21 reports of this reaction
2.1% of all POVIDONE IODINE 10% reports
#8 most reported adverse reaction
INTRAOCULAR PRESSURE INCREASED is the #8 most commonly reported adverse reaction for POVIDONE IODINE 10%, manufactured by Farmacias De Similares TX LLC. There are 21 FDA adverse event reports linking POVIDONE IODINE 10% to INTRAOCULAR PRESSURE INCREASED. This represents approximately 2.1% of all 1,006 adverse event reports for this drug.
Patients taking POVIDONE IODINE 10% who experience intraocular pressure increased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INTRAOCULAR PRESSURE INCREASED is a less commonly reported adverse event for POVIDONE IODINE 10%, but still significant enough to appear in the safety profile.
In addition to intraocular pressure increased, the following adverse reactions have been reported for POVIDONE IODINE 10%:
The following drugs have also been linked to intraocular pressure increased in FDA adverse event reports:
INTRAOCULAR PRESSURE INCREASED has been reported as an adverse event in 21 FDA reports for POVIDONE IODINE 10%. This does not prove causation, but indicates an association observed in post-market surveillance data.
INTRAOCULAR PRESSURE INCREASED accounts for approximately 2.1% of all adverse event reports for POVIDONE IODINE 10%, making it a notable side effect.
If you experience intraocular pressure increased 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.