Product image of Moxifloxacin Kabi (Moxifloxacin Hydrochloride) supplied by GNH India

Moxifloxacin Kabi

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacin Kabi (Moxifloxacin Hydrochloride)

Moxifloxacin, the active ingredient in Moxifloxacin Kabi, is a fluoroquinolone antibiotic presented as an intravenous solution for intravenous use. It treats a range of serious bacterial infections in adult patients, including community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, complicated skin and skin‑structure infections, and complicated intra‑abdominal infections.

GNH India supplies Moxifloxacin Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi Hungary Kft.

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Indications & Clinical Uses

Moxifloxacin is a fluoroquinolone antibiotic used to treat bacterial infections of the respiratory, skin and intra‑abdominal systems.

  • Community‑acquired pneumonia: achieves clinical cure and bacterial eradication in adult patients.
  • Acute bacterial sinusitis: reduces symptoms and eliminates causative pathogens.
  • Acute exacerbations of chronic bronchitis: improves lung function and shortens disease duration.
  • Complicated skin and skin structure infections: facilitates resolution of infection and promotes healing.
  • Complicated intra‑abdominal infections: supports clearance of intra‑abdominal pathogens and recovery.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling, replication and transcription. By binding to the ATP‑binding sites of these enzymes, it prevents DNA strand separation, leading to bactericidal activity against a broad spectrum of Gram‑positive, Gram‑negative and atypical organisms, including many resistant strains.

Side Effects

Moxifloxacin may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools, often self‑limiting.
  • Headache: transient cranial discomfort.
  • Rash: mild skin erythema or pruritus.

Serious or Rare Side Effects

  • Tendon rupture: sudden tendon pain or rupture, especially in the Achilles.
  • QT interval prolongation: risk of cardiac arrhythmia, monitor ECG.
  • Severe hypersensitivity reactions: anaphylaxis or Stevens‑Johnson syndrome.
  • Clostridioides difficile‑associated colitis: severe diarrhea due to gut flora disruption.

Precautions & Warnings

Use of Moxifloxacin requires careful assessment of patient-specific factors and monitoring for potential complications.

  • Renal impairment: adjust therapy and monitor renal function.
  • Hepatic dysfunction: use with caution; monitor liver enzymes.
  • History of tendon disorders: avoid use due to risk of tendon rupture.
  • Cardiac arrhythmias: assess QT interval before therapy.
  • Concomitant QT‑prolonging drugs: avoid combination to reduce arrhythmia risk.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Moxifloxacin can interact with several medicines, necessitating clinical vigilance.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce absorption, avoid concurrent use.
  • Warfarin: may increase INR, monitor coagulation.
  • Theophylline: increased plasma levels, monitor for toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase risk of central nervous system effects.
  • Corticosteroids: heightened risk of tendon rupture.
  • Oral contraceptives: possible reduction in efficacy, advise alternative contraception.

Frequently Asked Questions

Moxifloxacin Kabi is an intravenous fluoroquinolone antibiotic indicated for the treatment of adult patients with community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, complicated skin and skin‑structure infections, and complicated intra‑abdominal infections.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA supercoiling and replication. This dual inhibition halts bacterial DNA synthesis, producing a bactericidal effect against a broad range of Gram‑positive, Gram‑negative and atypical organisms.

The dosing regimen is determined by the prescribing clinician based on infection type, severity, renal and hepatic function, and individual patient factors. No fixed dose is provided here; the prescriber sets the appropriate regimen.

Safety data are limited and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies the potential risk to the fetus, and breastfeeding decisions should be made in consultation with a healthcare professional.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and the necessary import documentation.

Moxifloxacin provides broader coverage against atypical pathogens and higher potency against Gram‑positive organisms compared with older agents such as ciprofloxacin, while retaining the class‑related safety profile. Choice of agent depends on susceptibility data, infection site and clinical judgment.

Store the product at 2‑8 °C in a refrigerator, keep the vial in its original packaging, protect from light, and do not freeze or shake. Follow the manufacturer’s stability guidelines once the vial is removed from refrigeration.

Moxifloxacin Kabi is supplied as a sterile intravenous solution for infusion. Administration is performed by a qualified healthcare professional using aseptic technique, typically via a peripheral or central IV line, and follows the prescribed infusion rate and duration.

Serious adverse events include tendon rupture, QT‑interval prolongation leading to arrhythmias, severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome, and Clostridioides difficile‑associated colitis. Immediate medical evaluation is required if any of these occur.

Patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones, those with a history of fluoroquinolone‑related tendon disorders, and individuals with significant QT prolongation or uncontrolled cardiac arrhythmias should avoid this medication unless no suitable alternatives exist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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