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 adult patients, including community‑acquired pneumonia, acute bacterial sinusitis, skin and soft‑tissue infections, and complicated urinary tract infections.

GNH India supplies Levofloxacin Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance across Europe, Asia, Africa and the Americas.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

Levofloxacin is a fluoroquinolone antibacterial indicated for several serious bacterial infections.

  • Community‑acquired bacterial pneumonia: effective treatment to eradicate the causative pathogens and improve clinical outcomes.
  • Acute bacterial sinusitis: helps clear infection and relieve sinus inflammation.
  • Skin and soft‑tissue infections: provides bacterial eradication in cellulitis, abscesses, and wound infections.
  • Complicated urinary tract infections: targets resistant uropathogens to resolve infection.

How It Works

  • Levofloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By binding to the ATP‑binding sites of these enzymes, it prevents DNA strand separation, halting bacterial DNA synthesis and transcription, leading to bactericidal activity. The drug penetrates well into respiratory tissues, sinuses, skin, and the urinary tract, achieving concentrations above the minimum inhibitory concentrations for susceptible strains.

Side Effects

Levofloxacin may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, sometimes watery.
  • Headache: transient cranial discomfort.
  • Rash: mild skin erythema or itching.

Serious or Rare Side Effects

  • Tendon rupture: sudden tendon pain or swelling, especially in the Achilles.
  • QT prolongation: cardiac rhythm disturbances that may lead to arrhythmia.
  • Severe hypersensitivity: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.

Precautions & Warnings

Before using Levofloxacin, consider the following precautions to ensure safe administration.

  • Renal impairment: adjust dose or monitor renal function in patients with reduced kidney clearance.
  • History of tendon disorders: avoid in patients with prior tendon inflammation or recent corticosteroid therapy.
  • Cardiac risk: caution in individuals with known QT prolongation or electrolyte abnormalities.
  • Concomitant medications: review for drugs that may prolong QT interval or affect metabolism.
  • Pregnancy and lactation: use only if clearly needed, as safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: markedly reduce levofloxacin absorption; separate administration by at least 2 hours.
  • Warfarin: may enhance anticoagulant effect, increasing bleeding risk; monitor INR closely.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increased risk of central nervous system stimulation and seizures.

Moderate Interactions (Monitor Closely)

  • Theophylline: levofloxacin can raise plasma theophylline levels; monitor for toxicity.
  • Cyclosporine: may increase cyclosporine concentrations; adjust dose as needed.
  • Diabetic agents (e.g., insulin, sulfonylureas): possible hypoglycemia; monitor blood glucose.

Frequently Asked Questions

Levofloxacin Kabi is an intravenous fluoroquinolone antibacterial indicated for the treatment of serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, skin and soft‑tissue infections, and complicated urinary tract infections in adult patients.

Levofloxacin exerts its antibacterial effect by inhibiting the bacterial enzymes DNA gyrase (topoisomerase II) and topoisomerase IV. This blocks DNA supercoiling and replication, halting bacterial DNA synthesis and transcription, which leads to bacterial cell death.

The dose of Levofloxacin Kabi is determined by the prescribing clinician based on the specific infection, severity, patient weight, renal function, and other clinical factors. No fixed dosing regimen is provided here; the prescriber sets the appropriate regimen.

Safety data for levofloxacin in pregnancy and lactation are limited. It should be used only if clearly needed and the potential benefit justifies any potential risk to the fetus or infant. Consultation with a healthcare professional is essential.

To order Levofloxacin Kabi, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Levofloxacin offers broad‑spectrum activity against Gram‑positive and Gram‑negative bacteria and has excellent tissue penetration. Compared with older fluoroquinolones, it provides once‑daily dosing and a favorable safety profile, though class‑related risks such as tendon injury and QT prolongation remain. Choice of therapy depends on pathogen susceptibility, patient factors, and local resistance patterns.

Levofloxacin Kabi must be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution. Follow aseptic technique when preparing for intravenous administration.

Levofloxacin Kabi is administered by intravenous infusion. The solution is diluted in an appropriate compatible IV fluid and infused over the period recommended by the prescriber, typically 30‑60 minutes, under aseptic conditions.

Serious risks include tendon rupture (especially Achilles), QT interval prolongation leading to arrhythmias, and severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome. Patients should be advised to seek immediate medical attention if they experience sudden tendon pain, palpitations, or signs of an allergic reaction.

Levofloxacin Kabi should be avoided in patients with a known hypersensitivity to levofloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, and individuals with significant QT prolongation or uncontrolled electrolyte abnormalities. Caution is also advised in severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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