478 reports of this reaction
3.6% of all TRAVOPROST reports
#4 most reported adverse reaction
EYE IRRITATION is the #4 most commonly reported adverse reaction for TRAVOPROST, manufactured by Novartis Pharmaceuticals Corporation. There are 478 FDA adverse event reports linking TRAVOPROST to EYE IRRITATION. This represents approximately 3.6% of all 13,183 adverse event reports for this drug.
Patients taking TRAVOPROST 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 TRAVOPROST users, representing a notable but not dominant share of adverse events.
In addition to eye irritation, the following adverse reactions have been reported for TRAVOPROST:
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 478 FDA reports for TRAVOPROST. This does not prove causation, but indicates an association observed in post-market surveillance data.
EYE IRRITATION accounts for approximately 3.6% of all adverse event reports for TRAVOPROST, making it a notable side effect.
If you experience eye irritation while taking TRAVOPROST, 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.