Product image of Le-Vof (Levofloxacin Hemihydrate) supplied by GNH India

Le-Vof

Active Ingredient:
Levofloxacin Hemihydrate
Origin:
EU

Le-Vof (Levofloxacin Hemihydrate)

Levofloxacin, the active ingredient in Le-Vof, is a fluoroquinolone presented as a intravenous solution for intravenous use. It treats a range of bacterial infections in adult patients, including pneumonia, urinary and intra‑abdominal infections.

GNH India supplies Le-Vof as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Verisfield S.M.S.A

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Indications & Clinical Uses

Levofloxacin is a broad‑spectrum antibacterial indicated for several serious infections.

  • Community‑acquired pneumonia: achieves clinical cure and microbiological eradication.
  • Hospital‑acquired pneumonia: effective in treating resistant Gram‑negative pathogens.
  • Complicated urinary tract infections: resolves infection and prevents recurrence.
  • Complicated intra‑abdominal infections: provides rapid bacterial clearance.
  • Skin and soft tissue infections: reduces lesion size and bacterial load.
  • Acute bacterial sinusitis: improves symptoms and clears the causative organism.

How It Works

  • Levofloxacin 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 cell division and eventual cell death. This bactericidal action is effective against a wide range of Gram‑positive and Gram‑negative organisms.

Side Effects

Levofloxacin may cause a variety of adverse reactions, ranging from mild to severe.

Common Side Effects

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

Serious or Rare Side Effects

  • Tendon rupture: especially Achilles tendon, often linked to sudden activity.
  • QT interval prolongation: may predispose to cardiac arrhythmias.
  • Clostridioides difficile infection: severe colitis with watery diarrhea.
  • Severe allergic reactions: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Seizures: particularly in patients with CNS disorders.
  • Hepatic failure: rare but potentially life‑threatening liver injury.

Precautions & Warnings

Levofloxacin requires careful assessment of patient‑specific factors before use.

  • Renal impairment: dose adjustment may be necessary based on creatinine clearance.
  • History of tendon disorders: avoid use in patients with recent tendon injury or surgery.
  • QT prolongation risk: monitor ECG in patients with cardiac disease or electrolyte abnormalities.
  • Pregnancy and lactation: prescribe only if potential benefits outweigh risks.
  • Concomitant medications: review for interactions that may increase toxicity or reduce efficacy.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levofloxacin can affect the pharmacokinetics or pharmacodynamics of several drugs.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: markedly reduce levofloxacin absorption.
  • Warfarin: may increase INR and bleeding risk.
  • Cyclosporine: elevated serum levels can lead to nephrotoxicity.
  • Theophylline: increased risk of seizures and cardiac arrhythmias.
  • Other fluoroquinolones: additive toxicity, especially tendon and CNS effects.

Moderate Interactions (Monitor Closely)

  • NSAIDs: heightened risk of CNS stimulation and seizures.
  • Corticosteroids: increased chance of tendon rupture.
  • Diabetic agents (e.g., insulin, sulfonylureas): potential for hypoglycemia.
  • QT‑prolonging drugs (e.g., macrolides, antiarrhythmics): monitor cardiac rhythm.
  • Oral contraceptives: possible reduction in contraceptive efficacy.

Frequently Asked Questions

Le-Vof, containing levofloxacin, is indicated for serious bacterial infections such as community‑acquired and hospital‑acquired pneumonia, complicated urinary tract infections, complicated intra‑abdominal infections, skin and soft tissue infections, and acute bacterial sinusitis. It is administered intravenously to achieve rapid therapeutic concentrations in the bloodstream.

Levofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. By blocking these targets, the drug prevents bacterial cells from dividing and repairing DNA, leading to bactericidal activity against a broad spectrum of Gram‑positive and Gram‑negative organisms.

The specific dose and duration of Le-Vof are determined by the prescribing clinician based on the type and severity of infection, renal function, and patient characteristics. Healthcare professionals follow local guidelines and product labeling to select the appropriate regimen.

Levofloxacin is classified as a pregnancy category with unknown risk. It should be used only when the potential benefit justifies the potential risk to the fetus. Likewise, caution is advised during breastfeeding, and the decision should be made by the prescriber after evaluating maternal and infant health.

To request Le-Vof, 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.

Levofloxacin offers once‑daily dosing and a broad spectrum that includes many resistant Gram‑negative pathogens, often providing a more convenient regimen than older fluoroquinolones such as ciprofloxacin. Its pharmacokinetic profile yields high tissue penetration, making it a preferred option for severe infections requiring intravenous therapy.

Le-Vof should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the solution in its original packaging until use to maintain stability and sterility.

Le-Vof is given as an intravenous infusion by a qualified healthcare professional. The infusion rate and dilution are determined by the prescribing clinician and institutional protocols to ensure safe and effective delivery of the medication.

Serious risks include tendon rupture (especially Achilles), QT interval prolongation leading to arrhythmias, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and rare central nervous system effects like seizures. Patients should be monitored closely for these events.

Le-Vof 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 may cause dangerous interactions without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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