Product image of Levofloxacin Accord-Uk (Levofloxacin Hemihydrate) supplied by GNH India

Levofloxacin Accord-Uk

Active Ingredient:
Levofloxacin Hemihydrate
Origin:
EU

Levofloxacin Accord-Uk (Levofloxacin Hemihydrate)

Levofloxacin, the active ingredient in Levofloxacin Accord-Uk, is a fluoroquinolone antibiotic presented as a tablet for oral use. It treats a range of bacterial infections, especially in adults with respiratory, urinary, skin or prostate involvement.

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

Manufacturer / TM Owner

Accord-Uk Limited

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Indications & Clinical Uses

Levofloxacin, a fluoroquinolone antibacterial, is indicated for several common bacterial infection pathways.

  • Community‑acquired respiratory tract infections: eradicates the causative bacteria and improves respiratory symptoms.
  • Urinary tract infections: clears uropathogens and resolves dysuria and frequency.
  • Skin and soft‑tissue infections: eliminates skin‑resident bacteria, promoting wound healing.
  • Acute bacterial prostatitis: penetrates prostatic tissue to treat infection and reduce inflammation.

How It Works

  • Levofloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By binding to these targets, it prevents DNA synthesis and transcription, leading to bacterial cell death. The drug exhibits concentration‑dependent bactericidal activity against a broad spectrum 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 gastrointestinal upset.
  • Diarrhea: loose stools, often self‑limiting.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional vertigo or light‑headedness.
  • Rash: mild skin erythema.

Serious or Rare Side Effects

  • Tendon rupture: sudden pain or swelling, especially in the Achilles.
  • QT prolongation: cardiac rhythm disturbances that may cause palpitations.
  • Severe hypersensitivity: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Central nervous system effects: seizures or hallucinations.
  • Clostridioides difficile colitis: severe diarrhea with abdominal pain.

Precautions & Warnings

Before prescribing Levofloxacin, clinicians should consider several safety measures.

  • Assess renal function: dose adjustment may be required in impaired clearance.
  • Review cardiac history: avoid in patients with known QT prolongation.
  • Evaluate tendon health: discontinue if tendon pain or swelling occurs.
  • Monitor for hypersensitivity: discontinue at first sign of severe allergic reaction.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Levofloxacin can alter the activity of several co‑administered medicines.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: markedly reduce levofloxacin absorption.
  • Warfarin: may increase anticoagulant effect and bleeding risk.
  • Theophylline: can raise serum theophylline concentrations, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen): may increase risk of central nervous system stimulation.
  • Cyclosporine: potential for increased nephrotoxicity.
  • Oral contraceptives: efficacy may be reduced; advise alternative contraception.

Frequently Asked Questions

Levofloxacin Accord-Uk is a prescription‑only fluoroquinolone antibiotic used to treat a variety of bacterial infections, including community‑acquired respiratory tract infections, urinary tract infections, skin and soft‑tissue infections, and acute bacterial prostatitis in adult patients.

Levofloxacin works by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes that are essential for DNA replication and transcription. This inhibition prevents bacterial cells from multiplying, leading to their death and resolution of the infection.

The dosage of Levofloxacin Accord-Uk is determined by the prescribing clinician based on the type and severity of the infection, patient age, renal function, and other clinical factors. Patients should follow the prescriber’s instructions exactly.

Safety of levofloxacin in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and a healthcare professional should be consulted.

To place an 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 and any necessary import documentation.

Levofloxacin is a third‑generation fluoroquinolone with a broad spectrum of activity and once‑daily dosing for many infections, which can offer convenience over older agents like ciprofloxacin that may require multiple daily doses. Its pharmacokinetic profile provides higher tissue penetration in respiratory and urinary sites.

Store the tablets at ambient temperature, below 25 °C, in the original container. Protect them from moisture, heat and direct sunlight to maintain potency throughout the shelf life.

Levofloxacin Accord-Uk is taken orally, usually with a full glass of water. It may be taken with or without food, but antacids containing aluminum or magnesium should be avoided within two hours of dosing to ensure proper absorption.

Serious risks include tendon rupture (especially in the Achilles), QT‑interval prolongation leading to cardiac arrhythmias, severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome, and Clostridioides difficile‑associated colitis. Patients should seek immediate medical attention if they experience these symptoms.

Levofloxacin should be avoided in patients with a known hypersensitivity to fluoroquinolones, a history of tendon disorders related to fluoroquinolone use, uncontrolled epilepsy, or those taking medications that significantly prolong the QT interval. It is also contraindicated in patients with severe renal impairment unless dose‑adjusted.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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