212 reports of this reaction
2.1% of all VARENICLINE reports
#10 most reported adverse reaction
NIGHTMARE is the #10 most commonly reported adverse reaction for VARENICLINE, manufactured by Oyster Point Pharma, Inc.. There are 212 FDA adverse event reports linking VARENICLINE to NIGHTMARE. This represents approximately 2.1% of all 10,186 adverse event reports for this drug.
Patients taking VARENICLINE who experience nightmare should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NIGHTMARE is a less commonly reported adverse event for VARENICLINE, but still significant enough to appear in the safety profile.
In addition to nightmare, the following adverse reactions have been reported for VARENICLINE:
The following drugs have also been linked to nightmare in FDA adverse event reports:
NIGHTMARE has been reported as an adverse event in 212 FDA reports for VARENICLINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NIGHTMARE accounts for approximately 2.1% of all adverse event reports for VARENICLINE, making it a notable side effect.
If you experience nightmare while taking VARENICLINE, 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.