52 reports of this reaction
5.2% of all POVIDONE IODINE 10% reports
#1 most reported adverse reaction
TOXIC ANTERIOR SEGMENT SYNDROME is the #1 most commonly reported adverse reaction for POVIDONE IODINE 10%, manufactured by Farmacias De Similares TX LLC. There are 52 FDA adverse event reports linking POVIDONE IODINE 10% to TOXIC ANTERIOR SEGMENT SYNDROME. This represents approximately 5.2% of all 1,006 adverse event reports for this drug.
Patients taking POVIDONE IODINE 10% who experience toxic anterior segment syndrome should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TOXIC ANTERIOR SEGMENT SYNDROME is moderately reported among POVIDONE IODINE 10% users, representing a notable but not dominant share of adverse events.
In addition to toxic anterior segment syndrome, the following adverse reactions have been reported for POVIDONE IODINE 10%:
The following drugs have also been linked to toxic anterior segment syndrome in FDA adverse event reports:
TOXIC ANTERIOR SEGMENT SYNDROME has been reported as an adverse event in 52 FDA reports for POVIDONE IODINE 10%. This does not prove causation, but indicates an association observed in post-market surveillance data.
TOXIC ANTERIOR SEGMENT SYNDROME accounts for approximately 5.2% of all adverse event reports for POVIDONE IODINE 10%, making it one of the most commonly reported side effect.
If you experience toxic anterior segment syndrome 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.