2,185 reports of this reaction
5.0% of all ORLISTAT reports
#3 most reported adverse reaction
GASTROINTESTINAL DISORDER is the #3 most commonly reported adverse reaction for ORLISTAT, manufactured by Haleon US Holdings LLC. There are 2,185 FDA adverse event reports linking ORLISTAT to GASTROINTESTINAL DISORDER. This represents approximately 5.0% of all 43,367 adverse event reports for this drug.
Patients taking ORLISTAT who experience gastrointestinal disorder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GASTROINTESTINAL DISORDER is moderately reported among ORLISTAT users, representing a notable but not dominant share of adverse events.
In addition to gastrointestinal disorder, the following adverse reactions have been reported for ORLISTAT:
The following drugs have also been linked to gastrointestinal disorder in FDA adverse event reports:
GASTROINTESTINAL DISORDER has been reported as an adverse event in 2,185 FDA reports for ORLISTAT. This does not prove causation, but indicates an association observed in post-market surveillance data.
GASTROINTESTINAL DISORDER accounts for approximately 5.0% of all adverse event reports for ORLISTAT, making it one of the most commonly reported side effect.
If you experience gastrointestinal disorder while taking ORLISTAT, 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.