773 reports of this reaction
3.0% of all RALOXIFENE HYDROCHLORIDE reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for RALOXIFENE HYDROCHLORIDE, manufactured by Eli Lilly and Company. There are 773 FDA adverse event reports linking RALOXIFENE HYDROCHLORIDE to NAUSEA. This represents approximately 3.0% of all 26,004 adverse event reports for this drug.
Patients taking RALOXIFENE HYDROCHLORIDE 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 RALOXIFENE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for RALOXIFENE HYDROCHLORIDE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 773 FDA reports for RALOXIFENE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.0% of all adverse event reports for RALOXIFENE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience nausea while taking RALOXIFENE HYDROCHLORIDE, 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.