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

Moxifloxacine Fresenius Kabi

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacine Fresenius Kabi (Moxifloxacin Hydrochloride)

Moxifloxacin, the active ingredient in Moxifloxacine Fresenius Kabi, is a fluoroquinolone presented as an injectable solution for intravenous use. It treats a range of serious bacterial infections in adults, including community‑acquired pneumonia, acute bacterial sinusitis, exacerbations of chronic bronchitis, skin and soft‑tissue infections, and intra‑abdominal infections, and is indicated for severe infections requiring hospitalisation.

GNH India supplies Moxifloxacine Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and specialty clinics worldwide, ensuring quality and regulatory compliance across all markets.

Manufacturer / TM Owner

Fresenius Kabi Nederland B.V.

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Indications & Clinical Uses

Moxifloxacin is a fluoroquinolone antibiotic used to treat bacterial infections in several organ systems.

  • Community‑acquired bacterial pneumonia: achieves bacterial eradication and clinical cure in adult patients.
  • Acute bacterial sinusitis: reduces symptoms and eliminates the causative pathogens.
  • Acute exacerbations of chronic bronchitis: improves lung function and shortens disease duration.
  • Skin and skin structure infections: resolves infection and promotes tissue healing.
  • Intra‑abdominal infections: clears polymicrobial infection and supports recovery after surgery.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By binding to the quinolone‑binding site, it prevents DNA strand separation, halting bacterial DNA synthesis and transcription, leading to rapid bacterial cell death. This bactericidal activity is effective against a broad spectrum of Gram‑positive and Gram‑negative organisms.

Side Effects

Moxifloxacin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild 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, Stevens‑Johnson syndrome, or toxic epidermal necrolysis.

Precautions & Warnings

When using Moxifloxacine Fresenius Kabi, clinicians should consider several safety measures to minimize risk.

  • Renal function: assess and adjust in severe renal impairment.
  • QT prolongation: monitor ECG in patients with cardiac risk factors.
  • Allergy: discontinue immediately if hypersensitivity reaction occurs.
  • Concomitant corticosteroids: avoid or monitor for increased tendon rupture risk.
  • Pregnancy and lactation: use only if benefits outweigh potential risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • QT‑prolonging agents (e.g., quinidine, macrolides, antiarrhythmics): may increase risk of torsades de pointes.
  • Systemic corticosteroids: combined use raises tendon rupture risk.
  • Other fluoroquinolones: additive toxicity without added benefit.

Moderate Interactions (Monitor Closely)

  • Antacids or supplements containing magnesium or aluminum: reduce absorption; separate dosing by at least 2 hours.
  • Warfarin: may enhance anticoagulant effect; monitor INR closely.
  • Theophylline: may increase plasma concentrations; observe for signs of toxicity.

Frequently Asked Questions

Moxifloxacine Fresenius Kabi is an intravenous fluoroquinolone antibiotic indicated for the treatment of serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, skin and soft‑tissue infections, and intra‑abdominal infections in adult patients.

Moxifloxacin exerts its antibacterial effect by inhibiting the bacterial enzymes DNA gyrase (topoisomerase II) and topoisomerase IV. This blocks DNA supercoiling and replication, halting bacterial DNA synthesis and transcription, which leads to rapid bacterial cell death.

The appropriate dose and duration of therapy are determined by the prescribing clinician based on the infection type, severity, patient weight, renal function, and local guidelines. No specific dosing regimen is provided here.

The pregnancy category for this product is not definitively established. It should be used during pregnancy or lactation only when the potential benefits justify the potential risks, and after careful consideration by the treating physician.

To place an order, 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 where required) and necessary import documentation.

Moxifloxacin offers a broader spectrum against Gram‑positive organisms and better activity in respiratory infections compared with older fluoroquinolones such as ciprofloxacin. It also has a lower propensity for drug‑induced seizures but shares class‑related risks like tendon injury and QT prolongation, which must be weighed against alternatives.

The product should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use and discard any solution that appears discolored or contains particles.

Moxifloxacine Fresenius Kabi is supplied as an injectable solution for intravenous infusion. It is administered by a healthcare professional under aseptic conditions, typically as a slow infusion over a prescribed period, following the dosing instructions provided by the prescriber.

Serious adverse events include tendon rupture (especially Achilles), QT interval prolongation which can lead to life‑threatening arrhythmias, and severe hypersensitivity reactions such as anaphylaxis, Stevens‑Johnson syndrome, or toxic epidermal necrolysis. Prompt medical attention is required if any of these occur.

Patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones should avoid this product. It is also contraindicated in individuals with a history of QT prolongation, uncontrolled cardiac arrhythmias, or those taking other QT‑prolonging drugs unless benefits outweigh risks. Caution is advised in pregnant or lactating women and in patients with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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