1 reports of this reaction
2.1% of all LIDOCAINE HCI reports
#12 most reported adverse reaction
BRADYCARDIA is the #12 most commonly reported adverse reaction for LIDOCAINE HCI, manufactured by Aurobindo Pharma Limited. There are 1 FDA adverse event reports linking LIDOCAINE HCI to BRADYCARDIA. This represents approximately 2.1% of all 47 adverse event reports for this drug.
Patients taking LIDOCAINE HCI who experience bradycardia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BRADYCARDIA is a less commonly reported adverse event for LIDOCAINE HCI, but still significant enough to appear in the safety profile.
In addition to bradycardia, the following adverse reactions have been reported for LIDOCAINE HCI:
The following drugs have also been linked to bradycardia in FDA adverse event reports:
BRADYCARDIA has been reported as an adverse event in 1 FDA reports for LIDOCAINE HCI. This does not prove causation, but indicates an association observed in post-market surveillance data.
BRADYCARDIA accounts for approximately 2.1% of all adverse event reports for LIDOCAINE HCI, making it a notable side effect.
If you experience bradycardia while taking LIDOCAINE HCI, 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.