Drugplain

Zosyn in Galaxy Containers 2 g/50mL

TAZOBACTAM SODIUM and PIPERACILLIN SODIUM · INJECTION, SOLUTION · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

No Recall HistoryCurrently in Shortage
Plain English

Zosyn in Galaxy Containers is a injection, solution containing tazobactam sodium and piperacillin sodium at 2 g/50mL, taken intravenous. Manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..

Key Facts

Brand Name
Zosyn in Galaxy Containers
Generic Name
TAZOBACTAM SODIUM and PIPERACILLIN SODIUM
NDC Code (Product)
0206-8860
Manufacturer
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Strength
2 g/50mL
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
NDA050750
Marketing Start
03/01/1998

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

pyrexia549 reports
pneumonia535 reports
sepsis459 reports
acute kidney injury361 reports
diarrhoea353 reports
renal failure332 reports
dyspnoea323 reports
hypotension308 reports
nausea292 reports
anaemia273 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE ZOSYN is a combination of piperacillin, a penicillin-class antibacterial and tazobactam, a beta-lactamase inhibitor, indicated for the treatment of: • Intra-abdominal infections in adult and pediatric patients 2 months of age and older ( 1.1 ) • Nosocomial pneumonia in adult and pediatric patients 2 months of age and older ( 1.2 ) • Skin and skin structure infections in adults ( 1.3 ) • Female pelvic infections in adults ( 1.4 ) • Community-acquired pneumonia in adults ( 1.5 ) To reduce the development of drug-resistant bacteria and maintain the effectiveness of ZOSYN and other antibacterial drugs, ZOSYN should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. ( 1.6 ) 1.1 Intra-abdominal Infections ZOSYN 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 ZOSYN is indicated in adults a

Dosage & Administration

2 DOSAGE AND ADMINISTRATION • If a dose of ZOSYN is required that does not equal 2.25 g, 3.375 g, or 4.5 g, ZOSYN injection in GALAXY Containers is not recommended for use and an alternative formulation of ZOSYN should be considered. ( 2.1 ) • Adult Patients With Indications Other Than Nosocomial Pneumonia; The usual daily dosage of ZOSYN for adults is 3.375 g every six hours totaling 13.5 g (12.0 g piperacillin and 1.5 g tazobactam). ( 2.2 ) • Adult Patients with Nosocomial Pneumonia: Initial presumptive treatment of patients with nosocomial pneumonia should start with ZOSYN at a dosage of 4.5 g every six hours plus an aminoglycoside, totaling 18.0 g (16.0 g piperacillin and 2.0 g tazobactam). ( 2.3 ) • Adult 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. ( 2.4 ) • Pediatric Patients by Indication and Age: See Table below ( 2.5 ) Recommended Dosage of ZOSYN for Pediatric Patients 2 months of Age and Older, Weighing up to 40 Kg and With Normal Renal Function Age Appendicitis and /or Peritonitis Nosocomial Pneumonia 2 months to 9 months 90 mg

Contraindications

4 CONTRAINDICATIONS ZOSYN is contraindicated in patients with a history of allergic reactions to any of the penicillins, cephalosporins, or beta-lactamase inhibitors. Patients with a history of allergic reactions to any of the penicillins, cephalosporins, or beta-lactamase inhibitors. ( 4 )

Drug Interactions

7 DRUG INTERACTIONS • ZOSYN administration can significantly reduce tobramycin concentrations in hemodialysis patients. Monitor tobramycin concentrations in these patients. ( 7.1 ) • Probenecid prolongs the half-lives of piperacillin and tazobactam and should not be co-administered with ZOSYN unless the benefit outweighs the risk. ( 7.2 ) • Co-administration of ZOSYN with vancomycin may increase the incidence of acute kidney injury. Monitor kidney function in patients receiving ZOSYN and vancomycin. ( 7.3 ) • Monitor coagulation parameters in patients receiving ZOSYN and heparin or oral anticoagulants. ( 7.4 ) • ZOSYN may prolong the neuromuscular blockade of vecuronium and other non-depolarizing neuromuscular blockers. 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 inactivation : When 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.

Adverse Reactions

6 ADVERSE REACTIONS The following clinically significant adverse reactions are described elsewhere in the labeling: • Hypersensitivity Adverse Reactions [see Warnings and Precautions (5.1) ] • Severe Cutaneous Adverse Reactions [see Warnings and Precautions (5.2) ] • Hemophagocytic Lymphohistiocytosis [see Warnings and Precautions (5.3) ] • Hematologic Adverse Reactions [see Warnings and Precautions (5.4) ] • Central Nervous System Adverse Reactions [see Warnings and Precautions (5.5) ] • Nephrotoxicity in Critically Ill Patients [see Warnings and Precautions (5.6) ] • Clostridioides difficile- Associated Diarrhea [see Warnings and Precautions (5.8) ] The most common adverse reactions (incidence >5%) are diarrhea, constipation, nausea, headache, and insomnia. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc. at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 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.

Frequently Asked Questions

What is Zosyn in Galaxy Containers used for?

Zosyn in Galaxy Containers contains TAZOBACTAM SODIUM and PIPERACILLIN SODIUM. It is a injection, solution taken intravenous. Consult your doctor for specific uses.

Is Zosyn in Galaxy Containers a controlled substance?

Zosyn in Galaxy Containers is not classified as a controlled substance by the DEA.

What is the generic name for Zosyn in Galaxy Containers?

The generic name for Zosyn in Galaxy Containers is TAZOBACTAM SODIUM and PIPERACILLIN SODIUM. There are no other listed brand versions of TAZOBACTAM SODIUM and PIPERACILLIN SODIUM.

What is the NDC code for Zosyn in Galaxy Containers 2 g/50mL?

The NDC (National Drug Code) for Zosyn in Galaxy Containers 2 g/50mL is 0206-8860, listed by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..

Product NDC

0206-8860

Package NDC

0206-8860-02

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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