1,826 reports of this reaction
2.0% of all FENOFIBRATE reports
#9 most reported adverse reaction
ASTHENIA is the #9 most commonly reported adverse reaction for FENOFIBRATE, manufactured by AbbVie Inc.. There are 1,826 FDA adverse event reports linking FENOFIBRATE to ASTHENIA. This represents approximately 2.0% of all 92,182 adverse event reports for this drug.
Patients taking FENOFIBRATE who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for FENOFIBRATE, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for FENOFIBRATE:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 1,826 FDA reports for FENOFIBRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 2.0% of all adverse event reports for FENOFIBRATE, making it a notable side effect.
If you experience asthenia while taking FENOFIBRATE, 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.