196 reports of this reaction
1.2% of all BLINATUMOMAB reports
#19 most reported adverse reaction
PRODUCT STORAGE ERROR is the #19 most commonly reported adverse reaction for BLINATUMOMAB, manufactured by Amgen, Inc. There are 196 FDA adverse event reports linking BLINATUMOMAB to PRODUCT STORAGE ERROR. This represents approximately 1.2% of all 16,815 adverse event reports for this drug.
Patients taking BLINATUMOMAB 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 BLINATUMOMAB, but still significant enough to appear in the safety profile.
In addition to product storage error, the following adverse reactions have been reported for BLINATUMOMAB:
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 196 FDA reports for BLINATUMOMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT STORAGE ERROR accounts for approximately 1.2% of all adverse event reports for BLINATUMOMAB, making it a notable side effect.
If you experience product storage error while taking BLINATUMOMAB, 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.