Product image of Moxifloxacin Olikla (Moxifloxacin Hydrochloride) supplied by GNH India

Moxifloxacin Olikla

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacin Olikla (Moxifloxacin Hydrochloride)

Moxifloxacin, the active ingredient in Moxifloxacin Olikla, is a fluoroquinolone antibiotic presented as a sterile ophthalmic solution for ocular use. It treats bacterial eye infections such as conjunctivitis and keratitis in adult and pediatric patients, providing broad‑spectrum coverage against common ocular pathogens.

GNH India supplies Moxifloxacin Olikla as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Olikla S.R.O.

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Indications & Clinical Uses

  • Moxifloxacin Olikla is a fluoroquinolone antibiotic used to treat bacterial infections of the eye.
  • Bacterial conjunctivitis: reduces bacterial load and accelerates resolution of redness, discharge and irritation.
  • Bacterial keratitis: eradicates causative organisms to prevent corneal damage and preserve vision.
  • Other bacterial ocular infections: effective against susceptible Gram‑positive and Gram‑negative bacteria causing eyelid or surface infections.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription and repair. By binding to the quinolone‑resistance‑determining region of these enzymes, it prevents supercoiling of DNA, leading to bacterial cell death and providing bactericidal activity against a wide range of ocular pathogens.

Side Effects

Topical ocular administration of moxifloxacin may be associated with local and systemic adverse reactions.

Common Side Effects

  • Transient eye irritation: mild burning or stinging upon instillation.
  • Redness: temporary conjunctival hyperemia.
  • Blurred vision: short‑lasting visual disturbance.
  • Tearing: increased lacrimation.
  • Foreign body sensation: feeling of grit in the eye.

Serious or Rare Side Effects

  • Corneal ulceration: development of a non‑healing corneal lesion.
  • Severe allergic reaction: eyelid edema, hives or anaphylaxis.
  • Vision loss: rapid decrease in visual acuity.
  • Tendon rupture: rare systemic tendon injury.

Precautions & Warnings

  • Before prescribing Moxifloxacin Olikla, consider the following safety measures.
  • Allergy assessment: avoid use in patients with known hypersensitivity to fluoroquinolones.
  • Contact lens wearers: discontinue lenses before and after treatment to reduce risk of keratitis.
  • Pregnancy and lactation: use only if clearly needed, as safety data are limited.
  • Concurrent ocular surgery: postpone elective procedures until therapy is completed.
  • Systemic fluoroquinolone use: monitor for additive toxicity.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Moxifloxacin Olikla may interact with other ophthalmic or systemic agents.

Major Interactions (Avoid)

  • Systemic fluoroquinolones: increased risk of additive QT prolongation.
  • Corticosteroid eye drops: may mask signs of infection.
  • Anticholinergic agents: potential reduction in ocular surface lubrication.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory eye drops: may affect drug absorption.
  • Herbal supplements containing quinine: possible competitive inhibition.
  • High‑dose vitamin C: may alter ocular pH affecting drug stability.

Frequently Asked Questions

Moxifloxacin Olikla is a sterile ophthalmic solution indicated for the treatment of bacterial eye infections, principally bacterial conjunctivitis and bacterial keratitis. It is used to eliminate susceptible pathogens and promote healing of the ocular surface.

Moxifloxacin belongs to the fluoroquinolone class and exerts its antibacterial effect by inhibiting bacterial DNA gyrase and topoisomerase IV. This blocks DNA replication and transcription, leading to bacterial cell death and rapid reduction of the infection.

The dosing regimen for Moxifloxacin Olikla 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 data for ocular moxifloxacin in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision should 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 works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and import documentation.

Moxifloxacin offers a broader spectrum of activity and higher potency against Gram‑positive and Gram‑negative ocular pathogens compared with older agents such as ciprofloxacin. It also provides good corneal penetration, which can be advantageous in treating keratitis, while maintaining a convenient dosing schedule.

Store the ophthalmic solution at room temperature, below 25 °C, in its original container. Protect it from direct light and moisture. Do not freeze the product, and keep the vial tightly capped when not in use.

Moxifloxacin Olikla is applied as eye drops. The patient should wash hands, tilt the head back, pull down the lower eyelid to form a pocket, and instill the prescribed number of drops without touching the tip to the eye. The eye should be closed gently for a few seconds to allow absorption.

Serious adverse events, although rare, include corneal ulceration, severe allergic reactions such as anaphylaxis, sudden vision loss, and systemic tendon rupture. Any sudden worsening of vision or severe ocular pain should prompt immediate medical evaluation.

Patients with a known hypersensitivity to moxifloxacin, other fluoroquinolones, or any component of the formulation should avoid this product. It is also contraindicated in individuals with a history of tendon disorders related to fluoroquinolone use and in those for whom the risk outweighs the benefit, such as certain pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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