2 reports of this reaction
4.3% of all LIDOCAINE HCI reports
#3 most reported adverse reaction
DIARRHOEA is the #3 most commonly reported adverse reaction for LIDOCAINE HCI, manufactured by Aurobindo Pharma Limited. There are 2 FDA adverse event reports linking LIDOCAINE HCI to DIARRHOEA. This represents approximately 4.3% of all 47 adverse event reports for this drug.
Patients taking LIDOCAINE HCI 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 LIDOCAINE HCI users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for LIDOCAINE HCI:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 2 FDA reports for LIDOCAINE HCI. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 4.3% of all adverse event reports for LIDOCAINE HCI, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking LIDOCAINE HCI, 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.