for geriatric patients is not necessary.. Pediatric PatientsThe pharmacokinetics of linezolid following single intravenous dose were investigated in pediatric patients ranging in age from birth through 17 years (including premature and full-term neonates), in healthy adolescent subjects ranging in age from 12 through 17 years, and in pediatric patients ranging in age from week through 12 years. The pharmacokinetic parameters of linezolid are summarized in Table for the pediatric populations studied and healthy adult subjects after administration of single intravenous doses.The Cmax and the volume of distribution (Vss) of linezolid are similar regardless of age in pediatric patients. However, plasma clearance of linezolid varies as function of age. With the exclusion of pre-term neonates less than one week of age, weight-based clearance is most rapid in the youngest age groups ranging from 1 week old to 11 years, resulting in lower single-dose systemic exposure (AUC) and shorter half-life as compared with adults. As the age of pediatric patients increases, the weight-based clearance of linezolid gradually decreases, and by adolescence mean clearance values approach those observed for the adult population. There is increased inter-subject variability in linezolid clearance and systemic drug exposure (AUC) across all pediatric age groups as compared with adults.Similar mean daily AUC values were observed in pediatric patients from birth to 11 years of age dosed every hours relative to adolescents or adults dosed every 12 hours. Therefore, the dosage for pediatric patients up to 11 years of age should be 10 mg/kg every hours. Pediatric patients 12 years and older should receive 600 mg every 12 hours [see Dosage and Administration (2) ].Table 9. Pharmacokinetic Parameters of Linezolid in Pediatrics and Adults Following Single Intravenous Infusion of 10 mg/kg or 600 mg Linezolid (Mean: (%CV); [Min, Max Values])Age GroupCmax mcg/mLVss L/kgAUCAUC Single dose AUC0- mcgh/mLt 1/2 hrsCLmL/min/kgCmax Maximum plasma concentration; Vss= Volume of distribution; AUC Area under concentration-time curve; t1/2 Apparent elimination half-life; CL Systemic clearance normalized for body weightNeonatal PatientsPre-termIn this data set, pre-term is defined as <34 weeks gestational age (Note: Only patient enrolled was pre-term with postnatal age between week and 28 days) 1 week (N=9)Dose of 10 mg/kg 12.7 (30%)[9.6, 22.2]0.81 (24%)[0.43, 1.05]108 (47%)[41, 191]5.6 (46%)[2.4, 9.8]2.0 (52%)[0.9, 4.0]Full-termIn this data set, full-term is defined as >=34 weeks gestational age 1 week (N=10) 11.5 (24%)[8.0, 18.3]0.78 (20%)[0.45, 0.96]55 (47%)[19, 103]3.0 (55%)[1.3, 6.1]3.8 (55%)[1.5, 8.8]Full-term >= week to <= 28 days (N=10) 12.9 (28%)[7.7, 21.6]0.66 (29%)[0.35, 1.06]34 (21%)[23, 50]1.5 (17%)[1.2, 1.9]5.1 (22%)[3.3, 7.2]Infant Patients> 28 days to 3 Months (N=12) 11.0 (27%)[7.2, 18.0]0.79 (26%)[0.42, 1.08]33 (26%)[17, 48]1.8 (28%)[1.2, 2.8]5.4 (32%)[3.5, 9.9]Pediatric Patients months through 11 years (N=59)15.1 (30%)[6.8, 36.7]0.69 (28%)[0.31, 1.50]58 (54%)[19, 153]2.9 (53%)[0.9, 8.0]3.8 (53%)[1.0, 8.5]Adolescent Subjects and Patients 12 through 17 yearsDose of 600 mg or 10 mg/kg up to maximum of 600 mg (N=36)16.7 (24%)[9.9, 28.9]0.61 (15%)[0.44, 0.79]95 (44%)[32, 178]4.1 (46%)[1.3, 8.1]2.1 (53%)[0.9, 5.2]Adult SubjectsDose normalized to 600 mg (N= 29)12.5 (21%)[8.2, 19.3]0.65 (16%)[0.45, 0.84]91 (33%)[53, 155]4.9 (35%)[1.8, 8.3]1.7 (34%)[0.9, 3.3]. GenderFemales have slightly lower volume of distribution of linezolid than males. Plasma concentrations are higher in females than in males, which is partly due to body weight differences. After 600-mg dose, mean oral clearance is approximately 38% lower in females than in males. However, there are no significant gender differences in mean apparent elimination-rate constant or half-life. Thus, drug exposure in females is not expected to substantially increase beyond levels known to be well tolerated. Therefore, dose adjustment by gender does not appear to be necessary.. Renal ImpairmentThe pharmacokinetics of the parent drug, linezolid, are not altered in patients with any degree of renal impairment; however, the two primary metabolites of linezolid accumulate in patients with renal impairment, with the amount of accumulation increasing with the severity of renal dysfunction (see Table 10). The pharmacokinetics of linezolid and its two metabolites have also been studied in patients with end-stage renal disease (ESRD) receiving hemodialysis. In the ESRD study, 14 patients were dosed with linezolid 600 mg every 12 hours for 14.5 days (see Table 11). Because similar plasma concentrations of linezolid are achieved regardless of renal function, no dose adjustment is recommended for patients with renal impairment. However, given the absence of information on the clinical significance of accumulation of the primary metabolites, use of linezolid in patients with renal impairment should be weighed against the potential risks of accumulation of these metabolites. Both linezolid and the two metabolites are eliminated by hemodialysis. No information is available on the effect of peritoneal dialysis on the pharmacokinetics of linezolid. Approximately 30% of dose was eliminated in 3-hour hemodialysis session beginning hours after the dose of linezolid was administered; therefore, linezolid should be given after hemodialysis.Table 10. Mean (Standard Deviation) AUCs and Elimination Half-lives of Linezolid and Metabolites and in Patients with Varying Degrees of Renal Impairment After Single 600 mg Oral Dose of LinezolidParameterHealthy Subjects CLCR 80 mL/minModerate Renal Impairment 30 CLCR 80 mL/minSevere Renal Impairment 10 CLCR 30 mL/minLINEZOLIDAUC0-, mcg h/mL110 (22)128 (53)127 (66)t1/2, hours6.4 (2.2)6.1 (1.7)7.1 (3.7)METABOLITE AAUC0-48, mcg h/mL7.6 (1.9)11.7 (4.3)56.5 (30.6)t1/2, hours6.3 (2.1)6.6 (2.3)9.0 (4.6)METABOLITE BMetabolite is the major metabolite of linezolid. AUC0-48, mcg h/mL30.5 (6.2)51.1 (38.5)203 (92)t1/2, hours6.6 (2.7)9.9 (7.4)11.0 (3.9)Table 11. Mean (Standard Deviation) AUCs and Elimination Half-lives of Linezolid and Metabolites and in Subjects with End-Stage Renal Disease (ESRD) After the Administration of 600 mg Linezolid Every 12 Hours for 14.5 DaysParameterESRD Subjectsbetween hemodialysis sessions LINEZOLIDAUC0-12, mcg h/mL (after last dose)181 (52.3)t1/2, (after last dose)8.3 (2.4)METABOLITE AAUC0-12, mcg h/mL (after last dose)153 (40.6)t1/2, (after last dose)15.9 (8.5)METABOLITE BMetabolite is the major metabolite of linezolid. AUC0-12, mcg h/mL (after last dose)356 (99.7)t1/2, (after last dose)34.8 (23.1). Hepatic ImpairmentThe pharmacokinetics of linezolid are not altered in patients (n=7) with mild-to-moderate hepatic impairment (Child-Pugh class or B). On the basis of the available information, no dose adjustment is recommended for patients with mild-to-moderate hepatic impairment. The pharmacokinetics of linezolid in patients with severe hepatic impairment have not been evaluated.. Drug Interactions. Drugs Metabolized by Cytochrome P450Linezolid is not an inducer of cytochrome P450 (CYP450) in rats. In addition, linezolid does not inhibit the activities of clinically significant human CYP isoforms (e.g., 1A2, 2C9, 2C19, 2D6, 2E1, 3A4). Therefore, linezolid is not expected to affect the pharmacokinetics of other drugs metabolized by these major enzymes. Concurrent administration of linezolid does not substantially alter the pharmacokinetic characteristics of (S)-warfarin, which is extensively metabolized by CYP2C9. Drugs such as warfarin and phenytoin, which are CYP2C9 substrates, may be given with linezolid without changes in dosage regimen.. Antibacterial DrugsAztreonam: The pharmacokinetics of linezolid or aztreonam are not altered when administered together.Gentamicin: The pharmacokinetics of linezolid or gentamicin are not altered when administered together.. AntioxidantsThe potential for drug-drug interactions with linezolid and the antioxidants Vitamin and Vitamin was studied in healthy volunteers. Subjects were administered 600 mg oral dose of linezolid on Day 1, and another 600 mg dose of linezolid on Day 8. On Days 2-9, subjects were given either Vitamin (1,000 mg/day) or Vitamin (800 IU/ day). The AUC0- of linezolid increased 2.3% when co-administered with Vitamin and 10.9% when co-administered with Vitamin E. No linezolid dose adjustment is recommended during co-administration with Vitamin or Vitamin E.. Strong CYP 3A4 InducersRifampin: The effect of rifampin on the pharmacokinetics of linezolid was evaluated in study of 16 healthy adult males. Volunteers were administered oral linezolid 600 mg twice daily for doses with and without rifampin 600 mg once daily for days. Co-administration of rifampin with linezolid resulted in 21% decrease in linezolid Cmax [90% CI, 15% 27%] and 32% decrease in linezolid AUC0-12 [90% CI, 27% 37%]. The clinical significance of this interaction is unknown. The mechanism of this interaction is not fully understood and may be related to the induction of hepatic enzymes. Other strong inducers of hepatic enzymes (e.g. carbamazepine, phenytoin, phenobarbital) could cause similar or smaller decrease in linezolid exposure.. Monoamine Oxidase InhibitionLinezolid is reversible, nonselective inhibitor of monoamine oxidase. Therefore, linezolid has the potential for interaction with adrenergic and serotonergic agents.. Adrenergic AgentsSome individuals receiving ZYVOX may experience reversible enhancement of the pressor response to indirect-acting sympathomimetic agents, vasopressor or dopaminergic agents. Commonly used drugs such as phenylpropanolamine and pseudoephedrine have been specifically studied. Initial doses of adrenergic agents, such as dopamine or epinephrine, should be reduced and titrated to achieve the desired response.Tyramine: significant pressor response has been observed in normal adult subjects receiving linezolid and tyramine doses of more than 100 mg. Therefore, patients receiving linezolid need to avoid consuming large amounts of foods or beverages with high tyramine content [see Patient Counseling Information (17) ].Pseudoephedrine HCl or phenylpropanolamine HCl: reversible enhancement of the pressor response of either pseudoephedrine HCl (PSE) or phenylpropanolamine HCl (PPA) is observed when linezolid is administered to healthy normotensive subjects [see Warnings and Precautions (5.6) and Drug Interactions (7) ]. similar study has not been conducted in hypertensive patients. The interaction studies conducted in normotensive subjects evaluated the blood pressure and heart rate effects of placebo, PPA or PSE alone, linezolid alone, and the combination of steady-state linezolid (600 mg every 12 hours for days) with two doses of PPA (25 mg) or PSE (60 mg) given hours apart. Heart rate was not affected by any of the treatments. Blood pressure was increased with both combination treatments. Maximum blood pressure levels were seen to hours after the second dose of PPA or PSE, and returned to baseline to hours after peak. The results of the PPA study follow, showing the mean (and range) maximum systolic blood pressure in mm Hg: placebo 121 (103 to 158); linezolid alone 120 (107 to 135); PPA alone 125 (106 to 139); PPA with linezolid 147 (129 to 176). The results from the PSE study were similar to those in the PPA study. The mean maximum increase in systolic blood pressure over baseline was 32 mm Hg (range: 20-52 mm Hg) and 38 mm Hg (range: 18-79 mm Hg) during co-administration of linezolid with pseudoephedrine or phenylpropanolamine, respectively.. Serotonergic AgentsDextromethorphan: The potential drug-drug interaction with dextromethorphan was studied in healthy volunteers. Subjects were administered dextromethorphan (two 20-mg doses given hours apart) with or without linezolid. No serotonin syndrome effects (confusion, delirium, restlessness, tremors, blushing, diaphoresis, hyperpyrexia) have been observed in normal subjects receiving linezolid and dextromethorphan.. 12.4Microbiology. Mechanism of ActionLinezolid is synthetic antibacterial agent of the oxazolidinone class, which has clinical utility in the treatment of infections caused by aerobic Gram-positive bacteria. The in vitro spectrum of activity of linezolid also includes certain Gram-negative bacteria and anaerobic bacteria. Linezolid binds to site on the bacterial 23S ribosomal RNA of the 50S subunit and prevents the formation of functional 70S initiation complex, which is essential for bacterial reproduction. The results of time-kill studies have shown linezolid to be bacteriostatic against enterococci and staphylococci. For streptococci, linezolid was found to be bactericidal for the majority of isolates.. ResistanceIn vitro studies have shown that point mutations in the 23S rRNA are associated with linezolid resistance. Reports of vancomycin-resistant Enterococcus faecium becoming resistant to linezolid during its clinical use have been published. There are reports of Staphylococcus aureus (methicillin-resistant) developing resistance to linezolid during clinical use. The linezolid resistance in these organisms is associated with point mutation in the 23S rRNA (substitution of thymine for guanine at position 2576) of the organism. Organisms resistant to oxazolidinones via mutations in chromosomal genes encoding 23S rRNA or ribosomal proteins (L3 and L4) are generally cross-resistant to linezolid. Also linezolid resistance in staphylococci mediated by the enzyme methyltransferase has been reported. This resistance is mediated by the cfr (chloramphenicol-florfenicol) gene located on plasmid which is transferable between staphylococci.. Interaction with Other Antimicrobial DrugsIn vitro studies have demonstrated additivity or indifference between linezolid and vancomycin, gentamicin, rifampin, imipenem-cilastatin, aztreonam, ampicillin, or streptomycin.Linezolid 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) ].. Gram-positive bacteriaEnterococcus faecium (vancomycin-resistant isolates only)Staphylococcus aureus (including methicillin-resistant isolates)Streptococcus agalactiaeStreptococcus pneumoniaeStreptococcus pyogenesThe following in vitro data are available, but their clinical significance is unknown. Greater than 90% of the following bacteria exhibit an in vitro MIC less than or equal to the linezolid-susceptible breakpoint for organisms of similar genus. The safety and effectiveness of linezolid in treating clinical infections due to these bacteria have not been established in adequate and well-controlled clinical trials.. Gram-positive bacteriaEnterococcus faecalis (including vancomycin-resistant isolates)Enterococcus faecium (vancomycin-susceptible isolates)Staphylococcus epidermidis (including methicillin-resistant isolates)Staphylococcus haemolyticusViridans group streptococci. Gram-negative bacteriaPasteurella multocida. Susceptibility TestingFor 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.

14CLINICAL STUDIES. 14.1Adults. Nosocomial PneumoniaAdult patients with clinically and radiologically documented nosocomial pneumonia were enrolled in randomized, multi-center, double-blind trial. Patients were treated for to 21 days. One group received ZYVOX I.V. Injection 600 mg every 12 hours, and the other group received vancomycin g every 12 hours intravenously. Both groups received concomitant aztreonam (1 to g every hours intravenously), which could be continued if clinically indicated. There were 203 linezolid-treated and 193 vancomycin-treated patients enrolled in the study. One hundred twenty-two (60%) linezolid-treated patients and 103 (53%) vancomycin-treated patients were clinically evaluable. The cure rates in clinically evaluable patients were 57% for linezolid-treated patients and 60% for vancomycin-treated patients. The cure rates in clinically evaluable patients with ventilator-associated pneumonia were 47% for linezolid-treated patients and 40% for vancomycin-treated patients. modified intent-to-treat (MITT) analysis of 94 linezolid-treated patients and 83 vancomycin-treated patients included subjects who had pathogen isolated before treatment. The cure rates in the MITT analysis were 57% in linezolid-treated patients and 46% in vancomycin-treated patients. The cure rates by pathogen for microbiologically evaluable patients are presented in Table 12.Table 12. Cure Rates at the Test-of-Cure Visit for Microbiologically Evaluable Adult Patients with Nosocomial PneumoniaCuredPathogenZYVOXn/N (%)Vancomycinn/N (%)Staphylococcus aureus23/38 (61)14/23 (61)Methicillin-resistant S. aureus 13/22 (59)7/10 (70)Streptococcus pneumoniae9/9 (100)9/10 (90). Complicated Skin and Skin Structure InfectionsAdult patients with clinically documented complicated skin and skin structure infections were enrolled in randomized, multi-center, double-blind, double-dummy trial comparing study medications administered intravenously followed by medications given orally for total of 10 to 21 days of treatment. One group of patients received ZYVOX I.V. Injection 600 mg every 12 hours followed by ZYVOX Tablets 600 mg every 12 hours; the other group received oxacillin g every hours intravenously followed by dicloxacillin 500 mg every hours orally. Patients could receive concomitant aztreonam if clinically indicated. There were 400 linezolid-treated and 419 oxacillin-treated patients enrolled in the study. Two hundred forty-five (61%) linezolid-treated patients and 242 (58%) oxacillin-treated patients were clinically evaluable. The cure rates in clinically evaluable patients were 90% in linezolid-treated patients and 85% in oxacillin-treated patients. modified intent-to-treat (MITT) analysis of 316 linezolid-treated patients and 313 oxacillin-treated patients included subjects who met all criteria for study entry. The cure rates in the MITT analysis were 86% in linezolid-treated patients and 82% in oxacillin-treated patients. The cure rates by pathogen for microbiologically evaluable patients are presented in Table 13.Table 13. Cure Rates at the Test-of-Cure Visit for Microbiologically Evaluable Adult Patients with Complicated Skin and Skin Structure InfectionsCuredPathogenZYVOXn/N (%)Oxacillin/Dicloxacillinn/N (%)Staphylococcus aureus73/83 (88)72/84 (86)Methicillin-resistant S. aureus 2/3 (67)0/0 (-)Streptococcus agalactiae6/6 (100)3/6 (50)Streptococcus pyogenes18/26 (69)21/28 (75)A separate study provided additional experience with the use of ZYVOX in the treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections. This was randomized, open-label trial in hospitalized adult patients with documented or suspected MRSA infection.One group of patients received ZYVOX I.V. Injection 600 mg every 12 hours followed by ZYVOX Tablets 600 mg every 12 hours. The other group of patients received vancomycin g every 12 hours intravenously. Both groups were treated for to 28 days, and could receive concomitant aztreonam or gentamicin if clinically indicated. The cure rates in microbiologically evaluable patients with MRSA skin and skin structure infection were 26/33 (79%) for linezolid-treated patients and 24/33 (73%) for vancomycin-treated patients.. Diabetic Foot InfectionsAdult diabetic patients with clinically documented complicated skin and skin structure infections (diabetic foot infections) were enrolled in randomized (2:1 ratio), multi-center, open-label trial comparing study medications administered intravenously or orally for total of 14 to 28 days of treatment. One group of patients received ZYVOX 600 mg every 12 hours intravenously or orally; the other group received ampicillin/sulbactam 1.5 to g intravenously or amoxicillin/clavulanate 500 to 875 mg every to 12 hours orally. In countries where ampicillin/sulbactam is not marketed, amoxicillin/clavulanate 500 mg to g every hours was used for the intravenous regimen. Patients in the comparator group could also be treated with vancomycin g every 12 hours intravenously if MRSA was isolated from the foot infection. Patients in either treatment group who had Gram-negative bacilli isolated from the infection site could also receive aztreonam to g every 8-12 hours intravenously. All patients were eligible to receive appropriate adjunctive treatment methods, such as debridement and off-loading, as typically required in the treatment of diabetic foot infections, and most patients received these treatments. There were 241 linezolid-treated and 120 comparator-treated patients in the intent-to-treat (ITT) study population. Two hundred twelve (86%) linezolid-treated patients and 105 (85%) comparator-treated patients were clinically evaluable. In the ITT population, the cure rates were 68.5% (165/241) in linezolid-treated patients and 64% (77/120) in comparator-treated patients, where those with indeterminate and missing outcomes were considered failures. The cure rates in the clinically evaluable patients (excluding those with indeterminate and missing outcomes) were 83% (159/192) and 73% (74/101) in the linezolid- and comparator-treated patients, respectively. critical post-hoc analysis focused on 121 linezolid-treated and 60 comparator-treated patients who had Gram-positive pathogen isolated from the site of infection or from blood, who had less evidence of underlying osteomyelitis than the overall study population, and who did not receive prohibited antimicrobials. Based upon that analysis, the cure rates were 71% (86/121) in the linezolid-treated patients and 63% (38/60) in the comparator-treated patients. None of the above analyses were adjusted for the use of adjunctive therapies. The cure rates by pathogen for microbiologically evaluable patients are presented in Table 14.Table 14. Cure Rates at the Test-of-Cure Visit for Microbiologically Evaluable Adult Patients with Diabetic Foot InfectionsCuredPathogenZYVOXn/N (%)Comparatorn/N (%)Staphylococcus aureus49/63 (78)20/29 (69)Methicillin-resistant S. aureus 12/17 (71)2/3 (67)Streptococcus agalactiae25/29 (86)9/16 (56). Vancomycin-Resistant Enterococcal InfectionsAdult patients with documented or suspected vancomycin-resistant enterococcal infection were enrolled in randomized, multi-center, double-blind trial comparing high dose of ZYVOX (600 mg) with low dose of ZYVOX (200 mg) given every 12 hours either intravenously (IV) or orally for to 28 days. Patients could receive concomitant aztreonam or aminoglycosides. There were 79 patients randomized to high-dose linezolid and 66 to low-dose linezolid. The intent-to-treat (ITT) population with documented vancomycin-resistant enterococcal infection at baseline consisted of 65 patients in the high-dose arm and 52 in the low-dose arm.The cure rates for the ITT population with documented vancomycin-resistant enterococcal infection at baseline are presented in Table 15 by source of infection. These cure rates do not include patients with missing or indeterminate outcomes. The cure rate was higher in the high-dose arm than in the low-dose arm, although the difference was not statistically significant at the 0.05 level.Table 15. Cure Rates at the Test-of-Cure Visit for ITT Adult Patients with Documented Vancomycin-Resistant Enterococcal Infections at BaselineCuredSource of InfectionZYVOX 600 mg every 12 hoursn/N (%)ZYVOX 200 mg every 12 hoursn/N (%)Any site39/58 (67)24/46 (52)Any site with associated bacteremia10/17 (59)4/14 (29)Bacteremia of unknown origin5/10 (50)2/7 (29)Skin and skin structure9/13 (69)5/5 (100)Urinary tract12/19 (63)12/20 (60)Pneumonia2/3 (67)0/1 (0)OtherIncludes sources of infection such as hepatic abscess, biliary sepsis, necrotic gall bladder, pericolonic abscess, pancreatitis, and catheter-related infection. 11/13 (85)5/13 (39). 14.2Pediatric Patients. Infections due to Gram-positive BacteriaA safety and efficacy study provided experience on the use of ZYVOX in pediatric patients for the treatment of nosocomial pneumonia, complicated skin and skin structure infections, and other infections due to Gram-positive bacterial pathogens, including methicillin-resistant and -susceptible Staphylococcus aureus and vancomycin-resistant Enterococcus faecium. Pediatric patients ranging in age from birth through 11 years with infections caused by the documented or suspected Gram-positive bacteria were enrolled in randomized, open-label, comparator-controlled trial. One group of patients received ZYVOX I.V. Injection 10 mg/kg every hours followed by ZYVOX for Oral Suspension 10 mg/kg every hours. second group received vancomycin 10 to 15 mg/kg intravenously every to 24 hours, depending on age and renal clearance. Patients who had confirmed VRE infections were placed in third arm of the study and received ZYVOX 10 mg/kg every hours intravenously and/or orally. All patients were treated for total of 10 to 28 days and could receive concomitant Gram-negative antibacterial drugs if clinically indicated. In the intent-to-treat (ITT) population, there were 206 patients randomized to linezolid and 102 patients randomized to vancomycin. The cure rates for ITT, MITT, and clinically evaluable patients are presented in Table 16. After the study was completed, 13 additional patients ranging from days through 16 years of age were enrolled in an open-label extension of the VRE arm of the study. Table 17 provides clinical cure rates by pathogen for microbiologically evaluable patients including microbiologically evaluable patients with vancomycin-resistant Enterococcus faecium from the extension of this study.Table 16. Cure Rates at the Test-of-Cure Visit for Intent-to-Treat, Modified Intent-to-Treat, and Clinically Evaluable Pediatric Patients for the Overall Population and by Select Baseline DiagnosisITTMITTMITT ITT patients with an isolated Gram-positive pathogen at baseline Clinically EvaluablePopulationZYVOXn/N (%)Vancomycinn/N (%)ZYVOXn/N (%)Vancomycinn/N (%)ZYVOXn/N (%)Vancomycinn/N (%)Any diagnosis150/186 (81)69/83 (83)86/108 (80)44/49 (90)106/117 (91)49/54 (91)Complicated skin and skin structure infections61/72 (85)31/34 (91)37/43 (86)22/23 (96)46/49 (94)26/27 (96)Nosocomial pneumonia13/18 (72)11/12 (92)5/6 (83)4/4 (100)7/7 (100)5/5 (100)Table 17. Cure Rates at the Test-of-Cure Visit for Microbiologically Evaluable Pediatric Patients with Infections due to Gram-positive PathogensMicrobiologically EvaluablePathogenZYVOXn/N (%)Vancomycinn/N (%)Vancomycin-resistant Enterococcus faecium 6/8 (75)Includes data from patients enrolled in the open-label extension of this study. 0/0 (-)Staphylococcus aureus36/38 (95)23/24 (96)Methicillin-resistant S. aureus 16/17 (94)9/9 (100)Streptococcus pyogenes2/2 (100)1/2 (50).

CLINICAL TRIALS EXPERIENCE SECTION.

6.1Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.. AdultsThe safety of ZYVOX formulations was evaluated in 2,046 adult patients enrolled in seven Phase comparator-controlled clinical trials, who were treated for up to 28 days.Of the patients treated for uncomplicated skin and skin structure infections (uSSSIs), 25.4% of ZYVOX-treated and 19.6% of comparator-treated patients experienced at least one drug-related adverse event. For all other indications, 20.4% of ZYVOX -treated and 14.3% of comparator-treated patients experienced at least one drug-related adverse event.Table shows the incidence of all-causality, treatment-emergent adverse reactions reported in at least 1% of adult patients in these trials by dose of ZYVOX.Table 2. Incidence (%) of Treatment-Emergent Adverse Reactions Occurring in >1% of Adult Patients Treated with ZYVOX in Comparator-Controlled Clinical TrialsADVERSE REACTIONSUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg by mouth every 12 hours (n=548)Clarithromycin 250 mg by mouth every 12 hours (n=537)ZYVOX 600 mg every 12 hours (n=1498)All Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. (n=1464)Headache8.88.45.74.4Diarrhea8.26.18.36.4Nausea5.14.56.64.6Vomiting2.01.54.32.3Dizziness2.63.01.81.5Rash1.11.12.32.6Anemia0.402.11.4Taste alteration1.82.01.00.3Vaginal moniliasis1.81.31.10.5Oral moniliasis0.501.71.0Abnormal liver function tests0.40.21.60.8Fungal infection1.50.20.30.2Tongue discoloration1.300.30Localized abdominal pain1.30.61.20.8Generalized abdominal pain0.90.41.21.0Of the patients treated for uSSSIs, 3.5% of ZYVOX-treated and 2.4% of comparator-treated patients discontinued treatment due to drug-related adverse events. For all other indications, discontinuations due to drug-related adverse events occurred in 2.1% of ZYVOX-treated and 1.7% of comparator-treated patients. The most common reported drug-related adverse events leading to discontinuation of treatment were nausea, headache, diarrhea, and vomiting.. Pediatric PatientsThe safety of ZYVOX formulations was evaluated in 215 pediatric patients ranging in age from birth through 11 years, and in 248 pediatric patients aged through 17 years (146 of these 248 were age through 11 and 102 were age 12 to 17). These patients were enrolled in two Phase comparator-controlled clinical trials and were treated for up to 28 days. In the study of hospitalized pediatric patients (birth through 11 years) with Gram-positive infections, who were randomized to (linezolid: vancomycin), mortality was 6.0% (13/215) in the linezolid arm and 3.0% (3/101) in the vancomycin arm. However, given the severe underlying illness in the patient population, no causality could be established.Of the pediatric patients treated for uSSSIs, 19.2% of ZYVOX-treated and 14.1% of comparator-treated patients experienced at least one drug-related adverse event. For all other indications, 18.8% of ZYVOX-treated and 34.3% of comparator-treated patients experienced at least one drug-related adverse event.Table shows the incidence of all-causality, treatment-emergent adverse reactions reported in more than 1% of pediatric patients (and more than patient) in either treatment group in the comparator-controlled Phase trials.Table 3. Incidence (%) of Treatment-Emergent Adverse Reactions Occurring in 1% of Pediatric Patients (and >1 Patient) in Either Treatment Group in Comparator-Controlled Clinical TrialsADVERSE REACTIONSUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg by mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOX(n=248)Cefadroxil(n=251)ZYVOX(n=215)Vancomycin(n=101)Diarrhea7.88.010.812.1Vomiting2.96.49.49.1Headache6.54.00.90Anemia005.67.1Thrombocytopenia004.72.0Nausea3.73.21.90Generalized abdominal pain2.42.80.92.0Localized abdominal pain2.42.80.51.0Loose stools1.60.82.33.0Eosinophilia0.40.81.91.0Pruritus at non-application site0.80.41.42.0Vertigo1.20.400Of the pediatric patients treated for uSSSIs, 1.6% of ZYVOX-treated and 2.4% of comparator-treated patients discontinued treatment due to drug-related adverse events. For all other indications, discontinuations due to drug-related adverse events occurred in 0.9% of ZYVOX-treated and 6.1% of comparator-treated patients.. Laboratory AbnormalitiesZYVOX has been associated with thrombocytopenia when used in doses up to and including 600 mg every 12 hours for up to 28 days. In Phase comparator-controlled trials, the percentage of adult patients who developed substantially low platelet count (defined as less than 75% of lower limit of normal and/or baseline) was 2.4% (range among studies: 0.3 to 10.0%) with ZYVOX and 1.5% (range among studies: 0.4 to 7.0%) with comparator. In study of hospitalized pediatric patients ranging in age from birth through 11 years, the percentage of patients who developed substantially low platelet count (defined as less than 75% of lower limit of normal and/or baseline) was 12.9% with ZYVOX and 13.4% with vancomycin. In an outpatient study of pediatric patients aged from through 17 years, the percentage of patients who developed substantially low platelet count was 0% with ZYVOX and 0.4% with cefadroxil. Thrombocytopenia associated with the use of ZYVOX appears to be dependent on duration of therapy (generally greater than weeks of treatment). The platelet counts for most patients returned to the normal range/baseline during the follow-up period. No related clinical adverse events were identified in Phase clinical trials in patients developing thrombocytopenia. Bleeding events were identified in thrombocytopenic patients in compassionate use program for ZYVOX; the role of linezolid in these events cannot be determined [see Warning and Precautions (5.1) ].Changes seen in other laboratory parameters, without regard to drug relationship, revealed no substantial differences between ZYVOX and the comparators. These changes were generally not clinically significant, did not lead to discontinuation of therapy, and were reversible. The incidence of adult and pediatric patients with at least one substantially abnormal hematologic or serum chemistry value is presented in Tables 4, 5, 6, and 7.Table 4. Percent of Adult Patients who Experienced at Least One Substantially Abnormal<75% (<50% for neutrophils) of Lower Limit of Normal (LLN) for values normal at baseline; <75% (<50% for neutrophils) of LLN and of baseline for values abnormal at baseline. Hematology Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg every 12 hoursClarithromycin 250 mg every 12 hoursZYVOX 600 mg every 12 hoursAll Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. Hemoglobin (g/dL)0.90.07.16.6Platelet count (x 103/mm3)0.70.83.01.8WBC (x 103/mm3)0.20.62.21.3Neutrophils (x 103/mm3)0.00.21.11.2Table 5. Percent of Adult Patients who Experienced at Least One Substantially Abnormal>2 Upper Limit of Normal (ULN) for values normal at baseline; >2 ULN and >2 baseline for values abnormal at baseline. Serum Chemistry Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsAll Other IndicationsZYVOX 400 mg every 12 hoursClarithromycin 250 mg every 12 hoursZYVOX 600 mg every 12 hoursAll Other ComparatorsComparators included cefpodoxime proxetil 200 mg by mouth every 12 hours; ceftriaxone g intravenously every 12 hours; dicloxacillin 500 mg by mouth every hours; oxacillin g intravenously every hours; vancomycin g intravenously every 12 hours. AST (U/L)1.71.35.06.8ALT (U/L)1.71.79.69.3LDH (U/L)0.20.21.81.5Alkaline phosphatase (U/L)0.20.23.53.1Lipase (U/L)2.82.64.34.2Amylase (U/L)0.20.22.42.0Total bilirubin (mg/dL)0.20.00.91.1BUN (mg/dL)0.20.02.11.5Creatinine (mg/dL)0.20.00.20.6Table 6. Percent of Pediatric Patients who Experienced at Least One Substantially Abnormal<75% (<50% for neutrophils) of Lower Limit of Normal (LLN) for values normal at baseline;<75% (<50% for neutrophils) of LLN and <75% (<50% for neutrophils, <90% for hemoglobin if baseline <LLN) of baseline for values abnormal at baseline. Hematology Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg by mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOXCefadroxilZYVOXVancomycinHemoglobin (g/dL)0.00.015.712.4Platelet count (x 103/mm3)0.00.412.913.4WBC (x 103/mm3)0.80.812.410.3Neutrophils (x 103/mm3)1.20.85.94.3Table 7. Percent of Pediatric Patients who Experienced at Least One Substantially Abnormal>2 Upper Limit of Normal (ULN) for values normal at baseline; >2 ULN and >2 (>1.5 for total bilirubin) baseline for values abnormal at baseline. Serum Chemistry Laboratory Value in Comparator-Controlled Clinical Trials with ZYVOXLaboratory AssayUncomplicated Skin and Skin Structure InfectionsPatients through 11 years of age received ZYVOX 10 mg/kg by mouth every 12 hours or cefadroxil 15 mg/kg by mouth every 12 hours. Patients 12 years or older received ZYVOX 600 mg mouth every 12 hours or cefadroxil 500 mg by mouth every 12 hours. All Other IndicationsPatients from birth through 11 years of age received ZYVOX 10 mg/kg intravenously/by mouth every hours or vancomycin 10 to 15 mg/kg intravenously every 6-24 hours, depending on age and renal clearance. ZYVOX CefadroxilZYVOXVancomycinALT (U/L)0.00.010.112.5Lipase (U/L)0.41.2------Amylase (U/L)------0.61.3Total bilirubin (mg/dL)------6.35.2Creatinine (mg/dL)0.40.02.41.0.

CONTRAINDICATIONS SECTION.

4CONTRAINDICATIONS. Known hypersensitivity to linezolid or any of the other product components. (4.1)Patients taking any monoamine oxidase inhibitors (MAOI) or within two weeks of taking an MAOI. (4.2). Known hypersensitivity to linezolid or any of the other product components. (4.1). Patients taking any monoamine oxidase inhibitors (MAOI) or within two weeks of taking an MAOI. (4.2). 4.1Hypersensitivity. ZYVOX formulations are contraindicated for use in patients who have known hypersensitivity to linezolid or any of the other product components. 4.2Monoamine Oxidase Inhibitors. Linezolid should not be used in patients taking any medicinal product which inhibits monoamine oxidases or (e.g., phenelzine, isocarboxazid) or within two weeks of taking any such medicinal product.

DESCRIPTION SECTION.

11DESCRIPTION. ZYVOX I.V. Injection contains linezolid, which is synthetic antibacterial agent of the oxazolidinone class. The chemical name for linezolid is (S)-N-[[3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl] methyl]-acetamide.The empirical formula is C16H20FN3O4. Its molecular weight is 337.35, and its chemical structure is represented below:ZYVOX I.V. Injection is supplied as ready-to-use sterile isotonic solution for intravenous infusion. Each mL contains mg of linezolid. Inactive ingredients are dextrose monohydrate 50.24 mg/mL in an aqueous vehicle for intravenous administration, sodium citrate dihydrate 1.64 mg/mL, and citric acid anhydrous 0.85 mg/mL. Sodium hydroxide NF and/or hydrochloric acid NF are used to adjust the pH. The sodium (Na+) content is 0.38 mg/mL (5 mEq/300 mL bag).. Chemical Structure.

DOSAGE & ADMINISTRATION SECTION.

2DOSAGE AND ADMINISTRATION. Dosage, Route, and Frequency of AdministrationInfectionPediatric Patients (Birth through 11 years of Age)Adults and Adolescents (12 years and Older)Duration (days)Nosocomial pneumonia10 mg/kg intravenous or oral every hours600 mg intravenous or oral every 12 hours10 to 14Community-acquired pneumonia, including concurrent bacteremiaComplicated skin and skin structure infectionsVancomycin-resistant Enterococcus faecium infections, including concurrent bacteremia10 mg/kg intravenous or oral every hours600 mg intravenous or oral every 12 hours 14 to 28Uncomplicated skin and skin structure infectionsless than yrs: 10 mg/kg oral every hours5-11 yrs: 10 mg/kg oral every 12 hoursAdults: 400 mg oral every 12 hoursAdolescents: 600 mg oral every 12 hours10 to 14. 2.1General Dosage and Administration. The recommended dosage for ZYVOX formulations for the treatment of infections is described in Table 1.Table 1. Dosage Guidelines for ZYVOXInfectionDue to the designated pathogens [see Indications and Usage (1) Dosage, Route and Frequency of AdministrationRecommended Duration of Treatment (consecutive days)Pediatric PatientsNeonates less than7 days: Most pre-term neonates less than days of age (gestational age less than 34 weeks) have lower systemic linezolid clearance values and larger AUC values than many full-term neonates and older infants. These neonates should be initiated with dosing regimen of 10 mg/kg every 12 hours. Consideration may be given to the use of 10 mg/kg every hours regimen in neonates with sub-optimal clinical response. All neonatal patients should receive 10 mg/kg every hours by days of life [see Use in Specific Populations (8.4) and Clinical Pharmacology (12.3) ]. (Birth through 11 Years of Age)Adults and Adolescents(12 Years and Older)Nosocomial pneumonia10 mg/kg intravenously or oralOral dosing using either ZYVOX Tablets or ZYVOX for Oral Suspension [see How Supplied/Storage and Handling (16) ]. every hours600 mg intravenously or oral every 12 hours10 to 14Community-acquired pneumonia, including concurrent bacteremiaComplicated skin and skin structure infectionsVancomycin-resistant Enterococcus faecium infections, including concurrent bacteremia10 mg/kg intravenously or oral every hours600 mg intravenously or oral every 12 hours14 to 28Uncomplicated skin and skin structure infectionsless than yrs: 10 mg/kg oral every hours5-11 yrs: 10 mg/kg oral every 12 hoursAdults: 400 mg oral every 12 hoursAdolescents: 600 mg oral every 12 hours10 to 14No dose adjustment is necessary when switching from intravenous to oral administration.. 2.2Intravenous Administration. ZYVOX I.V. Injection is supplied in single-dose, ready-to-use infusion bags. Parenteral drug products should be inspected visually for particulate matter prior to administration. Check for minute leaks by firmly squeezing the bag. If leaks are detected, discard the solution, as sterility may be impaired. Keep the infusion bags in the overwrap until ready to use. Store at room temperature. Protect from freezing. ZYVOX I.V. Injection may exhibit yellow color that can intensify over time without adversely affecting potency.ZYVOX I.V. Injection should be administered by intravenous infusion over period of 30 to 120 minutes. Do not use this intravenous infusion bag in series connections. Additives should not be introduced into this solution. If ZYVOX I.V. Injection is to be given concomitantly with another drug, each drug should be given separately in accordance with the recommended dosage and route of administration for each product. Discard unused portion.If the same intravenous line is used for sequential infusion of several drugs, the line should be flushed before and after infusion of ZYVOX I.V. Injection with an infusion solution compatible with ZYVOX I.V. Injection and with any other drug(s) administered via this common line.. 2.3Compatibilities. Compatible intravenous solutions include 0.9% Sodium Chloride Injection, USP, 5% Dextrose Injection, USP, and Lactated Ringers Injection, USP.. 2.4Incompatibilities. Physical incompatibilities resulted when ZYVOX I.V. Injection was combined with the following drugs during simulated Y-site administration: amphotericin B, chlorpromazine HCl, diazepam, pentamidine isothionate, erythromycin lactobionate, phenytoin sodium, and trimethoprim-sulfamethoxazole. Additionally, chemical incompatibility resulted when ZYVOX I.V. Injection was combined with ceftriaxone sodium.

DOSAGE FORMS & STRENGTHS SECTION.

3DOSAGE FORMS AND STRENGTHS. ZYVOX I.V. Injection: 600 mg/300 mL (2 mg/mL) linezolid single-dose, ready-to-use flexible plastic infusion bags in foil laminate overwrap.. Injection: 600 mg/300 mL (2 mg/mL) linezolid. (3). Injection: 600 mg/300 mL (2 mg/mL) linezolid. (3).

DRUG INTERACTIONS SECTION.

7DRUG INTERACTIONS. Monoamine oxidase inhibitors and potential for interaction with adrenergic and serotonergic agents. (4.2, 5.3, 5.6, 7, 12.3). 7.1Monoamine Oxidase Inhibitors. Linezolid is reversible, nonselective inhibitor of monoamine oxidase [see Contraindications (4.2) and Clinical Pharmacology (12.3) ].. 7.2Adrenergic and Serotonergic Agents. Linezolid has the potential for interaction with adrenergic and serotonergic agents [see Warnings and Precautions (5.3, 5.6) and Clinical Pharmacology (12.3) ].

FEMALES & MALES OF REPRODUCTIVE POTENTIAL SECTION.

8.3Females and Males of Reproductive Potential. Infertility. MalesBased on findings from studies in rats, ZYVOX may reversibly impair fertility in male patients [see Nonclinical Toxicology (13.1) ].

GERIATRIC USE SECTION.

8.5Geriatric Use. Of the 2,046 patients treated with ZYVOX in Phase comparator-controlled clinical trials, 589 (29%) were 65 years or older and 253 (12%) were 75 years or older. No overall differences in safety or effectiveness were observed between these patients and younger patients, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

INFORMATION FOR PATIENTS SECTION.

17PATIENT COUNSELING INFORMATION. Important Administration InstructionsAdvise patients that ZYVOX may be taken with or without food.. Peripheral and Optic NeuropathyAdvise patients to inform their physician if they experience changes in vision while taking ZYVOX [see Warnings and Precautions (5.2) ]. Serotonin SyndromeAdvise patients to inform their physician if taking serotonergic agents, including serotonin re-uptake inhibitors or other antidepressants and opioids [see Warnings and Precautions (5.3) ]. Potential Interactions Producing Elevation of Blood PressureAdvise patients to inform their physician if they have history of hypertension.Advise patients to avoid large quantities of foods or beverages with high tyramine content while taking ZYVOX. Foods high in tyramine content include those that may have undergone protein changes by aging, fermentation, pickling, or smoking to improve flavor, such as aged cheeses, fermented or air-dried meats, sauerkraut, soy sauce, tap beers, and red wines. The tyramine content of any protein-rich food may be increased if stored for long periods or improperly refrigerated.Advise patients to inform their physician if taking medications containing pseudoephedrine HCl or phenylpropanolamine HCl, such as cold remedies and decongestants [see Warnings and Precautions (5.6) ].. Advise patients to inform their physician if they have history of hypertension.. Advise patients to avoid large quantities of foods or beverages with high tyramine content while taking ZYVOX. Foods high in tyramine content include those that may have undergone protein changes by aging, fermentation, pickling, or smoking to improve flavor, such as aged cheeses, fermented or air-dried meats, sauerkraut, soy sauce, tap beers, and red wines. The tyramine content of any protein-rich food may be increased if stored for long periods or improperly refrigerated.. Advise patients to inform their physician if taking medications containing pseudoephedrine HCl or phenylpropanolamine HCl, such as cold remedies and decongestants [see Warnings and Precautions (5.6) ].. Lactic AcidosisAdvise patients to inform their physician if they experience repeated episodes of nausea or vomiting while receiving ZYVOX [see Warnings and Precautions (5.7) ].. ConvulsionsAdvise patients to inform their physician if they have history of seizures or convulsions [see Warnings and Precautions (5.8) ].. HypoglycemiaAdvise patients to inform their physician if they have diabetes mellitus. Hypoglycemic reactions, such as diaphoresis and tremulousness, along with low blood glucose measurements may occur when treated with linezolid. If such reactions occur, patients should contact physician or other health professional for proper treatment [see Warnings and Precautions (5.9) ].. Hyponatremia and/or SIADHAdvise patients at risk for hyponatremia to inform their physician if they experience signs and symptoms of hyponatremia and/or SIADH, including confusion, somnolence, generalized weakness, and respiratory distress [see Warnings and Precautions (5.10) ].. PhenylketonuriaAdvise patients with phenylketonuria (PKU) that each mL of the 100 mg/5 mL ZYVOX for Oral Suspension contains 20 mg phenylalanine. The other ZYVOX formulations do not contain phenylalanine. Phenylalanine can be harmful to patients with phenylketonuria. Contact your physician or pharmacist when prescribed with ZYVOX oral suspension.. Antibacterial ResistancePatients should be counseled that antibacterial drugs including ZYVOX should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When ZYVOX is prescribed to treat bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by ZYVOX or other antibacterial drugs in the future.. DiarrheaDiarrhea is common problem caused by antibacterial drugs, which usually ends when the antibacterial drug is discontinued. Sometimes after starting treatment with antibacterial drugs, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibacterial drug. If this occurs, patients should contact their physician as soon as possible [see Warnings and Precautions (5.5) ].. InfertilityAdvise male patients that ZYVOX may reversibly impair fertility [see Use in Specific Populations (8.3) ].

MICROBIOLOGY SECTION.

12.4Microbiology. Mechanism of ActionLinezolid is synthetic antibacterial agent of the oxazolidinone class, which has clinical utility in the treatment of infections caused by aerobic Gram-positive bacteria. The in vitro spectrum of activity of linezolid also includes certain Gram-negative bacteria and anaerobic bacteria. Linezolid binds to site on the bacterial 23S ribosomal RNA of the 50S subunit and prevents the formation of functional 70S initiation complex, which is essential for bacterial reproduction. The results of time-kill studies have shown linezolid to be bacteriostatic against enterococci and staphylococci. For streptococci, linezolid was found to be bactericidal for the majority of isolates.. ResistanceIn vitro studies have shown that point mutations in the 23S rRNA are associated with linezolid resistance. Reports of vancomycin-resistant Enterococcus faecium becoming resistant to linezolid during its clinical use have been published. There are reports of Staphylococcus aureus (methicillin-resistant) developing resistance to linezolid during clinical use. The linezolid resistance in these organisms is associated with point mutation in the 23S rRNA (substitution of thymine for guanine at position 2576) of the organism. Organisms resistant to oxazolidinones via mutations in chromosomal genes encoding 23S rRNA or ribosomal proteins (L3 and L4) are generally cross-resistant to linezolid. Also linezolid resistance in staphylococci mediated by the enzyme methyltransferase has been reported. This resistance is mediated by the cfr (chloramphenicol-florfenicol) gene located on plasmid which is transferable between staphylococci.. Interaction with Other Antimicrobial DrugsIn vitro studies have demonstrated additivity or indifference between linezolid and vancomycin, gentamicin, rifampin, imipenem-cilastatin, aztreonam, ampicillin, or streptomycin.Linezolid 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) ].. Gram-positive bacteriaEnterococcus faecium (vancomycin-resistant isolates only)Staphylococcus aureus (including methicillin-resistant isolates)Streptococcus agalactiaeStreptococcus pneumoniaeStreptococcus pyogenesThe following in vitro data are available, but their clinical significance is unknown. Greater than 90% of the following bacteria exhibit an in vitro MIC less than or equal to the linezolid-susceptible breakpoint for organisms of similar genus. The safety and effectiveness of linezolid in treating clinical infections due to these bacteria have not been established in adequate and well-controlled clinical trials.. Gram-positive bacteriaEnterococcus faecalis (including vancomycin-resistant isolates)Enterococcus faecium (vancomycin-susceptible isolates)Staphylococcus epidermidis (including methicillin-resistant isolates)Staphylococcus haemolyticusViridans group streptococci. Gram-negative bacteriaPasteurella multocida. Susceptibility TestingFor 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.

NONCLINICAL TOXICOLOGY SECTION.

13NONCLINICAL TOXICOLOGY. 13.1Carcinogenesis, Mutagenesis, Impairment of Fertility. Lifetime studies in animals have not been conducted to evaluate the carcinogenic potential of linezolid. Neither mutagenic nor clastogenic potential was found in battery of tests including: assays for mutagenicity (Ames bacterial reversion and CHO cell mutation), an in vitro unscheduled DNA synthesis (UDS) assay, an in vitro chromosome aberration assay in human lymphocytes, and an in vivo mouse micronucleus assay.Linezolid did not affect the fertility or reproductive performance of adult female rats given oral doses of up to 100 mg/kg/day for 14 days prior to mating through Gestation Day 7. It reversibly decreased fertility and reproductive performance in adult male rats when given at doses >= 50 mg/kg/day, with exposures approximately equal to or greater than the expected human exposure level (exposure comparisons are based on AUCs). The reversible fertility effects were mediated through altered spermatogenesis. Affected spermatids contained abnormally formed and oriented mitochondria and were non-viable. Epithelial cell hypertrophy and hyperplasia in the epididymis was observed in conjunction with decreased fertility. Similar epididymal changes were not seen in dogs.In sexually mature male rats exposed to drug as juveniles, mildly decreased fertility was observed following treatment with linezolid through most of their period of sexual development (50 mg/kg/day from days to 36 of age, and 100 mg/kg/day from days 37 to 55 of age), with exposures up to 1.7 times greater than mean AUCs observed in pediatric patients aged months to 11 years. Decreased fertility was not observed with shorter treatment periods, corresponding to exposure in utero through the early neonatal period (gestation day through postnatal day 5), neonatal exposure (postnatal days to 21), or to juvenile exposure (postnatal days 22 to 35). Reversible reductions in sperm motility and altered sperm morphology were observed in rats treated from postnatal day 22 to 35.. 13.2Animal Toxicology and/or Pharmacology. Target organs of linezolid toxicity were similar in juvenile and adult rats and dogs. Dose- and time-dependent myelosuppression, as evidenced by bone marrow hypocellularity/decreased hematopoiesis, decreased extramedullary hematopoiesis in spleen and liver, and decreased levels of circulating erythrocytes, leukocytes, and platelets have been seen in animal studies. Lymphoid depletion occurred in thymus, lymph nodes, and spleen. Generally, the lymphoid findings were associated with anorexia, weight loss, and suppression of body weight gain, which may have contributed to the observed effects.In rats administered linezolid orally for months, non-reversible, minimal to mild axonal degeneration of sciatic nerves was observed at 80 mg/kg/day; minimal degeneration of the sciatic nerve was also observed in male at this dose level at 3-month interim necropsy. Sensitive morphologic evaluation of perfusion-fixed tissues was conducted to investigate evidence of optic nerve degeneration. Minimal to moderate optic nerve degeneration was evident in male rats after months of dosing, but the direct relationship to drug was equivocal because of the acute nature of the finding and its asymmetrical distribution. The nerve degeneration observed was microscopically comparable to spontaneous unilateral optic nerve degeneration reported in aging rats and may be an exacerbation of common background change.These effects were observed at exposure levels that are comparable to those observed in some human subjects. The hematopoietic and lymphoid effects were reversible, although in some studies, reversal was incomplete within the duration of the recovery period.

OVERDOSAGE SECTION.

10OVERDOSAGE. In the event of overdosage, supportive care is advised, with maintenance of glomerular filtration. Hemodialysis may facilitate more rapid elimination of linezolid. In Phase clinical trial, approximately 30% of dose of linezolid was removed during 3-hour hemodialysis session beginning hours after the dose of linezolid was administered. Data are not available for removal of linezolid with peritoneal dialysis or hemoperfusion. Clinical signs of acute toxicity in animals were decreased activity and ataxia in rats and vomiting and tremors in dogs treated with 3,000 mg/kg/day and 2,000 mg/kg/day, respectively.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

PRINCIPAL DISPLAY PANEL 300 mL Bag Label. NDC 0009-7807-01 Rx only ZYVOX(R) (linezolid) injection 600 mg/300 mL (2 mg/mL)Store at 25C (77F); excursions permitted to 15-30C (59-86F) [see USP Controlled Room Temperature]. Do not freeze. Each mL contains: linezolid mg dextrose, USP 50.24 mg sodium citrate, USP 1.64 mg citric acid, USP 0.85 mg water for injection, USP qspH adjusted to 4.8 with sodium hydroxide or hydrochloric acid. Sterile and nonpyrogenic. Single dose container. Do not add supplementary medication. Do not use in series connections. For intravenous administration Check for leaks by squeezing container. If leaks are found, discard, as sterility may be impaired. Check linezolid solution for clarity; it may exhibit yellow color that intensifies over time, with no adverse effect on potency. DOSAGE AND USE: See accompanying prescribing information. DISCARD UNUSED PORTION. The Infusion Bags and Ports are Not Made With Natural Rubber Latex. MADE IN SINGAPOREPREMIERProRx(R) freeflex1234567890 FSU 0703 01-68-26-050D7 OTHERDistributed by:Pharmacia Upjohn CoDivision of Pfizer Inc, NY, NY 10017PREMIERProRx(R) is registeredtrademark of Premier HealthcareAlliance, L.P., used under license.LOT EXP. PRINCIPAL DISPLAY PANEL 300 mL Bag Label.

PEDIATRIC USE SECTION.

8.4Pediatric Use. The safety and effectiveness of ZYVOX for the treatment of pediatric patients with the following infections are supported by evidence from adequate and well-controlled studies in adults, pharmacokinetic data in pediatric patients, and additional data from comparator-controlled study of Gram-positive infections in pediatric patients ranging in age from birth through 11 years [see Indications and Usage (1), Clinical Pharmacology (12.3) and Clinical Studies (14) ]:nosocomial pneumoniacomplicated skin and skin structure infectionscommunity-acquired pneumonia (also supported by evidence from an uncontrolled study in patients ranging in age from months through 12 years)vancomycin-resistant Enterococcus faecium infectionsThe safety and effectiveness of ZYVOX for the treatment of pediatric patients with the following infection have been established in comparator-controlled study in pediatric patients ranging in age from through 17 years [see Clinical Studies (14) ]:uncomplicated skin and skin structure infections caused by Staphylococcus aureus (methicillin-susceptible strains only) or Streptococcus pyogenes Pharmacokinetic information generated in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) linezolid concentrations following single and multiple dosing of linezolid; therapeutic concentrations were not consistently achieved or maintained in the CSF. Therefore, the use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended.The pharmacokinetics of linezolid have been evaluated in pediatric patients from birth to 17 years of age. In general, weight-based clearance of linezolid gradually decreases with increasing age of pediatric patients. However, in preterm (gestational age 34 weeks) neonates 7 days of age, linezolid clearance is often lower than in full-term neonates 7 days of age. Consequently, preterm neonates 7 days of age may need an alternative linezolid dosing regimen of 10 mg/kg every 12 hours [see Dosage and Administration (2.1) and Clinical Pharmacology (12.3) ].In limited clinical experience, out of (83%) pediatric patients with infections due to Gram-positive pathogens with minimum inhibitory concentrations (MICs) of mcg/mL treated with ZYVOX had clinical cures. However, pediatric patients exhibit wider variability in linezolid clearance and systemic exposure (AUC) compared with adults. In pediatric patients with sub-optimal clinical response, particularly those with pathogens with MIC of mcg/mL, lower systemic exposure, site and severity of infection, and the underlying medical condition should be considered when assessing clinical response [see Clinical Pharmacology (12.3) and Dosage and Administration (2) ].. nosocomial pneumonia. complicated skin and skin structure infections. community-acquired pneumonia (also supported by evidence from an uncontrolled study in patients ranging in age from months through 12 years). vancomycin-resistant Enterococcus faecium infections. uncomplicated skin and skin structure infections caused by Staphylococcus aureus (methicillin-susceptible strains only) or Streptococcus pyogenes.

PHARMACODYNAMICS SECTION.

12.2Pharmacodynamics. In randomized, positive- and placebo-controlled crossover thorough QT study, 40 healthy subjects were administered single ZYVOX 600 mg dose via 1 hour IV infusion, single ZYVOX 1,200 mg dose via 1 hour IV infusion, placebo, and single oral dose of positive control. At both the 600 mg and 1,200 mg ZYVOX doses, no significant effect on QTc interval was detected at peak plasma concentration or at any other time.

PHARMACOKINETICS SECTION.

12.3Pharmacokinetics. The mean pharmacokinetic parameters of linezolid in adults after single and multiple oral and intravenous doses are summarized in Table 8. Plasma concentrations of linezolid at steady-state after oral doses of 600 mg given every 12 hours are shown in Figure 1.Table 8. Mean (Standard Deviation) Pharmacokinetic Parameters of Linezolid in AdultsDose of LinezolidCmax mcg/mLCmin mcg/mLTmax hrsAUC AUC for single dose AUC0-; for multiple dose AUC0- mcgh/mLt1/2 hrsCLmL/minCmax Maximum plasma concentration; Cmin Minimum plasma concentration; Tmax Time to Cmax; AUC Area under concentration-time curve; t1/2 Elimination half-life; CL Systemic clearance400 mg tablet single dose Data dose-normalized from 375 mg 8.10(1.83)---1.52(1.01)55.10(25.00)5.20(1.50)146(67) every 12 hours11.00(4.37)3.08(2.25)1.12(0.47)73.40(33.50)4.69(1.70)110(49)600 mg tablet single dose12.70(3.96)---1.28(0.66)91.40(39.30)4.26(1.65)127(48) every 12 hours21.20(5.78)6.15(2.94)1.03(0.62)138.00(42.10)5.40(2.06)80(29)600 mg IV injection Data dose-normalized from 625 mg, intravenous dose was given as 0.5-hour infusion. single dose12.90(1.60)---0.50(0.10)80.20(33.30)4.40(2.40)138(39) every 12 hours15.10(2.52)3.68(2.36)0.51(0.03)89.70(31.00)4.80(1.70)123(40)600 mg oral suspension single dose11.00(2.76)---0.97(0.88)80.80(35.10)4.60(1.71)141(45)Figure 1. Plasma Concentrations of Linezolid in Adults at Steady-State Following Oral Dosing Every 12 Hours (Mean +- Standard Deviation, n=16). Figure 1. AbsorptionLinezolid is extensively absorbed after oral dosing. Maximum plasma concentrations are reached approximately to hours after dosing, and the absolute bioavailability is approximately 100%. Therefore, linezolid may be given orally or intravenously without dose adjustment.Linezolid may be administered without regard to the timing of meals. The time to reach the maximum concentration is delayed from 1.5 hours to 2.2 hours and Cmax is decreased by about 17% when high fat food is given with linezolid. However, the total exposure measured as AUC0- is similar under both conditions.. DistributionAnimal and human pharmacokinetic studies have demonstrated that linezolid readily distributes to well-perfused tissues. The plasma protein binding of linezolid is approximately 31% and is concentration-independent. The volume of distribution of linezolid at steady-state averaged 40 to 50 liters in healthy adult volunteers.Linezolid concentrations have been determined in various fluids from limited number of subjects in Phase volunteer studies following multiple dosing of linezolid. The ratio of linezolid in saliva relative to plasma was 1.2 to and the ratio of linezolid in sweat relative to plasma was 0.55 to 1.. MetabolismLinezolid is primarily metabolized by oxidation of the morpholine ring, which results in two inactive ring-opened carboxylic acid metabolites: the aminoethoxyacetic acid metabolite (A), and the hydroxyethyl glycine metabolite (B). Formation of metabolite is presumed to be formed via an enzymatic pathway whereas metabolite is mediated by non-enzymatic chemical oxidation mechanism in vitro. In vitro studies have demonstrated that linezolid is minimally metabolized and may be mediated by human cytochrome P450. However, the metabolic pathway of linezolid is not fully understood.. ExcretionNonrenal clearance accounts for approximately 65% of the total clearance of linezolid. Under steady-state conditions, approximately 30% of the dose appears in the urine as linezolid, 40% as metabolite B, and 10% as metabolite A. The mean renal clearance of linezolid is 40 mL/min which suggests net tubular reabsorption. Virtually no linezolid appears in the feces, while approximately 6% of the dose appears in the feces as metabolite B, and 3% as metabolite A.A small degree of nonlinearity in clearance was observed with increasing doses of linezolid, which appears to be due to lower renal and nonrenal clearance of linezolid at higher concentrations. However, the difference in clearance was small and was not reflected in the apparent elimination half-life.. Specific Populations. Geriatric PatientsThe pharmacokinetics of linezolid are not significantly altered in elderly patients (65 years or older). Therefore, dose adjustment for geriatric patients is not necessary.. Pediatric PatientsThe pharmacokinetics of linezolid following single intravenous dose were investigated in pediatric patients ranging in age from birth through 17 years (including premature and full-term neonates), in healthy adolescent subjects ranging in age from 12 through 17 years, and in pediatric patients ranging in age from week through 12 years. The pharmacokinetic parameters of linezolid are summarized in Table for the pediatric populations studied and healthy adult subjects after administration of single intravenous doses.The Cmax and the volume of distribution (Vss) of linezolid are similar regardless of age in pediatric patients. However, plasma clearance of linezolid varies as function of age. With the exclusion of pre-term neonates less than one week of age, weight-based clearance is most rapid in the youngest age groups ranging from 1 week old to 11 years, resulting in lower single-dose systemic exposure (AUC) and shorter half-life as compared with adults. As the age of pediatric patients increases, the weight-based clearance of linezolid gradually decreases, and by adolescence mean clearance values approach those observed for the adult population. There is increased inter-subject variability in linezolid clearance and systemic drug exposure (AUC) across all pediatric age groups as compared with adults.Similar mean daily AUC values were observed in pediatric patients from birth to 11 years of age dosed every hours relative to adolescents or adults dosed every 12 hours. Therefore, the dosage for pediatric patients up to 11 years of age should be 10 mg/kg every hours. Pediatric patients 12 years and older should receive 600 mg every 12 hours [see Dosage and Administration (2) ].Table 9. Pharmacokinetic Parameters of Linezolid in Pediatrics and Adults Following Single Intravenous Infusion of 10 mg/kg or 600 mg Linezolid (Mean: (%CV); [Min, Max Values])Age GroupCmax mcg/mLVss L/kgAUCAUC Single dose AUC0- mcgh/mLt 1/2 hrsCLmL/min/kgCmax Maximum plasma concentration; Vss= Volume of distribution; AUC Area under concentration-time curve; t1/2 Apparent elimination half-life; CL Systemic clearance normalized for body weightNeonatal PatientsPre-termIn this data set, pre-term is defined as <34 weeks gestational age (Note: Only patient enrolled was pre-term with postnatal age between week and 28 days) 1 week (N=9)Dose of 10 mg/kg 12.7 (30%)[9.6, 22.2]0.81 (24%)[0.43, 1.05]108 (47%)[41, 191]5.6 (46%)[2.4, 9.8]2.0 (52%)[0.9, 4.0]Full-termIn this data set, full-term is defined as >=34 weeks gestational age 1 week (N=10) 11.5 (24%)[8.0, 18.3]0.78 (20%)[0.45, 0.96]55 (47%)[19, 103]3.0 (55%)[1.3, 6.1]3.8 (55%)[1.5, 8.8]Full-term >= week to <= 28 days (N=10) 12.9 (28%)[7.7, 21.6]0.66 (29%)[0.35, 1.06]34 (21%)[23, 50]1.5 (17%)[1.2, 1.9]5.1 (22%)[3.3, 7.2]Infant Patients> 28 days to 3 Months (N=12) 11.0 (27%)[7.2, 18.0]0.79 (26%)[0.42, 1.08]33 (26%)[17, 48]1.8 (28%)[1.2, 2.8]5.4 (32%)[3.5, 9.9]Pediatric Patients months through 11 years (N=59)15.1 (30%)[6.8, 36.7]0.69 (28%)[0.31, 1.50]58 (54%)[19, 153]2.9 (53%)[0.9, 8.0]3.8 (53%)[1.0, 8.5]Adolescent Subjects and Patients 12 through 17 yearsDose of 600 mg or 10 mg/kg up to maximum of 600 mg (N=36)16.7 (24%)[9.9, 28.9]0.61 (15%)[0.44, 0.79]95 (44%)[32, 178]4.1 (46%)[1.3, 8.1]2.1 (53%)[0.9, 5.2]Adult SubjectsDose normalized to 600 mg (N= 29)12.5 (21%)[8.2, 19.3]0.65 (16%)[0.45, 0.84]91 (33%)[53, 155]4.9 (35%)[1.8, 8.3]1.7 (34%)[0.9, 3.3]. GenderFemales have slightly lower volume of distribution of linezolid than males. Plasma concentrations are higher in females than in males, which is partly due to body weight differences. After 600-mg dose, mean oral clearance is approximately 38% lower in females than in males. However, there are no significant gender differences in mean apparent elimination-rate constant or half-life. Thus, drug exposure in females is not expected to substantially increase beyond levels known to be well tolerated. Therefore, dose adjustment by gender does not appear to be necessary.. Renal ImpairmentThe pharmacokinetics of the parent drug, linezolid, are not altered in patients with any degree of renal impairment; however, the two primary metabolites of linezolid accumulate in patients with renal impairment, with the amount of accumulation increasing with the severity of renal dysfunction (see Table 10). The pharmacokinetics of linezolid and its two metabolites have also been studied in patients with end-stage renal disease (ESRD) receiving hemodialysis. In the ESRD study, 14 patients were dosed with linezolid 600 mg every 12 hours for 14.5 days (see Table 11). Because similar plasma concentrations of linezolid are achieved regardless of renal function, no dose adjustment is recommended for patients with renal impairment. However, given the absence of information on the clinical significance of accumulation of the primary metabolites, use of linezolid in patients with renal impairment should be weighed against the potential risks of accumulation of these metabolites. Both linezolid and the two metabolites are eliminated by hemodialysis. No information is available on the effect of peritoneal dialysis on the pharmacokinetics of linezolid. Approximately 30% of dose was eliminated in 3-hour hemodialysis session beginning hours after the dose of linezolid was administered; therefore, linezolid should be given after hemodialysis.Table 10. Mean (Standard Deviation) AUCs and Elimination Half-lives of Linezolid and Metabolites and in Patients with Varying Degrees of Renal Impairment After Single 600 mg Oral Dose of LinezolidParameterHealthy Subjects CLCR 80 mL/minModerate Renal Impairment 30 CLCR 80 mL/minSevere Renal Impairment 10 CLCR 30 mL/minLINEZOLIDAUC0-, mcg h/mL110 (22)128 (53)127 (66)t1/2, hours6.4 (2.2)6.1 (1.7)7.1 (3.7)METABOLITE AAUC0-48, mcg h/mL7.6 (1.9)11.7 (4.3)56.5 (30.6)t1/2, hours6.3 (2.1)6.6 (2.3)9.0 (4.6)METABOLITE BMetabolite is the major metabolite of linezolid. AUC0-48, mcg h/mL30.5 (6.2)51.1 (38.5)203 (92)t1/2, hours6.6 (2.7)9.9 (7.4)11.0 (3.9)Table 11. Mean (Standard Deviation) AUCs and Elimination Half-lives of Linezolid and Metabolites and in Subjects with End-Stage Renal Disease (ESRD) After the Administration of 600 mg Linezolid Every 12 Hours for 14.5 DaysParameterESRD Subjectsbetween hemodialysis sessions LINEZOLIDAUC0-12, mcg h/mL (after last dose)181 (52.3)t1/2, (after last dose)8.3 (2.4)METABOLITE AAUC0-12, mcg h/mL (after last dose)153 (40.6)t1/2, (after last dose)15.9 (8.5)METABOLITE BMetabolite is the major metabolite of linezolid. AUC0-12, mcg h/mL (after last dose)356 (99.7)t1/2, (after last dose)34.8 (23.1). Hepatic ImpairmentThe pharmacokinetics of linezolid are not altered in patients (n=7) with mild-to-moderate hepatic impairment (Child-Pugh class or B). On the basis of the available information, no dose adjustment is recommended for patients with mild-to-moderate hepatic impairment. The pharmacokinetics of linezolid in patients with severe hepatic impairment have not been evaluated.. Drug Interactions. Drugs Metabolized by Cytochrome P450Linezolid is not an inducer of cytochrome P450 (CYP450) in rats. In addition, linezolid does not inhibit the activities of clinically significant human CYP isoforms (e.g., 1A2, 2C9, 2C19, 2D6, 2E1, 3A4). Therefore, linezolid is not expected to affect the pharmacokinetics of other drugs metabolized by these major enzymes. Concurrent administration of linezolid does not substantially alter the pharmacokinetic characteristics of (S)-warfarin, which is extensively metabolized by CYP2C9. Drugs such as warfarin and phenytoin, which are CYP2C9 substrates, may be given with linezolid without changes in dosage regimen.. Antibacterial DrugsAztreonam: The pharmacokinetics of linezolid or aztreonam are not altered when administered together.Gentamicin: The pharmacokinetics of linezolid or gentamicin are not altered when administered together.. AntioxidantsThe potential for drug-drug interactions with linezolid and the antioxidants Vitamin and Vitamin was studied in healthy volunteers. Subjects were administered 600 mg oral dose of linezolid on Day 1, and another 600 mg dose of linezolid on Day 8. On Days 2-9, subjects were given either Vitamin (1,000 mg/day) or Vitamin (800 IU/ day). The AUC0- of linezolid increased 2.3% when co-administered with Vitamin and 10.9% when co-administered with Vitamin E. No linezolid dose adjustment is recommended during co-administration with Vitamin or Vitamin E.. Strong CYP 3A4 InducersRifampin: The effect of rifampin on the pharmacokinetics of linezolid was evaluated in study of 16 healthy adult males. Volunteers were administered oral linezolid 600 mg twice daily for doses with and without rifampin 600 mg once daily for days. Co-administration of rifampin with linezolid resulted in 21% decrease in linezolid Cmax [90% CI, 15% 27%] and 32% decrease in linezolid AUC0-12 [90% CI, 27% 37%]. The clinical significance of this interaction is unknown. The mechanism of this interaction is not fully understood and may be related to the induction of hepatic enzymes. Other strong inducers of hepatic enzymes (e.g. carbamazepine, phenytoin, phenobarbital) could cause similar or smaller decrease in linezolid exposure.. Monoamine Oxidase InhibitionLinezolid is reversible, nonselective inhibitor of monoamine oxidase. Therefore, linezolid has the potential for interaction with adrenergic and serotonergic agents.. Adrenergic AgentsSome individuals receiving ZYVOX may experience reversible enhancement of the pressor response to indirect-acting sympathomimetic agents, vasopressor or dopaminergic agents. Commonly used drugs such as phenylpropanolamine and pseudoephedrine have been specifically studied. Initial doses of adrenergic agents, such as dopamine or epinephrine, should be reduced and titrated to achieve the desired response.Tyramine: significant pressor response has been observed in normal adult subjects receiving linezolid and tyramine doses of more than 100 mg. Therefore, patients receiving linezolid need to avoid consuming large amounts of foods or beverages with high tyramine content [see Patient Counseling Information (17) ].Pseudoephedrine HCl or phenylpropanolamine HCl: reversible enhancement of the pressor response of either pseudoephedrine HCl (PSE) or phenylpropanolamine HCl (PPA) is observed when linezolid is administered to healthy normotensive subjects [see Warnings and Precautions (5.6) and Drug Interactions (7) ]. similar study has not been conducted in hypertensive patients. The interaction studies conducted in normotensive subjects evaluated the blood pressure and heart rate effects of placebo, PPA or PSE alone, linezolid alone, and the combination of steady-state linezolid (600 mg every 12 hours for days) with two doses of PPA (25 mg) or PSE (60 mg) given hours apart. Heart rate was not affected by any of the treatments. Blood pressure was increased with both combination treatments. Maximum blood pressure levels were seen to hours after the second dose of PPA or PSE, and returned to baseline to hours after peak. The results of the PPA study follow, showing the mean (and range) maximum systolic blood pressure in mm Hg: placebo 121 (103 to 158); linezolid alone 120 (107 to 135); PPA alone 125 (106 to 139); PPA with linezolid 147 (129 to 176). The results from the PSE study were similar to those in the PPA study. The mean maximum increase in systolic blood pressure over baseline was 32 mm Hg (range: 20-52 mm Hg) and 38 mm Hg (range: 18-79 mm Hg) during co-administration of linezolid with pseudoephedrine or phenylpropanolamine, respectively.. Serotonergic AgentsDextromethorphan: The potential drug-drug interaction with dextromethorphan was studied in healthy volunteers. Subjects were administered dextromethorphan (two 20-mg doses given hours apart) with or without linezolid. No serotonin syndrome effects (confusion, delirium, restlessness, tremors, blushing, diaphoresis, hyperpyrexia) have been observed in normal subjects receiving linezolid and dextromethorphan.

POSTMARKETING EXPERIENCE SECTION.

6.2Postmarketing Experience. The following adverse reactions have been identified during postapproval use of ZYVOX. Because these reactions are reported voluntarily from population of uncertain size, it is not always possible to reliably estimate their frequency or establish causal relationship to drug exposure;Myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) [see Warnings and Precautions (5.1) ]; sideroblastic anemia.Peripheral neuropathy, and optic neuropathy sometimes progressing to loss of vision [see Warnings and Precautions (5.2) ].Lactic acidosis [see Warnings and Precautions (5.7) ]. Although these reports have primarily been in patients treated for longer than the maximum recommended duration of 28 days, these events have also been reported in patients receiving shorter courses of therapy.Serotonin syndrome has been reported in patients receiving concomitant serotonergic agents, including antidepressants such as selective serotonin reuptake inhibitors (SSRIs) and opioids, and ZYVOX [see Warnings and Precautions (5.3) ].Convulsions [see Warnings and Precautions (5.8) ].Anaphylaxis, angioedema, bullous skin disorders including severe cutaneous adverse reactions (SCAR) such as toxic epidermal necrolysis and Stevens-Johnson syndrome, and hypersensitivity vasculitis.Superficial tooth discoloration and tongue discoloration have been reported with the use of linezolid. The tooth discoloration was removable with professional dental cleaning (manual descaling) in cases with known outcome.Hypoglycemia, including symptomatic episodes [see Warnings and Precautions (5.9) ].Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) [see Warnings and Precautions (5.10) ].. Myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) [see Warnings and Precautions (5.1) ]; sideroblastic anemia.. Peripheral neuropathy, and optic neuropathy sometimes progressing to loss of vision [see Warnings and Precautions (5.2) ].. Lactic acidosis [see Warnings and Precautions (5.7) ]. Although these reports have primarily been in patients treated for longer than the maximum recommended duration of 28 days, these events have also been reported in patients receiving shorter courses of therapy.. Serotonin syndrome has been reported in patients receiving concomitant serotonergic agents, including antidepressants such as selective serotonin reuptake inhibitors (SSRIs) and opioids, and ZYVOX [see Warnings and Precautions (5.3) ].. Convulsions [see Warnings and Precautions (5.8) ].. Anaphylaxis, angioedema, bullous skin disorders including severe cutaneous adverse reactions (SCAR) such as toxic epidermal necrolysis and Stevens-Johnson syndrome, and hypersensitivity vasculitis.. Superficial tooth discoloration and tongue discoloration have been reported with the use of linezolid. The tooth discoloration was removable with professional dental cleaning (manual descaling) in cases with known outcome.. Hypoglycemia, including symptomatic episodes [see Warnings and Precautions (5.9) ].. Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) [see Warnings and Precautions (5.10) ].

PREGNANCY SECTION.

8.1Pregnancy. Risk SummaryAvailable data from published and postmarketing case reports with linezolid use in pregnant women have not identified drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. When administered during organogenesis, linezolid did not cause malformations in mice, rats, or rabbits at maternal exposure levels approximately 6.5 times (mice), equivalent to (rats), or 0.06 times (rabbits) the clinical therapeutic exposure, based on AUCs. However, embryo-fetal lethality was observed in mice at 6.5 times the estimated human exposure. When female rats were dosed during organogenesis through lactation, postnatal survival of pups was decreased at doses approximately equivalent to the estimated human exposure based on AUCs (see Data ).The background risk of major birth defects and miscarriage for the indicated populations 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 2-4% and 15-20%, respectively.. Data. Animal DataIn mice, embryo-fetal toxicities were observed only at doses that caused maternal toxicity (clinical signs and reduced body weight gain). An oral dose of 450 mg/kg/day given from Gestation Day (GD) 6-16 (6.5 times the estimated human exposure based on AUCs) correlated with increased postimplantational embryo death, including total litter loss, decreased fetal body weights, and an increased incidence of costal cartilage fusion. Neither maternal nor embryo-fetal toxicities were observed at doses up to 150 mg/kg/day. Fetal malformations were not observed.In rats, fetal toxicity was observed at 15 and 50 mg/kg/day administered orally from GD 6-17 (exposures 0.22 times to approximately equivalent to the estimated human exposure, respectively, based on AUCs). The effects consisted of decreased fetal body weights and reduced ossification of sternebrae, finding often seen in association with decreased fetal body weights. Fetal malformations were not observed. Maternal toxicity, in the form of reduced body weight gain, was seen at 50 mg/kg/day.In rabbits, reduced fetal body weight occurred only in the presence of maternal toxicity (clinical signs, reduced body weight gain and food consumption) when administered at an oral dose of 15 mg/kg/day given from GD 6-20 (0.06 times the estimated human exposure based on AUCs). Fetal malformations were not observed.When female rats were treated with 50 mg/kg/day (approximately equivalent to the estimated human exposure based on AUCs) of linezolid during pregnancy and lactation (GD through Lactation Day 20), survival of pups was decreased on postnatal days to 4. Male and female pups permitted to mature to reproductive age, when mated, showed an increase in preimplantation loss.

RECENT MAJOR CHANGES SECTION.

Warnings and Precautions, Serotonin Syndrome (5.3)9/2021Warnings and Precautions, Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) (5.10)11/2021.

SPL UNCLASSIFIED SECTION.

1.1Nosocomial Pneumonia. ZYVOX is indicated for the treatment of nosocomial pneumonia caused by Staphylococcus aureus (methicillin-susceptible and -resistant isolates) or Streptococcus pneumoniae [see Clinical Studies (14) ].

STORAGE AND HANDLING SECTION.

Store at 25oC (77oF). Protect from light. It is recommended that the infusion bags be kept in the overwrap until ready to use. Protect infusion bags from freezing.

USE IN SPECIFIC POPULATIONS SECTION.

8USE IN SPECIFIC POPULATIONS. 8.1Pregnancy. Risk SummaryAvailable data from published and postmarketing case reports with linezolid use in pregnant women have not identified drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. When administered during organogenesis, linezolid did not cause malformations in mice, rats, or rabbits at maternal exposure levels approximately 6.5 times (mice), equivalent to (rats), or 0.06 times (rabbits) the clinical therapeutic exposure, based on AUCs. However, embryo-fetal lethality was observed in mice at 6.5 times the estimated human exposure. When female rats were dosed during organogenesis through lactation, postnatal survival of pups was decreased at doses approximately equivalent to the estimated human exposure based on AUCs (see Data ).The background risk of major birth defects and miscarriage for the indicated populations 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 2-4% and 15-20%, respectively.. Data. Animal DataIn mice, embryo-fetal toxicities were observed only at doses that caused maternal toxicity (clinical signs and reduced body weight gain). An oral dose of 450 mg/kg/day given from Gestation Day (GD) 6-16 (6.5 times the estimated human exposure based on AUCs) correlated with increased postimplantational embryo death, including total litter loss, decreased fetal body weights, and an increased incidence of costal cartilage fusion. Neither maternal nor embryo-fetal toxicities were observed at doses up to 150 mg/kg/day. Fetal malformations were not observed.In rats, fetal toxicity was observed at 15 and 50 mg/kg/day administered orally from GD 6-17 (exposures 0.22 times to approximately equivalent to the estimated human exposure, respectively, based on AUCs). The effects consisted of decreased fetal body weights and reduced ossification of sternebrae, finding often seen in association with decreased fetal body weights. Fetal malformations were not observed. Maternal toxicity, in the form of reduced body weight gain, was seen at 50 mg/kg/day.In rabbits, reduced fetal body weight occurred only in the presence of maternal toxicity (clinical signs, reduced body weight gain and food consumption) when administered at an oral dose of 15 mg/kg/day given from GD 6-20 (0.06 times the estimated human exposure based on AUCs). Fetal malformations were not observed.When female rats were treated with 50 mg/kg/day (approximately equivalent to the estimated human exposure based on AUCs) of linezolid during pregnancy and lactation (GD through Lactation Day 20), survival of pups was decreased on postnatal days to 4. Male and female pups permitted to mature to reproductive age, when mated, showed an increase in preimplantation loss.. 8.2Lactation. Risk SummaryLinezolid is present in breast milk. Based on data from available published case reports, the daily dose of linezolid that the infant would receive from breastmilk would be approximately 6% to 9% of the recommended therapeutic infant dose (10 mg/kg every hours). There is no information on the effects of linezolid on the breastfed infant; however, diarrhea and vomiting were the most common adverse reactions reported in clinical trials in infants receiving linezolid therapeutically [see Adverse Reactions (6.1) and (see Clinical Considerations). There is no information on the effects of linezolid on milk production. The developmental and health benefits of breastfeeding should be considered along with the mothers clinical need for linezolid and any potential adverse effects on the breastfed child from linezolid or from the underlying maternal condition.. Clinical ConsiderationsAdvise lactating women to monitor breastfed infant for diarrhea and vomiting.. 8.3Females and Males of Reproductive Potential. Infertility. MalesBased on findings from studies in rats, ZYVOX may reversibly impair fertility in male patients [see Nonclinical Toxicology (13.1) ].. 8.4Pediatric Use. The safety and effectiveness of ZYVOX for the treatment of pediatric patients with the following infections are supported by evidence from adequate and well-controlled studies in adults, pharmacokinetic data in pediatric patients, and additional data from comparator-controlled study of Gram-positive infections in pediatric patients ranging in age from birth through 11 years [see Indications and Usage (1), Clinical Pharmacology (12.3) and Clinical Studies (14) ]:nosocomial pneumoniacomplicated skin and skin structure infectionscommunity-acquired pneumonia (also supported by evidence from an uncontrolled study in patients ranging in age from months through 12 years)vancomycin-resistant Enterococcus faecium infectionsThe safety and effectiveness of ZYVOX for the treatment of pediatric patients with the following infection have been established in comparator-controlled study in pediatric patients ranging in age from through 17 years [see Clinical Studies (14) ]:uncomplicated skin and skin structure infections caused by Staphylococcus aureus (methicillin-susceptible strains only) or Streptococcus pyogenes Pharmacokinetic information generated in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) linezolid concentrations following single and multiple dosing of linezolid; therapeutic concentrations were not consistently achieved or maintained in the CSF. Therefore, the use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended.The pharmacokinetics of linezolid have been evaluated in pediatric patients from birth to 17 years of age. In general, weight-based clearance of linezolid gradually decreases with increasing age of pediatric patients. However, in preterm (gestational age 34 weeks) neonates 7 days of age, linezolid clearance is often lower than in full-term neonates 7 days of age. Consequently, preterm neonates 7 days of age may need an alternative linezolid dosing regimen of 10 mg/kg every 12 hours [see Dosage and Administration (2.1) and Clinical Pharmacology (12.3) ].In limited clinical experience, out of (83%) pediatric patients with infections due to Gram-positive pathogens with minimum inhibitory concentrations (MICs) of mcg/mL treated with ZYVOX had clinical cures. However, pediatric patients exhibit wider variability in linezolid clearance and systemic exposure (AUC) compared with adults. In pediatric patients with sub-optimal clinical response, particularly those with pathogens with MIC of mcg/mL, lower systemic exposure, site and severity of infection, and the underlying medical condition should be considered when assessing clinical response [see Clinical Pharmacology (12.3) and Dosage and Administration (2) ].. nosocomial pneumonia. complicated skin and skin structure infections. community-acquired pneumonia (also supported by evidence from an uncontrolled study in patients ranging in age from months through 12 years). vancomycin-resistant Enterococcus faecium infections. uncomplicated skin and skin structure infections caused by Staphylococcus aureus (methicillin-susceptible strains only) or Streptococcus pyogenes 8.5Geriatric Use. Of the 2,046 patients treated with ZYVOX in Phase comparator-controlled clinical trials, 589 (29%) were 65 years or older and 253 (12%) were 75 years or older. No overall differences in safety or effectiveness were observed between these patients and younger patients, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

WARNINGS AND PRECAUTIONS SECTION.

5WARNINGS AND PRECAUTIONS. Myelosuppression: Monitor complete blood counts weekly. Consider discontinuation in patients who develop or have worsening myelosuppression. (5.1)Peripheral and Optic Neuropathy: Reported primarily in patients treated for longer than 28 days. If patients experience symptoms of visual impairment, prompt ophthalmic evaluation is recommended. (5.2)Serotonin Syndrome: Monitor patients taking serotonergic agents, including antidepressants and opioids, for signs of serotonin syndrome. Patients taking serotonergic antidepressants should receive ZYVOX only if no other therapies are available. Discontinue serotonergic antidepressants and monitor patients for signs and symptoms of both serotonin syndrome and antidepressant discontinuation. (5.3)A mortality imbalance was seen in an investigational study in linezolid-treated patients with catheter-related bloodstream infections. (5.4)Clostridioides difficile-Associated Diarrhea: Evaluate if diarrhea occurs. (5.5)Potential interactions producing elevation of blood pressure: monitor blood pressure. (5.6)Hypoglycemia: Postmarketing cases of symptomatic hypoglycemia have been reported in patients with diabetes mellitus receiving insulin or oral hypoglycemic agents. (5.9)Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH): Monitor serum sodium levels regularly in patients at risk of hyponatremia and/or SIADH. (5.10). Myelosuppression: Monitor complete blood counts weekly. Consider discontinuation in patients who develop or have worsening myelosuppression. (5.1). Peripheral and Optic Neuropathy: Reported primarily in patients treated for longer than 28 days. If patients experience symptoms of visual impairment, prompt ophthalmic evaluation is recommended. (5.2). Serotonin Syndrome: Monitor patients taking serotonergic agents, including antidepressants and opioids, for signs of serotonin syndrome. Patients taking serotonergic antidepressants should receive ZYVOX only if no other therapies are available. Discontinue serotonergic antidepressants and monitor patients for signs and symptoms of both serotonin syndrome and antidepressant discontinuation. (5.3). mortality imbalance was seen in an investigational study in linezolid-treated patients with catheter-related bloodstream infections. (5.4). Clostridioides difficile-Associated Diarrhea: Evaluate if diarrhea occurs. (5.5). Potential interactions producing elevation of blood pressure: monitor blood pressure. (5.6). Hypoglycemia: Postmarketing cases of symptomatic hypoglycemia have been reported in patients with diabetes mellitus receiving insulin or oral hypoglycemic agents. (5.9). Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH): Monitor serum sodium levels regularly in patients at risk of hyponatremia and/or SIADH. (5.10). 5.1Myelosuppression. Myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) has been reported in patients receiving linezolid. In cases where the outcome is known, when linezolid was discontinued, the affected hematologic parameters have risen toward pretreatment levels. Complete blood counts should be monitored weekly in patients who receive linezolid, particularly in those who receive linezolid for longer than two weeks, those with pre-existing myelosuppression, those receiving concomitant drugs that produce bone marrow suppression, or those with chronic infection who have received previous or concomitant antibacterial drug therapy. Discontinuation of therapy with linezolid should be considered in patients who develop or have worsening myelosuppression. 5.2Peripheral and Optic Neuropathy. Peripheral and optic neuropathies have been reported in patients treated with ZYVOX, primarily in those patients treated for longer than the maximum recommended duration of 28 days. In cases of optic neuropathy that progressed to loss of vision, patients were treated for extended periods beyond the maximum recommended duration. Visual blurring has been reported in some patients treated with ZYVOX for less than 28 days. Peripheral and optic neuropathy has also been reported in children.If patients experience symptoms of visual impairment, such as changes in visual acuity, changes in color vision, blurred vision, or visual field defect, prompt ophthalmic evaluation is recommended. Visual function should be monitored in all patients taking ZYVOX for extended periods (>= months) and in all patients reporting new visual symptoms regardless of length of therapy with ZYVOX. If peripheral or optic neuropathy occurs, the continued use of ZYVOX in these patients should be weighed against the potential risks.. 5.3Serotonin Syndrome. Spontaneous reports of serotonin syndrome including fatal cases associated with the co-administration of ZYVOX and serotonergic agents, including antidepressants such as selective serotonin reuptake inhibitors (SSRIs), have been reported.Unless clinically appropriate and patients are carefully observed for signs and/or symptoms of serotonin syndrome or neuroleptic malignant syndrome-like (NMS-like) reactions, linezolid should not be administered to patients with carcinoid syndrome and/or patients taking any of the following medications: serotonin re-uptake inhibitors, tricyclic antidepressants, bupropion, buspirone, serotonin 5-HT1 receptor agonists (triptans), and opioids, including meperidine [see Drug Interactions (7) and Clinical Pharmacology (12.3) ].In some cases, patient already receiving serotonergic antidepressant or buspirone may require urgent treatment with linezolid. If alternatives to linezolid are not available and the potential benefits of linezolid outweigh the risks of serotonin syndrome or NMS-like reactions, the serotonergic antidepressant should be stopped promptly and linezolid administered. The patient should be monitored for two weeks (five weeks if fluoxetine was taken) or until 24 hours after the last dose of linezolid, whichever comes first. Symptoms of serotonin syndrome or NMS-like reactions include hyperthermia, rigidity, myoclonus, autonomic instability, and mental status changes that include extreme agitation progressing to delirium and coma. The patient should also be monitored for discontinuation symptoms of the antidepressant (see package insert of the specified agent(s) for description of the associated discontinuation symptoms).. 5.4Mortality Imbalance in an Investigational Study in Patients with Catheter-Related Bloodstream Infections, Including Those with Catheter-Site Infections. An imbalance in mortality was seen in patients treated with linezolid relative to vancomycin/dicloxacillin/oxacillin in an open-label study in seriously ill patients with intravascular catheter-related infections [78/363 (21.5%) vs. 58/363 (16.0%); odds ratio 1.426, 95% CI 0.970, 2.098]. While causality has not been established, this observed imbalance occurred primarily in linezolid-treated patients in whom either Gram-negative pathogens, mixed Gram-negative and Gram-positive pathogens, or no pathogen were identified at baseline, but was not seen in patients with Gram-positive infections only.Linezolid is not approved and should not be used for the treatment of patients with catheter-related bloodstream infections or catheter-site infections.Linezolid has no clinical activity against Gram-negative pathogens and is not indicated for the treatment of Gram-negative infections. It is critical that specific Gram-negative therapy be initiated immediately if concomitant Gram-negative pathogen is documented or suspected [see Indications and Usage (1) ].. 5.5Clostridioides difficile-Associated Diarrhea. Clostridioides difficile-Associated Diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including ZYVOX, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.C. difficile produces toxins and which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibacterial drug use.Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.If CDAD is suspected or confirmed, ongoing antibacterial drug use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibacterial drug treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.. 5.6Potential Interactions Producing Elevation of Blood Pressure. Unless patients are monitored for potential increases in blood pressure, linezolid should not be administered to patients with uncontrolled hypertension, pheochromocytoma, thyrotoxicosis and/or patients taking any of the following types of medications: directly and indirectly acting sympathomimetic agents (e.g., pseudoephedrine), vasopressive agents (e.g., epinephrine, norepinephrine), dopaminergic agents (e.g., dopamine, dobutamine) [see Drug Interactions (7) and Clinical Pharmacology (12.3) ]. 5.7Lactic Acidosis. Lactic acidosis has been reported with the use of ZYVOX. In reported cases, patients experienced repeated episodes of nausea and vomiting. Patients who develop recurrent nausea or vomiting, unexplained acidosis, or low bicarbonate level while receiving ZYVOX should receive immediate medical evaluation.. 5.8Convulsions. Convulsions have been reported in patients when treated with linezolid. In some of these cases, history of seizures or risk factors for seizures was reported.. 5.9Hypoglycemia. Postmarketing cases of symptomatic hypoglycemia have been reported in patients with diabetes mellitus receiving insulin or oral hypoglycemic agents when treated with linezolid, reversible, nonselective MAO inhibitor. Some MAO inhibitors have been associated with hypoglycemic episodes in diabetic patients receiving insulin or hypoglycemic agents. While causal relationship between linezolid and hypoglycemia has not been established, diabetic patients should be cautioned of potential hypoglycemic reactions when treated with linezolid.If hypoglycemia occurs, decrease in the dose of insulin or oral hypoglycemic agent, or discontinuation of oral hypoglycemic agent, insulin, or linezolid may be required.. 5.10Hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). Postmarketing cases of hyponatremia and/or Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) have been observed in patients treated with linezolid. In reported cases, the signs and symptoms included confusion, somnolence, generalized weakness, and in severe cases led to respiratory failure and even death. Monitor serum sodium levels regularly in the elderly, in patients taking diuretics, and in other patients at risk of hyponatremia and/or SIADH while taking ZYVOX. If signs and symptoms of hyponatremia and/or SIADH occur, discontinue ZYVOX, and institute appropriate supportive measures.. 5.11Development of Drug-Resistant Bacteria. Prescribing ZYVOX in the absence of proven or strongly suspected bacterial infection or prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.