853 reports of this reaction
3.1% of all OMEGA 3 ACID ETHYL ESTERS reports
#2 most reported adverse reaction
NAUSEA is the #2 most commonly reported adverse reaction for OMEGA 3 ACID ETHYL ESTERS, manufactured by Waylis Therapeutics LLC. There are 853 FDA adverse event reports linking OMEGA 3 ACID ETHYL ESTERS to NAUSEA. This represents approximately 3.1% of all 27,867 adverse event reports for this drug.
Patients taking OMEGA 3 ACID ETHYL ESTERS who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among OMEGA 3 ACID ETHYL ESTERS users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for OMEGA 3 ACID ETHYL ESTERS:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 853 FDA reports for OMEGA 3 ACID ETHYL ESTERS. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.1% of all adverse event reports for OMEGA 3 ACID ETHYL ESTERS, making it one of the most commonly reported side effect.
If you experience nausea while taking OMEGA 3 ACID ETHYL ESTERS, 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.