501 reports of this reaction
2.7% of all ICOSAPENT ETHYL reports
#6 most reported adverse reaction
POOR QUALITY PRODUCT ADMINISTERED is the #6 most commonly reported adverse reaction for ICOSAPENT ETHYL, manufactured by Amarin Pharma Inc.. There are 501 FDA adverse event reports linking ICOSAPENT ETHYL to POOR QUALITY PRODUCT ADMINISTERED. This represents approximately 2.7% of all 18,725 adverse event reports for this drug.
Patients taking ICOSAPENT ETHYL who experience poor quality product administered should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
POOR QUALITY PRODUCT ADMINISTERED is a less commonly reported adverse event for ICOSAPENT ETHYL, but still significant enough to appear in the safety profile.
In addition to poor quality product administered, the following adverse reactions have been reported for ICOSAPENT ETHYL:
The following drugs have also been linked to poor quality product administered in FDA adverse event reports:
POOR QUALITY PRODUCT ADMINISTERED has been reported as an adverse event in 501 FDA reports for ICOSAPENT ETHYL. This does not prove causation, but indicates an association observed in post-market surveillance data.
POOR QUALITY PRODUCT ADMINISTERED accounts for approximately 2.7% of all adverse event reports for ICOSAPENT ETHYL, making it a notable side effect.
If you experience poor quality product administered while taking ICOSAPENT ETHYL, 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.