6,524 reports of this reaction
4.3% of all ERENUMAB AOOE reports
#4 most reported adverse reaction
DRUG DOSE OMISSION BY DEVICE is the #4 most commonly reported adverse reaction for ERENUMAB AOOE, manufactured by Amgen Inc. There are 6,524 FDA adverse event reports linking ERENUMAB AOOE to DRUG DOSE OMISSION BY DEVICE. This represents approximately 4.3% of all 151,566 adverse event reports for this drug.
Patients taking ERENUMAB AOOE who experience drug dose omission by device should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG DOSE OMISSION BY DEVICE is moderately reported among ERENUMAB AOOE users, representing a notable but not dominant share of adverse events.
In addition to drug dose omission by device, the following adverse reactions have been reported for ERENUMAB AOOE:
The following drugs have also been linked to drug dose omission by device in FDA adverse event reports:
DRUG DOSE OMISSION BY DEVICE has been reported as an adverse event in 6,524 FDA reports for ERENUMAB AOOE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG DOSE OMISSION BY DEVICE accounts for approximately 4.3% of all adverse event reports for ERENUMAB AOOE, making it a notable side effect.
If you experience drug dose omission by device while taking ERENUMAB AOOE, 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.