129 reports of this reaction
1.5% of all DOPAMINE HYDROCHLORIDE reports
#17 most reported adverse reaction
BRADYCARDIA is the #17 most commonly reported adverse reaction for DOPAMINE HYDROCHLORIDE, manufactured by Deseret Biologicals, Inc.. There are 129 FDA adverse event reports linking DOPAMINE HYDROCHLORIDE to BRADYCARDIA. This represents approximately 1.5% of all 8,648 adverse event reports for this drug.
Patients taking DOPAMINE HYDROCHLORIDE who experience bradycardia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BRADYCARDIA is a less commonly reported adverse event for DOPAMINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to bradycardia, the following adverse reactions have been reported for DOPAMINE HYDROCHLORIDE:
The following drugs have also been linked to bradycardia in FDA adverse event reports:
BRADYCARDIA has been reported as an adverse event in 129 FDA reports for DOPAMINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BRADYCARDIA accounts for approximately 1.5% of all adverse event reports for DOPAMINE HYDROCHLORIDE, making it a notable side effect.
If you experience bradycardia while taking DOPAMINE HYDROCHLORIDE, 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.