7,812 reports of this reaction
3.1% of all ATENOLOL reports
#2 most reported adverse reaction
NAUSEA is the #2 most commonly reported adverse reaction for ATENOLOL, manufactured by Almatica Pharma LLC. There are 7,812 FDA adverse event reports linking ATENOLOL to NAUSEA. This represents approximately 3.1% of all 252,348 adverse event reports for this drug.
Patients taking ATENOLOL 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 ATENOLOL users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for ATENOLOL:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 7,812 FDA reports for ATENOLOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.1% of all adverse event reports for ATENOLOL, making it one of the most commonly reported side effect.
If you experience nausea while taking ATENOLOL, 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.