1 reports of this reaction
3.2% of all 5% LIDOCAINE reports
#9 most reported adverse reaction
DYSAESTHESIA is the #9 most commonly reported adverse reaction for 5% LIDOCAINE, manufactured by 100 KARMA INC. There are 1 FDA adverse event reports linking 5% LIDOCAINE to DYSAESTHESIA. This represents approximately 3.2% of all 31 adverse event reports for this drug.
Patients taking 5% LIDOCAINE who experience dysaesthesia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSAESTHESIA is moderately reported among 5% LIDOCAINE users, representing a notable but not dominant share of adverse events.
In addition to dysaesthesia, the following adverse reactions have been reported for 5% LIDOCAINE:
DYSAESTHESIA 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.
DYSAESTHESIA accounts for approximately 3.2% of all adverse event reports for 5% LIDOCAINE, making it a notable side effect.
If you experience dysaesthesia 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.