1 reports of this reaction
3.2% of all 5% LIDOCAINE reports
#3 most reported adverse reaction
BLOOD PRESSURE DECREASED is the #3 most commonly reported adverse reaction for 5% LIDOCAINE, manufactured by 100 KARMA INC. There are 1 FDA adverse event reports linking 5% LIDOCAINE to BLOOD PRESSURE DECREASED. This represents approximately 3.2% of all 31 adverse event reports for this drug.
Patients taking 5% LIDOCAINE who experience blood pressure decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BLOOD PRESSURE DECREASED is moderately reported among 5% LIDOCAINE users, representing a notable but not dominant share of adverse events.
In addition to blood pressure decreased, the following adverse reactions have been reported for 5% LIDOCAINE:
The following drugs have also been linked to blood pressure decreased in FDA adverse event reports:
BLOOD PRESSURE DECREASED 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.
BLOOD PRESSURE DECREASED 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 blood pressure decreased 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.