226 reports of this reaction
2.0% of all LOTEPREDNOL ETABONATE reports
#9 most reported adverse reaction
DRY EYE is the #9 most commonly reported adverse reaction for LOTEPREDNOL ETABONATE, manufactured by Bausch & Lomb Incorporated. There are 226 FDA adverse event reports linking LOTEPREDNOL ETABONATE to DRY EYE. This represents approximately 2.0% of all 11,509 adverse event reports for this drug.
Patients taking LOTEPREDNOL ETABONATE who experience dry eye should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY EYE is a less commonly reported adverse event for LOTEPREDNOL ETABONATE, but still significant enough to appear in the safety profile.
In addition to dry eye, the following adverse reactions have been reported for LOTEPREDNOL ETABONATE:
The following drugs have also been linked to dry eye in FDA adverse event reports:
DRY EYE has been reported as an adverse event in 226 FDA reports for LOTEPREDNOL ETABONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY EYE accounts for approximately 2.0% of all adverse event reports for LOTEPREDNOL ETABONATE, making it a notable side effect.
If you experience dry eye while taking LOTEPREDNOL ETABONATE, 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.