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VIGAMOX 0.5% EYE DROPS 5ML
- 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
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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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