4,237 reports of this reaction
2.0% of all FISH OIL reports
#10 most reported adverse reaction
PRURITUS is the #10 most commonly reported adverse reaction for FISH OIL, manufactured by Fresenius Kabi USA, LLC. There are 4,237 FDA adverse event reports linking FISH OIL to PRURITUS. This represents approximately 2.0% of all 214,316 adverse event reports for this drug.
Patients taking FISH OIL who experience pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRURITUS is a less commonly reported adverse event for FISH OIL, but still significant enough to appear in the safety profile.
In addition to pruritus, the following adverse reactions have been reported for FISH OIL:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 4,237 FDA reports for FISH OIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 2.0% of all adverse event reports for FISH OIL, making it a notable side effect.
If you experience pruritus 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.