5,912 reports of this reaction
2.8% of all FISH OIL reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for FISH OIL, manufactured by Fresenius Kabi USA, LLC. There are 5,912 FDA adverse event reports linking FISH OIL to NAUSEA. This represents approximately 2.8% of all 214,316 adverse event reports for this drug.
Patients taking FISH OIL 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 a less commonly reported adverse event for FISH OIL, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for FISH OIL:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 5,912 FDA reports for FISH OIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.8% of all adverse event reports for FISH OIL, making it one of the most commonly reported side effect.
If you experience nausea while taking FISH OIL, 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.