Index of reports
> Cases with Visual Acuity Reduced (3)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Betadine (Povidone-Iodine Ophthalmic) where reactions include visual acuity reduced. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Betadine side effects in female
Reported by a physician from United States on 2012-04-24
Patient: female
Reactions: Punctate Keratitis, Visual Acuity Reduced
Drug(s) suspected as cause:
Eylea
Dosage: intravitreal
Start date: 2012-01-30
Betadine
Possible Betadine side effects in 77 year old male
Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-27
Patient: 77 year old male, weighing 88.5 kg (194.6 pounds)
Reactions: Endophthalmitis, Medication Error, Eye Infection Bacterial, Visual Acuity Reduced, Streptococcal Infection, Treatment Noncompliance
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Vigamox
Dosage: (ophthalmic)
Indication: Intraocular Lens Implant
Start date: 2011-12-21
End date: 2011-12-21
Betadine
Dosage: (ophthalmic)
Indication: Intraocular Lens Implant
Start date: 2011-12-21
End date: 2011-12-21
BSS
Dosage: (intraocular)
Indication: Intraocular Lens Implant
Start date: 2011-12-21
End date: 2011-12-21
Other drugs received by patient: Epinephrine; Cefuroxime
Possible Betadine side effects in
Reported by a physician from United States on 2012-03-06
Patient:
Reactions: Visual Acuity Reduced, Corneal Deposits, Keratitis
Drug(s) suspected as cause:
Eylea
Dosage: intravitreal
Betadine
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