1,749 reports of this reaction
5.1% of all REGORAFENIB reports
#2 most reported adverse reaction
FATIGUE is the #2 most commonly reported adverse reaction for REGORAFENIB, manufactured by Bayer HealthCare Pharmaceuticals Inc.. There are 1,749 FDA adverse event reports linking REGORAFENIB to FATIGUE. This represents approximately 5.1% of all 34,211 adverse event reports for this drug.
Patients taking REGORAFENIB 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 moderately reported among REGORAFENIB users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for REGORAFENIB:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,749 FDA reports for REGORAFENIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 5.1% of all adverse event reports for REGORAFENIB, making it one of the most commonly reported side effect.
If you experience fatigue while taking REGORAFENIB, 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.