1 reports of this reaction
3.3% of all LIDOCAINE HYDROCHLORIDE, MENTHOL reports
#1 most reported adverse reaction
ABDOMINAL PAIN UPPER is the #1 most commonly reported adverse reaction for LIDOCAINE HYDROCHLORIDE, MENTHOL, manufactured by ANI Pharmaceuticals, Inc.. There are 1 FDA adverse event reports linking LIDOCAINE HYDROCHLORIDE, MENTHOL to ABDOMINAL PAIN UPPER. This represents approximately 3.3% of all 30 adverse event reports for this drug.
Patients taking LIDOCAINE HYDROCHLORIDE, MENTHOL who experience abdominal pain upper 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 UPPER is moderately reported among LIDOCAINE HYDROCHLORIDE, MENTHOL users, representing a notable but not dominant share of adverse events.
In addition to abdominal pain upper, the following adverse reactions have been reported for LIDOCAINE HYDROCHLORIDE, MENTHOL:
The following drugs have also been linked to abdominal pain upper in FDA adverse event reports:
ABDOMINAL PAIN UPPER has been reported as an adverse event in 1 FDA reports for LIDOCAINE HYDROCHLORIDE, MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN UPPER accounts for approximately 3.3% of all adverse event reports for LIDOCAINE HYDROCHLORIDE, MENTHOL, making it one of the most commonly reported side effect.
If you experience abdominal pain upper while taking LIDOCAINE HYDROCHLORIDE, MENTHOL, 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.