Product image of Levalox (Levofloxacin) supplied by GNH India

Levalox

Active Ingredient:
Levofloxacin
Origin:
EU

Levalox (Levofloxacin)

Levofloxacin, the active ingredient in Levalox, is a fluoroquinolone antibiotic presented as an intravenous solution for intravenous use. It treats a range of bacterial infections in adults, including community‑acquired and hospital‑acquired pneumonia, complicated urinary tract infections, skin and soft‑tissue infections, intra‑abdominal infections and bacterial prostatitis.

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

Manufacturer / TM Owner

Krka-Farma D.O.O.

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Indications & Clinical Uses

Levalox is a fluoroquinolone antibiotic used to treat serious bacterial infections across several organ systems.

  • Community‑acquired pneumonia: eradicates the causative pathogens and improves respiratory function.
  • Hospital‑acquired pneumonia: provides broad‑spectrum coverage for resistant organisms.
  • Complicated urinary tract infections: eliminates uropathogens in the upper and lower urinary tract.
  • Skin and soft‑tissue infections: resolves cellulitis, abscesses and other bacterial skin conditions.
  • Intra‑abdominal infections: targets mixed aerobic and anaerobic bacteria in the abdominal cavity.
  • Bacterial prostatitis: penetrates prostatic tissue to treat chronic bacterial infection.

How It Works

  • Levofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication and transcription. By binding to these enzymes, it prevents the supercoiling and relaxation of bacterial DNA, leading to inhibition of bacterial cell division and ultimately bacterial cell death. This bactericidal action is effective against a broad spectrum of Gram‑positive and Gram‑negative organisms.

Side Effects

Levalox may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, occasionally watery.
  • Headache: transient cranial discomfort.
  • Dizziness: sensation of light‑headedness.
  • Rash: mild skin erythema or itching.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Tendon rupture: especially Achilles tendon, may occur without warning.
  • QT interval prolongation: can precipitate cardiac arrhythmias.
  • Clostridioides difficile infection: severe colitis risk.
  • Severe allergic reactions: anaphylaxis, angioedema.
  • Hepatic failure: rare but potentially life‑threatening.
  • Seizures: particularly in patients with CNS disorders.

Precautions & Warnings

Levalox requires careful assessment of patient risk factors and monitoring during therapy.

  • Renal function: adjust therapy in patients with severe renal impairment.
  • History of tendon disorders: avoid use in individuals with prior tendon injury or tendon‑rupture risk.
  • Cardiac risk: monitor ECG in patients with known QT prolongation or electrolyte disturbances.
  • Concomitant NSAIDs or corticosteroids: increase risk of tendon rupture; use with caution.
  • Pregnancy and lactation: prescribe only when benefits outweigh potential risks.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Levalox can interact with several drug classes, requiring monitoring or avoidance.

Major Interactions (Avoid)

  • Co‑administration with other fluoroquinolones: additive toxicity.
  • Drugs that prolong QT interval (e.g., macrolides, antiarrhythmics): heightened arrhythmia risk.
  • Antacids or supplements containing aluminum, magnesium, calcium, or iron: reduce levofloxacin absorption.

Moderate Interactions (Monitor Closely)

  • Theophylline (CYP1A2 substrate): may increase serum theophylline levels.
  • Warfarin: monitor INR for potential anticoagulation changes.
  • Corticosteroids: observe for signs of tendon inflammation or rupture.

Frequently Asked Questions

Levalox, containing levofloxacin, is indicated for serious bacterial infections such as community‑acquired and hospital‑acquired pneumonia, complicated urinary tract infections, skin and soft‑tissue infections, intra‑abdominal infections, and bacterial prostatitis. It is administered intravenously under the direction of a qualified prescriber.

Levofloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes that control DNA supercoiling and replication. Inhibiting these enzymes prevents bacterial DNA synthesis, leading to bacterial cell death and eradication of the infection.

The dosage of Levalox is determined by the treating physician based on the type and severity of the infection, patient weight, renal function, and other clinical factors. Only a qualified prescriber may set the appropriate dosing regimen.

Levalox is classified as a prescription‑only medication and should be used in pregnancy or lactation only when the potential benefit justifies the potential risk to the fetus or infant. The prescriber must evaluate the risk‑benefit profile for each individual case.

To request Levalox, 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 import documentation.

Levalox (levofloxacin) offers broad‑spectrum coverage against many Gram‑positive and Gram‑negative pathogens, including atypical organisms, making it a convenient single‑agent option for both community‑acquired and hospital‑acquired pneumonia. Compared with beta‑lactams, it provides oral and IV formulations and does not require combination therapy for many typical pneumonia pathogens.

Levalox should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from direct light, moisture and extreme temperatures to maintain its stability and potency.

Levalox is supplied as an intravenous solution and is administered by a healthcare professional through a vein using a sterile infusion set. The infusion rate and duration are set according to the prescribing information and the patient’s clinical condition.

Serious adverse events linked to Levalox include tendon rupture (especially Achilles), QT interval prolongation leading to arrhythmias, Clostridioides difficile‑associated colitis, severe allergic reactions such as anaphylaxis, hepatic failure, and seizures. Patients should be monitored closely for these events during therapy.

Levalox is contraindicated in patients with a known hypersensitivity to levofloxacin or other fluoroquinolones. It should also be avoided in individuals with a history of tendon disorders related to fluoroquinolone use, uncontrolled QT prolongation, or those taking medications that significantly increase the risk of tendon injury.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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