51 reports of this reaction
5.1% of all POVIDONE IODINE 10% reports
#2 most reported adverse reaction
ENDOPHTHALMITIS is the #2 most commonly reported adverse reaction for POVIDONE IODINE 10%, manufactured by Farmacias De Similares TX LLC. There are 51 FDA adverse event reports linking POVIDONE IODINE 10% to ENDOPHTHALMITIS. This represents approximately 5.1% of all 1,006 adverse event reports for this drug.
Patients taking POVIDONE IODINE 10% who experience endophthalmitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ENDOPHTHALMITIS is moderately reported among POVIDONE IODINE 10% users, representing a notable but not dominant share of adverse events.
In addition to endophthalmitis, the following adverse reactions have been reported for POVIDONE IODINE 10%:
The following drugs have also been linked to endophthalmitis in FDA adverse event reports:
ENDOPHTHALMITIS has been reported as an adverse event in 51 FDA reports for POVIDONE IODINE 10%. This does not prove causation, but indicates an association observed in post-market surveillance data.
ENDOPHTHALMITIS accounts for approximately 5.1% of all adverse event reports for POVIDONE IODINE 10%, making it one of the most commonly reported side effect.
If you experience endophthalmitis while taking POVIDONE IODINE 10%, 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.