402 reports of this reaction
2.0% of all LANREOTIDE ACETATE reports
#9 most reported adverse reaction
MALAISE is the #9 most commonly reported adverse reaction for LANREOTIDE ACETATE, manufactured by Ipsen Biopharmaceuticals, Inc.. There are 402 FDA adverse event reports linking LANREOTIDE ACETATE to MALAISE. This represents approximately 2.0% of all 20,256 adverse event reports for this drug.
Patients taking LANREOTIDE ACETATE 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.
MALAISE is a less commonly reported adverse event for LANREOTIDE ACETATE, but still significant enough to appear in the safety profile.
In addition to malaise, the following adverse reactions have been reported for LANREOTIDE ACETATE:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 402 FDA reports for LANREOTIDE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 2.0% of all adverse event reports for LANREOTIDE ACETATE, making it a notable side effect.
If you experience malaise while taking LANREOTIDE ACETATE, 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.