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VIGAMOX 0.5% EYE DROPS 5ML
VIGAMOX 0.5% EYE DROPS 5ML
26.6
VIGAMOX 0.5% EYE DROPS 5ML

Frequently bought together

Brand : VIGAMOX

VIGAMOX 0.5% EYE DROPS 5ML

26.6
  • Sku : I-006689
  • Key features

    VIGAMOX 0.5% Eye Drops (moxifloxacin hydrochloride 0.5%) is an ophthalmic solution containing a fourth-generation fluoroquinolone antibiotic. It inhibits bacterial DNA gyrase and topoisomerase IV, disrupting DNA replication and preventing bacterial proliferation. It is indicated for the treatment of bacterial conjunctivitis caused by susceptible organisms. Available as a prescription-only 5 ml eye drop solution.

     

    • Brand: VIGAMOX
    • Active Ingredient: MOXIFLOXACIN HYDROCHLORIDE 0.5%
    • Strength: 0.5%
    • Dosage Form: Eye drops, solution
    • Pack Size: 5 ml
    • Route: Ocular use
    • Prescription Status: Prescription
    • Therapeutic Class: Ophthalmic
    • Pharmacological Group: Anti-infectives (Eye)
    • Drug Class: Fourth-generation Fluoroquinolone Antibiotic (Ophthalmic)
    • Manufacturer: NOVARTIS MANUFACTURING NV
    • Country of Origin: Belgium
    • SFDA Registration No.: 1707245591
    • Shelf Life: 24 months
    • Storage: store below 30°c
    • Target Organ: Eye
    • Preservative Free: Yes

Frequently bought together

Description
Specification

Indications

Approved Uses

Treatment of bacterial conjunctivitis caused by susceptible bacteria.

Dosage & Administration

Dosing by Condition

Bacterial conjunctivitis: Days 1-2: instill 1 drop in affected eye(s) 3 times daily; Days 3-7: instill 1 drop in affected eye(s) 3 times daily (total treatment 7 days)

Initial Dose

Instill one drop in the affected eye(s) 3 times a day.

Maintenance Dose

Instill one drop in the affected eye(s) 3 times a day for 7 days.

Maximum Dose

1 drop in the affected eye(s) three times daily; do not exceed the prescribed frequency/duration.

Children's Dosage

Approved for use in children aged 1 year and older: same dosing as adults - 1 drop in affected eye(s) 3 times daily for 7 days

How to Prepare

N/A - ready-to-use ophthalmic solution (no reconstitution or dilution required).

Side Effects

Common Side Effects

The most frequently reported adverse event is ocular discomfort.

Side Effect Frequency

Common (≥1%): eye irritation/burning, ocular pain, conjunctival hyperemia/redness, dry eye, pruritus, tearing, keratitis, blurred/decreased visual acuity, ocular discomfort, eye discharge; other reactions are uncommon (<1%).

Safety & Warnings

Contraindications

Hypersensitivity to moxifloxacin, other quinolone/fluoroquinolone antibiotics, or any component (excipient) of the formulation.

Warnings & Precautions

For topical ophthalmic use only (not for injection/oral use); discontinue at first sign of hypersensitivity; avoid contact lens wear during active infection; avoid contaminating the dropper tip; prolonged use may cause overgrowth of non-susceptible organisms including fungi.

Age Restriction

Approved for use in all ages (including pediatric patients); no minimum age restriction in labeling.

Drug Interactions

Drug Interactions

Clinically significant drug-drug interactions are unlikely due to minimal systemic absorption with ocular use.

Interaction Severity

No clinically significant drug interactions are expected with ophthalmic moxifloxacin due to minimal systemic absorption.

Food Interaction

No food interactions (ophthalmic administration).

Special Populations

Children

Approved for use in children aged 1 year and older: same dosing as adults - 1 drop in affected eye(s) 3 times daily for 7 days

Elderly

Standard adult dosing. No overall differences in safety and effectiveness have been observed between elderly and younger patients.

Storage & Patient Advice

Preparation Instructions

N/A - ready-to-use ophthalmic solution (no reconstitution or dilution required).

Stopping the Medicine

Complete the full prescribed course; do not stop early even if symptoms improve, and stop/seek care if hypersensitivity or severe irritation occurs.

Patient Counseling

Patients should be advised not to wear contact lenses if they have signs or symptoms of bacterial conjunctivitis.

Monitoring Requirements

Whenever clinical judgment dictates, the patient should be examined with the aid of magnification, such as slit-lamp biomicroscopy, and, where appropriate, fluorescein staining.

Pharmacology

Mechanism of Action

A fluoroquinolone antibiotic that inhibits the bacterial enzymes DNA gyrase (topoisomerase II) and topoisomerase IV, which are essential for bacterial DNA replication, transcription, and repair.

Onset of Action

Symptomatic improvement is typically seen within a few days; lack of improvement by about 2-3 days warrants reassessment.

Duration of Effect

Not well-defined clinically; dosing is based on labeled regimen rather than a specific per-dose duration (commonly dosed multiple times daily for conjunctivitis).

Product Information

Available Dosage Forms

Eye drops, solution (ophthalmic solution).

Composition per Dose

Ophthalmic solution containing moxifloxacin 0.5%.

Target Organ

Eye

Preservative Free

Yes

 

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The product information provided is derived from verified pharmaceutical references and is intended for general health education only. It is not a substitute for professional medical advice, diagnosis, or treatment.

Al Mujtama Pharmacy assumes no legal or medical liability for:

  • Any therapeutic decision made based on the information displayed without consulting a licensed physician or pharmacist
  • Any discrepancy between the information provided and the product's package insert or SFDA guidelines
  • Any misuse of medication resulting from personal interpretation of the content displayed

Important notice: Drug formulations and instructions may vary between production batches. Always rely on the leaflet included inside the product packaging you have, and consult your pharmacist or physician before starting, adjusting, or discontinuing any medication.

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