3,182 reports of this reaction
2.6% of all LIDOCAINE reports
#7 most reported adverse reaction
PRODUCT QUALITY ISSUE is the #7 most commonly reported adverse reaction for LIDOCAINE, manufactured by Shenzhen Finona Information Technology Co., Ltd. There are 3,182 FDA adverse event reports linking LIDOCAINE to PRODUCT QUALITY ISSUE. This represents approximately 2.6% of all 120,190 adverse event reports for this drug.
Patients taking LIDOCAINE who experience product quality issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT QUALITY ISSUE is a less commonly reported adverse event for LIDOCAINE, but still significant enough to appear in the safety profile.
In addition to product quality issue, the following adverse reactions have been reported for LIDOCAINE:
The following drugs have also been linked to product quality issue in FDA adverse event reports:
PRODUCT QUALITY ISSUE has been reported as an adverse event in 3,182 FDA reports for LIDOCAINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT QUALITY ISSUE accounts for approximately 2.6% of all adverse event reports for LIDOCAINE, making it a notable side effect.
If you experience product quality issue while taking 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.