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

Moxifloxacin Ab

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacin Ab (Moxifloxacin Hydrochloride)

Moxifloxacin, the active ingredient in Moxifloxacin Ab, is a fluoroquinolone antibiotic presented as an oral tablet for oral use. It is indicated for the treatment of several serious bacterial infections in adult patients, including community‑acquired pneumonia, acute bacterial sinusitis and complicated intra‑abdominal infections.

GNH India supplies Moxifloxacin Ab as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide under EU quality standards. The company maintains rigorous quality control and supports global distribution networks for reliable access.

Manufacturer / TM Owner

Aurobindo N.V.

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Indications & Clinical Uses

Moxifloxacin is a fluoroquinolone antibiotic used to treat bacterial infections in the respiratory, skin and intra‑abdominal 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 bacterial exacerbation of chronic bronchitis: improves lung function and shortens disease duration.
  • Skin and skin‑structure infections: provides effective antimicrobial coverage for Gram‑negative and Gram‑positive organisms.
  • Complicated intra‑abdominal infections: facilitates resolution of infection when combined with appropriate surgical management.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By binding to the ATP‑binding sites of these enzymes, it prevents unwinding and resealing of DNA strands, halting bacterial DNA synthesis and transcription. This bactericidal action is broad‑spectrum, affecting both Gram‑positive and Gram‑negative organisms, including atypical respiratory pathogens.

Side Effects

Moxifloxacin may cause 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.
  • Dizziness: occasional vertigo or light‑headedness.

Serious or Rare Side Effects

  • Tendon rupture: sudden pain and loss of function, especially in the Achilles.
  • QT interval prolongation: may lead to cardiac arrhythmias.
  • Severe hypersensitivity reactions: including Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

When prescribing Moxifloxacin, clinicians should consider several safety precautions to minimize risks.

  • Pregnancy: Category C; use only if potential benefits justify potential fetal risk.
  • Elderly patients: monitor for tendon disorders and CNS effects.
  • Renal impairment: dose adjustment may be required based on renal function.
  • History of QT prolongation: avoid or use with ECG monitoring.
  • Concomitant use with corticosteroids: increase risk of tendon rupture; assess benefits.
  • Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture and light.

Avoid Interactions

Moxifloxacin interacts with several drug classes; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce absorption of moxifloxacin.
  • Warfarin: may enhance anticoagulant effect, increasing bleeding risk.
  • Theophylline: increased serum levels leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: combined use raises tendon rupture risk.
  • Diabetic agents (e.g., insulin, sulfonylureas): may cause hypoglycemia.
  • Cyclosporine: may increase moxifloxacin plasma concentrations.

Frequently Asked Questions

Moxifloxacin Ab is indicated for adult patients with community‑acquired bacterial pneumonia, acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis, skin and skin‑structure infections, and complicated intra‑abdominal infections. It targets the bacteria responsible for these conditions.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. By inhibiting these enzymes, the drug prevents bacterial DNA from unwinding and re‑joining, leading to bacterial cell death.

The dosage of Moxifloxacin Ab is determined by the prescribing clinician based on the specific infection, patient characteristics, and local guidelines. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Moxifloxacin is classified as Pregnancy Category C, meaning it should be used only if the potential benefits justify the potential risk to the fetus. Limited data are available for breastfeeding; a risk‑benefit assessment by the healthcare provider is recommended.

To order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Moxifloxacin offers a broader spectrum against both Gram‑positive and Gram‑negative bacteria and has enhanced activity against atypical respiratory pathogens compared with older fluoroquinolones. Its pharmacokinetic profile allows once‑daily dosing for many indications.

Moxifloxacin Ab should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat and direct sunlight to maintain potency.

Moxifloxacin Ab is taken orally, usually with a full glass of water. It can be taken with or without food, but patients should avoid concomitant antacids containing aluminum or magnesium unless advised by a healthcare professional.

Serious risks include tendon rupture, especially of the Achilles tendon, QT interval prolongation that may lead to cardiac arrhythmias, and severe hypersensitivity reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, and individuals with significant QT prolongation should avoid Moxifloxacin Ab. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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