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

Moxifloxacin Accord

Active Ingredient:
Moxifloxacin
Origin:
EU

Moxifloxacin Accord (Moxifloxacin)

Moxifloxacin, the active ingredient in Moxifloxacin Accord, is a fluoroquinolone antibiotic presented as an oral tablet for oral use. It treats a range of bacterial infections, including community‑acquired pneumonia, acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis, and skin and soft‑tissue infections in adult patients.
GNH India supplies Moxifloxacin Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Moxifloxacin Accord is a fluoroquinolone antibiotic used to manage bacterial infections of the respiratory and skin systems.

  • Community‑acquired pneumonia: eradicates the causative bacteria and improves clinical outcomes.
  • Acute bacterial sinusitis: reduces sinus inflammation by eliminating pathogenic organisms.
  • Acute bacterial exacerbation of chronic bronchitis: controls bacterial overgrowth and relieves symptoms.
  • Skin and soft‑tissue infections: targets susceptible Gram‑positive and Gram‑negative bacteria to promote healing.

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, the drug prevents the supercoiling and separation of bacterial DNA strands, leading to halted bacterial cell division and eventual bacterial cell death. This bactericidal action is effective against a broad spectrum of Gram‑positive and Gram‑negative organisms.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, often self‑limiting.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional vertiginous sensation.
  • Rash: mild skin erythema or pruritus.
  • Elevated liver enzymes: transient laboratory changes.

Serious or Rare Side Effects

  • Tendon rupture: especially Achilles tendon, may occur without warning.
  • QT interval prolongation: can precipitate cardiac arrhythmias.
  • Severe allergic reaction: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Clostridioides difficile infection: colitis due to gut flora disruption.
  • Hepatotoxicity: significant liver injury in rare cases.
  • Peripheral neuropathy: persistent numbness or tingling.

Precautions & Warnings

Before prescribing Moxifloxacin Accord, clinicians should consider several safety measures.

  • Assess renal function: dose adjustment may be required in impaired clearance.
  • Monitor cardiac status: avoid in patients with known QT prolongation or electrolyte disturbances.
  • Evaluate hypersensitivity: discontinue if signs of allergic reaction appear.
  • Use cautiously in the elderly: increased risk of tendon injury and CNS effects.
  • Avoid concomitant use with other QT‑prolonging agents: risk of arrhythmia.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Moxifloxacin Accord can interact with other medicines, necessitating careful review.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce absorption of the drug.
  • Warfarin: may increase anticoagulant effect and bleeding risk.
  • Systemic corticosteroids: heightened risk of tendon rupture.
  • Other QT‑prolonging drugs (e.g., quinidine, amiodarone): may cause serious cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may enhance central nervous system stimulation.
  • Theophylline: increased plasma concentrations leading to toxicity.
  • Rifampin: may lower moxifloxacin levels, reducing efficacy.

Frequently Asked Questions

Moxifloxacin Accord is a prescription‑only fluoroquinolone antibiotic indicated for the treatment of adult patients with community‑acquired pneumonia, acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis, and skin or soft‑tissue infections caused by susceptible bacteria.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. By preventing DNA supercoiling and strand separation, the drug stops bacterial cell division, leading to bacterial death and resolution of the infection.

The specific dose and duration are determined by the prescribing clinician based on the infection type, severity, patient age, renal function, and local guidelines. Patients should follow the prescriber’s instructions and not alter the regimen without medical advice.

The pregnancy safety category for moxifloxacin is not definitively established. It should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult a healthcare professional, as the drug may be excreted in milk.

To place an order, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any 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 once‑daily dosing schedule, which can improve adherence, but shares class‑related safety considerations like tendon risk and QT prolongation.

Moxifloxacin Accord should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from excess moisture and direct sunlight to maintain stability throughout its shelf life.

The medication is supplied as an oral tablet that should be swallowed whole with a glass of water. It can be taken with or without food, but patients should avoid concurrent intake of antacids containing aluminum or magnesium, which may reduce absorption.

Serious adverse events include tendon rupture (especially in the Achilles tendon), QT interval prolongation that can lead to arrhythmias, severe allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome, and Clostridioides difficile‑associated colitis. Patients should seek immediate medical attention if they experience sudden tendon pain, palpitations, or severe skin reactions.

Moxifloxacin Accord is contraindicated in individuals with a known hypersensitivity to moxifloxacin or other fluoroquinolones, patients with a history of tendon disorders related to fluoroquinolone use, and those with established QT prolongation or uncorrected electrolyte abnormalities. Caution is also advised for patients with severe liver disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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