372 reports of this reaction
2.4% of all BUPIVACAINE reports
#6 most reported adverse reaction
HYPOAESTHESIA is the #6 most commonly reported adverse reaction for BUPIVACAINE, manufactured by Pacira Pharmaceuticals, Inc.. There are 372 FDA adverse event reports linking BUPIVACAINE to HYPOAESTHESIA. This represents approximately 2.4% of all 15,404 adverse event reports for this drug.
Patients taking BUPIVACAINE who experience hypoaesthesia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOAESTHESIA is a less commonly reported adverse event for BUPIVACAINE, but still significant enough to appear in the safety profile.
In addition to hypoaesthesia, the following adverse reactions have been reported for BUPIVACAINE:
The following drugs have also been linked to hypoaesthesia in FDA adverse event reports:
HYPOAESTHESIA has been reported as an adverse event in 372 FDA reports for BUPIVACAINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOAESTHESIA accounts for approximately 2.4% of all adverse event reports for BUPIVACAINE, making it a notable side effect.
If you experience hypoaesthesia while taking BUPIVACAINE, 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.