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Medically reviewed by Militian Inessa Mesropovna, PharmD. Last updated on 28.03.2022
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Piperacilin/Tazobaktam Actavis is a combination product consisting of a penicillin-class antibacterial, piperacillin, and a β-lactamase inhibitor, tazobactam, indicated for the treatment of patients with moderate to severe infections caused by susceptible isolates of the designated bacteria in the conditions listed below.
Intra-abdominal Infections
Appendicitis (complicated by rupture or abscess) and peritonitis caused by β-lactamase producing isolates of Escherichia coli or the following members of the Bacteroides fragilis group: B. fragilis, B. ovatus, B. thetaiotaomicron, or B. vulgatus. The individual members of this group were studied in fewer than 10 cases.
Skin And Skin Structure Infections
Uncomplicated and complicated skin and skin structure infections, including cellulitis, cutaneous abscesses and ischemic/diabetic foot infections caused by β-lactamase producing isolates of Staphylococcus aureus.
Female Pelvic Infections
Postpartum endometritis or pelvic inflammatory disease caused by β-lactamase producing isolates of Escherichia coli.
Community-acquired Pneumonia
Community-acquired pneumonia (moderate severity only) caused by β-lactamase producing isolates of Haemophilus influenzae.
Nosocomial Pneumonia
Nosocomial pneumonia (moderate to severe) caused by β-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).
Usage
To reduce the development of drug-resistant bacteria and maintain the effectiveness of Piperacilin/Tazobaktam Actavis and other antibacterial drugs, Piperacilin/Tazobaktam Actavis 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.
Piperacilin/Tazobaktam Actavis should be administered by intravenous infusion over 30 minutes.
Adult Patients
The usual total daily dose of Piperacilin/Tazobaktam Actavis for adults is 3.375 g every six hours totaling 13.5 g (12.0 g piperacillin/1.5 g tazobactam). The usual duration of Piperacilin/Tazobaktam Actavis treatment is from 7 to 10 days.
Piperacilin/Tazobaktam Actavis should be administered by intravenous infusion over 30 minutes.
Nosocomial Pneumonia
Initial presumptive treatment of patients with nosocomial pneumonia should start with Piperacilin/Tazobaktam Actavis at a dosage of 4.5 g every six hours plus an aminoglycoside, totaling 18.0 g (16.0 g piperacillin/2.0 g tazobactam). The recommended duration of Piperacilin/Tazobaktam Actavis treatment for nosocomial pneumonia is 7 to 14 days. Treatment with the aminoglycoside should be continued in patients from whom P. aeruginosa is isolated.
Renal Impairment
In patients with renal impairment (creatinine clearance ≤ 40 mL/min) and dialysis patients (hemodialysis and CAPD), the intravenous dose of Piperacilin/Tazobaktam Actavis should be reduced to the degree of actual renal function impairment. The recommended daily doses of Piperacilin/Tazobaktam Actavis for patients with renal impairment are as follows:
Table 1: Recommended Dosing of Piperacilin/Tazobaktam Actavis in Patients with Normal Renal Function and Renal- Impairment (As total grams piperacillin/tazobactam)
| Renal Function (creatinine clearance, mL/min) | All Indications (except nosocomial pneumonia) | Nosocomial Pneumonia |
| > 40 mL/min | 3.375 q 6 h | 4.5 q 6 h |
| 20-40 mL/min* | 2.25 q 6 h | 3.375 q 6 h |
| < 20 mL/min* | 2.25 q 8 h | 2.25 q 6 h |
| Hemodialysis** | 2.25 q 12 h | 2.25 q 8 h |
| CAPD | 2.25 q 12 h | 2.25 q 8 h |
| * Creatinine clearance for patients not receiving hemodialysis ** 0.75 g (0.67 g piperacillin/0.08 g tazobactam) should be administered following each hemodialysis session on hemodialysis days |
For patients on hemodialysis, the maximum dose is 2.25 g every twelve hours for all indications other than nosocomial pneumonia and 2.25 g every eight hours for nosocomial pneumonia. Since hemodialysis removes 30% to 40% of the administered dose, an additional dose of 0.75 g Piperacilin/Tazobaktam Actavis (0.67 g piperacillin/0.08 g tazobactam) should be administered following each dialysis period on hemodialysis days. No additional dosage of Piperacilin/Tazobaktam Actavis is necessary for CAPD patients.
Pediatric Patients
For children with appendicitis and/or peritonitis 9 months of age or older, weighing up to 40 kg, and with normal renal function, the recommended Piperacilin/Tazobaktam Actavis dosage is 100 mg piperacillin/12.5 mg tazobactam per kilogram of body weight, every 8 hours. For pediatric patients between 2 months and 9 months of age, the recommended Piperacilin/Tazobaktam Actavis dosage based on pharmacokinetic modeling, is 80 mg piperacillin/10 mg tazobactam per kilogram of body weight, every 8 hours. Pediatric patients weighing over 40 kg and with normal renal function should receive the adult dose.
It has not been determined how to adjust Piperacilin/Tazobaktam Actavis dosage in pediatric patients with renal impairment.
Reconstitution And Dilution Of Powder Formulations
Pharmacy Bulk Vials
Reconstituted stock solution must be transferred and further diluted for intravenous infusion.
The pharmacy bulk vial is for use in a hospital pharmacy admixture service only under a laminar flow hood. After reconstitution, entry into the vial must be made with a sterile transfer set or other sterile dispensing device, and contents should be dispensed as aliquots into intravenous solution using aseptic technique. Use entire contents of pharmacy bulk vial promptly. Discard unused portion after 24 hours if stored at room temperature (20°C to 25°C [68°F to 77°F]), or after 48 hours if stored at refrigerated temperature (2°C to 8°C [36°F to 46°F]).
Reconstitute the pharmacy bulk vial with exactly 152 mL of a compatible reconstitution diluent, listed below, to a concentration of 200 mg/mL of piperacillin and 25 mg/mL of tazobactam. Shake well until dissolved. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to and during administration whenever solution and container permit.
Single Dose Vials
Reconstitute Piperacilin/Tazobaktam Actavis vials with a compatible reconstitution diluent from the list provided below. 2.25 g, 3.375 g, and 4.5 g Piperacilin/Tazobaktam Actavis should be reconstituted with 10 mL, 15 mL, and 20 mL, respectively. Swirl until dissolved.
Compatible Reconstitution Diluents for Pharmacy and Single Dose Vials
0.9% sodium chloride for injection
Sterile water for injection
Dextrose 5%
Bacteriostatic saline/parabens
Bacteriostatic water/parabens
Bacteriostatic saline/benzyl alcohol
Bacteriostatic water/benzyl alcohol
Reconstituted Piperacilin/Tazobaktam Actavis solutions for both bulk and single dose vials should be further diluted (recommended volume per dose of 50 mL to 150 mL) in a compatible intravenous solution listed below. Administer by infusion over a period of at least 30 minutes. During the infusion it is desirable to discontinue the primary infusion solution.
Compatible Intravenous Solutions for Pharmacy and Single Dose Vials
0.9% sodium chloride for injection
sterile water for injection‡
Dextran 6% in saline
Dextrose 5%
Lactated Ringer's Solution (compatible only with reformulated Piperacilin/Tazobaktam Actavis containing EDTA and is compatible for co-administration via a Y-site)
‡ Maximum recommended volume per dose of sterile water for injection is 50 mL.
Piperacilin/Tazobaktam Actavis should not be mixed with other drugs in a syringe or infusion bottle since compatibility has not been established.
Piperacilin/Tazobaktam Actavis is not chemically stable in solutions that contain only sodium bicarbonate and solutions that significantly alter the pH.
Piperacilin/Tazobaktam Actavis 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 Piperacilin/Tazobaktam Actavis Powder Formulations Following Reconstitution
Piperacilin/Tazobaktam Actavis reconstituted from bulk and single vials is stable in glass and plastic containers (plastic syringes, I.V. bags and tubing) when used with compatible diluents. The pharmacy bulk vial should NOT be frozen after reconstitution. Discard unused portions after storage for 24 hours at room temperature or after storage for 48 hours at refrigerated temperature (2°C to 8°C [36°F to 46°F]).
Single dose or pharmacy vials should be used immediately after reconstitution. Discard any unused portion after 24 hours if stored at room temperature (20°C to 25°C [68°F to 77°F]), or after 48 hours if stored at refrigerated temperature (2°C to 8°C [36°F to 46°F]). Vials should not be frozen after reconstitution.
Stability studies in the I.V. bags have demonstrated chemical stability (potency, pH of reconstituted solution and clarity of solution) for up to 24 hours at room temperature and up to one week at refrigerated temperature. Piperacilin/Tazobaktam Actavis contains no preservatives. Appropriate consideration of aseptic technique should be used.
Piperacilin/Tazobaktam Actavis reconstituted from bulk and single vials can be used in ambulatory intravenous infusion pumps. Stability of Piperacilin/Tazobaktam Actavis in an ambulatory intravenous infusion pump has been demonstrated for a period of 12 hours at room temperature. Each dose was reconstituted and diluted to a volume of 37.5 mL or 25 mL. One-day supplies of dosing solution were aseptically transferred into the medication reservoir (I.V. bags or cartridge). The reservoir was fitted to a preprogrammed ambulatory intravenous infusion pump per the manufacturer's instructions. Stability of Piperacilin/Tazobaktam Actavis is not affected when administered using an ambulatory intravenous infusion pump.
Directions For Use Of Piperacilin/Tazobaktam Actavis In GALAXY Containers
Piperacilin/Tazobaktam Actavis Injection is to be administered using sterile equipment, after thawing to room temperature.
Piperacilin/Tazobaktam Actavis containing EDTA is compatible for co-administration via a Y-site intravenous tube with Lactated Ringer's injection, USP.
Do not add supplementary medication.
Unused portions of Piperacilin/Tazobaktam Actavis should be discarded.
CAUTION: Do not use plastic containers in series connections. Such use could result in air embolism due to residual air being drawn from the primary container before administration of the fluid from the secondary container is complete.
Thawing Of Plastic Container
Thaw frozen container at room temperature 20°C to 25°C [68°F to 77°F] or under refrigeration (2°C to 8°C [36°F to 46°F]). Do not force thaw by immersion in water baths or by microwave irradiation.
Check for minute leaks by squeezing container firmly. If leaks are detected, discard solution as sterility may be impaired.
The container should be visually inspected. Components of the solution may precipitate in the frozen state and will dissolve upon reaching room temperature with little or no agitation. Potency is not affected. Agitate after solution has reached room temperature. If after visual inspection, the solution remains cloudy or if an insoluble precipitate is noted or if any seals or outlet ports are not intact, the container should be discarded.
Administer by infusion over a period of at least 30 minutes. During the infusion it is desirable to discontinue the primary infusion solution.
Storage
Store in a freezer capable of maintaining a temperature of -20°C (-4°F).
For GALAXY containers, the thawed solution is stable for 14 days under refrigeration (2°C to 8°C [36°F to 46°F]) or 24 hours at room temperature 20°C to 25°C [68°F to 77°F]. Do not refreeze thawed Piperacilin/Tazobaktam Actavis.
Compatibility With Aminoglycosides
Due to the in vitro inactivation of aminoglycosides by piperacillin, Piperacilin/Tazobaktam Actavis and aminoglycosides are recommended for separate administration. Piperacilin/Tazobaktam Actavis and aminoglycosides should be reconstituted, diluted, and administered separately when concomitant therapy with aminoglycosides is indicated.
In circumstances where co-administration via Y-site is necessary, Piperacilin/Tazobaktam Actavis formulations containing EDTA are compatible for simultaneous co-administration via Y-site infusion only with the following aminoglycosides under the following conditions:
Table 2: Compatibility with Aminoglycosides
| Aminoglycoside | Piperacilin/Tazobaktam Actavis Dose (grams) | Piperacilin/Tazobaktam Actavis Diluent Volumea (mL) | Aminoglycoside Concentration Rangeb (mg/mL) | Acceptable Diluents |
| Amikacin | 2.25 | 50 | 1.75 - 7.5 | 0.9% sodium chloride or 5% dextrose |
| 3.375 | 100 | |||
| 4.5 | 150 | |||
| Gentamicin | 2.25 | 50 | 0.7 - 3.32 | 0.9% sodium chloride or 5% dextrose |
| 3.375c | 100 | |||
| 4.5 | 150 | |||
| a Diluent volumes apply only to single vials and bulk pharmacy containers b The concentration ranges in Table 2 are based on administration of the aminoglycoside in divided doses (10-15 mg/kg/day in two daily doses for amikacin and 3-5 mg/kg/day in three daily doses for gentamicin). Administration of amikacin or gentamicin in a single daily dose or in doses exceeding those stated above via Y-site with Piperacilin/Tazobaktam Actavis containing EDTA has not been evaluated. See package insert for each aminoglycoside for complete Dosage and Administration instructions. c Piperacilin/Tazobaktam Actavis 3.375 g per 50 mL GALAXY containers are NOT compatible with gentamicin for coadministration via a Y-site due to the higher concentrations of piperacillin and tazobactam. |
Only the concentration and diluents for amikacin or gentamicin with the dosages of Piperacilin/Tazobaktam Actavis 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 Piperacilin/Tazobaktam Actavis.
Piperacilin/Tazobaktam Actavis is not compatible with tobramycin for simultaneous co-administration via Y-site infusion. Compatibility of Piperacilin/Tazobaktam Actavis 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.
Piperacilin/Tazobaktam Actavis is contraindicated in patients with a history of allergic reactions to any of the penicillins, cephalosporins, or β-lactamase inhibitors.
WARNINGS
Included as part of the PRECAUTIONS section.
PRECAUTIONS
Hypersensitivity Adverse Reactions
Serious and occasionally fatal hypersensitivity (anaphylactic/anaphylactoid) reactions (including shock) have been reported in patients receiving therapy with Piperacilin/Tazobaktam Actavis. These reactions are more likely to occur in individuals with a history of penicillin, cephalosporin, or carbapenem hypersensitivity or a history of sensitivity to multiple allergens. Before initiating therapy with Piperacilin/Tazobaktam Actavis, careful inquiry should be made concerning previous hypersensitivity reactions. If an allergic reaction occurs, Piperacilin/Tazobaktam Actavis should be discontinued and appropriate therapy instituted.
Severe Cutaneous Adverse Reactions
Piperacilin/Tazobaktam Actavis 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 a skin rash they should be monitored closely and Piperacilin/Tazobaktam Actavis discontinued if lesions progress.
Hematologic Adverse Reactions
Bleeding manifestations have occurred in some patients receiving β-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, Piperacilin/Tazobaktam Actavis should be discontinued and appropriate therapy instituted.
The leukopenia/neutropenia associated with Piperacilin/Tazobaktam Actavis administration appears to be reversible and most frequently associated with prolonged administration.
Periodic assessment of hematopoietic function should be performed, especially with prolonged therapy, ie, ≥ 21 days.
Central Nervous System Adverse Reactions
As with other penicillins, patients may experience neuromuscular excitability or convulsions if higher than recommended doses are given intravenously (particularly in the presence of renal failure).
Nephrotoxicity In Critically Ill Patients
The use of Piperacilin/Tazobaktam Actavis 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 a 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 Piperacilin/Tazobaktam Actavis.
Combined use of piperacillin/tazobactam and vancomycin may be associated with an increased incidence of acute kidney injury.
Electrolyte Effects
Piperacilin/Tazobaktam Actavis contains a total of 2.84 mEq (65 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.
Clostridium Difficile Associated Diarrhea
Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Piperacilin/Tazobaktam Actavis, 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 A and B 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 C. difficile, and surgical evaluation should be instituted as clinically indicated.
Development Of Drug-Resistant Bacteria
Prescribing Piperacilin/Tazobaktam Actavis in the absence of a proven or strongly suspected bacterial infection is unlikely to provide benefit to the patient and increases the risk of development of drug-resistant bacteria.
Nonclinical Toxicology
Carcinogenesis, Mutagenesis, Impairment Of Fertility
Long-term carcinogenicity studies in animals have not been conducted with piperacillin/tazobactam, piperacillin, or tazobactam.
Piperacillin/Tazobactam
Piperacillin/tazobactam was negative in microbial mutagenicity assays, the unscheduled DNA synthesis (UDS) test, a mammalian point mutation (Chinese hamster ovary cell HPRT) assay, and a mammalian cell (BALB/c-3T3) transformation assay. In vivo, piperacillin/tazobactam did not induce chromosomal aberrations in rats.
Piperacillin/tazobactam
Reproduction studies have been performed in rats and have revealed no evidence of impaired fertility when piperacillin/tazobactam is administered intravenously up to a 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).
Use In Specific Populations
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 a 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 1 to 2 times and 2 to 3 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).
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 2-4% and 15-20%, respectively.
Data
Animal Data
In 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 1 to 2 times and 2 to 3 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 a 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 1 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 1 times the human dose of piperacillin and tazobactam, respectively, based on body-surface area) from gestation day 17 through lactation day 21.
Lactation
Risk Summary
Piperacillin 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 breastfed child or on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Piperacilin/Tazobaktam Actavis and any potential adverse effects on the breastfed child from Piperacilin/Tazobaktam Actavis or from the underlying maternal condition.
Pediatric Use
Use of Piperacilin/Tazobaktam Actavis in pediatric patients 2 months of age or older with appendicitis and/or peritonitis is supported by evidence from well-controlled studies and pharmacokinetic studies in adults and in pediatric patients. This includes a prospective, randomized, comparative, open-label clinical trial with 542 pediatric patients 2-12 years of age with complicated intra-abdominal infections, in which 273 pediatric patients received piperacillin/tazobactam. Safety and efficacy in pediatric patients less than 2 months of age have not been established.
It has not been determined how to adjust Piperacilin/Tazobaktam Actavis dosage in pediatric patients with renal impairment.
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.
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.
Piperacilin/Tazobaktam Actavis contains 65 mg (2.84 mEq) of sodium per gram of piperacillin in the combination product. At the usual recommended doses, patients would receive between 780 and 1040 mg/day (34.1 and 45.5 mEq) of sodium. The geriatric population may respond with a 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.
Renal Impairment
In patients with creatinine clearance ≤ 40 mL/min and dialysis patients (hemodialysis and CAPD), the intravenous dose of Piperacilin/Tazobaktam Actavis should be reduced to the degree of renal function impairment.
Hepatic Impairment
Dosage adjustment of Piperacilin/Tazobaktam Actavis is not warranted in patients with hepatic cirrhosis.
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.
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
During the initial clinical investigations, 2621 patients worldwide were treated with Piperacilin/Tazobaktam Actavis in phase 3 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, Piperacilin/Tazobaktam Actavis 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 3: Adverse Reactions from Piperacilin/Tazobaktam Actavis Monotherapy Clinical Trials
| System Organ Class/ Adverse Reaction | |
| Gastrointestinal disorders | |
| Diarrhea | (11.3%) |
| Constipation | (7.7%) |
| Nausea | (6.9%) |
| Vomiting | (3.3%) |
| Dyspepsia | (3.3%) |
| Abdominal pain | (1.3%) |
| General disorders and administration site conditions | |
| Fever | (2.4%) |
| Injection site reaction | ( ≤ 1%) |
| Rigors | ( ≤ 1%) |
| Immune system disorders | |
| Anaphylaxis | ( ≤ 1%) |
| Infections and infestations | |
| Candidiasis | (1.6%) |
| Pseudomembranous colitis | ( ≤ 1%) |
| Metabolism and nutrition disorders | |
| Hypoglycemia | ( ≤ 1%) |
| Musculoskeletal and connective tissue disorders | |
| Myalgia | ( ≤ 1%) |
| Arthralgia | ( ≤ 1%) |
| Nervous system disorders | |
| Headache | (7.7%) |
| Psychiatric disorders | |
| Insomnia | (6.6%) |
| Skin and subcutaneous tissue disorders | |
| Rash including maculopapular, bullous, and urticarial | (4.2%) |
| Pruritus | (3.1%) |
| Purpura | ( ≤ 1%) |
| Vascular disorders | |
| Phlebitis | (1.3%) |
| Thrombophlebitis | ( ≤ 1%) |
| Hypotension | ( ≤ 1%) |
| Flushing | ( ≤ 1%) |
| Respiratory, thoracic and mediastinal disorders | |
| Epistaxis | ( ≤ 1%) |
Nosocomial Pneumonia Trials
Two trials of nosocomial lower respiratory tract infections were conducted. In one study, 222 patients were treated with Piperacilin/Tazobaktam Actavis in a dosing regimen of 4.5 g every 6 hours in combination with an aminoglycoside and 215 patients were treated with imipenem/cilastatin (500 mg/500 mg q6h) 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 (11.0%) 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 a dosing regimen of 3.375 g given every 4 hours with an aminoglycoside.
Table 4: Adverse Reactions from Piperacilin/Tazobaktam Actavis Plus Aminoglycoside Clinical Trialsa
| System Organ Class Adverse Reaction | |
| Blood and lymphatic system disorders | |
| Thrombocythemia | (1.4%) |
| Anemia | ( ≤ 1%) |
| Thrombocytopenia | ( ≤ 1%) |
| Eosinophilia | ( ≤ 1%) |
| Gastrointestinal disorders | |
| Diarrhea | (20%) |
| Constipation | (8.4%) |
| Nausea | (5.8%) |
| Vomiting | (2.7%) |
| Dyspepsia | (1.9%) |
| Abdominal pain | (1.8%) |
| Stomatitis | ( ≤ 1%) |
| General disorders and administration site conditions | |
| Fever | (3.2%) |
| Injection site reaction | ( ≤ 1%) |
| Infections and infestations | |
| Oral candidiasis | (3.9%) |
| Candidiasis | (1.8%) |
| Investigations | |
| BUN 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 disorders | |
| Hypoglycemia | ( ≤ 1%) |
| Hypokalemia | ( ≤ 1%) |
| Nervous system disorders | |
| Headache | (4.5%) |
| Psychiatric disorders | |
| Insomnia | (4.5%) |
| Renal and urinary disorders | |
| Renal failure | ( ≤ 1%) |
| Skin and subcutaneous tissue disorders | |
| Rash | (3.9%) |
| Pruritus | (3.2%) |
| Vascular disorders | |
| Thrombophlebitis | (1.3%) |
| Hypotension | (1.3%) |
| a For adverse drug reactions that appeared in both studies the higher frequency is presented. | |
Other Trials: Nephrotoxicity
In a randomized, multicenter, controlled trial in 1200 adult critically ill patients, piperacillin/tazobactam was found to be a 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 betalactam antibacterial drugs.1.
Pediatrics
Studies of Piperacilin/Tazobaktam Actavis in pediatric patients suggest a similar safety profile to that seen in adults. In a prospective, randomized, comparative, open-label clinical trial of pediatric patients with severe intra-abdominal infections (including appendicitis and/or peritonitis), 273 patients were treated with Piperacilin/Tazobaktam Actavis (112.5 mg/kg every 8 hours) and 269 patients were treated with cefotaxime (50 mg/kg) plus metronidazole (7.5 mg/kg) every 8 hours. In this trial, treatment-emergent adverse events were reported by 146 patients, 73 (26.7%) in the Piperacilin/Tazobaktam Actavis group and 73 (27.1%) in the cefotaxime/metronidazole group. Six patients (2.2%) in the Piperacilin/Tazobaktam Actavis group and 5 patients (1.9%) in the cefotaxime/metronidazole group discontinued due to an adverse event.
Adverse Laboratory Events (Seen During Clinical Trials)
Of the trials reported, including that of nosocomial lower respiratory tract infections in which a higher dose of Piperacilin/Tazobaktam Actavis 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 time
Hepatic - transient elevations of AST (SGOT), ALT (SGPT), alkaline phosphatase, bilirubin
Renal - increases in serum creatinine, blood urea nitrogen
Additional 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.
Post-Marketing Experience
In addition to the adverse drug reactions identified in clinical trials in Table 3 and Table 4, the following adverse reactions have been identified during post-approval use of Piperacilin/Tazobaktam Actavis. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Hepatobiliary - hepatitis, jaundice
Hematologic - hemolytic anemia, agranulocytosis, pancytopenia
Immune - hypersensitivity reactions, anaphylactic/anaphylactoid reactions (including shock)
Renal - interstitial nephritis
Respiratory - eosinophilic pneumonia
Skin and Appendages - erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, (DRESS), acute generalized exanthematous pustulosis (AGEP), dermatitis exfoliative
Additional Experience With piperacillin
The following adverse reaction has also been reported for piperacillin for injection:
Skeletal - prolonged muscle relaxation.
Post-marketing experience with Piperacilin/Tazobaktam Actavis in pediatric patients suggests a similar safety profile to that seen in adults.
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 convulsions if higher than recommended doses are given intravenously (particularly in the presence of renal failure).
Treatment should be supportive and symptomatic according the patient's clinical presentation. Excessive serum concentrations of either piperacillin or tazobactam may be reduced by hemodialysis. Following a single 3.375 g dose of piperacillin/tazobactam, the percentage of the piperacillin and tazobactam dose removed by hemodialysis was approximately 31% and 39%, respectively.
The pharmacodynamic parameter for piperacillin/tazobactam that is most predictive of clinical and microbiological efficacy is time above MIC.
The mean and coefficients of variation (CV%) for the pharmacokinetic parameters of piperacillin and tazobactam after multiple intravenous doses are summarized in Table 6.
Table 6: Mean (CV%) Piperacillin and Tazobactam PK Parameters
| Piperacillin | ||||||
| Piperacillin/ Tazobactam Dosea | Cmax mcg/mL | AUCb mcg•h/mL | CL mL/min | VL | T½h | CLR mL/min |
| 2.25 g | 134 | 131 (14) | 257 | 17.4 | 0.79 | -- |
| 3.375 g | 242 | 242 (10) | 207 | 15.1 | 0.84 | 140 |
| 4.5 g | 298 | 322 (16) | 210 | 15.4 | 0.84 | -- |
| Tazobactam | ||||||
| Piperacillin/ Tazobactam Dosea | Cmax mcg/mL | AUCb mcg•h/mL | CL mL/min | VL | T½ | CLR% mL/min |
| 2.25 g | 15 | 16.0 (21) | 258 | 17.0 | 0.77 | -- |
| 3.375 g | 24 | 25.0 (8) | 251 | 14.8 | 0.68 | 166 |
| 4.5 g | 34 | 39.8 (15) | 206 | 14.7 | 0.82 | -- |
| a Piperacillin and tazobactam were given in combination, infused over 30 minutes. b Numbers in parentheses are coefficients of variation (CV%). | ||||||
Peak plasma concentrations of piperacillin and tazobactam are attained immediately after completion of an intravenous infusion of Piperacilin/Tazobaktam Actavis. Piperacillin plasma concentrations, following a 30-minute infusion of Piperacilin/Tazobaktam Actavis, 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.
Distribution
Both 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 7).
Table 7: Piperacillin/Tazobactam Concentrations in Selected Tissues and Fluids after Single 4 g/0.5 g 30-min IV Infusion of Piperacilin/Tazobaktam Actavis
| Tissue or Fluid | Na | Sampling periodb (h) | Mean PIP Concentration Range (mg/L) | Tissue:Plasma Range | Tazo Concentration Range (mg/L) | Tazo Tissue:Plasma Range |
| Skin | 35 | 0.5 - 4.5 | 34.8 - 94.2 | 0.60 - 1.1 | 4.0 - 7.7 | 0.49 - 0.93 |
| Fatty Tissue | 37 | 0.5 - 4.5 | 4.0 - 10.1 | 0.097 - 0.115 | 0.7 - 1.5 | 0.10 - 0.13 |
| Muscle | 36 | 0.5 - 4.5 | 9.4 - 23.3 | 0.29 - 0.18 | 1.4 - 2.7 | 0.18 - 0.30 |
| Proximal Intestinal Mucosa | 7 | 1.5 - 2.5 | 31.4 | 0.55 | 10.3 | 1.15 |
| Distal Intestinal Mucosa | 7 | 1.5 - 2.5 | 31.2 | 0.59 | 14.5 | 2.1 |
| Appendix | 22 | 0.5 - 2.5 | 26.5 - 64.1 | 0.43 - 0.53 | 9.1 - 18.6 | 0.80 - 1.35 |
| a Each subject provided a single sample. b Time from the start of the infusion |
Metabolism
Piperacillin is metabolized to a minor microbiologically active desethyl metabolite. Tazobactam is metabolized to a single metabolite that lacks pharmacological and antibacterial activities.
Excretion
Following single or multiple Piperacilin/Tazobaktam Actavis 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.
