Ocuflox Ophthalmic Drops, Solution 0.3pct Drug Medication Dosage Information
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Ocuflox: Ophthalmic drops, solution (0.3%)

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What is this Medicine?

OFLOXACIN (oh FLOKS a sin) is a quinolone antibiotic. It is used in the eye to treat bacterial infections.

In-Depth Information

Ocuflox 0.3% Ophthalmic Solution

NDC: 119800779
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Corneal Ulcer, Bacterial Conjunctivitis

Storage Information
Store between 59 to 77 degrees F
Ocuflox 0.3% Ophthalmic Solution

Reported Side Effects for Ocuflox 0.3% Ophthalmic Solution

Vesicular Rash Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Lyell'S Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Darkened Skin Patches Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Bruises Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Photosensitivity Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Heavy Menstrual Period Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Laryngeal Edema Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Rash Of Red Skin Bumps Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Diaphoresis Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Blistery Rash Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Breathing Difficulties Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Severe Allergy Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Angioedema Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Erythema Multiforme Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Exfoliative Dermatitis Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Light Sensitivity Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Serum Sickness Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Stevens-Johnson Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Hives Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Retinal Detachment Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Inflamed Blood Vessels Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Anaphylactoid Reactions Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Upset Stomach Incidence:
0.3-10.0%*
Severity: MILD
Onset: EARLY
Itching Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Skin Rash Incidence:
1.0-3.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


Learning More About
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