Product image of Moxifloxacin Eberth (Moxifloxacin) supplied by GNH India

Moxifloxacin Eberth

Active Ingredient:
Moxifloxacin
Origin:
EU

Moxifloxacin Eberth (Moxifloxacin)

Moxifloxacin, the active ingredient in Moxifloxacin Eberth, is a fluoroquinolone antibiotic presented as an injection for intravenous use. It treats a range of serious bacterial infections in adult patients, including pneumonia, sinusitis, and complicated skin or intra‑abdominal infections.

GNH India supplies Moxifloxacin Eberth as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Dr. Friedrich Eberth Arzneimittel Gmbh

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Indications & Clinical Uses

  • Moxifloxacin is a broad‑spectrum fluoroquinolone used to treat bacterial infections in various organ systems.
  • Community‑acquired bacterial pneumonia: effective eradication of susceptible pathogens causing lung infection.
  • Acute bacterial sinusitis: rapid bacterial clearance in sinus cavities.
  • Complicated skin and skin‑structure infections: treatment of severe dermal infections caused by susceptible organisms.
  • Complicated intra‑abdominal infections: control of mixed bacterial flora in abdominal cavities.
  • Acute exacerbations of chronic bronchitis: reduction of bacterial load during flare‑ups.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. By binding to these enzymes, it prevents the unwinding of bacterial DNA, leading to halted cell division and bacterial cell death. The drug displays concentration‑dependent bactericidal activity against a wide range of Gram‑positive and Gram‑negative organisms.

Side Effects

Moxifloxacin may cause a variety of adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea or vomiting
  • Diarrhea
  • Headache
  • Dizziness or vertigo
  • Rash or mild skin irritation
  • Elevated liver enzymes

Serious or Rare Side Effects

  • Tendon rupture or tendonitis, especially in the Achilles tendon
  • QT interval prolongation leading to cardiac arrhythmias
  • Severe hypersensitivity reactions (anaphylaxis, Stevens‑Johnson syndrome)
  • Clostridioides difficile‑associated colitis
  • Hepatic failure or jaundice
  • Peripheral neuropathy

Precautions & Warnings

  • Before initiating therapy, clinicians should assess patient‑specific risk factors and monitor for adverse events.
  • Renal impairment: adjust therapy and monitor renal function.
  • Hepatic impairment: use with caution; monitor liver enzymes.
  • QT prolongation risk: avoid in patients with known cardiac arrhythmias or electrolyte disturbances.
  • Elderly patients: increased susceptibility to tendon injury; advise caution.
  • Pregnancy and lactation: safety not established; use only if benefit outweighs risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Moxifloxacin can interact with several drug classes, altering efficacy or safety.

Major Interactions (Avoid)

  • Antacids or supplements containing aluminum, magnesium, calcium, or iron: reduce absorption.
  • Warfarin: may increase INR and bleeding risk.
  • Theophylline: increased plasma concentrations leading to toxicity.
  • Cyclosporine: elevated cyclosporine levels.
  • Amiodarone or other QT‑prolonging agents: heightened risk of arrhythmias.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase risk of CNS stimulation.
  • Oral contraceptives: reduced effectiveness, consider backup method.
  • Diabetic agents (e.g., sulfonylureas): potential hypoglycemia.
  • Corticosteroids: increased risk of tendon rupture.
  • Rifampin: may reduce moxifloxacin plasma levels.

Frequently Asked Questions

Moxifloxacin Eberth is indicated for serious bacterial infections such as community‑acquired bacterial pneumonia, acute bacterial sinusitis, complicated skin and skin‑structure infections, complicated intra‑abdominal infections, and acute exacerbations of chronic bronchitis in adult patients.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. This inhibition prevents bacterial cell division and leads to rapid bacterial death, providing a broad‑spectrum antibacterial effect.

The specific dose and duration are determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and other clinical factors. Healthcare professionals should follow local prescribing guidelines.

Safety data for moxifloxacin in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and under close medical supervision.

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 enhanced activity against atypical respiratory pathogens compared with older fluoroquinolones like ciprofloxacin. It also has a lower propensity for drug‑induced photosensitivity but shares class‑wide risks such as tendon injury and QT prolongation.

Moxifloxacin Eberth should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Maintain the cold chain during transport and keep the product in its original packaging until use.

The product is supplied as a sterile injection for intravenous infusion. Administration is performed by a qualified healthcare professional, typically over a period of 60 minutes, following aseptic technique and according to the prescribing information.

Serious risks include tendon rupture or tendonitis, QT interval prolongation leading to potentially fatal arrhythmias, severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome, Clostridioides difficile‑associated colitis, and hepatic failure. Patients should be monitored closely for these events.

Moxifloxacin Eberth is contraindicated in patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, and individuals with pre‑existing prolonged QT interval or receiving other QT‑prolonging drugs unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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