Product image of Kezutin (Piperacillin, Tazobactam) supplied by GNH India

Kezutin

Active Ingredient:
Piperacillin, Tazobactam
Origin:
EU

Kezutin (Piperacillin, Tazobactam)

Piperacillin, the active ingredient in Kezutin, is a penicillin β‑lactamase inhibitor combination presented as an intravenous solution for intravenous use. It provides broad‑spectrum antibacterial activity against Gram‑negative, Gram‑positive and anaerobic organisms and is employed in the treatment of serious infections in hospitalized patients.

GNH India supplies Kezutin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to EU quality standards and offers reliable global distribution to healthcare facilities.

Manufacturer / TM Owner

Ardez Pharma

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Indications & Clinical Uses

Kezutin (piperacillin/tazobactam) is used for a range of serious bacterial infections affecting various organ systems.

  • Complicated intra‑abdominal infections: delivers broad coverage against aerobic and anaerobic pathogens to resolve infection.
  • Complicated urinary tract infections: eradicates resistant Gram‑negative organisms causing pyelonephritis and cystitis.
  • Skin and soft tissue infections: treats mixed‑flora infections including MRSA‑susceptible strains.
  • Community‑acquired pneumonia: provides empiric therapy against typical and atypical respiratory pathogens.
  • Hospital‑acquired pneumonia: targets multidrug‑resistant Gram‑negative bacteria in intensive‑care settings.
  • Sepsis: offers rapid bactericidal activity to control systemic infection.

How It Works

  • Piperacillin binds to penicillin‑binding proteins, inhibiting the final step of bacterial cell‑wall peptidoglycan synthesis, which leads to cell lysis. Tazobactam, a β‑lactamase inhibitor, protects piperacillin from enzymatic degradation by many β‑lactamases, thereby extending the antibacterial spectrum to include organisms that would otherwise be resistant.

Side Effects

Adverse reactions may occur with any intravenous antibiotic and should be monitored.

Common Side Effects

  • Diarrhea: mild to moderate loose stools.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Rash or pruritus: mild skin irritation.
  • Elevated liver enzymes: transient hepatic enzyme rise.
  • Injection site pain: discomfort at the infusion site.
  • Mild electrolyte disturbances: occasional changes in sodium or potassium levels.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Clostridioides difficile‑associated diarrhea: potentially life‑threatening colitis.
  • Severe neutropenia or thrombocytopenia: marked reduction in white blood cells or platelets.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: severe skin reactions.
  • Acute renal impairment: sudden decline in kidney function.
  • Hepatotoxicity: significant liver injury.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dosage in patients with impaired kidney function.
  • Allergy history: avoid in individuals with known penicillin or β‑lactamase inhibitor hypersensitivity.
  • Hepatic function: monitor liver enzymes during prolonged treatment.
  • Clostridioides difficile risk: watch for new-onset diarrhea and treat promptly.
  • Pregnancy and lactation: use only when the potential benefit justifies the potential risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the solution.

Avoid Interactions

Drug‑drug interactions may alter efficacy or increase toxicity.

Major Interactions (Avoid)

  • Probenecid: can increase piperacillin plasma concentrations, raising toxicity risk.
  • Methotrexate: reduced clearance may lead to severe myelosuppression.
  • Warfarin: potentiates anticoagulant effect, increasing bleeding risk.
  • Live vaccines: may diminish vaccine efficacy.
  • Aminoglycosides: combined nephrotoxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect electrolyte balance and renal clearance.
  • Oral contraceptives: possible reduction in contraceptive effectiveness.
  • Vancomycin: additive nephrotoxic potential when used together.

Frequently Asked Questions

Kezutin is an intravenous antibiotic containing piperacillin and tazobactam. It is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft tissue infections, community‑acquired and hospital‑acquired pneumonia, and sepsis in hospitalized patients.

Piperacillin interferes with bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, causing cell lysis. Tazobactam inhibits a broad range of β‑lactamases, protecting piperacillin from enzymatic degradation and extending its activity against resistant organisms.

The dosage of Kezutin is individualized by the prescribing clinician based on infection severity, patient weight, renal function, and local antimicrobial guidelines. No fixed regimen is provided here; the prescriber determines the appropriate dose and infusion rate.

Safety data for piperacillin/tazobactam in pregnancy and lactation are limited. It should be used only when the potential therapeutic benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician.

To order Kezutin, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Compared with carbapenems, piperacillin/tazobactam offers a similar spectrum against many Gram‑negative and anaerobic pathogens but may have a lower risk of selecting carbapenem‑resistant organisms. It is generally less costly than newer agents, though resistance patterns and local guidelines dictate the optimal choice.

Kezutin must be stored at 2‑8 °C, protected from light, and kept in its original packaging. Do not freeze or shake the solution. Before administration, allow the product to reach room temperature if required and inspect for particulate matter or discoloration.

Kezutin is given by intravenous infusion. The infusion rate and duration are determined by the prescriber, typically over 30 minutes to 1 hour, depending on the dose and patient tolerance. It should be administered using aseptic technique and appropriate IV equipment.

Serious adverse events include anaphylaxis, Clostridioides difficile‑associated colitis, severe neutropenia or thrombocytopenia, Stevens‑Johnson syndrome, acute renal impairment, and hepatotoxicity. Immediate medical attention is required if any of these reactions are suspected.

Kezutin is contraindicated in patients with a documented hypersensitivity to piperacillin, other penicillins, β‑lactamase inhibitors, or any component of the formulation. Caution is also advised for patients with severe renal impairment, known hepatic disease, or a history of severe allergic reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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