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 injectable solution for intravenous use. It is employed to treat a range of serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, exacerbations of chronic bronchitis, skin‑structure infections and complicated intra‑abdominal infections.

GNH India supplies Moxifloxacin Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to stringent quality standards and provides reliable logistics for global healthcare institutions, including tertiary care centers and specialty clinics.

Manufacturer / TM Owner

Fresenius Kabi Bulgaria Eood

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Indications & Clinical Uses

Moxifloxacin is a fluoroquinolone antibiotic indicated for several bacterial infections affecting the respiratory, skin and intra‑abdominal systems.

  • Community‑acquired pneumonia: effective eradication of susceptible pathogens, leading to clinical improvement and resolution of infection.
  • Acute bacterial sinusitis: rapid reduction of sinus inflammation and bacterial load, relieving symptoms.
  • Acute bacterial exacerbation of chronic bronchitis: helps restore lung function by eliminating causative bacteria.
  • Skin and skin‑structure infections: provides bactericidal activity against common Gram‑positive and Gram‑negative organisms.
  • Complicated intra‑abdominal infections: achieves deep tissue penetration to treat polymicrobial infections following surgery.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription and repair. By stabilizing the enzyme–DNA complex, it prevents the resealing of DNA strands, leading to lethal double‑strand breaks and bacterial cell death. This dual‑target action provides broad‑spectrum activity against Gram‑positive, Gram‑negative and atypical pathogens.

Side Effects

Moxifloxacin may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea
  • Diarrhea
  • Headache
  • Injection site pain or phlebitis

Serious or Rare Side Effects

  • Tendon rupture or tendinitis
  • QT interval prolongation and cardiac arrhythmias
  • Clostridioides difficile–associated diarrhea
  • Severe hypersensitivity reactions including anaphylaxis

Precautions & Warnings

When using Moxifloxacin, clinicians should observe several safety considerations to minimize risk.

  • Assess renal function: adjust therapy in patients with impaired clearance.
  • Monitor cardiac rhythm: avoid use in patients with known QT prolongation.
  • Avoid concomitant QT‑prolonging drugs: limit risk of arrhythmias.
  • Use with caution in patients with tendon disorders: discontinue if pain or inflammation occurs.
  • Adjust dose in hepatic impairment: follow prescribing information for liver dysfunction.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Moxifloxacin can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Antacids or supplements containing aluminum, magnesium, calcium, or iron: chelate the drug and markedly reduce absorption.
  • Co‑administration with other fluoroquinolones: increases risk of additive toxicity.
  • Concurrent use with drugs that prolong QT interval (e.g., macrolides, antiarrhythmics): may cause serious cardiac events.
  • Warfarin: may enhance anticoagulant effect and raise INR.
  • Systemic corticosteroids: increase risk of tendon rupture.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase central nervous system stimulation.
  • Theophylline: elevated plasma concentrations can lead to toxicity.
  • Cyclosporine: higher levels may occur, requiring monitoring.
  • Oral contraceptives: reduced hormonal efficacy, consider alternative contraception.
  • Diabetic agents (e.g., insulin, sulfonylureas): potential for hypoglycemia, monitor glucose.

Frequently Asked Questions

Moxifloxacin Kabi is indicated for serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, skin and skin‑structure infections, and complicated intra‑abdominal infections. It is administered intravenously in a hospital setting to target susceptible pathogens.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. By preventing the resealing of DNA strands, it creates lethal double‑strand breaks, leading to rapid bacterial cell death and a broad spectrum of activity against Gram‑positive, Gram‑negative and atypical organisms.

The dosage of Moxifloxacin Kabi is determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and local guidelines. Healthcare professionals set the exact dose and infusion rate for each individual patient.

Safety data for Moxifloxacin Kabi in pregnancy and lactation are limited. The drug should be used only if the potential benefit justifies any potential risk to the fetus or infant. Clinicians must evaluate each case and consider alternative therapies when possible.

To request Moxifloxacin Kabi, submit an enquiry on the product page at gnhindia.com, specifying 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 if needed) and import documentation.

Moxifloxacin offers a broader spectrum against Gram‑positive and atypical pathogens compared with many earlier fluoroquinolones, and it achieves higher tissue concentrations in the lungs and sinuses. Its safety profile is similar, but it carries class‑related risks such as tendon injury and QT prolongation, which must be weighed against clinical benefits.

Moxifloxacin Kabi should be stored at 2‑8 °C in a refrigerator. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. Do not use the product if it has been exposed to temperatures outside the recommended range.

Moxifloxacin Kabi is given as an intravenous infusion. The healthcare professional prepares the solution according to the product label, selects an appropriate infusion set, and administers it over the recommended time period, typically under clinical monitoring for adverse reactions.

Serious risks include tendon rupture or tendinitis, QT interval prolongation leading to potentially fatal arrhythmias, severe hypersensitivity reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis. Patients should be monitored closely for signs of these events, especially if risk factors are present.

Moxifloxacin Kabi is contraindicated in patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones. It should be avoided in individuals with a history of tendon disorders related to fluoroquinolone use, uncontrolled QT prolongation, or those taking multiple QT‑prolonging agents without careful monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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