1,123 reports of this reaction
4.4% of all EPOETIN ALFA reports
#1 most reported adverse reaction
PRODUCT STORAGE ERROR is the #1 most commonly reported adverse reaction for EPOETIN ALFA, manufactured by Amgen, Inc. There are 1,123 FDA adverse event reports linking EPOETIN ALFA to PRODUCT STORAGE ERROR. This represents approximately 4.4% of all 25,704 adverse event reports for this drug.
Patients taking EPOETIN ALFA 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 moderately reported among EPOETIN ALFA users, representing a notable but not dominant share of adverse events.
In addition to product storage error, the following adverse reactions have been reported for EPOETIN ALFA:
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 1,123 FDA reports for EPOETIN ALFA. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT STORAGE ERROR accounts for approximately 4.4% of all adverse event reports for EPOETIN ALFA, making it one of the most commonly reported side effect.
If you experience product storage error while taking EPOETIN ALFA, 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.