PIPERACILLIN/TAZOBACTAM
(pi-per'a-cil-lin/taz-o-bac'tam)
Zosyn
Classifications: antiinfective; beta-lactam antibiotic; antipseudomonal penicillin
Prototype: Piperacillin Sodium
Pregnancy Category: B

Availability

2 g, 3 g, 4 g injection

Actions

Antibacterial combination product consisting of the semisynthetic piperacillin and the beta-lactamase inhibitor tazobactam. Tazobactam component does not decrease the activity of the piperacillin component against susceptible organisms.

Therapeutic Effects

Tazobactam is an inhibitor of a wide variety of bacterial beta–lactamases. It has little antibacterial activity itself; however, in combination with piperacillin, it extends the spectrum of bacteria that are susceptible to piperacillin. Two-drug combination has antibiotic activity against an extremely broad spectrum of gram-positive, gram-negative, and anaerobic bacteria.

Uses

Treatment of moderate to severe appendicitis, uncomplicated and complicated skin and skin structure infections, endometritis, pelvic inflammatory disease, or nosocomial or community-acquired pneumonia caused by piperacillin-resistant, piperacillin/tazobactam-susceptible, beta-lactamase-producing bacteria.

Contraindications

Hypersensitivity to piperacillin, tazobactam, penicillins, cephalosporins, or beta-lactamase inhibitors such as clavulanic acid and sulbactam.

Cautious Use

Kidney failure; pregnancy (category B), lactation.

Route & Dosage

Moderate to Severe Infections
Adult: IV 3.375 g q6h, infused over 30 min, for 7–10 d
Child: IV <6 mo, 150–300 mg piperacillin/kg/d divided q6–8h; 6 mo, 240 mg piperacillin component/kg/d divided q8h

Nosocomial Pneumonia
Adult: IV 4.5 g q6h, infused over 30 min, for 7–10 d

Renal Insufficiency
Clcr 20–40 mL/min: 2.25 g q6h; <20 mL/min: 2.25 g q8h

Administration

Note: Verify correct IV concentration and rate of infusion for administration to infants or children with physician.

Intravenous
  • For hemodialysis patients, the maximum dose is 2.25 g q8h; give one extra 0.75-g dose after each dialysis period.

PREPARE: Intermittent: Reconstitute powder with 5 mL of diluent (e.g., D5W, NS); shake well until dissolved. Further dilute to at least 50 mL of selected diluent. Use single-dose vials immediately after reconstitution.  

ADMINISTER: Intermittent: Give over at least 30 min.  

INCOMPATIBILITIES Solution/additive: Aminoglycosides, Lactated Ringer's, albumin, blood products, solutions containing sodium bicarbonate. Y-site: Acyclovir, aminoglycosides, amiodarone, amphotericin B, amphotericin B cholesteryl complex, azithromycin, chlorpromazine, cisplatin, dacarbazine, daunorubicin, doxorubicin, doxycycline, droperidol, famotidine, ganciclovir, gemcitabine, hydroxyzine, idarubicin, minocycline, mitomycin, mitoxantrone, nalbuphine, prochlorperazine, promethazine, vancomycin.

Adverse Effects (1%)

CNS: Headache, insomnia, fever. GI: Diarrhea, constipation, nausea, vomiting, dyspepsia, pseudomembranous colitis. Skin: Rash, pruritus, hypersensitivity reactions.

Interactions

Drug: May increase risk of bleeding with anticoagulants; probenecid decreases elimination of piperacillin.

Pharmacokinetics

Distribution: Distributes into many tissues, including lung, blister fluid, and bile; crosses placenta; distributed into breast milk. Metabolism: Metabolized in liver. Elimination: Piperacillin and tazobactam are excreted in urine. Half-Life: 0.7–1.2 h.

Nursing Implications

Assessment & Drug Effects

Patient & Family Education


Common adverse effects in italic, life-threatening effects underlined; generic names in bold; classifications in SMALL CAPS; Canadian drug name; Prototype drug