POVIDONE IODINE 10% and CONJUNCTIVAL OEDEMA

21 reports of this reaction

2.1% of all POVIDONE IODINE 10% reports

#7 most reported adverse reaction

Overview

CONJUNCTIVAL OEDEMA is the #7 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 CONJUNCTIVAL OEDEMA. This represents approximately 2.1% of all 1,006 adverse event reports for this drug.

Patients taking POVIDONE IODINE 10% who experience conjunctival oedema should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

CONJUNCTIVAL OEDEMA21 of 1,006 reports

CONJUNCTIVAL OEDEMA is a less commonly reported adverse event for POVIDONE IODINE 10%, but still significant enough to appear in the safety profile.

Other Side Effects of POVIDONE IODINE 10%

In addition to conjunctival oedema, the following adverse reactions have been reported for POVIDONE IODINE 10%:

Frequently Asked Questions

Does POVIDONE IODINE 10% cause CONJUNCTIVAL OEDEMA?

CONJUNCTIVAL OEDEMA 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.

How common is CONJUNCTIVAL OEDEMA with POVIDONE IODINE 10%?

CONJUNCTIVAL OEDEMA accounts for approximately 2.1% of all adverse event reports for POVIDONE IODINE 10%, making it a notable side effect.

What should I do if I experience CONJUNCTIVAL OEDEMA while taking POVIDONE IODINE 10%?

If you experience conjunctival oedema 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.

Related Pages

POVIDONE IODINE 10% Full ProfileAll Drugs Causing CONJUNCTIVAL OEDEMAFarmacias De Similares TX LLC Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.