6,806 reports of this reaction
2.7% of all BISOPROLOL FUMARATE reports
#3 most reported adverse reaction
FATIGUE is the #3 most commonly reported adverse reaction for BISOPROLOL FUMARATE, manufactured by TruPharma, LLC. There are 6,806 FDA adverse event reports linking BISOPROLOL FUMARATE to FATIGUE. This represents approximately 2.7% of all 256,068 adverse event reports for this drug.
Patients taking BISOPROLOL FUMARATE who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is a less commonly reported adverse event for BISOPROLOL FUMARATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for BISOPROLOL FUMARATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 6,806 FDA reports for BISOPROLOL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.7% of all adverse event reports for BISOPROLOL FUMARATE, making it one of the most commonly reported side effect.
If you experience fatigue while taking BISOPROLOL FUMARATE, 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.