14,427 reports of this reaction
8.6% of all VARENICLINE TARTRATE reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for VARENICLINE TARTRATE, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 14,427 FDA adverse event reports linking VARENICLINE TARTRATE to NAUSEA. This represents approximately 8.6% of all 167,559 adverse event reports for this drug.
VARENICLINE TARTRATE has an overall safety score of 85 out of 100. Patients taking VARENICLINE TARTRATE 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 VARENICLINE TARTRATE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for VARENICLINE TARTRATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 14,427 FDA reports for VARENICLINE TARTRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 8.6% of all adverse event reports for VARENICLINE TARTRATE, making it one of the most commonly reported side effect.
If you experience nausea while taking VARENICLINE TARTRATE, 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.