142 reports of this reaction
1.2% of all IVABRADINE reports
#20 most reported adverse reaction
HEART RATE INCREASED is the #20 most commonly reported adverse reaction for IVABRADINE, manufactured by Amgen Inc. There are 142 FDA adverse event reports linking IVABRADINE to HEART RATE INCREASED. This represents approximately 1.2% of all 12,129 adverse event reports for this drug.
Patients taking IVABRADINE who experience heart rate increased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HEART RATE INCREASED is a less commonly reported adverse event for IVABRADINE, but still significant enough to appear in the safety profile.
In addition to heart rate increased, the following adverse reactions have been reported for IVABRADINE:
The following drugs have also been linked to heart rate increased in FDA adverse event reports:
HEART RATE INCREASED has been reported as an adverse event in 142 FDA reports for IVABRADINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HEART RATE INCREASED accounts for approximately 1.2% of all adverse event reports for IVABRADINE, making it a notable side effect.
If you experience heart rate increased while taking IVABRADINE, 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.