Product image of Levofloxacin/Rafarm [pf] (Levofloxacin Hemihydrate) supplied by GNH India

Levofloxacin/Rafarm [pf]

Active Ingredient:
Levofloxacin Hemihydrate
Origin:
EU

Levofloxacin/Rafarm [pf] (Levofloxacin Hemihydrate)

Levofloxacin, the active ingredient in Levofloxacin/Rafarm [pf], is a fluoroquinolone presented as an ophthalmic preparation for ocular use. It treats bacterial eye infections such as conjunctivitis and keratitis in both adult and pediatric patients.

GNH India supplies Levofloxacin/Rafarm [pf] as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing quality‑assured products that meet EU regulatory standards.

Manufacturer / TM Owner

Rafarm Sa.

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Indications & Clinical Uses

Levofloxacin is a fluoroquinolone antibiotic indicated for bacterial infections of the eye.

  • Bacterial conjunctivitis: reduces bacterial load and alleviates symptoms such as redness, discharge and irritation.
  • Bacterial keratitis: eradicates causative organisms and supports corneal healing, helping to preserve visual acuity.

How It Works

  • Levofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication and transcription. By binding to these targets, it prevents bacterial DNA supercoiling and separation, leading to inhibition of bacterial cell division and ultimately bacterial death. The drug exhibits concentration‑dependent bactericidal activity against a broad spectrum of Gram‑positive and Gram‑negative ocular pathogens.

Side Effects

Levofloxacin ophthalmic solution may cause local and systemic adverse reactions.

Common Side Effects

  • Eye irritation or burning sensation.
  • Redness of the conjunctiva.
  • Tearing or increased lacrimation.
  • Transient blurred vision.
  • Foreign‑body sensation.
  • Mild itching.

Serious or Rare Side Effects

  • Allergic reactions such as eyelid edema, rash or urticaria.
  • Corneal ulceration or severe keratitis.
  • Vision loss or sudden decrease in visual acuity.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis involving the ocular surface.
  • Persistent severe eye pain.

Precautions & Warnings

Levofloxacin ophthalmic solution should be used with caution and under professional supervision.

  • Hypersensitivity: discontinue if any signs of allergic reaction appear.
  • Corneal disease: avoid in patients with active corneal ulcer unless specifically indicated.
  • Contact lenses: remove lenses during treatment and re‑insert only after therapy completion.
  • Concomitant steroids: monitor closely as combined use may increase risk of infection.
  • Pediatric use: follow ophthalmologist guidance for dosing and duration.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Levofloxacin ophthalmic solution can interact with other ocular or systemic agents.

Major Interactions (Avoid)

  • Co‑administration with other fluoroquinolone eye drops may increase local toxicity.
  • Systemic fluoroquinolones combined with corticosteroids can raise the risk of tendon rupture.

Moderate Interactions (Monitor Closely)

  • Use with anticholinergic eye drops may reduce drug penetration.
  • Concurrent use of non‑steroidal anti‑inflammatory eye drops may heighten irritation.
  • Systemic cation‑containing supplements (e.g., calcium, iron) can reduce overall fluoroquinolone exposure if systemic absorption occurs.

Frequently Asked Questions

Levofloxacin/Rafarm [pf] is an ophthalmic fluoroquinolone antibiotic indicated for the treatment of bacterial eye infections such as bacterial conjunctivitis and bacterial keratitis. It works by eliminating the causative bacteria, helping to reduce symptoms and prevent complications.

Levofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. By blocking these enzymes, the drug prevents bacterial cell division, leading to rapid bacterial death and clearance of the infection from ocular tissues.

The dosing regimen for Levofloxacin ophthalmic solution is determined by the prescribing ophthalmologist based on the severity of the infection, patient age, and response to therapy. The prescriber will specify the number of drops, frequency, and duration of treatment.

Safety of levofloxacin in pregnancy or lactation has not been definitively established. The drug should be used only if the potential benefit justifies any potential risk to the fetus or infant, and this decision must be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com, indicating the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Levofloxacin offers broad‑spectrum coverage against Gram‑positive and Gram‑negative ocular pathogens and provides convenient once‑ or twice‑daily dosing. Compared with older agents such as ciprofloxacin, it often achieves higher ocular tissue concentrations and may have a lower risk of resistance development.

Levofloxacin ophthalmic solution should be stored at room temperature, below 25 °C, in its original container. Protect the product from direct light and moisture, and keep the cap tightly closed when not in use.

The medication is applied as eye drops. The prescriber will instruct the patient on the number of drops per eye, the frequency (e.g., twice daily), and the total duration of therapy. Proper hand hygiene and avoidance of contamination are essential.

Serious risks include severe allergic reactions, corneal ulceration, vision loss, and rare systemic hypersensitivity syndromes such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience intense eye pain, worsening redness, swelling, or any signs of an allergic reaction.

Individuals with a known hypersensitivity to levofloxacin, other fluoroquinolones, or any component of the formulation should avoid using this product. It is also contraindicated in patients with active corneal ulcers unless specifically prescribed by an ophthalmologist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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