MALAISE is the #9 most commonly reported adverse reaction for NATALIZUMAB, manufactured by Biogen Inc.. There are 7,318 FDA adverse event reports linking NATALIZUMAB to MALAISE. This represents approximately 2.5% of all 289,050 adverse event reports for this drug.
NATALIZUMAB has an overall safety score of 75 out of 100. Patients taking NATALIZUMAB 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
MALAISE7,318 of 289,050 reports
MALAISE is a less commonly reported adverse event for NATALIZUMAB, but still significant enough to appear in the safety profile.
Other Side Effects of NATALIZUMAB
In addition to malaise, the following adverse reactions have been reported for NATALIZUMAB:
MALAISE has been reported as an adverse event in 7,318 FDA reports for NATALIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is MALAISE with NATALIZUMAB?
MALAISE accounts for approximately 2.5% of all adverse event reports for NATALIZUMAB, making it a notable side effect.
What should I do if I experience MALAISE while taking NATALIZUMAB?
If you experience malaise while taking NATALIZUMAB, 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.