221 reports of this reaction
12.2% of all BAYER GENUINE ASPIRIN reports
#1 most reported adverse reaction
PRODUCT USE ISSUE is the #1 most commonly reported adverse reaction for BAYER GENUINE ASPIRIN, manufactured by Bayer HealthCare LLC.. There are 221 FDA adverse event reports linking BAYER GENUINE ASPIRIN to PRODUCT USE ISSUE. This represents approximately 12.2% of all 1,811 adverse event reports for this drug.
Patients taking BAYER GENUINE ASPIRIN who experience product use 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 USE ISSUE is a frequently reported adverse event for BAYER GENUINE ASPIRIN, accounting for a significant proportion of all reports.
In addition to product use issue, the following adverse reactions have been reported for BAYER GENUINE ASPIRIN:
The following drugs have also been linked to product use issue in FDA adverse event reports:
PRODUCT USE ISSUE has been reported as an adverse event in 221 FDA reports for BAYER GENUINE ASPIRIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT USE ISSUE accounts for approximately 12.2% of all adverse event reports for BAYER GENUINE ASPIRIN, making it one of the most commonly reported side effect.
If you experience product use issue while taking BAYER GENUINE ASPIRIN, 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.