59 reports of this reaction
1.5% of all LIDOCAINE HCL reports
#10 most reported adverse reaction
HYPOTENSION is the #10 most commonly reported adverse reaction for LIDOCAINE HCL, manufactured by Chattem, Inc.. There are 59 FDA adverse event reports linking LIDOCAINE HCL to HYPOTENSION. This represents approximately 1.5% of all 3,987 adverse event reports for this drug.
LIDOCAINE HCL has an overall safety score of 72 out of 100. Patients taking LIDOCAINE HCL who experience hypotension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOTENSION is a less commonly reported adverse event for LIDOCAINE HCL, but still significant enough to appear in the safety profile.
In addition to hypotension, the following adverse reactions have been reported for LIDOCAINE HCL:
The following drugs have also been linked to hypotension in FDA adverse event reports:
HYPOTENSION has been reported as an adverse event in 59 FDA reports for LIDOCAINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTENSION accounts for approximately 1.5% of all adverse event reports for LIDOCAINE HCL, making it a notable side effect.
If you experience hypotension while taking LIDOCAINE 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.