Product image of Moxifloxacine Krka (Moxifloxacin) supplied by GNH India

Moxifloxacine Krka

Active Ingredient:
Moxifloxacin
Origin:
EU

Moxifloxacine Krka (Moxifloxacin)

Moxifloxacin, the active ingredient in Moxifloxacine Krka, is a fluoroquinolone presented as an oral tablet for oral use. It treats a variety of bacterial infections in adult patients, including respiratory, skin and intra‑abdominal infections.

GNH India supplies Moxifloxacine Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides reliable logistics for global distribution. Our network ensures timely delivery and regulatory support for each market.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

  • Moxifloxacin is indicated for several bacterial infections affecting the respiratory, skin and abdominal systems.
  • Community‑acquired pneumonia: reduces bacterial load and improves clinical outcomes in adult patients.
  • Acute bacterial sinusitis: eradicates the causative pathogens and relieves sinus inflammation.
  • Acute exacerbations of chronic bronchitis: shortens symptom duration and prevents disease progression.
  • Skin and soft tissue infections: eliminates susceptible organisms and promotes wound healing.
  • Complicated intra‑abdominal infections: provides broad‑spectrum coverage for mixed aerobic and anaerobic bacteria.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription and repair. By stabilizing the enzyme–DNA complex, it prevents the resealing of DNA strands, leading to halted bacterial replication and ultimately bacterial cell death.

Side Effects

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

Common Side Effects

  • Nausea
  • Diarrhea
  • Headache
  • Dizziness
  • Abdominal pain
  • Rash

Serious or Rare Side Effects

  • Tendon rupture or inflammation
  • QT interval prolongation leading to arrhythmia
  • Severe allergic reactions such as anaphylaxis
  • Clostridioides difficile‑associated colitis
  • Hepatic dysfunction
  • Peripheral neuropathy

Precautions & Warnings

  • When prescribing Moxifloxacine Krka, clinicians should observe several safety considerations.
  • Assess renal function: adjust therapy if renal impairment is present.
  • Check for hypersensitivity: discontinue if an allergic reaction occurs.
  • Monitor tendon health: advise patients to report tendon pain or swelling promptly.
  • Evaluate cardiac risk: avoid use in patients with known QT prolongation.
  • Store at room temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Moxifloxacin can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: markedly reduce oral absorption of moxifloxacin.
  • Warfarin: may increase anticoagulant effect and bleeding risk.
  • Theophylline: can raise serum theophylline concentrations, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: combined use may increase risk of tendon rupture.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may enhance central nervous system stimulation.

Frequently Asked Questions

Moxifloxacine Krka contains moxifloxacin, a fluoroquinolone antibiotic indicated for adult patients with community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, skin and soft‑tissue infections, and complicated intra‑abdominal infections. It targets susceptible bacteria to help resolve infection and improve clinical symptoms.

Moxifloxacin blocks bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes required for DNA replication and transcription. By preventing the resealing of DNA strands, the drug halts bacterial cell division, leading to bacterial death and clearance of the infection.

The specific dose of Moxifloxacine Krka is determined by the prescribing clinician based on the type and severity of infection, patient age, weight, renal function and local treatment guidelines. Healthcare providers select an appropriate regimen and duration for each individual case.

Safety data for moxifloxacin in pregnancy and lactation are limited. The drug should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Pregnant or nursing women should discuss treatment options with their healthcare professional.

To 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 broad spectrum of activity against both Gram‑positive and Gram‑negative organisms, including atypical pathogens, and has a once‑daily dosing schedule for many infections. Compared with older fluoroquinolones, it may have a lower risk of certain resistance patterns but shares class‑related safety considerations such as tendon toxicity and QT prolongation.

Store the tablets at room temperature, below 25 °C (77 °F). Keep them in the original container, protect from moisture, heat and direct sunlight. Do not store in the bathroom or near a kitchen sink where humidity is high.

Moxifloxacine Krka is taken orally as a whole tablet with a glass of water. It may be taken with or without food, but patients should follow any specific instructions from their prescriber. The tablet should be swallowed whole and not chewed or crushed.

Serious risks include tendon rupture or inflammation, especially in older adults or those on corticosteroids; QT interval prolongation that can lead to cardiac arrhythmias; severe allergic reactions such as anaphylaxis; Clostridioides difficile‑associated colitis; and rare cases of hepatic dysfunction or peripheral neuropathy.

Patients with a known hypersensitivity to moxifloxacin or any fluoroquinolone should avoid the drug. It is also contraindicated in individuals with a history of tendon disorders related to fluoroquinolone use, those with significant QT prolongation, and patients taking medications that strongly interact with moxifloxacin without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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