375 reports of this reaction
1.3% of all BRIMONIDINE TARTRATE reports
#20 most reported adverse reaction
VISUAL IMPAIRMENT is the #20 most commonly reported adverse reaction for BRIMONIDINE TARTRATE, manufactured by Sandoz Inc. There are 375 FDA adverse event reports linking BRIMONIDINE TARTRATE to VISUAL IMPAIRMENT. This represents approximately 1.3% of all 28,834 adverse event reports for this drug.
Patients taking BRIMONIDINE TARTRATE who experience visual impairment should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VISUAL IMPAIRMENT is a less commonly reported adverse event for BRIMONIDINE TARTRATE, but still significant enough to appear in the safety profile.
In addition to visual impairment, the following adverse reactions have been reported for BRIMONIDINE TARTRATE:
The following drugs have also been linked to visual impairment in FDA adverse event reports:
VISUAL IMPAIRMENT has been reported as an adverse event in 375 FDA reports for BRIMONIDINE TARTRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
VISUAL IMPAIRMENT accounts for approximately 1.3% of all adverse event reports for BRIMONIDINE TARTRATE, making it a notable side effect.
If you experience visual impairment while taking BRIMONIDINE TARTRATE, 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.