1,235 reports of this reaction
3.0% of all RANIBIZUMAB reports
#5 most reported adverse reaction
CEREBROVASCULAR ACCIDENT is the #5 most commonly reported adverse reaction for RANIBIZUMAB, manufactured by Genentech, Inc.. There are 1,235 FDA adverse event reports linking RANIBIZUMAB to CEREBROVASCULAR ACCIDENT. This represents approximately 3.0% of all 41,498 adverse event reports for this drug.
Patients taking RANIBIZUMAB 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 RANIBIZUMAB, but still significant enough to appear in the safety profile.
In addition to cerebrovascular accident, the following adverse reactions have been reported for RANIBIZUMAB:
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 1,235 FDA reports for RANIBIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
CEREBROVASCULAR ACCIDENT accounts for approximately 3.0% of all adverse event reports for RANIBIZUMAB, making it a notable side effect.
If you experience cerebrovascular accident while taking RANIBIZUMAB, 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.