23 reports of this reaction
3.8% of all LANOLIN, PETROLATUM reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for LANOLIN, PETROLATUM, manufactured by Family Dollar Services Inc. There are 23 FDA adverse event reports linking LANOLIN, PETROLATUM to NAUSEA. This represents approximately 3.8% of all 611 adverse event reports for this drug.
Patients taking LANOLIN, PETROLATUM 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 LANOLIN, PETROLATUM users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for LANOLIN, PETROLATUM:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 23 FDA reports for LANOLIN, PETROLATUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.8% of all adverse event reports for LANOLIN, PETROLATUM, making it one of the most commonly reported side effect.
If you experience nausea while taking LANOLIN, PETROLATUM, 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.