222 reports of this reaction
1.3% of all DOFETILIDE reports
#19 most reported adverse reaction
PALPITATIONS is the #19 most commonly reported adverse reaction for DOFETILIDE, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 222 FDA adverse event reports linking DOFETILIDE to PALPITATIONS. This represents approximately 1.3% of all 17,040 adverse event reports for this drug.
Patients taking DOFETILIDE who experience palpitations should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PALPITATIONS is a less commonly reported adverse event for DOFETILIDE, but still significant enough to appear in the safety profile.
In addition to palpitations, the following adverse reactions have been reported for DOFETILIDE:
The following drugs have also been linked to palpitations in FDA adverse event reports:
PALPITATIONS has been reported as an adverse event in 222 FDA reports for DOFETILIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PALPITATIONS accounts for approximately 1.3% of all adverse event reports for DOFETILIDE, making it a notable side effect.
If you experience palpitations while taking DOFETILIDE, 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.