430 reports of this reaction
2.3% of all ICOSAPENT ETHYL reports
#9 most reported adverse reaction
PRODUCT TASTE ABNORMAL is the #9 most commonly reported adverse reaction for ICOSAPENT ETHYL, manufactured by Amarin Pharma Inc.. There are 430 FDA adverse event reports linking ICOSAPENT ETHYL to PRODUCT TASTE ABNORMAL. This represents approximately 2.3% of all 18,725 adverse event reports for this drug.
Patients taking ICOSAPENT ETHYL who experience product taste abnormal 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 TASTE ABNORMAL is a less commonly reported adverse event for ICOSAPENT ETHYL, but still significant enough to appear in the safety profile.
In addition to product taste abnormal, the following adverse reactions have been reported for ICOSAPENT ETHYL:
The following drugs have also been linked to product taste abnormal in FDA adverse event reports:
PRODUCT TASTE ABNORMAL has been reported as an adverse event in 430 FDA reports for ICOSAPENT ETHYL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT TASTE ABNORMAL accounts for approximately 2.3% of all adverse event reports for ICOSAPENT ETHYL, making it a notable side effect.
If you experience product taste abnormal 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.