1 reports of this reaction
3.2% of all 5% LIDOCAINE reports
#2 most reported adverse reaction
ABDOMINAL PAIN is the #2 most commonly reported adverse reaction for 5% LIDOCAINE, manufactured by 100 KARMA INC. There are 1 FDA adverse event reports linking 5% LIDOCAINE to ABDOMINAL PAIN. This represents approximately 3.2% of all 31 adverse event reports for this drug.
Patients taking 5% LIDOCAINE 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 moderately reported among 5% LIDOCAINE users, representing a notable but not dominant share of adverse events.
In addition to abdominal pain, the following adverse reactions have been reported for 5% LIDOCAINE:
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 1 FDA reports for 5% LIDOCAINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN accounts for approximately 3.2% of all adverse event reports for 5% LIDOCAINE, making it one of the most commonly reported side effect.
If you experience abdominal pain while taking 5% LIDOCAINE, 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.