628 reports of this reaction
5.5% of all KETOTIFEN FUMARATE reports
#3 most reported adverse reaction
EYE IRRITATION is the #3 most commonly reported adverse reaction for KETOTIFEN FUMARATE, manufactured by Alcon Laboratories, Inc.. There are 628 FDA adverse event reports linking KETOTIFEN FUMARATE to EYE IRRITATION. This represents approximately 5.5% of all 11,458 adverse event reports for this drug.
Patients taking KETOTIFEN FUMARATE who experience eye irritation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
EYE IRRITATION is moderately reported among KETOTIFEN FUMARATE users, representing a notable but not dominant share of adverse events.
In addition to eye irritation, the following adverse reactions have been reported for KETOTIFEN FUMARATE:
The following drugs have also been linked to eye irritation in FDA adverse event reports:
EYE IRRITATION has been reported as an adverse event in 628 FDA reports for KETOTIFEN FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
EYE IRRITATION accounts for approximately 5.5% of all adverse event reports for KETOTIFEN FUMARATE, making it one of the most commonly reported side effect.
If you experience eye irritation while taking KETOTIFEN FUMARATE, 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.