450 reports of this reaction
1.7% of all LOPERAMIDE HCL reports
#11 most reported adverse reaction
ABDOMINAL PAIN is the #11 most commonly reported adverse reaction for LOPERAMIDE HCL, manufactured by Rite Aid Corporation. There are 450 FDA adverse event reports linking LOPERAMIDE HCL to ABDOMINAL PAIN. This represents approximately 1.7% of all 26,027 adverse event reports for this drug.
Patients taking LOPERAMIDE HCL who experience abdominal pain should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL PAIN is a less commonly reported adverse event for LOPERAMIDE HCL, but still significant enough to appear in the safety profile.
In addition to abdominal pain, the following adverse reactions have been reported for LOPERAMIDE HCL:
The following drugs have also been linked to abdominal pain in FDA adverse event reports:
ABDOMINAL PAIN has been reported as an adverse event in 450 FDA reports for LOPERAMIDE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN accounts for approximately 1.7% of all adverse event reports for LOPERAMIDE HCL, making it a notable side effect.
If you experience abdominal pain 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.