2 reports of this reaction
5.1% of all GELSEMIUM SEMPERVIRENS ROOT reports
#9 most reported adverse reaction
MALAISE is the #9 most commonly reported adverse reaction for GELSEMIUM SEMPERVIRENS ROOT, manufactured by Boiron. There are 2 FDA adverse event reports linking GELSEMIUM SEMPERVIRENS ROOT to MALAISE. This represents approximately 5.1% of all 39 adverse event reports for this drug.
Patients taking GELSEMIUM SEMPERVIRENS ROOT 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 moderately reported among GELSEMIUM SEMPERVIRENS ROOT users, representing a notable but not dominant share of adverse events.
In addition to malaise, the following adverse reactions have been reported for GELSEMIUM SEMPERVIRENS ROOT:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 2 FDA reports for GELSEMIUM SEMPERVIRENS ROOT. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 5.1% of all adverse event reports for GELSEMIUM SEMPERVIRENS ROOT, making it a notable side effect.
If you experience malaise while taking GELSEMIUM SEMPERVIRENS ROOT, 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.