ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The most common adverse reactions (incidence >5%) are diarrhea, constipation, nausea, headache and insomnia. (6.1)To report SUSPECTED ADVERSE REACTIONS, contact Hospira Inc. at 1-800-441-4100 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical 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.Clinical Trials in Adult PatientsDuring the initial clinical investigations, 2621 patients worldwide were treated with piperacillin and tazobactam for injection in phase trials. In the key North American monotherapy clinical trials (n=830 patients), 90% of the adverse events reported were mild to moderate in severity and transient in nature. However, in 3.2% of the patients treated worldwide, piperacillin and tazobactam for injection was discontinued because of adverse events primarily involving the skin (1.3%), including rash and pruritus; the gastrointestinal system (0.9%), including diarrhea, nausea, and vomiting; and allergic reactions (0.5%).Table 4: Adverse Reactions from Piperacillin and Tazobactam for Injection Monotherapy Clinical TrialsSystem Organ Class Adverse ReactionGastrointestinal disordersDiarrhea (11.3%)Constipation (7.7%)Nausea (6.9%)Vomiting (3.3%)Dyspepsia (3.3%)Abdominal pain (1.3%)General disorders and administration site conditionsFever (2.4%)Injection site reaction (<=1%)Rigors (<=1%)Immune system disordersAnaphylaxis (<=1%)Infections and infestationsCandidiasis (1.6%)Pseudomembranous colitis (<=1%)Metabolism and nutrition disordersHypoglycemia (<=1%)Musculoskeletal and connective tissue disordersMyalgia (<=1%)Arthralgia (<=1%)Nervous system disordersHeadache (7.7%)Psychiatric disordersInsomnia (6.6%)Skin and subcutaneous tissue disordersRash (4.2%, including maculopapular, bullous, and urticarial)Pruritus (3.1%)Purpura (<=1%)Vascular disordersPhlebitis (1.3%)Thrombophlebitis (<=1%)Hypotension (<=1%)Flushing (<=1%)Respiratory, thoracic and mediastinal disordersEpistaxis (<=1%)Nosocomial Pneumonia TrialsTwo trials of nosocomial lower respiratory tract infections were conducted. In one study, 222 patients were treated with piperacillin and tazobactam for injection in dosing regimen of 4.5 every hours in combination with an aminoglycoside and 215 patients were treated with imipenem/cilastatin (500 mg/500 mg every hours) in combination with an aminoglycoside. In this trial, treatment-emergent adverse events were reported by 402 patients, 204 (91.9%) in the piperacillin/tazobactam group and 198 (92.1%) in the imipenem/cilastatin group. Twenty-five (11%) patients in the piperacillin/tazobactam group and 14 (6.5%) in the imipenem/cilastatin group (p 0.05) discontinued treatment due to an adverse event.The second trial used dosing regimen of 3.375 given every hours with an aminoglycoside.Table 5: Adverse Reactions from Piperacillin and Tazobactam Injection plus Aminoglycoside Clinical TrialsSystem Organ Class Adverse ReactionBlood and lymphatic system disordersThrombocythemia (1.4%)Anemia (<=1%) Thrombocytopenia (<=1%)Eosinophilia (<=1%)Gastrointestinal disordersDiarrhea (20%)Constipation (8.4%)Nausea (5.8%)Vomiting (2.7%)Dyspepsia (1.9%)Abdominal pain (1.8%) Stomatitis (<=1%)General disorders and administration site conditionsFever (3.2%)Injection site reaction (<=1%)Infections and infestationsOral candidiasis (3.9%)Candidiasis (1.8%)InvestigationsBUN increased (1.8%)Blood creatinine increased (1.8%)Liver function test abnormal (1.4%)Alkaline phosphatase increased (<=1%)Aspartate aminotransferase increased (<=1%)Alanine aminotransferase increased (<=1%)Metabolism and nutrition disordersHypoglycemia (<=1%)Hypokalemia (<=1%)Nervous system disordersHeadache (4.5%)Psychiatric disordersInsomnia (4.5%)Renal and urinary disordersRenal failure (<=1%)Skin and subcutaneous tissue disordersRash (3.9%)Pruritus (3.2%)Vascular disordersThrombophlebitis (1.3%)Hypotension (1.3%) For adverse drug reactions that appeared in both studies the higher frequency is presented.Other Trials: NephrotoxicityIn randomized, multicenter, controlled trial in 1200 adult critically ill patients, piperacillin/tazobactam was found to be risk factor for renal failure (odds ratio 1.7, 95% CI 1.18 to 2.43), and associated with delayed recovery of renal function as compared to other beta-lactam antibacterial drugs.1 [see Warnings and Precautions (5.5)]. Adverse Laboratory Changes (Seen During Clinical Trials)Of the trials reported, including that of nosocomial lower respiratory tract infections in which higher dose of piperacillin and tazobactam for injection was used in combination with an aminoglycoside, changes in laboratory parameters include:Hematologic-decreases in hemoglobin and hematocrit, thrombocytopenia, increases in platelet count, eosinophilia, leukopenia, neutropenia. These patients were withdrawn from therapy; some had accompanying systemic symptoms (e.g., fever, rigors, chills).Coagulation-positive direct Coombs test, prolonged prothrombin time, prolonged partial thromboplastin timeHepatic-transient elevations of AST (SGOT), ALT (SGPT), alkaline phosphatase, bilirubinRenal-increases in serum creatinine, blood urea nitrogenAdditional laboratory events include abnormalities in electrolytes (i.e., increases and decreases in sodium, potassium, and calcium), hyperglycemia, decreases in total protein or albumin, blood glucose decreased, gamma-glutamyltransferase increased, hypokalemia, and bleeding time prolonged.Clinical Trials in Pediatric PatientsClinical studies of piperacillin and tazobactam in pediatric patients suggest similar safety profile to that seen in adults.In prospective, randomized, comparative, open-label clinical trial of pediatric patients, to 12 years of age, with intra-abdominal infections (including appendicitis and/or peritonitis), 273 patients were treated with piperacillin and tazobactam 112.5 mg/kg given IV every hours and 269 patients were treated with cefotaxime (50 mg/kg) plus metronidazole (7.5 mg/kg) every hours. In this trial, treatment-emergent adverse events were reported by 146 patients, 73 (26.7%) in the piperacillin and tazobactam group and 73 (27.1%) in the cefotaxime/metronidazole group. Six patients (2.2%) in the piperacillin and tazobactam group and patients (1.9%) in the cefotaxime/metronidazole group discontinued due to an adverse event.In retrospective, cohort study, 140 pediatric patients months to less than 18 years of age with nosocomial pneumonia were treated with piperacillin and tazobactam and 267 patients were treated with comparators (which included ticarcillin-clavulanate, carbapenems, ceftazidime, cefepime, or ciprofloxacin). The rates of serious adverse reactions were generally similar between the piperacillin and tazobactam and comparator groups, including patients aged months to months treated with piperacillin and tazobactam 90 mg/kg IV every hours and patients older than months and less than 18 years of age treated with piperacillin and tazobactam 112.5 mg/kg IV every hours.. 6.2 Post-Marketing Experience. In addition to the adverse drug reactions identified in clinical trials in Table and Table 5, the following adverse reactions have been identified during post-approval use of piperacillin and tazobactam for injection. 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.Hepatobiliary-hepatitis, jaundiceHematologic-hemolytic anemia, agranulocytosis, pancytopeniaImmune-hypersensitivity reactions, anaphylactic/anaphylactoid reactions (including shock)Renal-interstitial nephritisNervous system disorders seizuresPsychiatric disorders deliriumRespiratory-eosinophilic pneumoniaSkin and Appendages-erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, (DRESS), acute generalized exanthematous pustulosis (AGEP), dermatitis exfoliativePost-marketing experience with piperacillin and tazobactam for injection in pediatric patients suggests similar safety profile to that seen in adults.. 6.3 Additional Experience with Piperacillin. The following adverse reaction has also been reported for piperacillin for injection:Skeletal-prolonged muscle relaxation [see Drug Interactions 7.5 )].

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility. CarcinogenesisLong-term carcinogenicity studies in animals have not been conducted with piperacillin/tazobactam, piperacillin, or tazobactam.MutagenesisPiperacillin/tazobactam was negative in microbial mutagenicity assays, the unscheduled DNA synthesis (UDS) test, mammalian point mutation (Chinese hamster ovary cell HPRT) assay, and mammalian cell (BALB/c-3T3) transformation assay. In vivo, piperacillin/tazobactam did not induce chromosomal aberrations in rats.FertilityReproduction studies have been performed in rats and have revealed no evidence of impaired fertility when piperacillin/tazobactam is administered intravenously up to dose of 1280/320 mg/kg piperacillin/tazobactam, which is similar to the maximum recommended human daily dose based on body-surface area (mg/m2).

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. Piperacillin and tazobactam for injection is an antibacterial drug see Microbiology (12.4)].. 12.2 Pharmacodynamics. The pharmacodynamic parameter for piperacillin/tazobactam that is most predictive of clinical and microbiological efficacy is time above MIC.. 12.3 Pharmacokinetics. The mean and coefficients of variation (CV%) for the pharmacokinetic parameters of piperacillin and tazobactam after multiple intravenous doses are summarized in Table 7. Table 7: Mean (CV%) Piperacillin and Tazobactam PK ParametersPiperacillinPiperacillin/TazobactamDose Cmax(mcg/mL)AUC+(mcgoh/mL)CL(mL/min)V(L)T1/2(h)CLR(mL/min)2.25 g134131 [14]25717.40.79-3.375 g242242 [10]20715.10.841404.5 g298322 [16]21015.40.84-TazobactamPiperacillin/TazobactamDose Cmax(mcg/mL)AUC+(mcgoh/mL)CL(mL/min)V(L)T1/2(h)CLR(mL/min)2.25 g1516 [21]258170.77-3.375 g2425 [8]25114.80.681664.5 g3439.8 [15]20614.70.82- Piperacillin and tazobactam were given in combination, infused over 30 minutes.+ Numbers in ] parentheses are coefficients of variation [CV%].Cmax: maximum observed concentration, AUC: Area under the curve, CL=clearance, CLR= Renal clearanceV=volume of distribution, T1/2 elimination half-lifePeak plasma concentrations of piperacillin and tazobactam are attained immediately after completion of an intravenous infusion of piperacillin and tazobactam for injection. Piperacillin plasma concentrations, following 30-minute infusion of piperacillin and tazobactam for injection, were similar to those attained when equivalent doses of piperacillin were administered alone. Steady-state plasma concentrations of piperacillin and tazobactam were similar to those attained after the first dose due to the short half-lives of piperacillin and tazobactam.DistributionBoth piperacillin and tazobactam are approximately 30% bound to plasma proteins. The protein binding of either piperacillin or tazobactam is unaffected by the presence of the other compound. Protein binding of the tazobactam metabolite is negligible.Piperacillin and tazobactam are widely distributed into tissues and body fluids including intestinal mucosa, gallbladder, lung, female reproductive tissues (uterus, ovary, and fallopian tube), interstitial fluid, and bile. Mean tissue concentrations are generally 50% to 100% of those in plasma. Distribution of piperacillin and tazobactam into cerebrospinal fluid is low in subjects with non-inflamed meninges, as with other penicillins (see Table 8).Table 8: Piperacillin/Tazobactam Concentrations in Selected Tissues and Fluids after Single g/0.5 30-min IV Infusion of Piperacillin and Tazobactam for InjectionTissueor FluidNSamplingperiod+(h)Mean PIPConcentrationRange(mg/L)Tissue:PlasmaRangeTazoConcentrationRange(mg/L)TazoTissue:PlasmaRangeSkin350.5 4.534.8 94.20.6 1.14 7.70.49 0.93Fatty Tissue370.5 4.54 10.10.097 0.1150.7 1.50.1 0.13Muscle360.5 4.59.4 23.30.29 0.181.4 2.70.18 0.3Proximal Intestinal Mucosa71.5 2.531.40.5510.31.15Distal Intestinal Mucosa71.5 2.531.20.5914.52.1Appendix220.5 2.526.5 64.10.43 0.539.1 18.60.8 1.35 Each subject provided single sample.+ Time from the start of the infusion.MetabolismPiperacillin is metabolized to minor microbiologically active desethyl metabolite. Tazobactam is metabolized to single metabolite that lacks pharmacological and antibacterial activities.ExcretionFollowing single or multiple piperacillin and tazobactam for injection doses to healthy subjects, the plasma half-life of piperacillin and of tazobactam ranged from 0.7 to 1.2 hours and was unaffected by dose or duration of infusion.Both piperacillin and tazobactam are eliminated via the kidney by glomerular filtration and tubular secretion. Piperacillin is excreted rapidly as unchanged drug with 68% of the administered dose excreted in the urine. Tazobactam and its metabolite are eliminated primarily by renal excretion with 80% of the administered dose excreted as unchanged drug and the remainder as the single metabolite. Piperacillin, tazobactam and desethyl piperacillin are also secreted into the bile.Specific PopulationsRenal ImpairmentAfter the administration of single doses of piperacillin/tazobactam to subjects with renal impairment, the half-life of piperacillin and of tazobactam increases with decreasing creatinine clearance. At creatinine clearance below 20 mL/min, the increase in half-life is twofold for piperacillin and fourfold for tazobactam compared to subjects with normal renal function. Dosage adjustments for piperacillin and tazobactam for injection are recommended when creatinine clearance is below 40 mL/min in patients receiving the usual recommended daily dose of piperacillin and tazobactam for injection. See Dosage and Administration (2) for specific recommendations for the treatment of patients with renal impairment.Hemodialysis removes 30% to 40% of piperacillin/tazobactam dose with an additional 5% of the tazobactam dose removed as the tazobactam metabolite. Peritoneal dialysis removes approximately 6% and 21% of the piperacillin and tazobactam doses, respectively, with up to 16% of the tazobactam dose removed as the tazobactam metabolite. For dosage recommendations for patients undergoing hemodialysis [see Dosage and Administration (2)].Hepatic ImpairmentThe half-life of piperacillin and of tazobactam increases by approximately 25% and 18%, respectively, in patients with hepatic cirrhosis compared to healthy subjects. However, this difference does not warrant dosage adjustment of piperacillin and tazobactam for injection due to hepatic cirrhosis.PediatricsPiperacillin and tazobactam pharmacokinetics were studied in pediatric patients months of age and older. The clearance of both compounds is slower in the younger patients compared to older children and adults.In population PK analysis, estimated clearance for month-old to 12 year-old patients was comparable to adults, with population mean (SE) value of 5.64 (0.34) mL/min/kg. The piperacillin clearance estimate is 80% of this value for pediatric patients to months old. In patients younger than months of age, clearance of piperacillin is slower compared to older children; however, it is not adequately characterized for dosing recommendations. The population mean (SE) for piperacillin volume of distribution is 0.243 (0.011) L/kg and is independent of age.GeriatricsThe impact of age on the pharmacokinetics of piperacillin and tazobactam was evaluated in healthy male subjects, aged 18 to 35 years (n=6) and aged 65 to 80 years (n=12). Mean half-life for piperacilln and tazobactam was 32% and 55% higher, respectively, in the elderly compared to the younger subjects. This difference may be due to age-related changes in creatinine clearance.RaceThe effect of race on piperacillin and tazobactam was evaluated in healthy male volunteers. No difference in piperacillin or tazobactam pharmacokinetics was observed between Asian (n=9) and Caucasian (n=9) healthy volunteers who received single 4/0.5 doses.Drug InteractionsThe potential for pharmacokinetic drug interactions between piperacillin and tazobactam for injection and aminoglycosides, probenecid, vancomycin, heparin, vecuronium, and methotrexate has been evaluated [see Drug Interactions (7)].. 12.4 Microbiology. Mechanism of ActionPiperacillin sodium exerts bactericidal activity by inhibiting septum formation and cell wall synthesis of susceptible bacteria. n vitro, piperacillin is active against variety of Gram-positive and Gram-negative aerobic and anaerobic bacteria. Tazobactam sodium has little clinically relevant in vitro activity against bacteria due to its reduced affinity to penicillin-binding proteins. It is, however, beta-lactamase inhibitor of the Molecular class enzymes, including Richmond- Sykes class III (Bush class 2b 2b) penicillinases and cephalosporinases. It varies in its ability to inhibit class II and IV (2a 4) penicillinases. Tazobactam does not induce chromosomally- mediated beta-lactamases at tazobactam concentrations achieved with the recommended dosage regimen.Antimicrobial ActivityPiperacillin/tazobactam 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)].Aerobic BacteriaGram-positive bacteria:Staphylococcus aureus (methicillin susceptible isolates only)Gram-negative bacteria:Acinetobacter baumanniiEscherichia coliHaemophilus influenzae (excluding beta-lactamase negative, ampicillin-resistant isolates)Klebsiella pneumoniaePseudomonas aeruginosa (given in combination with an aminoglycoside to which the isolate is susceptible)Anaerobic Bacteria:Bacteroides fragilis group (B. fragilis, B. ovatus, B. thetaiotaomicron, and B. vulgatus)The following in vitro data are available, but their clinical significance is unknown. At least 90 percent of the following bacteria exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for piperacillin/tazobactam against isolates of similar genus or organism group. However, the efficacy of piperacillin/tazobactam in treating clinical infections caused by these bacteria has not been established in adequate and well-controlled clinical trials.Aerobic BacteriaGram-positive bacteria:Enterococcus faecalis (ampicillin or penicillin-susceptible isolates only)Staphylococcus epidermidis (methicillin susceptible isolates only)Streptococcus agalactiae+Streptococcus pneumoniae+ (penicillin-susceptible isolates only)Streptococcus pyogenes+Viridans group streptococci Gram-negative bacteria:Citrobacter koseriMoraxella catarrhalisMorganella morganiiNeisseria gonorrhoeaeProteus mirabilisProteus vulgarisSerratia marcescensProvidencia stuartiiProvidencia rettgeriSalmonella entericaAnaerobic Bacteria:Clostridium perfringensBacteroides distasonisPrevotella melaninogenica+These are not beta-lactamase producing bacteria and, therefore, are susceptible to piperacillin alone.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.

CONTRAINDICATIONS SECTION.

4 CONTRAINDICATIONS. Piperacillin and tazobactam for injection is contraindicated in patients with history of allergic reactions to any of the penicillins, cephalosporins, or beta-lactamase inhibitors.. Patients with history of allergic reactions to any of the penicillins, cephalosporins, or beta-lactamase inhibitors. (4).

DESCRIPTION SECTION.

11 DESCRIPTION. Piperacillin and tazobactam for injection, USP is an injectable antibacterial combination products consisting of the semisynthetic antibacterial piperacillin sodium and the beta-lactamase inhibitor tazobactam sodium for intravenous administration.Piperacillin sodium is derived from D(-)--aminobenzyl-penicillin. The chemical name of piperacillin sodium is sodium (2S,5R,6R)-6-[(R)-2-(4-ethyl-2,3-dioxo-1-piperazine-carboxamido)-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. The chemical formula is C23H26N5NaO7S and the molecular weight is 539.5. The chemical structure of piperacillin sodium is:Tazobactam sodium, derivative of the penicillin nucleus, is penicillanic acid sulfone. Its chemical name is sodium (2S,3S,5R)-3-methyl-7-oxo-3-(1H-1,2,3-triazol-1-ylmethyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4,4-dioxide. The chemical formula is C10H11N4NaO5S and the molecular weight is 322.3. The chemical structure of tazobactam sodium is:Piperacillin and tazobactam for injection, USP, is white to yellowish sterile, cryodesiccated powder consisting of piperacillin and tazobactam as their sodium salts packaged in glass vials. The product does not contain excipients or preservatives. Dilute solutions are colorless to yellowish.Each piperacillin and tazobactam for injection, USP 2.25 ADD-Vantage(R) vial contains an amount of drug sufficient for withdrawal of piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.25 of tazobactam. Each vial contains 4.69 mEq (108 mg) of sodium.Each piperacillin and tazobactam for injection, USP 3.375 ADD-Vantage(R) vial contains an amount of drug sufficient for withdrawal of piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.375 of tazobactam. Each vial contains 7.04 mEq (162 mg) of sodium.Each piperacillin and tazobactam for injection, USP 4.5 ADD-Vantage(R) vial contains an amount of drug sufficient for withdrawal of piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.5 of tazobactam. Each vial contains 9.39 mEq (216 mg) of sodium.Piperacillin and tazobactam for injection, USP contains total of 2.35 mEq (54 mg) of sodium (Na+) per gram of piperacillin in the combination product.Meets USP Organic Impurities Procedure 3.. Piperacillin Chemical Structure. Tazobactam Chemical Structure.

DOSAGE & ADMINISTRATION SECTION.

2 DOSAGE AND ADMINISTRATION. oAdult Patients with Indications Other Than Nosocomial Pneumonia: The usual daily dosage of piperacillin and tazobactam for injection for adults is 3.375 every six hours totaling 13.5 (12 piperacillin/1.5 tazobactam). (2.1)oAdult Patients with Nosocomial Pneumonia: Initial presumptive treatment of patients with nosocomial pneumonia should start with piperacillin and tazobactam for injection at dosage of 4.5 every six hours plus an aminoglycoside, totaling 18 (16 piperacillin/2 tazobactam). (2.2)oAdult Patients with Renal Impairment: Dosage in patients with renal impairment (creatinine clearance <= 40 mL/min) and dialysis patients should be reduced, based on the degree of renal impairment. (2.3)oPediatric Patients by Indication and Age: See Table below (2.4)Recommended Dosage of Piperacillin and Tazobactam for Injection for Pediatric Patients months of Age and Older, Weighing up to 40 kg and With Normal Renal FunctionAgeAppendicitis and /or PeritonitisNosocomial Pneumonia2 months to months90 mg/kg (80 mg piperacillin/10 mg tazobactam) every (eight) hours 90 mg/kg (80 mg piperacillin/10 mg tazobactam) every (six) hours Older than months112.5 mg/kg (100 mg piperacillin/12.5 mg tazobactam) every (eight) hours 112.5 mg/kg (100 mg piperacillin/12.5 mg tazobactam) every (six) hours oAdminister piperacillin and tazobactam for injection by intravenous infusion over 30 minutes to both adult and pediatric patients. (2.1, 2.2, 2.3, 2.4)oPiperacillin and tazobactam for injection and aminoglycosides should be reconstituted, diluted, and administered separately. Co-administration via Y-site can be done under certain conditions. (2.7)oSee the full prescribing information for the preparation and administration instructions for piperacillin and tazobactam for injection ADD-Vantage(R) system.. oAdult Patients with Indications Other Than Nosocomial Pneumonia: The usual daily dosage of piperacillin and tazobactam for injection for adults is 3.375 every six hours totaling 13.5 (12 piperacillin/1.5 tazobactam). (2.1). oAdult Patients with Nosocomial Pneumonia: Initial presumptive treatment of patients with nosocomial pneumonia should start with piperacillin and tazobactam for injection at dosage of 4.5 every six hours plus an aminoglycoside, totaling 18 (16 piperacillin/2 tazobactam). (2.2). oAdult Patients with Renal Impairment: Dosage in patients with renal impairment (creatinine clearance <= 40 mL/min) and dialysis patients should be reduced, based on the degree of renal impairment. (2.3). oPediatric Patients by Indication and Age: See Table below (2.4). oAdminister piperacillin and tazobactam for injection by intravenous infusion over 30 minutes to both adult and pediatric patients. (2.1, 2.2, 2.3, 2.4). oPiperacillin and tazobactam for injection and aminoglycosides should be reconstituted, diluted, and administered separately. Co-administration via Y-site can be done under certain conditions. (2.7). oSee the full prescribing information for the preparation and administration instructions for piperacillin and tazobactam for injection ADD-Vantage(R) system.. 2.1 Dosage in Adult Patients with Indications Other Than Nosocomial Pneumonia. The usual total daily dosage of piperacillin and tazobactam for injection for adult patients with indications other than nosocomial pneumonia is 3.375 every six hours [totaling 13.5 (12 piperacillin/1.5 tazobactam)], to be administered by intravenous infusion over 30 minutes. The usual duration of piperacillin and tazobactam for injection treatment is from to 10 days.. 2.2 Dosage in Adult Patients with Nosocomial Pneumonia. Initial presumptive treatment of adult patients with nosocomial pneumonia should start with piperacillin and tazobactam for injection at dosage of 4.5 every six hours plus an aminoglycoside, [totaling 18 (16 piperacillin/2 tazobactam)], administered by intravenous infusion over 30 minutes. The recommended duration of piperacillin and tazobactam for injection treatment for nosocomial pneumonia is to 14 days. Treatment with the aminoglycoside should be continued in patients from whom P. aeruginosa is isolated.. 2.3 Dosage in Adult Patients with Renal Impairment. In adult patients with renal impairment (creatinine clearance <= 40 mL/min) and dialysis patients (hemodialysis and CAPD), the intravenous dose of piperacillin and tazobactam for injection should be reduced based on the degree of renal impairment. The recommended daily dosage of piperacillin and tazobactam for injection for patients with renal impairment administered by intravenous infusion over 30 minutes is described in Table 1.Table 1: Recommended Dosage of Piperacillin and Tazobactam for Injection in Patients with Normal Renal Function and Renal Impairment (As total grams piperacillin/tazobactam) Creatinine Clearance,mL/minAll Indications(except nosocomialpneumonia)NosocomialPneumoniaGreater than 40 mL/min3.375 every hours4.5 every hours20 to 40 mL/min+ 2.25 every hours3.375 every hoursLess than 20 mL/min+ 2.25 every hours2.25 every hoursHemodialysis 2.25 every 12 hours2.25 every hoursCAPD2.25 every 12 hours2.25 every hours Administer piperacillin and tazobactam for injection by intravenous infusion over 30 minutes.+ Creatinine clearance for patients not receiving hemodialysis. 0.75 (0.67 piperacillin/0.08 tazobactam) should be administered following each hemodialysis session on hemodialysis days.For patients on hemodialysis, the maximum dose is 2.25 every twelve hours for all indications other than nosocomial pneumonia and 2.25 every eight hours for nosocomial pneumonia. Since hemodialysis removes 30% to 40% of the administered dose, an additional dose of 0.75 piperacillin and tazobactam for injection (0.67 piperacillin/0.08 tazobactam) should be administered following each dialysis period on hemodialysis days. No additional dosage of piperacillin and tazobactam for injection is necessary for CAPD patients.. 2.4 Dosage in Pediatric Patients with Appendicitis/Peritonitis or Nosocomial Pneumonia. The recommended dosage for pediatric patients with appendicitis and/or peritonitis or nosocomial pneumonia aged months of age and older, weighing up to 40 kg, and with normal renal function, is described in Table [see Use in Specific Populations (8.4) and Clinical Pharmacology (12.3)].Table 2: Recommended Dosage of Piperacillin and Tazobactam for Injection in Pediatric Patients Months of Age and Older, Weighing up to 40 kg and With Normal Renal Function AgeAppendicitis and /or PeritonitisNosocomial Pneumonia2 months to months90 mg/kg (80 mg piperacillin/10 mg tazobactam) every (eight) hours 90 mg/kg (80 mg piperacillin/10 mg tazobactam) every (six) hours Older than months of age112.5 mg/kg (100 mg piperacillin/12.5 mg tazobactam) every (eight) hours 112.5 mg/kg (100 mg piperacillin/12.5 mg tazobactam) every (six) hours Administer piperacillin and tazobactam for injection by intravenous infusion over 30 minutes.Pediatric patients weighing over 40 kg and with normal renal function should receive the adult dose [see Dosage and Administration (2.1, 2.2)].Dosage of piperacillin and tazobactam for injection in pediatric patients with renal impairment has not been determined.. 2.5 Directions for Reconstitution and Dilution for Use. ADD-Vantage(R) System AdmixturesDextrose 5% in Water (50 or 100 mL)0.9% Sodium Chloride (50 or 100 mL)For ADD-Vantage(R) vials reconstitution directions see Instructions for Use of the ADD-Vantage(R) System LACTATED RINGERS SOLUTION IS NOT COMPATIBLE WITH PIPERACILLIN AND TAZOBACTAM FOR INJECTION.Piperacillin and tazobactam for injection should not be mixed with other drugs in syringe or infusion bottle since compatibility has not been established.Piperacillin and tazobactam for injection is not chemically stable in solutions that contain only sodium bicarbonate and solutions that significantly alter the pH.Piperacillin and tazobactam for injection should not be added to blood products or albumin hydrolysates. Parenteral drug products should be inspected visually for particulate matter or discoloration prior to administration, whenever solution and container permit.Stability of Piperacillin and Tazobactam for Injection Powder Formulations Following ReconstitutionPiperacillin and tazobactam for injection is stable in glass and plastic containers (plastic syringes, I.V. bags and tubing) when used with compatible diluents.Stability studies with the admixed ADD-Vantage(R) system have demonstrated chemical stability (potency, pH of reconstituted solution and clarity of solution) for up to 24 hours at room temperature. (Note: The admixed ADD-Vantage(R) should not be refrigerated or frozen after reconstitution.). Piperacillin and tazobactam for injection contains no preservatives. Appropriate consideration of aseptic technique should be used.. 2.6 Instructions for Use of the ADD-Vantage(R) System. To Open Diluent Container:Peel overwrap from the corner and remove container. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually.To Assemble Vial and Flexible Diluent Container (Use Aseptic Technique):1.Remove the protective covers from the top of the vial and the vial port on the diluent container as follows:A.To remove the breakaway vial cap, swing the pull ring over the top of the vial and pull down far enough to start the opening (SEE FIGURE 1.), then pull straight up to remove the cap. (SEE FIGURE 2.) NOTE: Do not access vial with syringe.B.To remove the vial port cover, grasp the tab on the pull ring, pull up to break the three tie strings, then pull back to remove the cover. (SEE FIGURE 3.)2.Screw the vial into the vial port until it will go no further. THE VIAL MUST BE SCREWED IN TIGHTLY TO ASSURE SEAL. This occurs approximately 1/2 turn (180) after the first audible click. (SEE FIGURE 4.) The clicking sound does not assure seal; the vial must be turned as far as it will go. NOTE: Once vial is seated, do not attempt to remove. (SEE FIGURE 4.)3.Recheck the vial to assure that it is tight by trying to turn it further in the direction of assembly.4.Label appropriately.To Prepare Admixture:1.Squeeze the bottom of the diluent container gently to inflate the portion of the container surrounding the end of the drug vial.2.With the other hand, push the drug vial down into the container telescoping the walls of the container. Grasp the inner cap of the vial through the walls of the container. (SEE FIGURE 5.)3.Pull the inner cap from the drug vial. (SEE FIGURE 6.) Verify that the rubber stopper has been pulled out, allowing the drug and diluent to mix.4.Mix container contents thoroughly and use within the specified time.Preparation for Administration (Use Aseptic Technique):1.Confirm the activation and admixture of vial contents.2.Check for leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired.3.Close flow control clamp of administration set.4.Remove cover from outlet port at bottom of container.5.Insert piercing pin of administration set into port with twisting motion until the pin is firmly seated. NOTE: See full directions on administration set carton.6.Lift the free end of the hanger loop on the bottom of the vial, breaking the two tie strings. Bend the loop outward to lock it in the upright position, then suspend container from hanger. 7.Squeeze and release drip chamber to establish proper fluid level in chamber.8.Open flow control clamp and clear air from set. Close clamp.9.Attach set to venipuncture device. If device is not indwelling, prime and make venipuncture.10.Regulate rate of administration with flow control clamp.WARNING: Do not use flexible container in series connections.. 1.Remove the protective covers from the top of the vial and the vial port on the diluent container as follows:A.To remove the breakaway vial cap, swing the pull ring over the top of the vial and pull down far enough to start the opening (SEE FIGURE 1.), then pull straight up to remove the cap. (SEE FIGURE 2.) NOTE: Do not access vial with syringe.B.To remove the vial port cover, grasp the tab on the pull ring, pull up to break the three tie strings, then pull back to remove the cover. (SEE FIGURE 3.). A.To remove the breakaway vial cap, swing the pull ring over the top of the vial and pull down far enough to start the opening (SEE FIGURE 1.), then pull straight up to remove the cap. (SEE FIGURE 2.) NOTE: Do not access vial with syringe.. B.To remove the vial port cover, grasp the tab on the pull ring, pull up to break the three tie strings, then pull back to remove the cover. (SEE FIGURE 3.). 2.Screw the vial into the vial port until it will go no further. THE VIAL MUST BE SCREWED IN TIGHTLY TO ASSURE SEAL. This occurs approximately 1/2 turn (180) after the first audible click. (SEE FIGURE 4.) The clicking sound does not assure seal; the vial must be turned as far as it will go. NOTE: Once vial is seated, do not attempt to remove. (SEE FIGURE 4.). 3.Recheck the vial to assure that it is tight by trying to turn it further in the direction of assembly.. 4.Label appropriately.. 1.Squeeze the bottom of the diluent container gently to inflate the portion of the container surrounding the end of the drug vial.. 2.With the other hand, push the drug vial down into the container telescoping the walls of the container. Grasp the inner cap of the vial through the walls of the container. (SEE FIGURE 5.). 3.Pull the inner cap from the drug vial. (SEE FIGURE 6.) Verify that the rubber stopper has been pulled out, allowing the drug and diluent to mix.. 4.Mix container contents thoroughly and use within the specified time.. 1.Confirm the activation and admixture of vial contents.. 2.Check for leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired.. 3.Close flow control clamp of administration set.. 4.Remove cover from outlet port at bottom of container.. 5.Insert piercing pin of administration set into port with twisting motion until the pin is firmly seated. NOTE: See full directions on administration set carton.. 6.Lift the free end of the hanger loop on the bottom of the vial, breaking the two tie strings. Bend the loop outward to lock it in the upright position, then suspend container from hanger. 7.Squeeze and release drip chamber to establish proper fluid level in chamber.. 8.Open flow control clamp and clear air from set. Close clamp.. 9.Attach set to venipuncture device. If device is not indwelling, prime and make venipuncture.. 10.Regulate rate of administration with flow control clamp.. Figure and 2. Figure and 4. Figure and 6. 2.7 Compatibility with Aminoglycosides. Due to the in vitro inactivation of aminoglycosides by piperacillin, piperacillin and tazobactam for injection and aminoglycosides are recommended for separate administration. Piperacillin and tazobactam for injection and aminoglycosides should be reconstituted, diluted, and administered separately when concomitant therapy with aminoglycosides is indicated [see Drug Interactions (7.1)].In circumstances where co-administration via Y-site is necessary, piperacillin and tazobactam for injection can be administered via Y-site infusion only with the following aminoglycosides under the following conditions:Table 3: Compatibility with AminoglycosidesAminoglycosidePiperacillin andTazobactam forInjection Dose(grams)Piperacillin andTazobactam forInjection DiluentVolume (mL)AminoglycosideConcentrationRange+ (mg/mL)AcceptableDiluentsAmikacin2.253.3754.5501001501.75 7.50.9% sodium chloride or 5% dextroseGentamicin2.253.3754.5501001500.7 3.320.9% sodium chloride or 5% dextrose Diluent volumes apply only to single vials and bulk pharmacy containers.+ The concentration ranges in Table are based on administration of the aminoglycoside in divided doses (10 to 15 mg/kg/day in two daily doses for amikacin and to mg/kg/day in three daily doses for gentamicin). Administration of amikacin or gentamicin in single daily dose or in doses exceeding those stated above via Y-site with piperacillin and tazobactam for injection has not been evaluated. See package insert for each aminoglycoside for complete Dosage and Administration instructions.Only the concentration and diluents for amikacin or gentamicin with the dosages of piperacillin and tazobactam for injection listed above have been established as compatible for co-administration via Y-site infusion. Simultaneous co-administration via Y-site infusion in any manner other than listed above may result in inactivation of the aminoglycoside by piperacillin and tazobactam for injection.Piperacillin and tazobactam for injection is not compatible with tobramycin for simultaneous co-administration via Y-site infusion. Compatibility of piperacillin and tazobactam for injection with other aminoglycosides has not been established.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

DOSAGE FORMS & STRENGTHS SECTION.

3 DOSAGE FORMS AND STRENGTHS. Piperacillin and tazobactam for injection, USP is supplied as white to yellowish powder in vials of the following sizes:Each piperacillin and tazobactam for injection, USP 2.25 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.25 of tazobactam.Each piperacillin and tazobactam for injection, USP 3.375 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.375 of tazobactam.Each piperacillin and tazobactam for injection, USP 4.5 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.5 of tazobactam.. Piperacillin and tazobactam for injection: 2.25 g, 3.375 g, and 4.5 lyophilized powder for reconstitution in ADD-Vantage(R) vials. (3).

DRUG INTERACTIONS SECTION.

7 DRUG INTERACTIONS. oPiperacillin and tazobactam for injection administration can significantly reduce tobramycin concentrations in hemodialysis patients. Monitor tobramycin concentrations in these patients. (7.1)oProbenecid prolongs the half-lives of piperacillin and tazobactam and should not be co-administered with piperacillin and tazobactam for injection unless the benefit outweighs the risk. (7.2)oCo-administration of piperacillin and tazobactam with vancomycin may increase the incidence of acute kidney injury. Monitor kidney function in patients receiving piperacillin and tazobactam and vancomycin. (7.3)oMonitor coagulation parameters in patients receiving piperacillin and tazobactam for injection and heparin or oral anticoagulants. (7.4)oPiperacillin and tazobactam for injection may prolong the neuromuscular blockade of vecuronium and other non-depolarizing muscle relaxants. Monitor for adverse reactions related to neuromuscular blockade. (7.5). oPiperacillin and tazobactam for injection administration can significantly reduce tobramycin concentrations in hemodialysis patients. Monitor tobramycin concentrations in these patients. (7.1). oProbenecid prolongs the half-lives of piperacillin and tazobactam and should not be co-administered with piperacillin and tazobactam for injection unless the benefit outweighs the risk. (7.2). oCo-administration of piperacillin and tazobactam with vancomycin may increase the incidence of acute kidney injury. Monitor kidney function in patients receiving piperacillin and tazobactam and vancomycin. (7.3). oMonitor coagulation parameters in patients receiving piperacillin and tazobactam for injection and heparin or oral anticoagulants. (7.4). oPiperacillin and tazobactam for injection may prolong the neuromuscular blockade of vecuronium and other non-depolarizing muscle relaxants. Monitor for adverse reactions related to neuromuscular blockade. (7.5). 7.1 Aminoglycosides. Piperacillin may inactivate aminoglycosides by converting them to microbiologically inert amides.In vivo inactivationWhen aminoglycosides are administered in conjunction with piperacillin to patients with end-stage renal disease requiring hemodialysis, the concentrations of the aminoglycosides (especially tobramycin) may be significantly reduced and should be monitored.Sequential administration of piperacillin and tazobactam for injection and tobramycin to patients with either normal renal function or mild to moderate renal impairment has been shown to modestly decrease serum concentrations of tobramycin but no dosage adjustment is considered necessary.In vitro inactivationDue to the in vitro inactivation of aminoglycosides by piperacillin, piperacillin and tazobactam for injection and aminoglycosides are recommended for separate administration. Piperacillin and tazobactam for injection and aminoglycosides should be reconstituted, diluted, and administered separately when concomitant therapy with aminoglycosides is indicated. Piperacillin and tazobactam for injection is compatible with amikacin and gentamicin for simultaneous Y-site infusion in certain diluents and at specific concentrations. Piperacillin and tazobactam for injection is not compatible with tobramycin for simultaneous Y-site infusion [see Dosage and Administration (2.7)].. 7.2 Probenecid. Probenecid administered concomitantly with piperacillin and tazobactam for injection prolongs the half-life of piperacillin by 21% and that of tazobactam by 71% because probenecid inhibits tubular renal secretion of both piperacillin and tazobactam. Probenecid should not be co-administered with piperacillin and tazobactam for injection unless the benefit outweighs the risk.. 7.3 Vancomycin Studies have detected an increased incidence of acute kidney injury in patients concomitantly administered piperacillin/tazobactam and vancomycin as compared to vancomycin alone [see Warnings and Precautions (5.5)]. Monitor kidney function in patients concomitantly administered with piperacillin/tazobactam and vancomycin. No pharmacokinetic interactions have been noted between piperacillin/tazobactam and vancomycin.. 7.4 Anticoagulants. Coagulation parameters should be tested more frequently and monitored regularly during simultaneous administration of high doses of heparin, oral anticoagulants, or other drugs that may affect the blood coagulation system or the thrombocyte function [see Warnings and Precautions 5.3 )]. 7.5 Vecuronium. Piperacillin when used concomitantly with vecuronium has been implicated in the prolongation of the neuromuscular blockade of vecuronium. Piperacillin and tazobactam for injection could produce the same phenomenon if given along with vecuronium. Due to their similar mechanism of action, it is expected that the neuromuscular blockade produced by any of the non-depolarizing muscle relaxants could be prolonged in the presence of piperacillin. Monitor for adverse reactions related to neuromuscular blockade (see package insert for vecuronium bromide).. 7.6 Methotrexate. Limited data suggests that co-administration of methotrexate and piperacillin may reduce the clearance of methotrexate due to competition for renal secretion. The impact of tazobactam on the elimination of methotrexate has not been evaluated. If concurrent therapy is necessary, serum concentrations of methotrexate as well as the signs and symptoms of methotrexate toxicity should be frequently monitored.. 7.7 Effects on Laboratory Tests. There have been reports of positive test results using the Bio-Rad Laboratories Platelia Aspergillus EIA test in patients receiving piperacillin/tazobactam injection who were subsequently found to be free of Aspergillus infection. Cross-reactions with non-Aspergillus polysaccharides and polyfuranoses with the Bio-Rad Laboratories Platelia Aspergillus EIA test have been reported. Therefore, positive test results in patients receiving piperacillin/tazobactam should be interpreted cautiously and confirmed by other diagnostic methods.As with other penicillins, the administration of piperacillin and tazobactam for injection may result in false-positive reaction for glucose in the urine using copper-reduction method (CLINITEST(R)). It is recommended that glucose tests based on enzymatic glucose oxidase reactions be used.

GERIATRIC USE SECTION.

8.5 Geriatric Use. Patients over 65 years are not at an increased risk of developing adverse effects solely because of age. However, dosage should be adjusted in the presence of renal impairment [see Dosage and Administration (2)].In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.Piperacillin and tazobactam for injection contains 54 mg (2.35 mEq) of sodium per gram of piperacillin in the combination product. At the usual recommended doses, patients would receive between 648 and 864 mg/day (28.2 and 37.6 mEq) of sodium. The geriatric population may respond with blunted natriuresis to salt loading. This may be clinically important with regard to such diseases as congestive heart failure.This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

HOW SUPPLIED SECTION.

16 HOW SUPPLIED/STORAGE AND HANDLING. Piperacillin and tazobactam for injection, USP is supplied as ADD-Vantage(R) vials in the following sizes:Each piperacillin and tazobactam for injection, USP 2.25 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.25 of tazobactam. Each ADD-Vantage(R) vial contains 4.69 mEq (108 mg) of sodium.Supplied 10 per box NDC 0409-3374-02Each piperacillin and tazobactam for injection, USP 3.375 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.375 of tazobactam. Each ADD-Vantage(R) vial contains 7.04 mEq (162 mg) of sodium.Supplied 10 per box NDC 0409-3378-13Each piperacillin and tazobactam for injection, USP 4.5 ADD-Vantage(R) vial provides piperacillin sodium equivalent to grams of piperacillin and tazobactam sodium equivalent to 0.5 of tazobactam. Each ADD-Vantage(R) vial contains 9.39 mEq (216 mg) of sodium.Supplied 10 per box NDC 0409-3379-04Piperacillin and tazobactam for injection, USP ADD-Vantage(R) vials should be stored at 20 to 25C (68 to 77F) [see USP Controlled Room Temperature] prior to reconstitution.

INDICATIONS & USAGE SECTION.

1 INDICATIONS AND USAGE. Piperacillin and tazobactam for injection is combination of piperacillin, penicillin-class antibacterial and tazobactam, beta-lactamase inhibitor, indicated for the treatment of:oIntra-abdominal infections in adult and pediatric patients months of age and older (1.1)oNosocomial pneumonia in adult and pediatric patients months of age and older (1.2)oSkin and skin structure infections in adults (1.3)oFemale pelvic infections in adults (1.4)oCommunity-acquired pneumonia in adults (1.5)To reduce the development of drug-resistant bacteria and maintain the effectiveness of piperacillin and tazobactam for injection and other antibacterial drugs, piperacillin and tazobactam for injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. (1.6). oIntra-abdominal infections in adult and pediatric patients months of age and older (1.1). oNosocomial pneumonia in adult and pediatric patients months of age and older (1.2). oSkin and skin structure infections in adults (1.3). oFemale pelvic infections in adults (1.4). oCommunity-acquired pneumonia in adults (1.5). 1.1 Intra-abdominal Infections. Piperacillin and tazobactam for injection is indicated in adults and pediatric patients (2 months of age and older) for the treatment of appendicitis (complicated by rupture or abscess) and peritonitis caused by beta-lactamase producing isolates of Escherichia coli or the following members of the Bacteroides fragilis group: B. fragilis, B. ovatus, B. thetaiotaomicron, or B. vulgatus.. 1.2 Nosocomial Pneumonia. Piperacillin and tazobactam for injection is indicated in adults and pediatric patients (2 months of age and older) for the treatment of nosocomial pneumonia (moderate to severe) caused by beta-lactamase producing isolates of Staphylococcus aureus and by piperacillin/tazobactam-susceptible Acinetobacter baumannii, Haemophilus influenzae, Klebsiella pneumoniae, and Pseudomonas aeruginosa (Nosocomial pneumonia caused by P. aeruginosa should be treated in combination with an aminoglycoside) [see Dosage and Administration (2)].. 1.3 Skin and Skin Structure Infections. Piperacillin and tazobactam for injection is indicated in adults for the treatment of uncomplicated and complicated skin and skin structure infections, including cellulitis, cutaneous abscesses and ischemic/diabetic foot infections caused by beta-lactamase producing isolates of Staphylococcus aureus.. 1.4 Female Pelvic Infections. Piperacillin and tazobactam for injection is indicated in adults for the treatment of postpartum endometritis or pelvic inflammatory disease caused by beta-lactamase producing isolates of Escherichia coli.. 1.5 Community-acquired Pneumonia. Piperacillin and tazobactam for injection is indicated in adults for the treatment of community-acquired pneumonia (moderate severity only) caused by beta-lactamase producing isolates of Haemophilus influenzae.. 1.6 Usage To reduce the development of drug-resistant bacteria and maintain the effectiveness of piperacillin and tazobactam for injection and other antibacterial drugs, piperacillin and tazobactam for injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by 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.

INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. Serious Hypersensitivity ReactionsAdvise patients, their families, or caregivers that serious hypersensitivity reactions, including serious allergic cutaneous reactions, could occur that require immediate treatment. Ask them about any previous hypersensitivity reactions to piperacillin and tazobactam for injection, other beta-lactams (including cephalosporins), or other allergens [see Warnings and Precautions (5.2)]. DiarrheaAdvise patients, their families, or caregivers that diarrhea is common problem caused by antibacterial drugs which usually ends when the 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 drug. If this occurs, patients should contact their physician as soon as possible. Antibacterial ResistanceCounsel patients that antibacterial drugs including piperacillin and tazobactam for injection should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When piperacillin and tazobactam for injection 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 piperacillin and tazobactam for injection or other antibacterial drugs in the future.Counsel patients that piperacillin and tazobactam can cross the placenta in humans and is excreted in human milk.CLINITEST(R) is registered trademark of Siemens Healthcare Diagnostics Inc.ADD-Vantage(R) is registered trademark of Hospira, Inc.46269527Manufactured by Sandoz GmbH for Hospira, Inc.,Lake Forest, IL 60045, USA.

MECHANISM OF ACTION SECTION.

12.1 Mechanism of Action. Piperacillin and tazobactam for injection is an antibacterial drug see Microbiology (12.4)].

NONCLINICAL TOXICOLOGY SECTION.

13 NONCLINICAL TOXICOLOGY. 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility. CarcinogenesisLong-term carcinogenicity studies in animals have not been conducted with piperacillin/tazobactam, piperacillin, or tazobactam.MutagenesisPiperacillin/tazobactam was negative in microbial mutagenicity assays, the unscheduled DNA synthesis (UDS) test, mammalian point mutation (Chinese hamster ovary cell HPRT) assay, and mammalian cell (BALB/c-3T3) transformation assay. In vivo, piperacillin/tazobactam did not induce chromosomal aberrations in rats.FertilityReproduction studies have been performed in rats and have revealed no evidence of impaired fertility when piperacillin/tazobactam is administered intravenously up to dose of 1280/320 mg/kg piperacillin/tazobactam, which is similar to the maximum recommended human daily dose based on body-surface area (mg/m2).

OVERDOSAGE SECTION.

10 OVERDOSAGE. There have been postmarketing reports of overdose with piperacillin/tazobactam. The majority of those events experienced, including nausea, vomiting, and diarrhea, have also been reported with the usual recommended dosages. Patients may experience neuromuscular excitability or seizures if higher than recommended doses are given intravenously (particularly in the presence of renal failure) see Warnings and Precautions (5.4)].Treatment should be supportive and symptomatic according the patients clinical presentation. Excessive serum concentrations of either piperacillin or tazobactam may be reduced by hemodialysis. Following single 3.375 dose of piperacillin/tazobactam, the percentage of the piperacillin and tazobactam dose removed by hemodialysis was approximately 31% and 39%, respectively see Clinical Pharmacology (12)].

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

2.25 grams Label. NDC 0409-3374-02 Rx onlyPiperacillin and Tazobactamfor Injection, USP2.25 gramsper ADD-Vantage(R) vial10 2.25 gram Single-Dose ADD-Vantage(R) VialsFor Intravenous UseHospira. 2.25g-case-label.

PEDIATRIC USE SECTION.

8.4 Pediatric Use. The safety and effectiveness of piperacillin and tazobactam for injection for intra-abdominal infections, and nosocomial pneumonia have been established in pediatric patients months of age and older.Use of piperacillin and tazobactam for injection in pediatric patients months of age and older with intra-abdominal infections including appendicitis and/or peritonitis is supported by evidence from well-controlled studies and pharmacokinetic studies in adults and in pediatric patients. This includes prospective, randomized, comparative, open-label clinical trial with 542 pediatric patients to 12 years of age with intra-abdominal infections (including appendicitis and/or peritonitis), in which 273 pediatric patients received piperacillin/tazobactam [see Adverse Reactions (6.1) and Clinical Pharmacology (12.3)]. Use of piperacillin and tazobactam for injection in pediatric patients months of age and older with nosocomial pneumonia is supported by evidence from well-controlled studies in adults with nosocomial pneumonia, simulation study performed with population pharmacokinetic model, and retrospective, cohort study of pediatric patients with nosocomial pneumonia in which 140 pediatric patients were treated with piperacillin and tazobactam for injection and 267 patients treated with comparators (which included ticarcillin-clavulanate, carbapenems, ceftazidime, cefepime, or ciprofloxacin) [see Adverse Reactions (6.1) and Clinical Pharmacology (12.3)]. The safety and effectiveness of piperacillin and tazobactam for injection have not been established in pediatric patients less than months of age [see Clinical Pharmacology (12) and Dosage and Administration (2)]. Dosage of piperacillin and tazobactam for injection in pediatric patients with renal impairment has not been determined.

PHARMACODYNAMICS SECTION.

12.2 Pharmacodynamics. The pharmacodynamic parameter for piperacillin/tazobactam that is most predictive of clinical and microbiological efficacy is time above MIC.

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics. The mean and coefficients of variation (CV%) for the pharmacokinetic parameters of piperacillin and tazobactam after multiple intravenous doses are summarized in Table 7. Table 7: Mean (CV%) Piperacillin and Tazobactam PK ParametersPiperacillinPiperacillin/TazobactamDose Cmax(mcg/mL)AUC+(mcgoh/mL)CL(mL/min)V(L)T1/2(h)CLR(mL/min)2.25 g134131 [14]25717.40.79-3.375 g242242 [10]20715.10.841404.5 g298322 [16]21015.40.84-TazobactamPiperacillin/TazobactamDose Cmax(mcg/mL)AUC+(mcgoh/mL)CL(mL/min)V(L)T1/2(h)CLR(mL/min)2.25 g1516 [21]258170.77-3.375 g2425 [8]25114.80.681664.5 g3439.8 [15]20614.70.82- Piperacillin and tazobactam were given in combination, infused over 30 minutes.+ Numbers in ] parentheses are coefficients of variation [CV%].Cmax: maximum observed concentration, AUC: Area under the curve, CL=clearance, CLR= Renal clearanceV=volume of distribution, T1/2 elimination half-lifePeak plasma concentrations of piperacillin and tazobactam are attained immediately after completion of an intravenous infusion of piperacillin and tazobactam for injection. Piperacillin plasma concentrations, following 30-minute infusion of piperacillin and tazobactam for injection, were similar to those attained when equivalent doses of piperacillin were administered alone. Steady-state plasma concentrations of piperacillin and tazobactam were similar to those attained after the first dose due to the short half-lives of piperacillin and tazobactam.DistributionBoth piperacillin and tazobactam are approximately 30% bound to plasma proteins. The protein binding of either piperacillin or tazobactam is unaffected by the presence of the other compound. Protein binding of the tazobactam metabolite is negligible.Piperacillin and tazobactam are widely distributed into tissues and body fluids including intestinal mucosa, gallbladder, lung, female reproductive tissues (uterus, ovary, and fallopian tube), interstitial fluid, and bile. Mean tissue concentrations are generally 50% to 100% of those in plasma. Distribution of piperacillin and tazobactam into cerebrospinal fluid is low in subjects with non-inflamed meninges, as with other penicillins (see Table 8).Table 8: Piperacillin/Tazobactam Concentrations in Selected Tissues and Fluids after Single g/0.5 30-min IV Infusion of Piperacillin and Tazobactam for InjectionTissueor FluidNSamplingperiod+(h)Mean PIPConcentrationRange(mg/L)Tissue:PlasmaRangeTazoConcentrationRange(mg/L)TazoTissue:PlasmaRangeSkin350.5 4.534.8 94.20.6 1.14 7.70.49 0.93Fatty Tissue370.5 4.54 10.10.097 0.1150.7 1.50.1 0.13Muscle360.5 4.59.4 23.30.29 0.181.4 2.70.18 0.3Proximal Intestinal Mucosa71.5 2.531.40.5510.31.15Distal Intestinal Mucosa71.5 2.531.20.5914.52.1Appendix220.5 2.526.5 64.10.43 0.539.1 18.60.8 1.35 Each subject provided single sample.+ Time from the start of the infusion.MetabolismPiperacillin is metabolized to minor microbiologically active desethyl metabolite. Tazobactam is metabolized to single metabolite that lacks pharmacological and antibacterial activities.ExcretionFollowing single or multiple piperacillin and tazobactam for injection doses to healthy subjects, the plasma half-life of piperacillin and of tazobactam ranged from 0.7 to 1.2 hours and was unaffected by dose or duration of infusion.Both piperacillin and tazobactam are eliminated via the kidney by glomerular filtration and tubular secretion. Piperacillin is excreted rapidly as unchanged drug with 68% of the administered dose excreted in the urine. Tazobactam and its metabolite are eliminated primarily by renal excretion with 80% of the administered dose excreted as unchanged drug and the remainder as the single metabolite. Piperacillin, tazobactam and desethyl piperacillin are also secreted into the bile.Specific PopulationsRenal ImpairmentAfter the administration of single doses of piperacillin/tazobactam to subjects with renal impairment, the half-life of piperacillin and of tazobactam increases with decreasing creatinine clearance. At creatinine clearance below 20 mL/min, the increase in half-life is twofold for piperacillin and fourfold for tazobactam compared to subjects with normal renal function. Dosage adjustments for piperacillin and tazobactam for injection are recommended when creatinine clearance is below 40 mL/min in patients receiving the usual recommended daily dose of piperacillin and tazobactam for injection. See Dosage and Administration (2) for specific recommendations for the treatment of patients with renal impairment.Hemodialysis removes 30% to 40% of piperacillin/tazobactam dose with an additional 5% of the tazobactam dose removed as the tazobactam metabolite. Peritoneal dialysis removes approximately 6% and 21% of the piperacillin and tazobactam doses, respectively, with up to 16% of the tazobactam dose removed as the tazobactam metabolite. For dosage recommendations for patients undergoing hemodialysis [see Dosage and Administration (2)].Hepatic ImpairmentThe half-life of piperacillin and of tazobactam increases by approximately 25% and 18%, respectively, in patients with hepatic cirrhosis compared to healthy subjects. However, this difference does not warrant dosage adjustment of piperacillin and tazobactam for injection due to hepatic cirrhosis.PediatricsPiperacillin and tazobactam pharmacokinetics were studied in pediatric patients months of age and older. The clearance of both compounds is slower in the younger patients compared to older children and adults.In population PK analysis, estimated clearance for month-old to 12 year-old patients was comparable to adults, with population mean (SE) value of 5.64 (0.34) mL/min/kg. The piperacillin clearance estimate is 80% of this value for pediatric patients to months old. In patients younger than months of age, clearance of piperacillin is slower compared to older children; however, it is not adequately characterized for dosing recommendations. The population mean (SE) for piperacillin volume of distribution is 0.243 (0.011) L/kg and is independent of age.GeriatricsThe impact of age on the pharmacokinetics of piperacillin and tazobactam was evaluated in healthy male subjects, aged 18 to 35 years (n=6) and aged 65 to 80 years (n=12). Mean half-life for piperacilln and tazobactam was 32% and 55% higher, respectively, in the elderly compared to the younger subjects. This difference may be due to age-related changes in creatinine clearance.RaceThe effect of race on piperacillin and tazobactam was evaluated in healthy male volunteers. No difference in piperacillin or tazobactam pharmacokinetics was observed between Asian (n=9) and Caucasian (n=9) healthy volunteers who received single 4/0.5 doses.Drug InteractionsThe potential for pharmacokinetic drug interactions between piperacillin and tazobactam for injection and aminoglycosides, probenecid, vancomycin, heparin, vecuronium, and methotrexate has been evaluated [see Drug Interactions (7)].

PREGNANCY SECTION.

8.1 Pregnancy. Risk Summary. Piperacillin and tazobactam cross the placenta in humans. However, there are insufficient data with piperacillin and/or tazobactam in pregnant women to inform drug-associated risk for major birth defects and miscarriage. No fetal structural abnormalities were observed in rats or mice when piperacillin/tazobactam was administered intravenously during organogenesis at doses to times and to times the human dose of piperacillin and tazobactam, respectively, based on body-surface area (mg/m2). However, fetotoxicity in the presence of maternal toxicity was observed in developmental toxicity and peri/postnatal studies conducted in rats (intraperitoneal administration prior to mating and throughout gestation or from gestation day 17 through lactation day 21) at doses less than the maximum recommended human daily dose based on body-surface area (mg/m2) [see Data]. The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is to 4% and 15 to 20%, respectively.DataAnimal DataIn embryo-fetal development studies in mice and rats, pregnant animals received intravenous doses of piperacillin/tazobactam up to 3000/750 mg/kg/day during the period of organogenesis. There was no evidence of teratogenicity up to the highest dose evaluated, which is to times and to times the human dose of piperacillin and tazobactam, in mice and rats respectively, based on body-surface area (mg/m2). Fetal body weights were reduced in rats at maternally toxic doses at or above 500/62.5 mg/kg/day, minimally representing 0.4 times the human dose of both piperacillin and tazobactam based on body-surface area (mg/m2).A fertility and general reproduction study in rats using intraperitoneal administration of tazobactam or the combination piperacillin/tazobactam prior to mating and through the end of gestation, reported decrease in litter size in the presence of maternal toxicity at 640 mg/kg/day tazobactam (4 times the human dose of tazobactam based on body-surface area), and decreased litter size and an increase in fetuses with ossification delays and variations of ribs, concurrent with maternal toxicity at >=640/160 mg/kg/day piperacillin/tazobactam (0.5 times and times the human dose of piperacillin and tazobactam, respectively, based on body-surface area).Peri/postnatal development in rats was impaired with reduced pup weights, increased stillbirths, and increased pup mortality concurrent with maternal toxicity after intraperitoneal administration of tazobactam alone at doses >=320 mg/kg/day (2 times the human dose based on body surface area) or of the combination piperacillin/tazobactam at doses >=640/160 mg/kg/day (0.5 times and times the human dose of piperacillin and tazobactam, respectively, based on body-surface area) from gestation day 17 through lactation day 21.

RECENT MAJOR CHANGES SECTION.

Indications and Usage (1) 5/2020Dosage and Administration (2) 5/2020Warnings and Precautions, Central Nervous System Adverse Reactions (5.4) 5/2020.

REFERENCES SECTION.

15 REFERENCES. 1.Jensen J-US, Hein L, Lundgren B, et al. BMJ Open 2012; 2:e000635. doi:10.1136.. 1.Jensen J-US, Hein L, Lundgren B, et al. BMJ Open 2012; 2:e000635. doi:10.1136.

SPL UNCLASSIFIED SECTION.

1.1 Intra-abdominal Infections. Piperacillin and tazobactam for injection is indicated in adults and pediatric patients (2 months of age and older) for the treatment of appendicitis (complicated by rupture or abscess) and peritonitis caused by beta-lactamase producing isolates of Escherichia coli or the following members of the Bacteroides fragilis group: B. fragilis, B. ovatus, B. thetaiotaomicron, or B. vulgatus.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Dosage in patients with renal impairment (creatinine clearance <= 40 mL/min) should be reduced based on the degree of renal impairment. (2.3, 8.6). Dosage in patients with renal impairment (creatinine clearance <= 40 mL/min) should be reduced based on the degree of renal impairment. (2.3, 8.6). 8.1 Pregnancy. Risk Summary. Piperacillin and tazobactam cross the placenta in humans. However, there are insufficient data with piperacillin and/or tazobactam in pregnant women to inform drug-associated risk for major birth defects and miscarriage. No fetal structural abnormalities were observed in rats or mice when piperacillin/tazobactam was administered intravenously during organogenesis at doses to times and to times the human dose of piperacillin and tazobactam, respectively, based on body-surface area (mg/m2). However, fetotoxicity in the presence of maternal toxicity was observed in developmental toxicity and peri/postnatal studies conducted in rats (intraperitoneal administration prior to mating and throughout gestation or from gestation day 17 through lactation day 21) at doses less than the maximum recommended human daily dose based on body-surface area (mg/m2) [see Data]. The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is to 4% and 15 to 20%, respectively.DataAnimal DataIn embryo-fetal development studies in mice and rats, pregnant animals received intravenous doses of piperacillin/tazobactam up to 3000/750 mg/kg/day during the period of organogenesis. There was no evidence of teratogenicity up to the highest dose evaluated, which is to times and to times the human dose of piperacillin and tazobactam, in mice and rats respectively, based on body-surface area (mg/m2). Fetal body weights were reduced in rats at maternally toxic doses at or above 500/62.5 mg/kg/day, minimally representing 0.4 times the human dose of both piperacillin and tazobactam based on body-surface area (mg/m2).A fertility and general reproduction study in rats using intraperitoneal administration of tazobactam or the combination piperacillin/tazobactam prior to mating and through the end of gestation, reported decrease in litter size in the presence of maternal toxicity at 640 mg/kg/day tazobactam (4 times the human dose of tazobactam based on body-surface area), and decreased litter size and an increase in fetuses with ossification delays and variations of ribs, concurrent with maternal toxicity at >=640/160 mg/kg/day piperacillin/tazobactam (0.5 times and times the human dose of piperacillin and tazobactam, respectively, based on body-surface area).Peri/postnatal development in rats was impaired with reduced pup weights, increased stillbirths, and increased pup mortality concurrent with maternal toxicity after intraperitoneal administration of tazobactam alone at doses >=320 mg/kg/day (2 times the human dose based on body surface area) or of the combination piperacillin/tazobactam at doses >=640/160 mg/kg/day (0.5 times and times the human dose of piperacillin and tazobactam, respectively, based on body-surface area) from gestation day 17 through lactation day 21. 8.2 Lactation Risk SummaryPiperacillin is excreted in human milk; tazobactam concentrations in human milk have not been studied. No information is available on the effects of piperacillin and tazobactam on the breast-fed child or on milk production. The developmental and health benefits of breastfeeding should be considered along with the mothers clinical need for piperacillin and tazobactam for injection and any potential adverse effects on the breastfed child from Piperacillin and tazobactam for injection or from the underlying maternal condition. 8.4 Pediatric Use. The safety and effectiveness of piperacillin and tazobactam for injection for intra-abdominal infections, and nosocomial pneumonia have been established in pediatric patients months of age and older.Use of piperacillin and tazobactam for injection in pediatric patients months of age and older with intra-abdominal infections including appendicitis and/or peritonitis is supported by evidence from well-controlled studies and pharmacokinetic studies in adults and in pediatric patients. This includes prospective, randomized, comparative, open-label clinical trial with 542 pediatric patients to 12 years of age with intra-abdominal infections (including appendicitis and/or peritonitis), in which 273 pediatric patients received piperacillin/tazobactam [see Adverse Reactions (6.1) and Clinical Pharmacology (12.3)]. Use of piperacillin and tazobactam for injection in pediatric patients months of age and older with nosocomial pneumonia is supported by evidence from well-controlled studies in adults with nosocomial pneumonia, simulation study performed with population pharmacokinetic model, and retrospective, cohort study of pediatric patients with nosocomial pneumonia in which 140 pediatric patients were treated with piperacillin and tazobactam for injection and 267 patients treated with comparators (which included ticarcillin-clavulanate, carbapenems, ceftazidime, cefepime, or ciprofloxacin) [see Adverse Reactions (6.1) and Clinical Pharmacology (12.3)]. The safety and effectiveness of piperacillin and tazobactam for injection have not been established in pediatric patients less than months of age [see Clinical Pharmacology (12) and Dosage and Administration (2)]. Dosage of piperacillin and tazobactam for injection in pediatric patients with renal impairment has not been determined.. 8.5 Geriatric Use. Patients over 65 years are not at an increased risk of developing adverse effects solely because of age. However, dosage should be adjusted in the presence of renal impairment [see Dosage and Administration (2)].In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.Piperacillin and tazobactam for injection contains 54 mg (2.35 mEq) of sodium per gram of piperacillin in the combination product. At the usual recommended doses, patients would receive between 648 and 864 mg/day (28.2 and 37.6 mEq) of sodium. The geriatric population may respond with blunted natriuresis to salt loading. This may be clinically important with regard to such diseases as congestive heart failure.This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.. 8.6 Renal Impairment. In patients with creatinine clearance <= 40 mL/min and dialysis patients (hemodialysis and CAPD), the intravenous dose of piperacillin and tazobactam for injection should be reduced to the degree of renal function impairment [see Dosage and Administration (2)].. 8.7 Hepatic Impairment. Dosage adjustment of piperacillin and tazobactam for injection is not warranted in patients with hepatic cirrhosis [see Clinical Pharmacology (12.3)].. 8.8 Patients with Cystic Fibrosis. As with other semisynthetic penicillins, piperacillin therapy has been associated with an increased incidence of fever and rash in cystic fibrosis patients.

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. oSerious hypersensitivity reactions (anaphylactic/anaphylactoid) reactions have been reported in patients receiving piperacillin and tazobactam for injection. Discontinue piperacillin and tazobactam for injection if reaction occurs. (5.1)oPiperacillin and tazobactam for injection may cause severe cutaneous adverse reactions, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, and acute generalized exanthematous pustulosis. Discontinue piperacillin and tazobactam for injection for progressive rashes. (5.2)oHematological effects (including bleeding, leukopenia and neutropenia) have occurred. Monitor hematologic tests during prolonged therapy. (5.3)oAs with other penicillins, piperacillin and tazobactam for injection may cause neuromuscular excitability or seizures. Patients receiving higher doses, especially in the presence of renal impairment may be at greater risk. Closely monitor patients with renal impairment or seizure disorders for signs and symptoms of neuromuscular excitability or seizures. (5.4)oNephrotoxicity in critically ill patients has been observed; the use of piperacillin and tazobactam for injection was found to be an independent risk factor for renal failure and was associated with delayed recovery of renal function as compared to other beta-lactam antibacterial drugs in randomized, multicenter, controlled trial in critically ill patients. Based on this study, alternative treatment options should be considered in the critically ill population. If alternative treatment options are inadequate or unavailable, monitor renal function during treatment with Piperacillin and tazobactam for injection. (5.5)oClostridioides difficile associated diarrhea: evaluate patients if diarrhea occurs. (5.7). oSerious hypersensitivity reactions (anaphylactic/anaphylactoid) reactions have been reported in patients receiving piperacillin and tazobactam for injection. Discontinue piperacillin and tazobactam for injection if reaction occurs. (5.1). oPiperacillin and tazobactam for injection may cause severe cutaneous adverse reactions, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, and acute generalized exanthematous pustulosis. Discontinue piperacillin and tazobactam for injection for progressive rashes. (5.2). oHematological effects (including bleeding, leukopenia and neutropenia) have occurred. Monitor hematologic tests during prolonged therapy. (5.3). oAs with other penicillins, piperacillin and tazobactam for injection may cause neuromuscular excitability or seizures. Patients receiving higher doses, especially in the presence of renal impairment may be at greater risk. Closely monitor patients with renal impairment or seizure disorders for signs and symptoms of neuromuscular excitability or seizures. (5.4). oNephrotoxicity in critically ill patients has been observed; the use of piperacillin and tazobactam for injection was found to be an independent risk factor for renal failure and was associated with delayed recovery of renal function as compared to other beta-lactam antibacterial drugs in randomized, multicenter, controlled trial in critically ill patients. Based on this study, alternative treatment options should be considered in the critically ill population. If alternative treatment options are inadequate or unavailable, monitor renal function during treatment with Piperacillin and tazobactam for injection. (5.5). oClostridioides difficile associated diarrhea: evaluate patients if diarrhea occurs. (5.7). 5.1 Hypersensitivity Adverse Reactions. Serious and occasionally fatal hypersensitivity (anaphylactic/anaphylactoid) reactions (including shock) have been reported in patients receiving therapy with piperacillin and tazobactam for injection. These reactions are more likely to occur in individuals with history of penicillin, cephalosporin, or carbapenem hypersensitivity or history of sensitivity to multiple allergens. Before initiating therapy with piperacillin and tazobactam for injection, careful inquiry should be made concerning previous hypersensitivity reactions. If an allergic reaction occurs, piperacillin and tazobactam for injection should be discontinued and appropriate therapy instituted.. 5.2 Severe Cutaneous Adverse Reactions. Piperacillin and tazobactam for injection may cause severe cutaneous adverse reactions, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, and acute generalized exanthematous pustulosis. If patients develop skin rash they should be monitored closely and piperacillin and tazobactam for injection discontinued if lesions progress.. 5.3 Hematologic Adverse Reactions. Bleeding manifestations have occurred in some patients receiving beta-lactam drugs, including piperacillin. These reactions have sometimes been associated with abnormalities of coagulation tests such as clotting time, platelet aggregation and prothrombin time, and are more likely to occur in patients with renal failure. If bleeding manifestations occur, piperacillin and tazobactam for injection should be discontinued and appropriate therapy instituted.The leukopenia/neutropenia associated with piperacillin and tazobactam for injection administration appears to be reversible and most frequently associated with prolonged administration.Periodic assessment of hematopoietic function should be performed, especially with prolonged therapy, i.e., >= 21 days [see Adverse Reactions (6.1)].. 5.4 Central Nervous System Adverse Reactions. As with other penicillins, piperacillin and tazobactam for injection may cause neuromuscular excitability or seizures. Patients receiving higher doses, especially patients with renal impairment may be at greater risk for central nervous system adverse reactions. Closely monitor patients with renal impairment or seizure disorders for signs and symptoms of neuromuscular excitability or seizures [see Adverse Reactions (6.2)].. 5.5 Nephrotoxicity in Critically ill Patients The use of Piperacillin and tazobactam for injection was found to be an independent risk factor for renal failure and was associated with delayed recovery of renal function as compared to other beta-lactam antibacterial drugs in randomized, multicenter, controlled trial in critically ill patients [see Adverse Reactions (6.1)]. Based on this study, alternative treatment options should be considered in the critically ill population. If alternative treatment options are inadequate or unavailable, monitor renal function during treatment with Piperacillin and tazobactam for injection [see Dosage and Administration (2.3)]. Combined use of piperacillin/tazobactam and vancomycin may be associated with an increased incidence of acute kidney injury [see Drug Interactions (7.3)]. 5.6 Electrolyte Effects. Piperacillin and tazobactam for injection contains total of 2.35 mEq (54 mg) of Na+ (sodium) per gram of piperacillin in the combination product. This should be considered when treating patients requiring restricted salt intake. Periodic electrolyte determinations should be performed in patients with low potassium reserves, and the possibility of hypokalemia should be kept in mind with patients who have potentially low potassium reserves and who are receiving cytotoxic therapy or diuretics.. 5.7 Clostridioides difficile Associated Diarrhea. Clostridioides difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including piperacillin and tazobactam for injection, 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 treatment of . difficile, and surgical evaluation should be instituted as clinically indicated.. 5.8 Development of Drug-Resistant Bacteria. Prescribing piperacillin and tazobactam for injection in the absence of proven or strongly suspected bacterial infection is unlikely to provide benefit to the patient and increases the risk of development of drug-resistant bacteria.