135 reports of this reaction
1.3% of all POVIDONE IODINE reports
#15 most reported adverse reaction
VISUAL IMPAIRMENT is the #15 most commonly reported adverse reaction for POVIDONE IODINE, manufactured by Alcon Laboratories, Inc.. There are 135 FDA adverse event reports linking POVIDONE IODINE to VISUAL IMPAIRMENT. This represents approximately 1.3% of all 10,103 adverse event reports for this drug.
Patients taking POVIDONE IODINE who experience visual impairment should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VISUAL IMPAIRMENT is a less commonly reported adverse event for POVIDONE IODINE, but still significant enough to appear in the safety profile.
In addition to visual impairment, the following adverse reactions have been reported for POVIDONE IODINE:
The following drugs have also been linked to visual impairment in FDA adverse event reports:
VISUAL IMPAIRMENT has been reported as an adverse event in 135 FDA reports for POVIDONE IODINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
VISUAL IMPAIRMENT accounts for approximately 1.3% of all adverse event reports for POVIDONE IODINE, making it a notable side effect.
If you experience visual impairment while taking POVIDONE IODINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.