3,948 reports of this reaction
3.8% of all FINASTERIDE reports
#1 most reported adverse reaction
FATIGUE is the #1 most commonly reported adverse reaction for FINASTERIDE, manufactured by Organon LLC. There are 3,948 FDA adverse event reports linking FINASTERIDE to FATIGUE. This represents approximately 3.8% of all 103,583 adverse event reports for this drug.
Patients taking FINASTERIDE 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 FINASTERIDE users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for FINASTERIDE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 3,948 FDA reports for FINASTERIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.8% of all adverse event reports for FINASTERIDE, making it one of the most commonly reported side effect.
If you experience fatigue while taking FINASTERIDE, 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.