Product image of Oxalux Unit Dose (Levofloxacin Hemihydrate) supplied by GNH India

Oxalux Unit Dose

Active Ingredient:
Levofloxacin Hemihydrate
Origin:
EU

Oxalux Unit Dose (Levofloxacin Hemihydrate)

Levofloxacin hemihydrate, the active ingredient in Oxalux Unit Dose, is a fluoroquinolone antibiotic presented as a unit dose for oral use. It treats a variety of bacterial infections in adults and children when indicated. GNH India supplies Oxalux Unit Dose as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Manufacturer / TM Owner

Kestrel Ophthalmics Ltd

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Indications & Clinical Uses

Levofloxacin is a broad‑spectrum fluoroquinolone used to treat infections caused by susceptible bacteria in several organ systems.

  • Community‑acquired bacterial pneumonia: helps eradicate the causative pathogens and improve respiratory symptoms.
  • Acute bacterial sinusitis: reduces sinus inflammation and clears the infection.
  • Uncomplicated urinary tract infection: eliminates the uropathogen and relieves dysuria and frequency.
  • Skin and soft‑tissue infections: targets common Gram‑positive and Gram‑negative organisms to promote healing.
  • Chronic bronchitis exacerbations: controls bacterial overgrowth and improves airflow.
  • Complicated intra‑abdominal infections (as part of combination therapy): contributes to bacterial clearance when used with other agents.

How It Works

  • Levofloxacin hemihydrate inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. By stabilising the DNA‑enzyme complex, it prevents strand re‑ligation, leading to bacterial cell death and a bactericidal effect against a wide range of Gram‑positive and Gram‑negative organisms.

Side Effects

Levofloxacin may cause a range of adverse reactions, from mild to severe, that vary with individual susceptibility and treatment duration.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, occasionally watery.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional sense of light‑headedness.
  • Insomnia: difficulty falling or staying asleep.
  • Rash: mild skin erythema or itching.

Serious or Rare Side Effects

  • Tendon rupture: sudden pain or loss of function, especially in the Achilles.
  • QT interval prolongation: cardiac rhythm changes detectable on ECG.
  • Severe hypersensitivity: anaphylaxis, angio‑edema, or Stevens‑Johnson syndrome.
  • Peripheral neuropathy: numbness or tingling in extremities.
  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • Clostridioides difficile infection: persistent watery diarrhea with abdominal cramping.

Precautions & Warnings

Levofloxacin should be used with caution in patients with certain risk factors and medical histories.

  • Renal impairment: dose adjustment may be required based on kidney function.
  • History of tendon disorders: avoid use in patients with prior tendon inflammation or rupture.
  • Cardiac arrhythmia risk: monitor QT interval in patients with known prolongation.
  • Seizure history: use cautiously in individuals with a history of seizures.
  • Pregnancy and lactation: assess risk‑benefit ratio before prescribing.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levofloxacin can interact with several medicines, altering its efficacy or increasing toxicity risk.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce levofloxacin absorption.
  • Warfarin: may enhance anticoagulant effect, increasing bleeding risk.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): heighten risk of central nervous system stimulation.

Moderate Interactions (Monitor Closely)

  • Theophylline: may increase serum theophylline concentrations.
  • Cyclosporine: potential for increased nephrotoxicity.
  • Diabetic agents (sulfonylureas, insulin): may cause hypoglycaemia.
  • Corticosteroids: combined use may raise tendon‑rupture risk.

Frequently Asked Questions

Oxalux Unit Dose contains levofloxacin hemihydrate, a fluoroquinolone antibiotic used to treat bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, uncomplicated urinary tract infections, skin and soft‑tissue infections, and certain exacerbations of chronic bronchitis.

Levofloxacin hemihydrate blocks bacterial DNA gyrase and topoisomerase IV, enzymes needed for DNA replication and transcription. This inhibition prevents bacterial DNA from re‑joining after being cut, leading to bacterial cell death and a bactericidal effect.

The specific dose and duration of Oxalux Unit Dose are determined by the prescribing clinician based on the infection type, severity, patient age, kidney function, and other clinical factors. The prescriber sets the appropriate regimen.

Levofloxacin is classified as pregnancy‑category C in many regions, indicating that risk cannot be ruled out. It should only be used when the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult a healthcare professional, as the drug may pass into breast milk.

To place an order, submit an enquiry on the Oxalux Unit Dose 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 and any required import documentation.

Levofloxacin offers a once‑daily dosing option and broad‑spectrum coverage against both Gram‑positive and Gram‑negative bacteria, often allowing shorter treatment courses compared with older fluoroquinolones such as ciprofloxacin. Its pharmacokinetic profile provides high tissue penetration, making it suitable for respiratory and urinary infections.

Oxalux Unit Dose should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the tablet’s potency and stability throughout its shelf life.

Oxalux Unit Dose is supplied as an oral tablet intended for swallowing with a full glass of water. It may be taken with or without food, but patients should follow the prescribing clinician’s instructions regarding timing relative to meals.

Serious adverse events linked to levofloxacin include tendon rupture, QT‑interval prolongation leading to cardiac arrhythmias, severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome, peripheral neuropathy, and Clostridioides difficile‑associated colitis. Patients should seek immediate medical attention if they experience any of these symptoms.

Oxalux Unit Dose should be avoided in individuals with a known hypersensitivity to levofloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, and patients with certain cardiac conditions that predispose them to QT prolongation. Clinicians must also assess risks in pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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