196 reports of this reaction
4.1% of all MECLIZINE HCL reports
#1 most reported adverse reaction
FATIGUE is the #1 most commonly reported adverse reaction for MECLIZINE HCL, manufactured by Rising Pharma Holdings, Inc.. There are 196 FDA adverse event reports linking MECLIZINE HCL to FATIGUE. This represents approximately 4.1% of all 4,811 adverse event reports for this drug.
Patients taking MECLIZINE HCL 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 MECLIZINE HCL users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for MECLIZINE HCL:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 196 FDA reports for MECLIZINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 4.1% of all adverse event reports for MECLIZINE HCL, making it one of the most commonly reported side effect.
If you experience fatigue while taking MECLIZINE HCL, 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.