301 reports of this reaction
1.6% of all ICOSAPENT ETHYL reports
#11 most reported adverse reaction
PRESCRIBED UNDERDOSE is the #11 most commonly reported adverse reaction for ICOSAPENT ETHYL, manufactured by Amarin Pharma Inc.. There are 301 FDA adverse event reports linking ICOSAPENT ETHYL to PRESCRIBED UNDERDOSE. This represents approximately 1.6% of all 18,725 adverse event reports for this drug.
Patients taking ICOSAPENT ETHYL who experience prescribed underdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRESCRIBED UNDERDOSE is a less commonly reported adverse event for ICOSAPENT ETHYL, but still significant enough to appear in the safety profile.
In addition to prescribed underdose, the following adverse reactions have been reported for ICOSAPENT ETHYL:
PRESCRIBED UNDERDOSE has been reported as an adverse event in 301 FDA reports for ICOSAPENT ETHYL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRESCRIBED UNDERDOSE accounts for approximately 1.6% of all adverse event reports for ICOSAPENT ETHYL, making it a notable side effect.
If you experience prescribed underdose 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.