548 reports of this reaction
1.7% of all NICOTINE POLACRILEX MINI reports
#13 most reported adverse reaction
MACULAR DEGENERATION is the #13 most commonly reported adverse reaction for NICOTINE POLACRILEX MINI, manufactured by AmerisourceBergen (Good Neighbor Pharmacy) 46122. There are 548 FDA adverse event reports linking NICOTINE POLACRILEX MINI to MACULAR DEGENERATION. This represents approximately 1.7% of all 31,749 adverse event reports for this drug.
Patients taking NICOTINE POLACRILEX MINI who experience macular degeneration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MACULAR DEGENERATION is a less commonly reported adverse event for NICOTINE POLACRILEX MINI, but still significant enough to appear in the safety profile.
In addition to macular degeneration, the following adverse reactions have been reported for NICOTINE POLACRILEX MINI:
The following drugs have also been linked to macular degeneration in FDA adverse event reports:
MACULAR DEGENERATION has been reported as an adverse event in 548 FDA reports for NICOTINE POLACRILEX MINI. This does not prove causation, but indicates an association observed in post-market surveillance data.
MACULAR DEGENERATION accounts for approximately 1.7% of all adverse event reports for NICOTINE POLACRILEX MINI, making it a notable side effect.
If you experience macular degeneration while taking NICOTINE POLACRILEX MINI, 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.