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

Moxifloxacin Kabi

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacin Kabi (Moxifloxacin Hydrochloride)

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

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 Deutschland Gmbh

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Indications & Clinical Uses

Moxifloxacin Kabi is a fluoroquinolone antibacterial indicated for several serious bacterial infections.

  • Community‑acquired bacterial pneumonia: provides rapid bactericidal activity to resolve pulmonary infection and improve respiratory function.
  • Complicated intra‑abdominal infections: achieves broad‑spectrum coverage of aerobic and anaerobic pathogens involved in intra‑abdominal sepsis.
  • Complicated skin and soft tissue infections: eliminates resistant Gram‑positive and Gram‑negative organisms to promote wound healing.
  • Acute bacterial sinusitis: eradicates the causative bacteria, relieving sinus inflammation and congestion.

How It Works

  • Moxifloxacin Hydrochloride inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By blocking these targets, the drug prevents bacterial DNA synthesis and transcription, leading to rapid bactericidal activity against susceptible Gram‑positive and Gram‑negative organisms.

Side Effects

Moxifloxacin Kabi may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: often self‑limiting, may be watery.
  • Headache: transient and usually resolves without intervention.
  • Injection site reactions: erythema or discomfort at the infusion site.

Serious or Rare Side Effects

  • Tendon rupture or tendinitis: especially in the Achilles tendon, may occur during or after therapy.
  • QT interval prolongation: can precipitate ventricular arrhythmias, particularly in patients with cardiac risk factors.
  • Severe hypersensitivity reactions: including anaphylaxis, Stevens‑Johnson syndrome, or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • History of tendon disorders: avoid use in patients with prior tendon injury or tendon‑related conditions.
  • QT prolongation risk: obtain baseline ECG and avoid concomitant QT‑prolonging agents.
  • Concurrent use with antacids containing aluminum or magnesium: separate administration by at least 2 hours to prevent reduced absorption.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk to the fetus or infant.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Moxifloxacin Kabi can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Co‑administration with other fluoroquinolones: increased risk of additive toxicity.
  • Concurrent use with drugs that prolong the QT interval (e.g., macrolides, antiarrhythmics): heightened risk of cardiac arrhythmias.
  • Combination with non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase the likelihood of central nervous system adverse effects.

Moderate Interactions (Monitor Closely)

  • Antacids or supplements containing divalent cations (calcium, iron, magnesium, zinc): may reduce drug absorption; separate dosing by at least 2 hours.
  • Warfarin: may enhance anticoagulant effect; monitor INR closely.
  • Theophylline: possible increase in serum theophylline levels; observe for signs of toxicity.

Frequently Asked Questions

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

Moxifloxacin Hydrochloride blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. This inhibition halts bacterial cell division, resulting in rapid bactericidal activity against a broad range of Gram‑positive and Gram‑negative pathogens.

The prescribed dose of Moxifloxacin Kabi is determined by the treating physician based on the type and severity of infection, patient weight, renal function, and other clinical factors. Dosage regimens are individualized and should follow the prescriber's instructions.

Safety data for Moxifloxacin Kabi during pregnancy and lactation are limited. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Moxifloxacin Kabi, 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 import documentation.

Moxifloxacin Kabi offers a broad spectrum of activity, including enhanced coverage of atypical respiratory pathogens and anaerobes, and is available as an injectable formulation for rapid intravenous delivery. Compared with older fluoroquinolones, it has a lower propensity for certain resistance mechanisms but shares class‑related safety considerations.

Moxifloxacin Kabi must 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.

Moxifloxacin Kabi is administered by intravenous infusion. The vial is reconstituted with the appropriate diluent, then infused over the period recommended by the prescriber, typically 30‑60 minutes, under aseptic conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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