26 reports of this reaction
1.4% of all BAYER GENUINE ASPIRIN reports
#17 most reported adverse reaction
CEREBROVASCULAR ACCIDENT is the #17 most commonly reported adverse reaction for BAYER GENUINE ASPIRIN, manufactured by Bayer HealthCare LLC.. There are 26 FDA adverse event reports linking BAYER GENUINE ASPIRIN to CEREBROVASCULAR ACCIDENT. This represents approximately 1.4% of all 1,811 adverse event reports for this drug.
Patients taking BAYER GENUINE ASPIRIN who experience cerebrovascular accident should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CEREBROVASCULAR ACCIDENT is a less commonly reported adverse event for BAYER GENUINE ASPIRIN, but still significant enough to appear in the safety profile.
In addition to cerebrovascular accident, the following adverse reactions have been reported for BAYER GENUINE ASPIRIN:
The following drugs have also been linked to cerebrovascular accident in FDA adverse event reports:
CEREBROVASCULAR ACCIDENT has been reported as an adverse event in 26 FDA reports for BAYER GENUINE ASPIRIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
CEREBROVASCULAR ACCIDENT accounts for approximately 1.4% of all adverse event reports for BAYER GENUINE ASPIRIN, making it a notable side effect.
If you experience cerebrovascular accident 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.