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$8 – $97
In the Deductible co-pay stage, you are responsible for the full cost of your prescriptions. Your Medicare deductible cannot exceed $360 in 2016.
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Note: This document contains side effect information about moxifloxacin ophthalmic. Some of the dosage forms listed on this page may not apply to the brand name Vigamox.For the Consumer
Applies to moxifloxacin ophthalmic: ophthalmic solution
Along with its needed effects, moxifloxacin ophthalmic (the active ingredient contained in Vigamox) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking moxifloxacin ophthalmic:
Incidence not known
Some side effects of moxifloxacin ophthalmic may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
For Healthcare Professionals
Applies to moxifloxacin ophthalmic: intraocular solution, ophthalmic solutionGeneral
The most common side effects were eye irritation and eye pain.Ocular
Common (1% to 10%): Conjunctivitis, decreased visual acuity, dry eye, keratitis, ocular discomfort, ocular hyperemia, ocular pain, ocular pruritus, subconjunctival hemorrhage, tearing, eye irritation, eye pain
Uncommon (0.1% to 1%): Punctuate keratitis, eye pruritus, conjunctival hemorrhage, eyelid edema
Rare (less than 0.1%): Corneal epithelium defect, corneal disorder, blepharitis, eye swelling, conjunctival edema, blurred vision, asthenopia, erythema of eyelid
Frequency not reported: Endophthalmitis, ulcerative keratitis, corneal erosion, corneal abrasion, intraocular pressure increased, corneal opacity, corneal infiltrates, corneal deposits, eye allergy, corneal edema, photophobia, lacrimation increased, eye discharge, foreign body sensation in eyes, corneal staining, eyelid disorder, abnormal sensation in eyeRespiratory
Common (1% to 10%): Increased cough, pharyngitis, rhinitis
Rare (less than 0.1%): Nasal discomfort, pharyngolaryngeal pain, sensation of foreign body (throat)
Frequency not reported: DyspneaDermatologic
Common (1% to 10%): Rash
Frequency not reported: Erythema, pruritus, urticariaOther
Common (1% to 10%): Otitis media, fever/pyrexia, infectionNervous system
Uncommon (0.1% to 1%): Dysgeusia, headache
Rare (less than 0.1%): Paresthesia
Frequency not reported: DizzinessGastrointestinal
Rare (less than 0.1%): Vomiting
Frequency not reported: NauseaHematologic
Rare (less than 0.1%): Decreased hemoglobinHepatic
Rare (less than 0.1%): Increased ALT, increased GGTHypersensitivity
Serious and occasionally fatal hypersensitivity (anaphylactic) reactions (some after first dose) have been reported with systemic quinolones.
Frequency not reported: Hypersensitivity
-Frequency not reported: Hypersensitivity (anaphylactic) reactionsCardiovascular
Frequency not reported: PalpitationsMusculoskeletal
-Frequency not reported: Tendon ruptures
Ruptures of the shoulder, hand, Achilles, or other tendons (requiring surgical repair or resulting in prolonged disability) have been reported with systemic fluoroquinolones. Risk of such ruptures may be increased in patients using concomitant corticosteroids, especially geriatric patients and in tendons under high stress (including the Achilles tendon).
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