MALAISE is the #11 most commonly reported adverse reaction for VEDOLIZUMAB, manufactured by Takeda Pharmaceuticals America, Inc.. There are 4,083 FDA adverse event reports linking VEDOLIZUMAB to MALAISE. This represents approximately 1.8% of all 224,197 adverse event reports for this drug.
VEDOLIZUMAB has an overall safety score of 88 out of 100. Patients taking VEDOLIZUMAB who experience malaise should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
MALAISE4,083 of 224,197 reports
MALAISE is a less commonly reported adverse event for VEDOLIZUMAB, but still significant enough to appear in the safety profile.
Other Side Effects of VEDOLIZUMAB
In addition to malaise, the following adverse reactions have been reported for VEDOLIZUMAB:
MALAISE has been reported as an adverse event in 4,083 FDA reports for VEDOLIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is MALAISE with VEDOLIZUMAB?
MALAISE accounts for approximately 1.8% of all adverse event reports for VEDOLIZUMAB, making it a notable side effect.
What should I do if I experience MALAISE while taking VEDOLIZUMAB?
If you experience malaise while taking VEDOLIZUMAB, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.