Product image of Levofloxacin Kabi (Levofloxacin Hemihydrate) supplied by GNH India

Levofloxacin Kabi

Active Ingredient:
Levofloxacin Hemihydrate
Origin:
EU

Levofloxacin Kabi (Levofloxacin Hemihydrate)

Levofloxacin, the active ingredient in Levofloxacin Kabi, is a fluoroquinolone presented as an injectable solution for intravenous use. It treats a range of bacterial infections in adults and children as prescribed by a healthcare professional.

GNH India supplies Levofloxacin Kabi as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

  • Levofloxacin is a fluoroquinolone antibiotic used to treat infections caused by susceptible bacteria.
  • Community-acquired pneumonia: effective therapy to eradicate the causative bacterial pathogens and improve clinical outcomes.
  • Complicated urinary tract infections: eradicates Gram‑negative and Gram‑positive organisms, facilitating resolution of infection.
  • Skin and soft tissue infections: provides rapid bacterial clearance and promotes wound healing.
  • Acute bacterial sinusitis: reduces bacterial load and alleviates sinus inflammation.
  • Acute exacerbations of chronic bronchitis: shortens symptom duration and prevents further pulmonary deterioration.

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 bacterial cell death. This bactericidal action is broad‑spectrum, affecting both Gram‑negative and Gram‑positive organisms that are susceptible to fluoroquinolones.

Side Effects

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

Common Side Effects

  • Nausea or vomiting
  • Diarrhea or loose stools
  • Headache or dizziness
  • Rash or mild skin irritation
  • Elevated liver enzymes
  • Transient increase in serum creatinine

Serious or Rare Side Effects

  • Tendon rupture or tendonitis, especially in the Achilles tendon
  • QT interval prolongation leading to cardiac arrhythmias
  • Clostridioides difficile‑associated colitis
  • Severe hypersensitivity reactions such as Stevens‑Johnson syndrome
  • Peripheral neuropathy or central nervous system effects

Precautions & Warnings

  • Levofloxacin should be used with caution in specific patient populations and clinical situations.
  • Renal impairment: adjust dose or monitor renal function closely.
  • History of tendon disorders: avoid use due to risk of tendon rupture.
  • QT prolongation risk: avoid in patients with known cardiac arrhythmias or electrolyte disturbances.
  • Concurrent NSAIDs or corticosteroids: monitor for additive CNS or tendon toxicity.
  • Pregnancy and lactation: prescribe only if potential benefit outweighs potential risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levofloxacin can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Other fluoroquinolones or quinolone‑containing products: additive risk of QT prolongation.
  • Anti‑arrhythmic agents (e.g., sotalol, amiodarone): may precipitate serious cardiac rhythm disturbances.
  • Antacids or supplements containing magnesium, aluminum, calcium, or iron: markedly reduce levofloxacin absorption.

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect, requiring INR monitoring.
  • Theophylline: levofloxacin can increase serum theophylline levels, risking toxicity.
  • NSAIDs: combined use may increase risk of CNS stimulation and seizures.
  • Corticosteroids: concurrent therapy may raise the likelihood of tendon injury.

Frequently Asked Questions

Levofloxacin Kabi is an intravenous fluoroquinolone indicated for the treatment of serious bacterial infections such as community‑acquired pneumonia, complicated urinary tract infections, skin and soft‑tissue infections, acute bacterial sinusitis, and acute exacerbations of chronic bronchitis, when a parenteral route is required.

Levofloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes that unwind and reseal DNA during replication and transcription. This inhibition prevents bacterial DNA synthesis, leading to rapid bactericidal activity against a broad range of susceptible Gram‑negative and Gram‑positive organisms.

The dose of Levofloxacin Kabi is determined by the prescribing clinician based on the infection type, severity, patient weight, renal function, and local susceptibility patterns. Healthcare professionals adjust the regimen to achieve optimal therapeutic outcomes while minimizing toxicity.

Safety data for levofloxacin in pregnancy and lactation are limited. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and only under direct medical supervision.

To order, 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 handling if needed), and required import documentation.

Levofloxacin offers once‑daily dosing and a broad spectrum that includes many respiratory and urinary pathogens, similar to moxifloxacin but with a slightly different activity profile against Gram‑positive organisms. Compared with older fluoroquinolones, it has improved pharmacokinetics and a lower propensity for drug‑induced photosensitivity.

Levofloxacin Kabi must be stored refrigerated between 2 °C and 8 °C, protected from light, and must not be frozen or shaken. Before use, the solution should be inspected for particulate matter and administered according to aseptic technique.

Levofloxacin Kabi is given as an intravenous infusion. The product is diluted in an appropriate compatible IV fluid and infused over 30‑60 minutes, depending on the prescribed dose and patient tolerance. Administration should be performed by qualified healthcare personnel.

Serious adverse events include tendon rupture or tendonitis, especially in the Achilles tendon, QT interval prolongation leading to arrhythmias, Clostridioides difficile‑associated colitis, severe hypersensitivity reactions such as Stevens‑Johnson syndrome, and peripheral neuropathy. Prompt medical evaluation is required if any of these occur.

Levofloxacin Kabi is contraindicated in patients with a known hypersensitivity to levofloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone therapy, and individuals with established QT prolongation or receiving drugs that significantly prolong the QT interval.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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