9,454 reports of this reaction
6.2% of all ERENUMAB AOOE reports
#3 most reported adverse reaction
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is the #3 most commonly reported adverse reaction for ERENUMAB AOOE, manufactured by Amgen Inc. There are 9,454 FDA adverse event reports linking ERENUMAB AOOE to WRONG TECHNIQUE IN PRODUCT USAGE PROCESS. This represents approximately 6.2% of all 151,566 adverse event reports for this drug.
Patients taking ERENUMAB AOOE who experience wrong technique in product usage process should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is moderately reported among ERENUMAB AOOE users, representing a notable but not dominant share of adverse events.
In addition to wrong technique in product usage process, the following adverse reactions have been reported for ERENUMAB AOOE:
The following drugs have also been linked to wrong technique in product usage process in FDA adverse event reports:
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS has been reported as an adverse event in 9,454 FDA reports for ERENUMAB AOOE. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS accounts for approximately 6.2% of all adverse event reports for ERENUMAB AOOE, making it one of the most commonly reported side effect.
If you experience wrong technique in product usage process 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.