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PIPTASIGN INJECTION

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PIPTASIGN Injection is a combination of Piperacillin and Tazobactam, formulated for the effective treatment of severe bacterial infections. Manufactured and globally exported by BLUEPILL EXPRESS, this broad-spectrum antibiotic injection ensures optimal treatment outcomes in hospital and critical care settings.

Description

PIPTASIGN Injection is a potent broad-spectrum β-lactam/β-lactamase inhibitor combination that consists of Piperacillin (a ureidopenicillin antibiotic) and Tazobactam (a β-lactamase inhibitor). This synergistic formulation enhances the activity of Piperacillin by preventing bacterial resistance mechanisms, particularly against organisms producing β-lactamase enzymes.

PIPTASIGN is widely used in the treatment of moderate to severe bacterial infections, including those of the respiratory tract, urinary tract, intra-abdominal area, skin and soft tissues, and gynecological infections. It is also commonly administered in cases of hospital-acquired infections, neutropenic fever, and sepsis.

This injection is manufactured under WHO-GMP, ISO, and stringent regulatory standards by BLUEPILL EXPRESS, a trusted global pharmaceutical manufacturer and exporter. The company offers PIPTASIGN Injection for third-party manufacturing, international distribution, and custom-label partnerships.

  • Broad-Spectrum Antibiotic

  • Anti-infective

  • β-lactam/β-lactamase Inhibitor Combination

  • Piperacillin: 4 g

  • Tazobactam: 0.5 g

  • Also available in 2.25 g and 1.125 g strengths (on request)

  • Effective against resistant gram-positive and gram-negative bacteria

  • Inhibits β-lactamase enzymes, enhancing antibiotic spectrum

  • Ideal for life-threatening infections in ICU and hospital settings

  • Reliable treatment for both aerobic and anaerobic pathogens

  • Injectable dosage ensures rapid systemic availability

  • Community-acquired and hospital-acquired pneumonia

  • Severe urinary tract infections (UTIs)

  • Intra-abdominal infections (including peritonitis)

  • Pelvic inflammatory disease

  • Complicated skin and soft tissue infections

  • Febrile neutropenia

  • Sepsis and bacteremia

  • Adults: Typically 4.5 g IV every 6–8 hours

  • Children: Dose based on body weight, under physician guidance

  • Administer via intravenous infusion over 20–30 minutes

  • Dosage adjustment may be required in renal impairment

  • Reconstitute with sterile water or appropriate IV diluent

  • Administer under medical supervision in sterile conditions

  • Complete full course even if symptoms improve early

  • Do not mix with other drugs in the same IV line unless confirmed compatible

  • Hypersensitivity to penicillins or cephalosporins

  • Caution in patients with renal dysfunction or electrolyte imbalance

  • Monitor liver enzymes and blood counts during prolonged therapy

  • Not recommended in viral infections (e.g., influenza)

  • Diarrhea

  • Injection site reactions

  • Nausea or vomiting

  • Elevated liver enzymes

  • Rare: Hypersensitivity reactions, thrombocytopenia

  • Form: Dry powder for IV injection

  • Strengths: 4.5 g / 2.25 g / 1.125 g

  • Pack Type: Glass vial with sterile water for injection (if required)

  • Shelf Life: 24 months

  • Storage: Store below 25°C; protect from light and moisture

  • Certifications: WHO-GMP, ISO 9001:2015, FDA (India)

BLUEPILL EXPRESS – A global leader in third-party pharmaceutical manufacturing and merchant export of high-quality medical formulations. Backed by state-of-the-art infrastructure and international certifications, BLUEPILL EXPRESS is committed to quality, safety, and efficacy in healthcare exports.

  • WHO-GMP certified global manufacturing facility

  • Customizable formulations and labeling for clients

  • Strict adherence to international pharmacopeial standards

  • Available for bulk export, contract manufacturing, and tender supply

  • Supported with complete COA, MSDS, and export documentation

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