Product image of Moxifloxacina Anfarm (Moxifloxacin) supplied by GNH India

Moxifloxacina Anfarm

Active Ingredient:
Moxifloxacin
Origin:
EU

Moxifloxacina Anfarm (Moxifloxacin)

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

GNH India supplies Moxifloxacina Anfarm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Anfarm Hellas Sa

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Indications & Clinical Uses

Moxifloxacin is a broad‑spectrum fluoroquinolone used to treat bacterial infections in the respiratory, skin and abdominal systems.

  • Community‑acquired pneumonia: achieves bacterial eradication and clinical recovery.
  • Acute bacterial sinusitis: reduces sinus inflammation and clears infection.
  • Acute bacterial exacerbation of chronic bronchitis: improves lung function and resolves bacterial load.
  • Complicated skin and skin‑structure infections: eliminates pathogenic bacteria and promotes wound healing.
  • Complicated intra‑abdominal infections: provides systemic antibacterial activity against mixed flora.

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 DNA, leading to halted bacterial cell division and ultimately bacterial cell death. This bactericidal action is effective 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: mild gastrointestinal upset.
  • Diarrhea: loose stools, often self‑limiting.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional vertiginous sensation.
  • Rash: mild skin erythema.
  • Elevated liver enzymes: transient hepatic enzyme rise.

Serious or Rare Side Effects

  • Tendon rupture: sudden tendon pain or rupture, especially in the Achilles.
  • QT interval prolongation: risk of cardiac arrhythmias.
  • Clostridioides difficile infection: severe colitis.
  • Severe allergic reactions: anaphylaxis, angioedema.
  • Hepatic failure: marked liver dysfunction.
  • Seizures: rare neurologic events.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Assess renal function: adjust therapy if renal impairment is present.
  • Monitor for tendon pain: discontinue if signs of tendonitis or rupture appear.
  • Avoid concomitant QT‑prolonging drugs: reduce risk of arrhythmia.
  • Use with caution in elderly patients: higher susceptibility to adverse events.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Moxifloxacin can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Co‑administration with other fluoroquinolones: increased risk of toxicity.
  • Concurrent systemic corticosteroids: heightened tendon rupture risk.
  • Combination with other QT‑prolonging agents: potential for serious cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may diminish antibacterial activity.
  • Antacids containing magnesium or aluminum: reduce oral absorption (relevant for oral forms).
  • Warfarin: may enhance anticoagulant effect, requiring INR monitoring.

Frequently Asked Questions

Moxifloxacina Anfarm, containing the fluoroquinolone moxifloxacin, is indicated for serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, complicated skin and skin‑structure infections, and complicated intra‑abdominal infections.

Moxifloxacin blocks bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes required for DNA replication and transcription. This inhibition prevents bacterial cell division, leading to rapid bactericidal activity against a broad spectrum of Gram‑positive and Gram‑negative organisms.

The dosage of Moxifloxacina Anfarm is determined by the prescribing clinician based on the infection type, severity, patient weight, renal function and local guidelines. Only a qualified healthcare professional should set the exact regimen.

The safety of moxifloxacin in pregnancy and lactation has not been definitively established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made 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 if needed) and any required import documentation.

Moxifloxacin offers a broader spectrum against Gram‑positive organisms and better activity in respiratory infections compared with older fluoroquinolones such as ciprofloxacin. Its pharmacokinetic profile allows once‑daily dosing, but it shares class‑related safety considerations like tendon toxicity and QT prolongation.

Moxifloxacina Anfarm should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial, and keep it in the original packaging to maintain stability.

The product is supplied as an injectable solution for intravenous infusion. Administration is performed by a qualified healthcare professional, typically over a prescribed period of time, following aseptic technique and appropriate infusion guidelines.

Serious risks include tendon rupture, especially in the Achilles tendon, QT interval prolongation leading to arrhythmias, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, hepatic failure, and rare neurologic events like seizures.

Patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, individuals with significant QT prolongation, and patients receiving concomitant medications that strongly prolong the QT interval should avoid this product unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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