6,630 reports of this reaction
2.5% of all EVOLOCUMAB reports
#6 most reported adverse reaction
PRODUCT STORAGE ERROR is the #6 most commonly reported adverse reaction for EVOLOCUMAB, manufactured by Amgen USA Inc.. There are 6,630 FDA adverse event reports linking EVOLOCUMAB to PRODUCT STORAGE ERROR. This represents approximately 2.5% of all 266,603 adverse event reports for this drug.
Patients taking EVOLOCUMAB who experience product storage 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 STORAGE ERROR is a less commonly reported adverse event for EVOLOCUMAB, but still significant enough to appear in the safety profile.
In addition to product storage error, the following adverse reactions have been reported for EVOLOCUMAB:
The following drugs have also been linked to product storage error in FDA adverse event reports:
PRODUCT STORAGE ERROR has been reported as an adverse event in 6,630 FDA reports for EVOLOCUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT STORAGE ERROR accounts for approximately 2.5% of all adverse event reports for EVOLOCUMAB, making it a notable side effect.
If you experience product storage error while taking EVOLOCUMAB, 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.