3,628 reports of this reaction
2.9% of all ONABOTULINUMTOXINA reports
#5 most reported adverse reaction
PRODUCT PREPARATION ERROR is the #5 most commonly reported adverse reaction for ONABOTULINUMTOXINA, manufactured by Allergan, Inc.. There are 3,628 FDA adverse event reports linking ONABOTULINUMTOXINA to PRODUCT PREPARATION ERROR. This represents approximately 2.9% of all 126,795 adverse event reports for this drug.
ONABOTULINUMTOXINA has an overall safety score of 78 out of 100. Patients taking ONABOTULINUMTOXINA who experience product preparation error 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 PREPARATION ERROR is a less commonly reported adverse event for ONABOTULINUMTOXINA, but still significant enough to appear in the safety profile.
In addition to product preparation error, the following adverse reactions have been reported for ONABOTULINUMTOXINA:
PRODUCT PREPARATION ERROR has been reported as an adverse event in 3,628 FDA reports for ONABOTULINUMTOXINA. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT PREPARATION ERROR accounts for approximately 2.9% of all adverse event reports for ONABOTULINUMTOXINA, making it a notable side effect.
If you experience product preparation error while taking ONABOTULINUMTOXINA, 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.