1 reports of this reaction
1.7% of all BEVACIZUMAB TNJN reports
#16 most reported adverse reaction
BLOOD PRESSURE DECREASED is the #16 most commonly reported adverse reaction for BEVACIZUMAB TNJN, manufactured by Bio-Thera Solutions, Ltd.. There are 1 FDA adverse event reports linking BEVACIZUMAB TNJN to BLOOD PRESSURE DECREASED. This represents approximately 1.7% of all 59 adverse event reports for this drug.
Patients taking BEVACIZUMAB TNJN who experience blood pressure decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BLOOD PRESSURE DECREASED is a less commonly reported adverse event for BEVACIZUMAB TNJN, but still significant enough to appear in the safety profile.
In addition to blood pressure decreased, the following adverse reactions have been reported for BEVACIZUMAB TNJN:
The following drugs have also been linked to blood pressure decreased in FDA adverse event reports:
BLOOD PRESSURE DECREASED has been reported as an adverse event in 1 FDA reports for BEVACIZUMAB TNJN. This does not prove causation, but indicates an association observed in post-market surveillance data.
BLOOD PRESSURE DECREASED accounts for approximately 1.7% of all adverse event reports for BEVACIZUMAB TNJN, making it a notable side effect.
If you experience blood pressure decreased while taking BEVACIZUMAB TNJN, 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.