1,592 reports of this reaction
6.1% of all LOPERAMIDE HCL reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for LOPERAMIDE HCL, manufactured by Rite Aid Corporation. There are 1,592 FDA adverse event reports linking LOPERAMIDE HCL to DIARRHOEA. This represents approximately 6.1% of all 26,027 adverse event reports for this drug.
Patients taking LOPERAMIDE HCL 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 HCL users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for LOPERAMIDE HCL:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 1,592 FDA reports for LOPERAMIDE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 6.1% of all adverse event reports for LOPERAMIDE HCL, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking LOPERAMIDE HCL, 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.