414 reports of this reaction
3.8% of all SIMETHICONE reports
#3 most reported adverse reaction
FATIGUE is the #3 most commonly reported adverse reaction for SIMETHICONE, manufactured by Haleon US Holdings LLC. There are 414 FDA adverse event reports linking SIMETHICONE to FATIGUE. This represents approximately 3.8% of all 10,965 adverse event reports for this drug.
Patients taking SIMETHICONE who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is moderately reported among SIMETHICONE users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for SIMETHICONE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 414 FDA reports for SIMETHICONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.8% of all adverse event reports for SIMETHICONE, making it one of the most commonly reported side effect.
If you experience fatigue while taking SIMETHICONE, 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.