22,053 reports of this reaction
8.2% of all Repatha reports
#3 most reported adverse reaction
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is the #3 most commonly reported adverse reaction for Repatha, manufactured by Amgen USA Inc.. There are 22,053 FDA adverse event reports linking Repatha to WRONG TECHNIQUE IN PRODUCT USAGE PROCESS. This represents approximately 8.2% of all 269,908 adverse event reports for this drug.
Patients taking Repatha 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 Repatha 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 Repatha:
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 22,053 FDA reports for Repatha. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS accounts for approximately 8.2% of all adverse event reports for Repatha, making it one of the most commonly reported side effect.
If you experience wrong technique in product usage process while taking Repatha, 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.