3,689 reports of this reaction
1.5% of all ATENOLOL reports
#17 most reported adverse reaction
HYPOTENSION is the #17 most commonly reported adverse reaction for ATENOLOL, manufactured by Almatica Pharma LLC. There are 3,689 FDA adverse event reports linking ATENOLOL to HYPOTENSION. This represents approximately 1.5% of all 252,348 adverse event reports for this drug.
Patients taking ATENOLOL who experience hypotension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOTENSION is a less commonly reported adverse event for ATENOLOL, but still significant enough to appear in the safety profile.
In addition to hypotension, the following adverse reactions have been reported for ATENOLOL:
The following drugs have also been linked to hypotension in FDA adverse event reports:
HYPOTENSION has been reported as an adverse event in 3,689 FDA reports for ATENOLOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTENSION accounts for approximately 1.5% of all adverse event reports for ATENOLOL, making it a notable side effect.
If you experience hypotension 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.