6 reports of this reaction
4.2% of all LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE, manufactured by Aurohealth LLC. There are 6 FDA adverse event reports linking LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE to DIARRHOEA. This represents approximately 4.2% of all 142 adverse event reports for this drug.
Patients taking LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is moderately reported among LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 6 FDA reports for LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 4.2% of all adverse event reports for LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking LOPERAMIDE HYDROCHLORIDE AND 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.