998 reports of this reaction
1.3% of all NICOTINE reports
#20 most reported adverse reaction
PRODUCT ADHESION ISSUE is the #20 most commonly reported adverse reaction for NICOTINE, manufactured by Haleon US Holdings LLC. There are 998 FDA adverse event reports linking NICOTINE to PRODUCT ADHESION ISSUE. This represents approximately 1.3% of all 74,737 adverse event reports for this drug.
NICOTINE has an overall safety score of 78 out of 100. Patients taking NICOTINE who experience product adhesion issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT ADHESION ISSUE is a less commonly reported adverse event for NICOTINE, but still significant enough to appear in the safety profile.
In addition to product adhesion issue, the following adverse reactions have been reported for NICOTINE:
The following drugs have also been linked to product adhesion issue in FDA adverse event reports:
PRODUCT ADHESION ISSUE has been reported as an adverse event in 998 FDA reports for NICOTINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT ADHESION ISSUE accounts for approximately 1.3% of all adverse event reports for NICOTINE, making it a notable side effect.
If you experience product adhesion issue while taking NICOTINE, 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.