25 reports of this reaction
2.5% of all POVIDONE IODINE 10% reports
#4 most reported adverse reaction
POST PROCEDURAL COMPLICATION is the #4 most commonly reported adverse reaction for POVIDONE IODINE 10%, manufactured by Farmacias De Similares TX LLC. There are 25 FDA adverse event reports linking POVIDONE IODINE 10% to POST PROCEDURAL COMPLICATION. This represents approximately 2.5% of all 1,006 adverse event reports for this drug.
Patients taking POVIDONE IODINE 10% who experience post procedural complication should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
POST PROCEDURAL COMPLICATION is a less commonly reported adverse event for POVIDONE IODINE 10%, but still significant enough to appear in the safety profile.
In addition to post procedural complication, the following adverse reactions have been reported for POVIDONE IODINE 10%:
The following drugs have also been linked to post procedural complication in FDA adverse event reports:
POST PROCEDURAL COMPLICATION has been reported as an adverse event in 25 FDA reports for POVIDONE IODINE 10%. This does not prove causation, but indicates an association observed in post-market surveillance data.
POST PROCEDURAL COMPLICATION accounts for approximately 2.5% of all adverse event reports for POVIDONE IODINE 10%, making it a notable side effect.
If you experience post procedural complication 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.