180 reports of this reaction
1.6% of all FLUVASTATIN SODIUM reports
#14 most reported adverse reaction
CEREBROVASCULAR ACCIDENT is the #14 most commonly reported adverse reaction for FLUVASTATIN SODIUM, manufactured by Sandoz Inc. There are 180 FDA adverse event reports linking FLUVASTATIN SODIUM to CEREBROVASCULAR ACCIDENT. This represents approximately 1.6% of all 11,133 adverse event reports for this drug.
Patients taking FLUVASTATIN SODIUM 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 FLUVASTATIN SODIUM, but still significant enough to appear in the safety profile.
In addition to cerebrovascular accident, the following adverse reactions have been reported for FLUVASTATIN SODIUM:
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 180 FDA reports for FLUVASTATIN SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
CEREBROVASCULAR ACCIDENT accounts for approximately 1.6% of all adverse event reports for FLUVASTATIN SODIUM, making it a notable side effect.
If you experience cerebrovascular accident while taking FLUVASTATIN SODIUM, 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.