17 reports of this reaction
1.9% of all TETRACAINE reports
#12 most reported adverse reaction
EYE DISORDER is the #12 most commonly reported adverse reaction for TETRACAINE, manufactured by Bellus Medical, LLC. There are 17 FDA adverse event reports linking TETRACAINE to EYE DISORDER. This represents approximately 1.9% of all 876 adverse event reports for this drug.
Patients taking TETRACAINE who experience eye disorder 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 DISORDER is a less commonly reported adverse event for TETRACAINE, but still significant enough to appear in the safety profile.
In addition to eye disorder, the following adverse reactions have been reported for TETRACAINE:
The following drugs have also been linked to eye disorder in FDA adverse event reports:
EYE DISORDER has been reported as an adverse event in 17 FDA reports for TETRACAINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
EYE DISORDER accounts for approximately 1.9% of all adverse event reports for TETRACAINE, making it a notable side effect.
If you experience eye disorder while taking TETRACAINE, 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.