218 reports of this reaction
1.8% of all RAMELTEON reports
#11 most reported adverse reaction
POOR QUALITY SLEEP is the #11 most commonly reported adverse reaction for RAMELTEON, manufactured by Takeda Pharmaceuticals America, Inc.. There are 218 FDA adverse event reports linking RAMELTEON to POOR QUALITY SLEEP. This represents approximately 1.8% of all 11,977 adverse event reports for this drug.
Patients taking RAMELTEON who experience poor quality sleep should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
POOR QUALITY SLEEP is a less commonly reported adverse event for RAMELTEON, but still significant enough to appear in the safety profile.
In addition to poor quality sleep, the following adverse reactions have been reported for RAMELTEON:
The following drugs have also been linked to poor quality sleep in FDA adverse event reports:
POOR QUALITY SLEEP has been reported as an adverse event in 218 FDA reports for RAMELTEON. This does not prove causation, but indicates an association observed in post-market surveillance data.
POOR QUALITY SLEEP accounts for approximately 1.8% of all adverse event reports for RAMELTEON, making it a notable side effect.
If you experience poor quality sleep while taking RAMELTEON, 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.